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Plinabulin Granted FDA Breakthrough Therapy Designation for Chemotherapy-Induced Neutropenia – Targeted Oncology

A Breakthrough Therapy designation was granted to plinabulin as treatment of chemotherapy-induced neutropenia (CIN) from both the FDA in the United States and Chinas Center for Drug Evaluation of the National Medical Products Administration, announced BeyondSpring Inc, developer of the drug, in a press release.1

Should this agent be approved, it would fulfill a significant unmet medical need for CIN.

"Receipt of Breakthrough Therapy Designation from the FDA acknowledges both the significant unmet need among patients with CIN and the highly encouraging clinical results generated by Plinabulin, said Douglas Blayney, MD, global principal investigator for the CIN studies pf Plinabulin and professor of Medicine at the Stanford University School of Medicine, in a statement.

This should expedite Plinabulins move into the clinic, which is beneficial for patients. The currently approved CIN prevention agents are all G-CSF-based and not available to all patients. Even with the use of G-CSFs, over 80 percent of cancer patients undergoing chemotherapy may still experience Grade 4 neutropenia, which could lead to severe infection, hospitalization, and even death. Thus, CIN still represents an unmet medical need.

The designation was based on findings from the phase 3 PROTECTIVE-2 clinical trial (NCT03294577), which achieved a clinically meaningful primary end point of prevention of severe neutropenia. In combination with pegfilgrastim (Neulasta), plinabulin was significantly better at achieving the primary end point (P <.01). The safety profile also appeared well-tolerated with few adverse events of grade 4 severity in the combination arm compared with the control.

These results are supported by other studies in CIN that have confirmed early action of plinabulin in week 1 by protecting neutrophils in various cancer types with a variety of chemotherapy agents. This is complementary to week 2 neutrophil protection with granulocyte colony-stimulating factors (G-CSFs).2

The superiority study, PROTECTIVE-2, was designed to assess both the safety and efficacy of plinabulin as treatment of patients with breast cancer treated with docetaxel, doxorubicin, and cyclophosphamide (TAC) in a 21-day cycle. Plinabulin was administered in a 40 mg dose on day 1 with a 6 mg dose of pegfilgrastim on day 2, while pegfilgrastim was administered in the control arm at 6 mg dose as well on day 2. TAC is considered a high-risk chemotherapy regimen associated with neutropenia.

BeyondSpring announced the interim findings of this study in June 2020, which demonstrated a significant enhancement of G-CSFs with the plinabulin combination, which supports the potential for superiority of this treatment compared with pegfilgrastim alone.

The primary end point of severe neutropenia prevention in cycle 1 demonstrated a P value<.01. The key secondary end points of this study included duration of severe neutropenia in cycle 1 (P<.05) and duration of severe neutropenia in the first 8 days of cycle 1 (P <.05). The achievement of these end points demonstrates the agents ability to provide early protection against severe neutropenia induced by chemotherapy.

The rate of grade 4 neutropenia for TAC and pegfilgrastim is observed in 83% to 93% of patients, according to the interim findings.

Plinabulin is a first-in-class differentiated immune and stem cell modulator. The agent is currently in late-stage clinical development for its opportunity to improve overall survival in patients with cancer, as well as to alleviate CIN. Plinabulin and G-CSFs have complementary mechanisms of action for preventing chemotherapy-induced neutropenia.1

"The clinical profile Plinabulin has shown truly represents a breakthrough in the CIN space since G-CSFs," said Ramon Mohanlal, MD, PhD, MBA, chief medical officer, and executive vice president, Research and Development, BeyondSpring, in a statement. We look forward to continuing to work with the FDA as we advance the development of Plinabulin to address this urgent medical need.

References

1. BeyondSpring receives breakthrough therapy designations from both US FDA and China NMPA for plinabulin in chemotherapy-induced neutropenia indication. News Release. BeyondSpring. September 8, 2020. Accessed September 10, 2020

2. BeyondSpring Announces Positive Topline Interim Results from PROTECTIVE-2 (Study 106) Phase 3 Trial Evaluating Superiority of Plinabulin in Combination with Neulasta for Chemotherapy-Induced Neutropenia Prevention. News Release. BeyondSpring. June 15, 2020. Accessed September 10, 2020. https://bit.ly/2YDJbiQ

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Plinabulin Granted FDA Breakthrough Therapy Designation for Chemotherapy-Induced Neutropenia - Targeted Oncology

GSK and J&J alum Vijay Reddy to take control of R&D at Tmunity; Andrew Hirsch exits Agios for CEO job at C4 Therapeutics – Endpoints News

Vijay Reddy was seeking a return to the US when he left his role as CMO at London-based Autolus this summer. Philadelphia is that landing spot, as the T cell immunotherapy player Tmunity has put him in charge of R&D.

Reddy arrives at the Penn spinout with plenty of Big Pharma bona fides after developing the CAR-T cell clinical program at Autolus. Tmunitys new chief R&D officer was a senior director and led early clinical development at J&J subsidiary Janssen from 2013-16, and from 2009-13, he was GSKs medical director, cancer research and clinical development.

Tmunity also added to their leadership team by selecting Simona King as their CFO. A nearly 20-year vet of Bristol Myers Squibb in various financial roles, King just had a brief run as VP, finance and assistant treasurer at Emergent BioSolutions.

Co-founded by CAR-T inventors Carl June and Bruce Levine, Tmunity has racked up $231 million in total funding.

Completing a 4-year run as CFO at Agios, Andrew Hirsch has made the jump to CEO of protein degradation pioneer C4 Therapeutics. Hirsch takes the helm at another biotech after a brief tenure as president and CEO of Bind Therapeutics, where he spent 4 years overall. C4 just penciled in $100 million for an IPO and back in June, the biotech raked in a $170 million raise, $150 million of that from a Series B round. Hirsch succeeds Andrew Phillips, who bolts after 2 years on the job.

Maryland-based CavoGene LifeSciences, whose lead program for ALS is slated for clinical trials by early 2022, has a new CEO with Daniel Jorgensen now at the helm. A former senior director at Pfizer, Jorgensen was the pharma giants first vaccine development team leader, and he also served as global clinical leader for azithromycin. Elsewhere, hes been CMO and SVP, clinical development at PolyMedix and VP, clinical research for AMAG Pharmaceuticals.

Ex-Dendreon CEO Jim Caggiano is back at the helm of another biotech, this time at Targazyme, an immunotherapy and stem cell transplantation outfit in San Diego using enzyme-based platform technologies. Before Caggianos tenure at Dendreon, the former US Army officer was president of Valeant Pharmaceuticals and also held positions at Allergan for more than 5 years.

No doubt getting a boost from Akebias Phase III vadadustat fail last week, roxadustat developer FibroGen has plucked Big Pharma vet Percy Carter from Janssen for the newly-created CSO post. Carter was previously Janssens global head of discovery sciences, and prior to that, he spent nearly 20 years at Bristol Myers Squibb in several roles, namely head of discovery and head of discovery chemistry & molecular technologies.

Young oncology company Black Diamond Therapeutics, which collected over $200 million for their IPO in January, has locked in Rachel Humphrey as CMO. Humphrey is taking over from Karsten Witt, who has been serving as acting CMO along with his duties as the companys SVP of clinical development. Humphrey brings to the table experience from a long list of roles at CytomX Therapeutics where she served as CMO Eli Lilly, AstraZeneca, Mirati Therapeutics, Bristol Myers Squibb and Bayer.

Ali Fattaey is now leading cancer metabolism player MetaboMed as their CEO. His predecessor, co-founder Simone Botti, is moving to a senior position at an undisclosed European VC. Fattaey previously led therapeutics discovery and development at Scipher Medicine and was the president and CEO at Curis. He started his career at Onyx Pharmaceuticals as VP, research.

Some hard times have befallen DBV Technologies, whose peanut allergy skin patch was rebuffed in a CRL from the FDA in August. Now, a couple of execs have headed for the exits with CFO Ramzi Benamar and CCO Kevin Trapp walking out the door of the French biotech. Sbastien Robitaille will be filling in as CFO on an interim basis effective Oct 2. The Ipsen vet, who started out at DBV 5 years ago as SVP, group controller and information systems, was promoted to chief of staff to CEO Daniel Tass a year ago.

Molly Henderson is resigning from her role as CFO at Princeton, NJ biotech Advaxis, effective Sept 25, to become CFO at UroGen beginning the following week. President and CEO Kenneth Berlin will function as interim CFO until her replacement is found. Advaxis has had a rough go of it with its ill-fated Amgen partnership and multiple FDA holds on their lead asset axalimogene.

Elsewhere at UroGen, Polly Murphy has taken on the role of CBO and Jason Smith will be general counsel and chief compliance officer. Murphy and Smith are both Pfizer alums: Murphy spent 12 years in a series of VP roles at the pharma giant and was most recently their VP for early commercial development in the oncology business unit, while Smith logged 11 years at Pfizer, the last 4 of those as their chief counsel, oncology. Before that, Smith was legal lead for the North American region of Pfizer Essential Health.

Back in May, Spruce Biosciences introduced Samir Gharib as their CFO, and theres another change at the San Francisco biotechs C-suite with Rosh Dias coming in as CMO. Before joining Spruce, which targets rare endocrine disorders and revealed positive Phase II data a year ago with lead candidate tildacerfont, Dias a Novartis vet spent the last year in the same role at Indivior. From 2015-18, he was Amgens VP, global scientific affairs. In other Spruce developments, ex-BioMarin CFO Dan Spiegelman was added to their board of directors.

Forging ahead in Phase III of their Covid-19 vaccine and ranking No. 2 on our list of the 29 vaccine players, Moderna has tapped Michael Mullette as managing director, Canada. After nearly 2 decades at Sanofi, with the last 2 years as general manager and country chair for Sanofi Canada in Montreal, Mullette came to Moderna in August as VP, market access, and he will carry on in that role in addition to his new appointment.

Raising $16 million in a Series B last week in an effort to democratize biologics, Seattle-based Lumen Bioscience has given the nod to Mike Spigarelli to be their CMO. Spigarelli is coming off 4 years as VP, medical affairs for diagnostics company Immucor.

Respiratory disease-centered genetic medicines player ReCode Therapeutics has a trifecta of appointments with Mukul Agarwal, CBO; Vladimir Kharitonov, SVP, chemistry, manufacturing and controls (CMC); and Brandon Wustman, SVP, R&D. Agarwal heads to ReCode after a little over a year as VP, corporate development at Forty Seven, which Gilead bought in March for $4.9 billion. Kharitonov had spent 20 years at Pacira Pharmaceuticals, the last 10 as their VP of R&D. And Wustman had been with the company as VP of R&D before ReCode joined forces with TranscripTx in March. From 2002-14, he was senior director, preclinical biology at Amicus Therapeutics.

Ex-Millipore chairman, president and CEO Martin Madaus is making his way to Feng Zhangs CRISPR-based diagnostics player Sherlock Biosciences as COO. Madaus has been interim CEO and executive chairman at Ultivue and Emulate Bio of late, and from 2014-19, he was chairman and CEO at Ortho Clinical Diagnostics.

UK clinical AI company Sensyne Health has tapped Michael Macdonnell as COO. Macdonnell currently heads Google Health as director of global deployment. Prior to his position at Google Health, Macdonnell was at Google DeepMind and held roles at Accenture, NHS England and Imperial College London among others.

Longtime Merck vet Ercem Atillasoy is on board at cell therapy company AlloVir as chief regulatory and safety officer. At Merck Research Laboratories, Atillasoy was VP and therapeutic area head of vaccines and infectious disease and VP, global regulatory affairs and clinical safety. He ran Keytrudas first IND filing for melanoma and was involved in the approval of such medicines as the Ebola vaccine Ervebo and the HPV vaccine Gardasil.

Tillman Gerngross new endeavor, Adagio Therapeutics, has locked in Eric Kimble as chief commercial officer and Ed Campanaro as SVP of clinical operations. Kimble and Campanaro worked at Cubist Pharmaceuticals in VP positions at the same time Kimble from 2004-13, and Campanaro from 2000-14. Before Adagio, which focuses on antibodies as an avenue to combat Covid-19, Kimble was the CCO at Entasis Therapeutics, while Campanaro was SVP of clinical operations at Artugen Therapeutics.

Olema Oncology, working on the development of targeted therapies for womens cancers, has made several new additions to its executive team with the appointment of Shane Kovacs as COO/CFO, Genentech vet Kinney Horn as CBO, and John Moriarty as EVP, chief legal officer. In addition, Pamela Klein has been named CMO and David Myles has been promoted to chief development officer. Kovacs joins the company from BlueRock Therapeutics (acquired by Bayer), where he served as CBO and CFO. Horn held a 16-year stint at Genentech, while Moriarty was most recently EVP and general counsel at Portola Pharmaceuticals.

Klein joins the company with experience from Syndax Pharmaceuticals and Genentech where she most recently served as VP, development among others. Myles moves up to his new role after serving as Olemas EVP, drug discovery and development.

New York-based Phosplatin Therapeutics, which has obtained exclusive license to a family of compounds known as phosphaplatins that may aid in treating cancer, has made Joseph ODonnell their interim CMO, and Jason Summa has gotten the call to be VP of clinical development. ODonnell has long been in academia at Dartmouth Universitys Geisel School of Medicine, where he started teaching in 1978. A Bind and Momenta alum, Summa was previously oncology director and clinical project scientist at Janssen.

Australian CRO Avance Clinical has corralled Jorgen Mould as a scientific affairs specialist. Mould was previously with Merck (KGaA) Healthcare as an associate medical manager and medical science liaison, neurology and immunology.

Cell engineering service provider MaxCyte has snagged Amanda Murphy as CFO, succeeding Ron Holtz who has been promoted to the position of SVP and chief accounting officer. Prior to MaxCyte, Murphy was managing director at BTIG and was partner and healthcare analyst at William Blair & Company.

Prilenia Therapeutics, focused on treatments for neurodegenerative and neurodevelopmental disorders, has welcomed Henk Schuring as chief regulatory and commercialization officer. Schuring hails from Sanofi Genzyme, where he had a 21-year career and managed the rare nephrological diseases business and rare neurological diseases business.

Paul Bavier has been appointed general counsel at cancer-focused VelosBio, which racked up $137 million in a Series B round a couple months ago. Before he set off for VelosBio, Bavier spent 3 years at Avedro as their general counsel and chief compliance officer. He also held similar roles at Biodel from 2007-16 and was also their VP, corporate development.

With Rich Heyman now chairman of the board and a $70 million Series D in the hopper, NJ-based PMV Pharma has brought in Robert Ticktin as general counsel. Ticktin was previously associate general counsel, corporate at Tesaro (and then GSK after the buyout). PMV Pharma, which targets p53 mutations, has also selected Arena Pharmaceuticals CFO Laurie Stelzer to the board of directors as audit committee chair.

Sygnature Discovery, a Nottingham-based provider of drug discovery and preclinical services, has reeled in Andy Mead as director and head of drug abuse and substance use disorders at its integrated vivopharmacology company, RenaSci. Mead jumps aboard Sygnature from Sosei Heptares, where he served as director of discovery and translational safety. In addition, he brings experience from roles at Merck, Pfizer and AstraZeneca among others.

UKs PrecisionLife has appointed Simon Beaulah as SVP of healthcare and head of US operations. Most recently, Beaulah was director of healthcare at Linguamatics and prior to that was at IDBS Healthcare.

VC and growth equity firm SV has brought on Alex Badamchi-Zadeh as senior associate. Badamchi-Zadeh hops aboard with experience from Xilio Therapeutics where he helped guide the Kendall Square-based company through their $100.5 million Series B financing round and LEK Consulting.

Dean Mitchell has been named chairman of the board at Kinnate, which just nabbed a $98 million Series C in August. The GSK and Bristol Myers Squibb vet is the former president and CEO of Lux Biosciences and Alpharma.

Blueprint Medicines president and CEO Jeff Albers has joined the board of directors at Kymera Therapeutics. The newly public protein degradation player also added Replimune CBO Pamela Esposito to the board.

After penciling in a $150 million IPO in June, Forma Therapeutics has recruited Thomas Wiggans to its board of directors. Wiggans is the former chairman and CEO of Dermira (acquired by Eli Lilly) and helped in the formation of the Biotechnology Industry Organization, now Biotechnology Innovation Organization (BIO).

Bonnie Anderson has been elected to the board of directors at Bruker Corporation, a scientific instrument manufacturer. Anderson co-founded Veracyte in 2008 and is their chairman and CEO.

UK-based GW Pharmaceuticals has tapped ex-Incyte and Celgene CFO David Gryska to be on their board of directors. Gryska is also on the boards of Seattle Genetics, PDL BioPharma and Aerie Pharmaceuticals.

Joseph Bower has announced his decision to retire as chairman of the board at orthopedic-focused Anika Therapeutics after his term is up in 2021. Bower, a professor emeritus at Harvard Business School, has served on the board since 1993. Anika is also bringing in Jack Henneman and Stephen Richard as new board members.

AAV-based gene therapies-focused Prevail Therapeutics has added William Carson to its board of directors. Most recently, Carson served as president and CEO of Otsuka Pharmaceutical Development & Commercialization and draws from experience from a stint at Bristol Myers Squibb.

Hematology biotech Starton Therapeutics has chosen Kenneth Anderson and Asher Chanan-Khan to sit on their board of directors. Anderson is director of the Jerome Lipper Multiple Myeloma Center and LeBow Institute for Myeloma Therapeutics at Dana-Farber, while Chanan-Khan is a professor of medicine at Mayo Clinic Cancer Center in Jacksonville.

Retinal gene therapy company Gyroscope Therapeutics has brought on Sean Bohen to its board of directors.Bohen is the former CMO and EVP, global medicines development at AstraZeneca and previously served as SVP of Genentech early development (gRED).

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GSK and J&J alum Vijay Reddy to take control of R&D at Tmunity; Andrew Hirsch exits Agios for CEO job at C4 Therapeutics - Endpoints News

New Data Further Reinforce Genentech’s Ocrevus (ocrelizumab) as a Highly Effective Treatment for People With Multiple Sclerosis – BioSpace

Sept. 11, 2020 05:00 UTC

SOUTH SAN FRANCISCO, Calif.--(BUSINESS WIRE)-- Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), today announced new data that show Ocrevus (ocrelizumab) is a highly effective treatment option for people with relapsing-remitting multiple sclerosis (RRMS) who experienced a suboptimal response to their prior disease modifying therapy (DMT). Subgroup analysis from the two-year open-label Phase IIIb CASTING study also demonstrates that patients benefit across a wide range of disease related and demographic subgroups, regardless of prior treatment background. Findings will be presented at MSVirtual2020, the 8th Joint Meeting of the Americas Committee for Treatment and Research in Multiple Sclerosis (ACTRIMS) and the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS).

For a wide range of people with MS who experienced a suboptimal response to prior treatment, we continue to see evidence that Ocrevus provides significant benefit in slowing disease progression, said Levi Garraway, M.D., Ph.D., chief medical officer and head of Global Product Development. New real-world Ocrevus data show high persistence and adherence to the only B-cell therapy with a twice-yearly dosing schedule, which we know can be very important to both people with MS and their physicians.

Phase IIIb open-label CASTING study

Approximately 75% of RRMS patients (492/658) had no evidence of disease activity (NEDA; brain lesions, relapses and worsening of disability) two years after switching to twice-yearly Ocrevus treatment (with prespecified MRI re-baselining at 8 weeks) in the primary analysis of the CASTING study. Patients enrolled in the study had prior suboptimal response to at least six months of treatment with up to two DMTs. The analysis also showed the proportion of patients achieving NEDA remained consistently high across all measured patient subgroups, including baseline MRI activity, relapse activity, disability level, age and the number of prior DMTs. Further, 78% of patients treated with only one prior DMT compared with 70% of patients treated with two prior DMTs achieved NEDA.

Additionally, patients treated with Ocrevus experienced an improvement in the majority of symptoms measured by SymptoMScreen after two years. SymptoMScreen is a patient-reported outcome tool to assess symptom severity across twelve domains. The most pronounced significant improvements (p<0.001) were seen in sensory symptoms, fatigue and vision, which are important for daily living.

CONFIDENCE real-world safety study

A 97% treatment persistence for Ocrevus patients at 18 months, and strong adherence to infusions every six months, was seen in an interim analysis of more than 1,600 patients in the ongoing German CONFIDENCE study. Separate data from a U.S. commercial claims database that support high persistence and sustained adherence to Ocrevus treatment will also be presented.

Ocrevus longer-term safety data

New safety data as of January 2020 will be presented, representing 5,680 patients with RMS and PPMS and 18,218 patient-years of exposure to Ocrevus, across all Ocrevus clinical trials. These findings further demonstrate the consistently favorable benefit:risk profile of Ocrevus over seven years.

With rapidly growing real-world experience and more than 170,000 people treated globally, Ocrevus has twice-yearly (six-monthly) dosing and is the first and only therapy approved for RMS (including relapsing-remitting MS [RRMS] and active, or relapsing, secondary progressive MS [SPMS], in addition to clinically isolated syndrome [CIS] in the U.S.) and primary progressive MS (PPMS). Ocrevus is approved in 92 countries across North America, South America, the Middle East, Eastern Europe, as well as in Australia, Switzerland and the European Union.

About multiple sclerosis

Multiple sclerosis (MS) is a chronic disease that affects nearly one million people in the United States, for which there is currently no cure. MS occurs when the immune system abnormally attacks the insulation and support around nerve cells (myelin sheath) in the brain, spinal cord and optic nerves, causing inflammation and consequent damage. This damage can cause a wide range of symptoms, including muscle weakness, fatigue and difficulty seeing, and may eventually lead to disability. Most people with MS experience their first symptom between 20 and 40 years of age, making the disease the leading cause of non-traumatic disability in younger adults.

Relapsing-remitting MS (RRMS) is the most common form of the disease and is characterized by episodes of new or worsening signs or symptoms (relapses) followed by periods of recovery. Approximately 85 percent of people with MS are initially diagnosed with RRMS. The majority of people who are diagnosed with RRMS will eventually transition to secondary progressive MS (SPMS), in which they experience steadily worsening disability over time. Relapsing forms of MS (RMS) include people with RRMS and people with SPMS who continue to experience relapses. Primary progressive MS (PPMS) is a debilitating form of the disease marked by steadily worsening symptoms but typically without distinct relapses or periods of remission. Approximately 15 percent of people with MS are diagnosed with the primary progressive form of the disease. Until the FDA approval of Ocrevus, there had been no FDA approved treatments for PPMS.

People with all forms of MS experience disease activity inflammation in the nervous system and permanent loss of nerve cells in the brain even when their clinical symptoms arent apparent or dont appear to be getting worse. An important goal of treating MS is to reduce disease activity as soon as possible to slow how quickly a persons disability progresses. Despite available disease-modifying treatments (DMTs), some people with RMS continue to experience disease activity and disability progression.

About Ocrevus(ocrelizumab)

Ocrevus is the first and only therapy approved for both RMS (including clinically isolated syndrome, RRMS and active, or relapsing, SPMS) and PPMS, with dosing every six months. Ocrevus is a humanized monoclonal antibody designed to target CD20-positive B cells, a specific type of immune cell thought to be a key contributor to myelin (nerve cell insulation and support) and axonal (nerve cell) damage. This nerve cell damage can lead to disability in people with MS. Based on preclinical studies, Ocrevus binds to CD20 cell surface proteins expressed on certain B cells, but not on stem cells or plasma cells, suggesting that important functions of the immune system may be preserved.

Ocrevus is administered by intravenous infusion every six months. The initial dose is given as two 300 mg infusions given two weeks apart. Subsequent doses are given as single 600 mg infusions.

Important Safety Information

What is Ocrevus?

Ocrevus is a prescription medicine used to treat:

It is not known if Ocrevus is safe or effective in children.

Who should not receive Ocrevus?

Do not receive Ocrevus if you have an active hepatitis B virus (HBV) infection.

Do not receive Ocrevus if you have had a life threatening allergic reaction to Ocrevus. Tell your healthcare provider if you have had an allergic reaction to Ocrevus or any of its ingredients in the past.

What is the most important information I should know about Ocrevus?

Ocrevus can cause serious side effects, including:

These infusion reactions can happen for up to 24 hours after your infusion. It is important that you call your healthcare provider right away if you get any of the signs or symptoms listed above after each infusion.

If you get infusion reactions, your healthcare provider may need to stop or slow down the rate of your infusion.

Before receiving Ocrevus, tell your healthcare provider about all of your medical conditions, including if you:

Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.

What are the possible side effects of Ocrevus?

Ocrevus may cause serious side effects, including:

Most common side effects include infusion reactions and infections.

These are not all the possible side effects of Ocrevus.

Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

For more information, go to http://www.Ocrevus.com or call 1-844-627-3887.

For additional safety information, please see the full Prescribing Information and Medication Guide.

About Genentech in neuroscience

Neuroscience is a major focus of research and development at Genentech and Roche. Our goal is to pursue groundbreaking science to develop new treatments that help improve the lives of people with chronic and potentially devastating diseases.

Genentech and Roche are investigating more than a dozen medicines for neurological disorders, including multiple sclerosis, stroke, Alzheimers disease, Huntingtons disease, Parkinsons disease, Duchenne muscular dystrophy and autism spectrum disorder. Together with our partners, we are committed to pushing the boundaries of scientific understanding to solve some of the most difficult challenges in neuroscience today.

About Genentech

Founded more than 40 years ago, Genentech is a leading biotechnology company that discovers, develops, manufactures and commercializes medicines to treat patients with serious and life-threatening medical conditions. The company, a member of the Roche Group, has headquarters in South San Francisco, California. For additional information about the company, please visit http://www.gene.com.

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New Data Further Reinforce Genentech's Ocrevus (ocrelizumab) as a Highly Effective Treatment for People With Multiple Sclerosis - BioSpace

Stem Cells Market Report, History and Forecast 2020-2027, Data Breakdown by Manufacturers, Key Regions, Types and Application – News Degree

Stem Cells Market Report

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The Stem Cells market has witnessed dynamic changes in trends and demands owing to the ongoing COVID-19 pandemic. The report provides a detailed outlook on how the pandemic has affected the key segments of the Stem Cells industry. The report includes an in-depth impact analysis of the COVID-19 pandemic on the overall Stem Cells industry and covers a futuristic impact scenario.

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The report covers extensive analysis of the key market players in the market, along with their business overview, expansion plans, and strategies. The key players studied in the report include:

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The report offers a comprehensive analysis of the Stem Cells market inclusive of product portfolio, categories, applications, and a comprehensive analysis of the value chain structure. The study investigates several factors influencing the growth of the market and provides a competitive advantage to the readers.

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Product Outlook (Revenue, USD Billion; 2017-2027)

Technology Outlook (Revenue, USD Billion; 2017-2027)

Therapy Outlook (Revenue, USD Billion; 2017-2027)

Application Outlook (Revenue, USD Billion; 2017-2027)

The report covers an extensive regional analysis and market estimation in each region and covers key geographical regions such as North America, Europe, Asia-Pacific, Latin America, and Middle East & Africa.

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Stem Cells Market Report, History and Forecast 2020-2027, Data Breakdown by Manufacturers, Key Regions, Types and Application - News Degree

Adipose Tissue-Derived Stem Cells (ADSCS) Market to Witness High Growth in Near Future – Good Night, Good Hockey

Data Bridge Market Research has recently published the Global research Report TitledAdipose Tissue-Derived Stem Cells (ADSCS) Market. The study provides an overview of current statistics and future predictions of the Global Adipose Tissue-Derived Stem Cells (ADSCS) Market.The study highlights a detailed assessment of the Market and displays market sizing trends by revenue & volume (if applicable), current growth factors, expert opinions, facts, and industry validated market development data.

Adipose tissue-derived stem cells (ADSCS) market is expected to gain market growth in the forecast period of 2020 to 2027. Data Bridge Market Research analyses the market to account grow at a CAGR of 6.1% in the above-mentioned forecast period. The accelerating application of adipose tissue-derived stem cells (ADSCS) in the regenerative medicines research, development of cell linage, tissue engendering, bone and cartilage regeneration are driving the exponential growth of adipose tissue-derived stem cells (ADSCS) market during the forecast period of 2020 to 2027.

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The report gives explanations about market definition, currency and pricing, market segmentation, market overview, premium insights, key insights and company profile of the key market players. With this large scale Adipose Tissue-Derived Stem Cells (ADSCS) Marketreport, it can also be estimated how the actions of key players are affecting the sales, import, export, revenue and CAGR values. The report also helps analyse the most appropriate method for the distribution of certain products. This market study also estimates the market status, market share, growth rate, sales volume, future trends, market drivers, market restraints, revenue generation, opportunities and challenges, risks and entry barriers, sales channels, and distributors

Top Key Vendors Covered in the report:

Antria Inc., CELGENE CORPORATION, pluristem, Tissue Genesis, Cytori Therapeutics Inc., PRECIGEN, Mesoblast Ltd, CORESTEM, Inc, among other domestic and global players.

Regions included:

North America (United States, Canada, and Mexico)

Europe (Germany, France, UK, Russia, and Italy)

Asia-Pacific (China, Japan, Korea, India, and Southeast Asia)

South America (Brazil, Argentina, Colombia)

The Middle East and Africa (Saudi Arabia, UAE, Egypt, Nigeria, and South Africa)

How Does This Market Insights Help?

Key Pointers Covered in the Adipose Tissue-Derived Stem Cells (ADSCS) Market Industry Trends and Forecast to 2026

Reasons to Purchase this Report

A complete value chain of the global Adipose Tissue-Derived Stem Cells (ADSCS) market is presented in the research report. It is associated with the review of the downstream and upstream components of the Adipose Tissue-Derived Stem Cells (ADSCS) Market. The market is bifurcated on the basis of the categories of products and customer application segments. The market analysis demonstrates the expansion of each segment of the global Adipose Tissue-Derived Stem Cells (ADSCS) market. The research report assists the user in taking a decisive step that will be a milestone in developing and expanding their businesses in the global Adipose Tissue-Derived Stem Cells (ADSCS) market.

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TABLE OF CONTENTS

Part 01:Executive Summary

Part 02:Scope of the Report

Part 03:Research Methodology

Part 04:Market Landscape

Part 05:Pipeline Analysis

Pipeline Analysis

Part 06:Market Sizing

Market Definition

Market Sizing

Market Size And Forecast

Part 07:Five Forces Analysis

Bargaining Power Of Buyers

Bargaining Power Of Suppliers

Threat Of New Entrants

Threat Of Substitutes

Threat Of Rivalry

Market Condition

Part 08:Market Segmentation

Segmentation

Comparison

Market Opportunity

Part 09:Customer Landscape

Part 10:Regional Landscape

Part 11:Decision Framework

Part 12:Drivers and Challenges

Market Drivers

Market Challenges

Part 13:Market Trends

Part 14:Vendor Landscape

Part 15:Vendor Analysis

Vendors Covered

Vendor Classification

Market Positioning Of Vendors

Part 16:Appendix

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Adipose Tissue-Derived Stem Cells (ADSCS) Market to Witness High Growth in Near Future - Good Night, Good Hockey

New Age Meats: "There’s a Reason We’re Called New Age Meats. The Definition of Meat is Changing." – vegconomist – the vegan business…

New Age Meats: Theres a Reason Were Called New Age Meats. The Definition of Meat is Changing.

We were fascinated to speak with New Age Meats CEO Brian Spears.

You have created a pork sausage already, what other products are you currently working on?One of the reasons we chose pork is that its the most commonly consumed animal in the world. Were working on other pork products for both Western and Asian markets. Weve also done work with other animals.

We understand that your product development is focused on interrogating the science of meat, to understand why it tastes and feels the way it does, can you tell us more about that?How do cells make the sensory characteristics that we care about? To understand that, we start with the human perception of meat. This allows us to see the biomarkers that we can then have the cells make more efficiently.

Why is cellbased meat important right now and how much potential to disrupt animal agriculture do you believe it offers as a segment?Were pretty open that we make blended products of cultivated and plant based meat, but the real question is that of demand and our planets ability to supply the food required to feed ourselves. The UNFAO predicts that we will need to grow our food supply by 70% by 2050, a growth rate which outpaces our land and resource availability. Were not seeking disruption so much as augmentation to meet that increased demand.

We covered a report from the GAO back in May that stated that cell-based meat is stuck in the Research and Development stage, what are your thoughts on this?The GAO performs invaluable services, but innovation is not one of them. Thinking that the pathway forward is to convert existing technologies in industries like biopharma and cellular therapeutics leads one to believe that the industry has a long way to go. Creating new pathways through whitespace is what startups do.

New Age Meats has secured $5M in funding to date; investors seem keen to be a part of this fledgling industry despite concerns noted from the GAO, will you be announcing further funding rounds? Absolutely. Alternative proteins comprise less than half a percent of the massive worldwide meat market. Well never make a dent in that market if we grow slowly. We make the future of meat, and investors are eager to join us in that journey.

Can we expect to see your pork sausage in the market in the near future? What challenges do you face with this?Yes! Were continually dropping the cost and ramping up production. Here in the US, regulators are moving quickly to allow us to come to market, and thats mirrored by other countries, notably in Asia.

Where do you see New Age Meats in the next five years?Pork products are where we start. In the next five years, well have multiple types of meat products in different geographies and distribution channels.

Link:
New Age Meats: "There's a Reason We're Called New Age Meats. The Definition of Meat is Changing." - vegconomist - the vegan business...

Global Wearable Artificial Organs Market Is Expected to Reach USD 17.48 billion by 2027 : Fior Markets – GlobeNewswire

September 08, 2020 08:02 ET | Source: Fior Markets

Newark, NJ, Sept. 08, 2020 (GLOBE NEWSWIRE) -- As per the report published by Fior Markets, theglobal wearable artificial organs market is expected to grow from USD 5.26 billion in 2019 and to reach USD 17.48 billion by 2027, growing at a CAGR of 16.20% during the forecast period 2020-2027.

The rising demand and supply gap of organ donors, along with the increasing frequency of organ failure, is driving the market growth. Technological advancement and continuous investments in research and development activities for wearable artificial organs also boost the market growth. The artificial organ is an engineered tool integrated into human living tissues to substitute the human organ. The requirement for wearable artificial organs is increasing due to less cost of wearable artificial organs than organ transplantation and the growing number of geriatric populations prone to kidney failure. Leading players in the industry are emphasizing on the advancement of wearable artificial organs for the disease that cannot be cured with alternative techniques. Wearable and portable devices would potentially enhance the quality of life by enabling patients to continue their daily activities while undergoing therapy or dialysis. Improvement in the field of stem cell, microelectronics, nanotechnology, artificial intelligence, genetic engineering, genomics, proteomics, and bioinformatics is generating new avenues for wearable artificial organs.

Artificial organs are synthetic machines or devices that replace several human organs that undergo from the malfunctioning or loss of complete functioning ability. Artificial organs are constructed from human stem cells and then developed in laboratories. However, advancements and innovation of modern artificial organs are still improving, offering significant growth outlooks to the global artificial organs market during the forecast period. An artificial organ is an engineered tissue or tool that is implanted into the human body. The artificial organs replace a natural organ to replicate a distinct function so that the patient can return to a healthy life. It is a remedial tool with a biochemical or mechanical function such as lung, heart, liver, kidney, or neurosensory organs.

Producers in the industry are focused on organ repair and biological replacement that will operate as a tissue-based artificial organ and simulates a physiological function of an organ. The devices are customized to the changing needs of the patients. The market for wearable artificial organs is shifting from mechanical alternative towards original biological replacement. Moreover, the machines are less expensive than organ transplants, thereby generating new opportunities and demand in the market. Improving healthcare infrastructure and decreasing waiting time for FDA permission are also factors that augment market growth. For instance, in August 2019, FDA authorized MED-EL Cochlear Implant System for asymmetric hearing loss. The system is utilized for children five years and older. A high number of permanent injuries, as well as rising incidence of road accidence, are also creating demand for wearable artificial organs.

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Key players operating in the global wearable artificial organs market include Medtronic, AWAK Technology, Second Sight Medical Products, Inc., Cochlear Ltd., Ekso bionics, MED-EL, Abbott Laboratories, Boston Scientific, HDT Global, Touch Bionics, Inc., Neurotron Biotechnology, Retina Implant AG, ReWalk Robotics, Rex Bionics Plc., Suit X (U.S. Bionics Inc.) and Lockheed Martin Corporation. To gain a significant market share in the global wearable artificial organs market, the key players are now focusing on adopting strategies such as product innovations, mergers & acquisitions, recent developments, joint ventures, collaborations, and partnerships.

The cochlear implant segment dominated the market and held the largest market share of 19.07% in the year 2019 The product segment includes vision bionics, brain bionics, bionic limbs, exoskeleton, cochlear implants, pancreas and kidney. The cochlear implants segment held the highest share of 19.07% in the wearable artificial organs market in 2019 due to frequent product launches. In December 2019, the FDA authorized the first active Osseointegrated steady-state implant, which can be utilized for children of 12 years and older with single-sided sensorineural deafness. The device would help in enhancing the patients capacity to hear in both quiet and noisy situations.

The electronic segment dominated the market and valued at USD 2.85 billion in the year 2019 The technology segment includes electronic and mechanical. The electronic segment held the highest share of UDS 2.85 billion in the wearable artificial organs market in 2019. It is due to the rising adoption of electronic wearable artificial organs and technological advancement. The need for electronic wearable artificial organs among amputees is rising. Electronic and battery systems are utilized to generate muscle and nerve movement in the remaining organ. The devices are creating a revolution in the therapeutic electronics industry. The market is anticipated to observe innovative product launches over the forecast period. For instance, in June 2020, Medtronic exhibited the positive results of MiniMed 780G System, its artificial pancreas. The device would give both basal insulin and correction boluses every five minutes to serve patients to avoid high and lows of insulin with greater comfort.

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Regional Segment Analysis of Global Wearable Artificial Organs Market

On the basis of geography, the global wearable artificial organs market is classified into North America, Europe, South America, Asia Pacific, and Middle East and Africa. North America had the largest share of 26.38% in the wearable artificial organs market in 2019. Rising research and development investment and speedy FDA permissions of the wearable artificial organs boost the demand in the region. The presence of significant market players and extremely modern healthcare infrastructure is also increasing the application in the region. In North America, the U.S. dominated the market due to factors such as favorable reimbursement policies, large patient pool, and deepening shortage of organ donors.

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About the report: The global wearable artificial organs market is analyzed on the basis of value (USD Billion), export (K Units), and import (K Units). All the segments have been analyzed on global, regional and country basis. The study includes an analysis of more than 30 countries for each segment. The report offers in-depth analysis of driving factors, opportunities, restraints, and challenges for gaining the key insight of the market. The study includes porters five forces model, attractiveness analysis, raw material analysis, and competitor position grid analysis.

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The report can be customized as per client requirements. For further queries, you can contact us onsales@fiormarkets.comor +1-201-465-4211. Our executives will be pleased to understand your requirements and offer you the best-suited reports.

About Fior Markets

Fior Markets is a futuristic market intelligence company, helping customers flourish their business strategies and make better decisions using actionable intelligence. With transparent information pool, we meet clients objectives, commitments on high standard and targeting possible prospects for SWOT analysis and market research reports. Fior Markets deploys a wide range of regional and global market intelligence research reports including industries like technology, pharmaceutical, consumer goods, food and beverages, chemicals, media, materials and many others. Our Strategic Intelligence capabilities are purposely planned to boost your business extension and elucidate the vigor of diverse industry. We hold distinguished units of highly expert analysts and consultants according to their respective domains. The global market research reports we provide involve both qualitative and quantitative analysis of current market scenario as per the geographical regions segregated and comprehensive performance in different regions with global approach. In addition, our syndicated research reports offer a packaged guide to keep companies abreast of the upcoming major restyle in their domains. Fior Markets facilitates clients with research analysis that are customized to their exact requirements, specifications and challenges, whether it is comprehensive desk research, survey work, composition of multiple methods, in-detailed interviewing or competitive intelligence. Our research experts are experienced in matching the exact personnel and methodology to your business need.

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Global Wearable Artificial Organs Market Is Expected to Reach USD 17.48 billion by 2027 : Fior Markets - GlobeNewswire

Global Organoids and Spheroids Market Is Expected to Reach USD 2794.79 Million by 2027 : Fior Markets – Yahoo Finance

Organoids and Spheroids Market by Type (Organoids and Spheroids), Application (Personalized Medicine, Developmental Biology, Drug Toxicity and Efficacy Testing, Disease Pathology Testing and Regenerative Medicine), End-Use, Region, Global Industry Analysis, Market Size, Share, Growth, Trends, and Forecast 2020 to 2027

Newark, NJ, Sept. 08, 2020 (GLOBE NEWSWIRE) -- As per the report published by Fior Markets, the global organoids and spheroids market is expected to grow from USD 502.92 million in 2019 and to reach USD 2794.79 million by 2027, growing at a CAGR of 23.91 % during the forecast period 2020-2027.

The growing prevalence of chronic disorders in recent times has increased the demand for effective drugs. The organoids and spheroids model is increasingly becoming popular as they provide a better perspective for human developmental biology research. The organoids model reveals the effects of covid-19 on several intestinal cells. Thus, these models are playing a significant role in the vaccine development process. The rise in demand for diagnostics and therapeutics solutions for these chronic diseases is fuelling market growth.

The organoids and spheroids are the three-dimensional structures that replicate the condition of different tissues present in the human body. The organoids model works as an in-vitro model for the study of biological development. The organoids can be established for organs such as kidney, retina, brain, liver, small and large intestine, lungs, etc. The organoids can be derived from a single adult stem cell or the embryonic stem cell. On the other hand, spheroids consist of a cluster of cells. These are derived from both the single-cell type and multi-cellular stems. The organoids and spheroids differ in the driving force required for the development. The organoids are formed by internal development processes and spheroids forms by adhesion of cells to each other. These also differ in the time duration for which the 3D culture can be maintained.

The human organoids have helped in the analysis of many tissues, which helps in a better understanding of the working of the organs. The 3D models of human organs have opened up opportunities for conducting various studies and experiments to analyze the effects of drugs on different organs. It also has provided potential ways of organ transplantation. Further, the growing technological advancements in the spheroid and organoid 3D models are fuelling the market growth. Apart from this, the major players operating in the market are also focusing on facilitating cell activities by taking control of the microenvironment of the culture.

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Key players operating in the organoids and spheroids market are 3D Biotek LLC, 3D Biomatrix, ATCC, Cellesce Ltd., Hubrecht Organoid Technology (HUB), Merck KGaA, STEMCELL Technologies Inc., Corning Incorporated, AMS Biotechnology Limited, Perkin Elmer, Kuraray, Thermo Fisher Scientific, Inc., Greiner Bio-One, Prellis Biologics, Lonza and others. The major players in the organoids and spheroids market are focusing on expansionary strategies such as mergers & acquisitions, recent developments, joint ventures, collaborations, product innovations and partnerships. These strategies would extract higher market shares for the players and thus strengthen their position in the global market. Thermo Fisher Scientific and Corning Incorporated are some of the biggest manufacturers and suppliers of organoids and spheroids in the global market.

Spheroids segment dominated the market and held the largest market share of 54.92% in the year 2019

On the basis of type segment, the global organoids and spheroids market includes organoids and spheroids. The organoids are segmented into product type, techniques and source. The product type of organoids includes neural organoids, intestinal organoids, hepatic organoids and others. The techniques include crypt organoid culture techniques, general submerged technique, clonal organoid from Lgr5+ cells, air-liquid interface (ALI) method and brain and retina organoid formation protocol. The sources segment includes primary tissues and stem cells. The spheroids are also segmented into product type, techniques and source. The product type of spheroids includes mammospheres, neurospheres, embryoid bodies, multi-cellular tumor spheroids and hepatospheres. The techniques segment includes hanging drop method, micropatterned plates, low cell attachment plates and others. The source of spheroid includes primary cells, cell line and iPSCs derived cells. Spheroids dominated the market and held the largest market share of 54.92% in the year 2019. The spheroids are in high demand owing to its increased application in cancer research and drug discovery. The spheroids can be cultured to produce cells of consistent shape, which can be used for thorough analysis. Further, the organoids segment is projected to register an impressive growth rate as these are used as in-vitro models in the process of drug discovery. The segment is expected to be driven by the intestinal organoids type owing to the increased application is cell biology and disease modeling.

Story continues

Developmental biology segment dominated the market and held the largest market share of 28.65% in the year 2019

On the basis of the application segment, the global organoids and spheroids market includes personalized medicine, developmental biology, drug toxicity and efficacy testing, disease pathology testing and regenerative medicine. Developmental biology dominated the market and held the largest market share of 28.65% in the year 2019. The organoids which are derived from induced pluripotent stem cells and embryonic stem cells are useful in human developmental biology. The spheroids and organoids have been increasingly used in the development biology study of the pancreas, kidney, stomach, liver, etc. for the purpose of embryonic development, tissue homeostasis and lineage specification.

Biotechnology and pharmaceutical companies segment dominated the market and held the largest market share of 39.82% in the year 2019

The end-user segment includes academic and research institutes, hospitals and diagnostic centers and biotechnology and pharmaceutical companies. Biotechnology and pharmaceutical companies segment dominated the market and held the largest market share of 39.82% in the year 2019. The organoids and spheroids are mainly used in clinical applications owing to the vast scope of the experiment. Thus, the biotechnology and pharmaceutical companies are using these increasingly in the drug discovery processes.

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Regional Segment Analysis of the Organoids and Spheroids Market

On the basis of geography, the global organoids and spheroids market is classified into North America, Europe, South America, Asia Pacific, and the Middle East and Africa. North America region accounted for a significant market share of 43.02% in the year 2019. The region has been lately, investing in the organoid and spheroids based research models. Further, the growing technological advancements provides a platform for extensive research on 3D models of human tissue structure for the development of personalized and regenerative medicines. However, Asia-Pacific is expected to register the highest growth rate during the forecast period. The growing patient population owing to the prevalence of chronic diseases has led to the development of the market in the region. Further, the growth of stem cell research has increased the demand for organoids and spheroids.

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About the report:

The global organoids and spheroids market is analyzed on the basis of value (USD Million). All the segments have been analyzed on global, regional and country basis. The study includes an analysis of more than 30 countries for each segment. The report offers in-depth analysis of driving factors, opportunities, restraints, and challenges for gaining the key insight of the market. The study includes porter's five forces model, attractiveness analysis, raw material analysis, and competitor position grid analysis.

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Customization of the Report:

The report can be customized as per client requirements. For further queries, you can contact us onsales@fiormarkets.comor +1-201-465-4211. Our executives will be pleased to understand your requirements and offer you the best-suited reports.

About Fior Markets

Fior Markets is a futuristic market intelligence company, helping customers flourish their business strategies and make better decisions using actionable intelligence. With transparent information pool, we meet clients objectives, commitments on high standard and targeting possible prospects for SWOT analysis and market research reports. Fior Markets deploys a wide range of regional and global market intelligence research reports including industries like technology, pharmaceutical, consumer goods, food and beverages, chemicals, media, materials and many others. Our Strategic Intelligence capabilities are purposely planned to boost your business extension and elucidate the vigor of diverse industry. We hold distinguished units of highly expert analysts and consultants according to their respective domains. The global market research reports we provide involve both qualitative and quantitative analysis of current market scenario as per the geographical regions segregated and comprehensive performance in different regions with global approach. In addition, our syndicated research reports offer a packaged guide to keep companies abreast of the upcoming major restyle in their domains. Fior Markets facilitates clients with research analysis that are customized to their exact requirements, specifications and challenges, whether it is comprehensive desk research, survey work, composition of multiple methods, in-detailed interviewing or competitive intelligence. Our research experts are experienced in matching the exact personnel and methodology to your business need.

Contact Us

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Original post:
Global Organoids and Spheroids Market Is Expected to Reach USD 2794.79 Million by 2027 : Fior Markets - Yahoo Finance

Competitive Scenario of Animal Stem Cell Therapy Market Growth, Size, Demand, Forecast with Depth Assessment by Top Key Players 2025 – Scientect

Key Questions Answered in The Report:

Purchase this report (Price With the slowdown in world economic growth, the Animal Stem Cell Therapy industry has also suffered a certain impact, but still maintained a relatively optimistic growth, the past four years, Animal Stem Cell Therapy market size to maintain the average annual growth rate of 0.148698354997 from 8.0 million USD in 2014 to 16.0 million USD in 2019, Report analysts believe that in the next few years, Animal Stem Cell Therapy market size will be further expanded, we expect that by 2024, The market size of the Animal Stem Cell Therapy will reach 80.0 million USD. USD for single user license)https://www.360researchreports.com/purchase/15079719

Major Highlights of TOC:

1 Report Overview

1.1 Study Scope

1.2 Key Market Segments

1.3 Regulatory Scenario by Region/Country

1.4 Market Investment Scenario Strategic

1.5 Market Analysis by Type

1.5.1 Global Animal Stem Cell Therapy Market Share by Type (2020-2026)

1.6 Market by Application

1.6.1 Global Animal Stem Cell Therapy Market Share by Application (2020-2026)

2.Global Market Growth Trends

2.1 Industry Trends

2.1.1 SWOT Analysis

2.1.2 Porters Five Forces Analysis

2.2 Potential Market and Growth Potential Analysis

2.3 Industry News and Policies by Regions

2.3.1 Industry News

2.3.2 Industry Policies

3 Value Chain of Animal Stem Cell Therapy Market

3.1 Value Chain Status

3.2 Animal Stem Cell Therapy Manufacturing Cost Structure Analysis

3.2.1 Production Process Analysis

3.2.2 Manufacturing Cost Structure of Electric Cookers

3.2.3 Labor Cost of Electric Cookers

4 Players Profiles

4.1 Media

4.1.1 Medea Basic Information

4.1.2 Animal Stem Cell Therapy Product Profiles, Application and Specification

4.1.3 Medea Animal Stem Cell Therapy Market Performance (2015-2020)

4.1.4 Medea Business Overview

5 Global Animal Stem Cell Therapy Market Analysis by Regions

5.1 Global Animal Stem Cell Therapy Sales, Revenue and Market Share by Regions

5.1.1 Global Animal Stem Cell Therapy Sales by Regions (2015-2020)

5.1.2 Global Animal Stem Cell Therapy Revenue by Regions (2015-2020)

5.2 North America Animal Stem Cell Therapy Sales and Growth Rate (2015-2020)

5.3 Europe Animal Stem Cell Therapy Sales and Growth Rate (2015-2020)

5.4 Asia-Pacific Animal Stem Cell Therapy Sales and Growth Rate (2015-2020)

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6 North America Animal Stem Cell Therapy Market Analysis by Countries

6.1 North America Animal Stem Cell Therapy Sales, Revenue and Market Share by Countries

6.1.1 North America Animal Stem Cell Therapy Sales by Countries (2015-2020)

6.1.2 North America Animal Stem Cell Therapy Revenue by Countries (2015-2020)

6.2 United States Animal Stem Cell Therapy Sales and Growth Rate (2015-2020)

7 Europe Animal Stem Cell Therapy Market Analysis by Countries

7.1 Europe Animal Stem Cell Therapy Sales, Revenue and Market Share by Countries

7.1.1 Europe Animal Stem Cell Therapy Sales by Countries (2015-2020)

7.1.2 Europe Animal Stem Cell Therapy Revenue by Countries (2015-2020)

7.2 Germany Animal Stem Cell Therapy Sales and Growth Rate (2015-2020)

7.3 UK Animal Stem Cell Therapy Sales and Growth Rate (2015-2020)

7.4 France Animal Stem Cell Therapy Sales and Growth Rate (2015-2020)

7.5 Italy Animal Stem Cell Therapy Sales and Growth Rate (2015-2020)

8 Asia-Pacific Animal Stem Cell Therapy Market Analysis by Countries

8.1 Asia-Pacific Animal Stem Cell Therapy Sales, Revenue and Market Share by Countries

8.1.1 Asia-Pacific Animal Stem Cell Therapy Sales by Countries (2015-2020)

8.1.2 Asia-Pacific Animal Stem Cell Therapy Revenue by Countries (2015-2020

8.2 China Animal Stem Cell Therapy Sales and Growth Rate (2015-2020)

8.3 Japan Animal Stem Cell Therapy Sales and Growth Rate (2015-2020)

Continued.

Animal Stem Cell Therapy Market Key Benefits

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D&D Pharmatech Announces Launch of Valted Seq Subsidiary Focusing on Discovery of Neurodegenerative Disease Pathways and Biomarkers to Support…

GYEONGGI-DO, South Korea & GAITHERSBURG, Md.--(BUSINESS WIRE)--D&D Pharmatech, Inc. (D&D), a clinical-stage biotechnology company focused on development and commercialization of revolutionary medicines, today announced the launch of their fourth subsidiary, Valted Seq. D&D Pharmatech is also the parent company of Neuraly, Precision Molecular, and Theraly Fibrosis.

Valted Seq is focused on the discovery of neurodegenerative pathways and biomarkers to inform and accelerate development of new therapeutics and diagnostics, including companion diagnostics which play a critical role in enabling advanced therapeutics. To achieve this, the company has created the worlds largest repository of single-cell sequencing data from high-quality, clinically characterized brain tissues of patients with neurodegenerative diseases including Alzheimers and Parkinsons.

We are excited to be a member of the D&D Pharmatech family of companies and are grateful for their investment which will ultimately improve our ability to diagnose and treat neurodegenerative diseases, said Valina Dawson, Ph.D., Interim Chief Executive Officer of Valted Seq. Valted Seq was founded on the belief that a deeper understanding of neurodegenerative pathways is essential to develop precision therapeutics and identify novel biomarkers to diagnose, guide therapies and monitor some of our most challenging and devastating diseases. We expect this unprecedented repository of single-cell genomics, which Valted Seq will explore using advanced big data analytics, will accelerate progress towards better outcomes for patients. Dr. Dawson is Director of the Neuroregeneration and Stem Cell Programs in the Institute for Cell Engineering at the Johns Hopkins University.

The ongoing collection and comprehensive analysis of thousands of brain tissue samples using Valted Seqs state-of-the-art single-cell analysis technology will support a number of projects including development of a first-in-class liquid biopsy assay for blood-based biomarkers for detection and monitoring of Parkinsons disease. The assay is being developed to be utilized in both internal and external clinical trials for emerging Parkinsons therapies; Valted Seq has already been approached by pharmaceutical companies seeking access to the proprietary biomarker assays. The company continues to expand and has added experienced leaders in bioinformatics and diagnostics to advance the technology through product development and towards commercialization.

We are excited to introduce Valted Seq as one of D&Ds companies, said Dr. Seulki Lee, Chief Executive Officer of D&D Pharmatech. Our subsidiaries, which to date have originated from technologies from leading research institutes, are examples of how D&D and academia have worked in close collaboration to build a powerful engine to accelerate translation of innovation from the academic setting into a framework for commercialization. The launch of Valted Seq exemplifies this successful type of collaboration and represents a model that D&D is extending to other preeminent universities.

In recent years, D&D has invested more than $7 million in sponsored research at leading medical research institutions to advance potentially game-changing healthcare innovations.

By establishing a set of subsidiaries that cover the full spectrum of screening, diagnosis, therapy and therapeutic monitoring of diseases affecting the central nervous system, D&D is creating synergies that would not otherwise be achievable. Three subsidiaries are enabling a comprehensive Total Care approach to neurodegeneration: Valted Seq is identifying novel biomarkers for diagnosing and screening Parkinsons and Alzheimers disease; Precision Molecular is advancing neuromolecular imaging to identify and/or follow patients for therapies being developed by Neuraly and is developing new imaging biomarkers based on Valted Seq discoveries. The academic founders of these subsidiaries remain deeply engaged with each other and industry experts, enabling D&D to create a continuum from groundbreaking science to innovative pipelines.

About D&D Pharmatech

D&D Pharmatech is a clinical-stage global biotech company that funds the development of revolutionary medicines through disease-specific subsidiary companies founded and guided by top-tier medical research faculty. This corporate structure creates a unique opportunity to accelerate translation of cutting-edge research into lifesaving therapeutic products for patients. The companys product pipeline focuses on a range of indications including neurodegenerative and fibrotic diseases. D&D Pharmatech is the parent company of U.S.-based Neuraly Inc., Theraly Fibrosis Inc., Precision Molecular Inc. and Valted Seq, Inc. For more information, please visit http://www.ddpharmatech.com/

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D&D Pharmatech Announces Launch of Valted Seq Subsidiary Focusing on Discovery of Neurodegenerative Disease Pathways and Biomarkers to Support...