Serving every person in the Summit County community – Summit Daily News

Panorama Summit Orthopedics has moved into its brand new, permanent clinic where it can continue to provide top notch orthopedic care to the entire community in a more spacious setting.

The number one goal of our practice from the start is to take care of this community, and that means all people, said Dr. Aaron Black, a sports medicine and orthopedic trauma specialist at Panorama Summit Orthopedics who has been with the Summit County practice since it opened. We dont turn anybody away. Were a top rate facility thats easily accessible and were here to take care of the entire community.

The entire Panorama Summit Orthopedics team knows and understands that being there for the community means committing to patients by providing same day appointments, timeliness in authorizing procedures, communication, efficiency, friendliness and follow-through, said Amy Manske, director of operations.

We are here for them to help them feel better so they can do more, she said.

Open in Frisco

With the completion of its brand new clinic on School Drive in Frisco, Panorama Summit Orthopedics is now able to offer more appointments and longer hours. This is especially helpful during COVID-19 thanks to a nearly 300% increase in the number of office exam rooms.

We went from seven rooms in the old office to 20, Dr. Black said. This facility also has a lot more space, which gives us a better ability to socially distance.

The new building also offers X-ray imaging and direct access to physical therapy services. Theres a procedure suite focusing on orthopedic biologics such as platelet-rich plasma and stem cell injections, as well as other small in-office procedures.

Its a really beautiful building and a much nicer facility with a lot more space, Dr. Black said of the practices new home.

Inclusive care

Panorama Summit Orthopedics believes that all treatment decisions shouldnt have anything to do with a patients insurance status or ability to pay. Dr. Black said this belief is also how hes ethically driven as a physician.

My goal has never been to look at how people pay, he said. Regardless of where people come from or what they do for a living, I know were taking care of the entire community and trying to make the right decisions for people.

Walk-in OrthoCare Clinic

Panorama Summit Orthopedics offers walk-in services for all orthopedic concerns except for spine (the practice is currently seeking a spine physician to add to its team). All walk-in patients will be seen by one of the clinics orthopedic surgeons.

This is a full orthopedic clinic visit, Dr. Black said. You see a doctor, and were there to perform a full history, imaging, small procedures, casting, splinting and small reductions.

Hours are Monday through Thursday from 4 to 6 p.m.; and 11 a.m. to 6 p.m. on Saturday.

On-site physical therapy

Physical therapy, which is an essential part of orthopaedic patients recovery, is now offered in the same building as the clinic. Dr. Black said just about every physical therapist in the county already has his cell phone number and can call anytime, but this new access adds another dimension to quality care.

Therapists can walk directly over and talk to us about patient questions, he said. If a wound looks funny or theres anything the therapist wants to talk about or show us, we can just walk over and look.

Added safety for staff and patients

Every patient who visits the Frisco clinic will get their temperature taken upon arrival. All patients and staff are required to wear face masks in the clinic (the clinic will provide masks for patients who need them).

Patients will also go straight to a private room to wait for their doctor rather than sit in a waiting room with others, Dr. Black said. All surfaces and equipment are also being frequently sanitized.

Weve done our best to keep everyone away from any interaction that isnt necessary, Dr. Black said. Some of my patients have said this feels like the safest place theyve been to in the county.

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Serving every person in the Summit County community - Summit Daily News

Coronavirus Disease (COVID-19) Impact Global Canine Stem Cell Therapy Market Report Top Companies like VETSTEM BIOPHARMA, Cell Therapy Sciences,…

Global Coronavirus pandemic has impacted all industries across the globe, Canine Stem Cell Therapy market being no exception. As Global economy heads towards major recession post 2009 crisis, Cognitive Market Research has published a recent study which meticulously studies impact of this crisis on Global Canine Stem Cell Therapy market and suggests possible measures to curtail them. This press release is a snapshot of research study and further information can be gathered by accessing complete report. To Contact Research Advisor Mail us @ [emailprotected] or call us on +1-312-376-8303.

The research report on global Canine Stem Cell Therapy market as well as industry is a detailed study that provides detailed information of major key players, product types & applications/end-users; historical figures, region analysis, market drivers/opportunities & restraints forecast scenarios, strategic planning, and a precise section for the effect of Covid-19 on the market. Our research analysts intensively determine the significant outlook of the global Canine Stem Cell Therapy market study with regard to primary & secondary data and they have represented it in the form of graphs, pie charts, tables & other pictorial representations for better understanding.

Allogeneic Stem Cells, Autologous Stem cells are some of the key types of market. All the type segments have been analyzed based on present and future trends and the market is estimated from 2020 to 2027. Based on the application segment, the global market can be classified into Veterinary Hospitals, Veterinary Clinics, Veterinary Research Institutes . The analysis of application segment will help to analyze the demand for market across different end-use industries.

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Amid the COVID-19 pandemic, the industry is witnessing a major change in operations.Some of the key players include VETSTEM BIOPHARMA, Cell Therapy Sciences, Regeneus, Aratana Therapeutics, Medivet Biologics, Okyanos, Vetbiologics, VetMatrix, Magellan Stem Cells, ANIMAL CELL THERAPIES, Stemcellvet . key players are changing their recruitment practices to comply with the social distancing norms enforced across several regions to mitigate the risk of infection. Additionally, companies are emphasizing on using advanced recruiting solutions and digital assets to avoid in-person meetings. Advanced technologies and manufacturing process are expected to play a decisive role in influencing the competitiveness of the market players.

Regional Analysis for Canine Stem Cell Therapy Market: North America (United States, Canada) Europe (Germany, Spain, France, UK, Russia, and Italy) Asia-Pacific (China, Japan, India, Australia, and South Korea) Latin America (Brazil, Mexico, etc.) The Middle East and Africa (GCC and South Africa)

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NOTE: Whole world is experiencing the impact of Covid-19 pandemic due to its increasing spread hence, the report comprises of an up to date scenario of the Canine Stem Cell Therapy market report. Research analyst team of our company is understanding & reviewing the Covid19 Impact on Market and all the necessary areas of the market that have been altered due to the change caused by Covid19 impact. Get in touch with us for more precise/in-depth information of the Canine Stem Cell Therapy market.

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At the end of May, many states began lifting lockdown restrictions and reopening in order to revive their economies, despite warnings that it was still too early. As a result, by mid-July, around 33 states were reporting higher rates of new cases compared to the previous week with only three states reporting declining rates. Due to this Covid-19 pandemic, there has been disruptions in the supply chain which have made end-use businesses realize destructive in the manufacturing and business process. During this lockdown period, the plastic packaging helps the products to have longer shelf life as the public would not be able to buy new replacements for the expired products because most of the production units are closed.

About Us: Cognitive Market Research is one of the finest and most efficient Market Research and Consulting firm. The company strives to provide research studies which include syndicate research, customized research, round the clock assistance service, monthly subscription services, and consulting services to our clients. We focus on making sure that based on our reports, our clients are enabled to make most vital business decisions in easiest and yet effective way. Hence, we are committed to delivering them outcomes from market intelligence studies which are based on relevant and fact-based research across the global market. Contact Us: +1-312-376-8303 Email: [emailprotected] Web: https://www.cognitivemarketresearch.com/

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Coronavirus Disease (COVID-19) Impact Global Canine Stem Cell Therapy Market Report Top Companies like VETSTEM BIOPHARMA, Cell Therapy Sciences,...

Global Stem Cells Market Report, History And Forecast 2020-2027, Breakdown Data By Manufacturers, Key Regions, Types And Application – Bulletin Line

Reportspedia, a prominent market research firm, has published a detailed report on Stem Cells Market. This market research report provides an all-inclusive and detailed study on the market which can probably help an enterprise to identify lucrative opportunities and assist them with manufacturing creative business tactics. The market report provides information about the up-to-date market situation about the global supply and demand, key market trends and prospects in the market, and challenges and threats faced by the industry players.

TheStem Cells Markethas observed huge growth from USD XX million to USD XX million from 2014 to 2020 With the CAGR of X.X%, this Industry is anticipated to reach USD XX million in 2027.

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Top Key Players of Stem Cells Market are:

Neuralstem, Inc. Stempeutics Research Pvt. Ltd. Reneuron Group Plc Mesoblast Neostem Oncology, Llc Pluristem Therapeutics Inc. Stemcells, Inc. Gamida Cell Ltd. Anterogen Co., Ltd. Orthocyte Corporation Pharmicell Co., Ltd. Apceth GmbHCompany KG Ocata Therapeutics, Inc. U.S. Stem Cell, Inc. (Bioheart) Medipost Co., Ltd. Biotime, Inc. Cell Cure Neurosciences Ltd.

The research revision comprises the market drivers, current as well as future growth opportunities, segment-wise, and region wise challenges faced by Stem Cells Market, competitive scenario in the global market. The regional landscape of the report covers market size and comparison of regions namely, North America, Europe, Asia Pacific (APAC), Middle East, and Africa (MEA), and Latin America.

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Types of Stem Cells covered are:

Adult Stem Cell Human Embryonic Stem Cell Induced Pluripotent Stem Cell Rat Neural Stem Cell Other

Applications of Stem Cells covered are:

Drug Discovery and Development Stem Cells Regenerative Medicine

Thus, the report takes a dashboard view of an entire Stem Cells Market by widely studying market conditions and situations and the numerous actions of leading players in the market such as mergers, partnerships, and achievements. This exclusive report explains the present industry situations that give a clear picture of the global Stem Cells Market to the clients. The thorough database which has given in this report helps the customers to get detailed information about the Stem Cells. It is the most substantial influence in any report to provide client/s information and Reportspedia committedly follows this basic principle of the market research industry.

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Global Stem Cells Market Report, History And Forecast 2020-2027, Breakdown Data By Manufacturers, Key Regions, Types And Application - Bulletin Line

New DNA Recovery Technique Reveals Richer Picture of the Past – Lab Manager Magazine

Tyler Murchie, a PhD candidate in the Department of Anthropology and a lead author of the study.

Emil Karpinski, McMaster University

Researchers at McMaster University have developed a new technique to tease ancient DNA from soil, pulling the genomes of hundreds of animals and thousands of plantsmany of them long extinctfrom less than a gram of sediment.

The DNA extraction method, outlined in the journalQuarternary Research, allows scientists to reconstruct the most advanced picture ever of environments that existed thousands of years ago.

The researchers analyzed permafrost samples from four sites in the Yukon, each representing different points in the Pleistocene-Halocene transition, which occurred approximately 11,000 years ago.

This transition featured the extinction of a large number of animal species such as mammoths, mastodons, and ground sloths, and the new process has yielded some surprising new information about the way events unfolded, say the researchers. They suggest, for example, that the woolly mammoth survived far longer than originally believed.

In the Yukon samples, they found the genetic remnants of a vast array of animals, including mammoths, horses, bison, reindeer, and thousands of varieties of plants, all from as little as 0.2 grams of sediment.

The Klondike region in the Yukon, where the permafrost samples containing sediment DNA, were collected.

Tyler Murchie, McMaster University

The scientists determined that woolly mammoths and horses were likely still present in the Yukon's Klondike region as recently as 9,700 years ago, thousands of years later than previous research using fossilized remains had suggested.

"That a few grams of soil contains the DNA of giant extinct animals and plants from another time and place, enables a new kind of detective work to uncover our frozen past," says evolutionary geneticist Hendrik Poinar, a lead author on the paper and director of the McMaster Ancient DNA Centre. "This research allows us to maximize DNA retention and fine-tune our understanding of change through time, which includes climate events and human migration patterns, without preserved remains."

The technique resolves a longstanding problem for scientists, who must separate DNA from other substances mixed in with sediment. The process has typically required harsh treatments that actually destroyed much of the usable DNA they were looking for. But by using the new combination of extraction strategies, the McMaster researchers have demonstrated it is possible to preserve much more DNA than ever.

"All of the DNA from those animals and plants is bound up in a tiny speck of dirt," explains Tyler Murchie, a PhD candidate in the Department of Anthropology and a lead author of the study.

"Organisms are constantly shedding cells throughout their lives. Humans, for example, shed some half a billion skin cells every day. Much of this genetic material is quickly degraded, but some small fraction is safeguarded for millenia through sedimentary mineral-binding and is out there waiting for us to recover and study it. Now, we can conduct some remarkable research by recovering an immense diversity of environmental DNA from very small amounts of sediment, and in the total absence of any surviving biological tissues."

- This press release was originally published onMcMaster University's Brighter World website

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New DNA Recovery Technique Reveals Richer Picture of the Past - Lab Manager Magazine

The Tax Watchers: How would you spend other people’s money? – Fairfield Daily Republic

Gay Eckman, The Tax Watchers

We are being asked in November to approve Proposition 14 an issue of $5.5 billion in general obligation bonds for California Stem Cell Research, Treatments and Cures.

Californians approved Proposition 71 for $3 billion in bonds in 2004 and the creation of the California Institute of Regenerative Medicine. The institutes appointed board members are charged with reviewing stem cell research and therapy proposals and selecting who will receive grants and for how much. This board also has the responsibility to oversee those grants. Operation of the institute itself technically has no oversight at all.

Proposition 14 is essentially a continuation of Proposition 71, which is out of money.

Robert Klein II, a staunch advocate for stem cell research whose personal fortune came from real estate, was the principal author of Proposition 71, and even though he now serves only in an advisory capacity to the California Institute of Regenerative Medicine, has once again authored Proposition 14 of 2020. Simply speaking Proposition 14 of 2020 is a continuation and mark-up of what the voters approved in 2004.

Klein, like many others back in 2004, believed embryonic stem cells might provide a miracle cure for almost everything. The federal government however had placed severe restrictions on the lines of embryonic stem cells available for research. But as a shrewd businessman, he could avoid these restrictions with a California project and could use the California initiative process to leverage millions of his own into billions of public dollars in support of this cause.

Klein claimed the advances made through his initiative would be self-supporting by stipulating a portion of receipts earned from the cures would be returned to the states general fund in 15 years and for about $5 billion of Californians money (including interest to bond holders), the general fund has received $352,560. Not a single federally approved therapy has resulted from stem cell science from the institute under Proposition 71.

Federal restrictions on embryonic stem cell research pertinent to drafting of Proposition 71 in 2004 were totally eliminated in 2009. Harnessing the hoped-for potential of stem cells remains elusive, and according to the Food and Drug Administration, these therapies do include risks. Stem cell research will not end . . . the National Institutes of Health and myriad charities aligned with specific diseases or conditions will continue with stem cell research. Their knowledge is more focused and better suited to solve these problems and utilizes the best medical science worldwide, including California scientists.

If Proposition 14 passes, California voters are risking $5.5 billion plus bond interest that could have been used for immediate needs such as education, housing and medical care. General obligation commitments take precedence over other funds we would like to spend or possibly even take away from what we planned to spend.

Do not be fooled again. Vote no on Proposition 14.

Gary Eckman is a member of the Central Solano Citizens/Taxpayer Group.

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The Tax Watchers: How would you spend other people's money? - Fairfield Daily Republic

Global Stem Cell Reconstructive Market- Industry Analysis and Forecast (2020-2027) – Kewaskum Statesman News Journal

Global Stem Cell Reconstructive Marketwas valued US$ XX Mn in 2019 and is expected to reach US$ XX Mn by 2027, at a CAGR of 24.5% during a forecast period.

Market Dynamics

The Research Report gives an in-depth account of the drivers and restraints in the stem cell reconstructive market. Stem cell reconstructive surgery includes the treatment of injured or dented part of body. Stem cells are undifferentiated biological cells, which divide to produce more stem cells. Growing reconstructive surgeries led by the rising number of limbs elimination and implants and accidents are boosting the growth in the stem cell reconstructive market. Additionally, rising number of aged population, number of patients suffering from chronic diseases, and unceasing development in the technology, these are factors which promoting the growth of the stem cell reconstructive market. Stem cell reconstructive is a procedure containing the use of a patients own adipose tissue to rise the fat volume in the area of reconstruction and therefore helping 3Dimentional reconstruction in patients who have experienced a trauma or in a post-surgical event such as a mastectomy or lumpectomy, brain surgery, or reconstructive surgery as a result of an accident or injury. Stem cell reconstructive surgeries are also used in plastic or cosmetic surgeries as well. Stem cell and regenerative therapies gives many opportunities for development in the practice of medicine and the possibility of an array of novel treatment options for patients experiencing a variety of symptoms and conditions. Stem cell therapy, also recognised as regenerative medicine, promotes the repair response of diseased, dysfunctional or injured tissue using stem cells or their derivatives.

The common guarantee of all the undifferentiated embryonic stem cells (ESCs), foetal, amniotic, UCB, and adult stem cell types is their indefinite self-renewal capacity and high multilineage differentiation potential that confer them a primitive and dynamic role throughout the developmental process and the lifespan in adult mammal. However, the high expenditure of stem cell reconstructive surgeries and strict regulatory approvals are restraining the market growth.

The report study has analyzed revenue impact of covid-19 pandemic on the sales revenue of market leaders, market followers and disrupters in the report and same is reflected in our analysis.

Global Stem Cell Reconstructive Market Segment analysis

Based on Cell Type, the embryonic stem cells segment is expected to grow at a CAGR of XX% during the forecast period. Embryonic stem cells (ESCs), derived from the blastocyst stage of early mammalian embryos, are distinguished by their capability to distinguish into any embryonic cell type and by their ability to self-renew. Owing to their plasticity and potentially limitless capacity for self-renewal, embryonic stem cell therapies have been suggested for regenerative medicine and tissue replacement after injury or disease. Additionally, their potential in regenerative medicine, embryonic stem cells provide a possible another source of tissue/organs which serves as a possible solution to the donor shortage dilemma. Researchers have differentiated ESCs into dopamine-producing cells with the hope that these neurons could be used in the treatment of Parkinsons disease. Upsurge occurrence of cardiac and malignant diseases is promoting the segment growth. Rapid developments in this vertical contain protocols for directed differentiation, defined culture systems, demonstration of applications in drug screening, establishment of several disease models, and evaluation of therapeutic potential in treating incurable diseases.

Global Stem Cell Reconstructive Market Regional analysis

The North American region has dominated the market with US$ XX Mn. America accounts for the largest and fastest-growing market of stem cell reconstructive because of the huge patient population and well-built healthcare sector. Americas stem cell reconstructive market is segmented into two major regions such as North America and South America. More than 80% of the market is shared by North America due to the presence of the US and Canada.

Europe accounts for the second-largest market which is followed by the Asia Pacific. Germany and UK account for the major share in the European market due to government support for research and development, well-developed technology and high healthcare expenditure have fuelled the growth of the market. This growing occurrence of cancer and diabetes in America is the main boosting factor for the growth of this market.

The objective of the report is to present a comprehensive analysis of the Global Stem Cell Reconstructive Market including all the stakeholders of the industry. The past and current status of the industry with forecasted market size and trends are presented in the report with the analysis of complicated data in simple language. The report covers all the aspects of the industry with a dedicated study of key players that includes market leaders, followers and new entrants. PORTER, SVOR, PESTEL analysis with the potential impact of micro-economic factors of the market has been presented in the report. External as well as internal factors that are supposed to affect the business positively or negatively have been analysed, which will give a clear futuristic view of the industry to the decision-makers.

The report also helps in understanding Global Stem Cell Reconstructive Market dynamics, structure by analysing the market segments and projects the Global Stem Cell Reconstructive Market size. Clear representation of competitive analysis of key players by Application, price, financial position, Product portfolio, growth strategies, and regional presence in the Global Stem Cell Reconstructive Market make the report investors guide. Scope of the Global Stem Cell Reconstructive Market

Global Stem Cell Reconstructive Market, By Sources

Allogeneic Autologous o Bone Marrow o Adipose Tissue o Blood Syngeneic Other Global Stem Cell Reconstructive Market, By Cell Type

Embryonic Stem Cell Adult Stem Cell Global Stem Cell Reconstructive Market, By Application

Cancer Diabetes Traumatic Skin Defect Severe Burn Other Global Stem Cell Reconstructive Market, By End-User

Hospitals Research Institute Others Global Stem Cell Reconstructive Market, By Regions

North America Europe Asia-Pacific South America Middle East and Africa (MEA) Key Players operating the Global Stem Cell Reconstructive Market

Osiris Therapeutics NuVasives Cytori Therapeutics Takeda (TiGenix) Cynata Celyad Medi-post Anterogen Molmed Baxter Eleveflow Mesoblast Ltd. Micronit Microfluidics TAKARA BIO INC. Tigenix Capricor Therapeutics Astellas Pharma US, Inc. Pfizer Inc. STEMCELL Technologies Inc.

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Global Stem Cell Reconstructive Market- Industry Analysis and Forecast (2020-2027) - Kewaskum Statesman News Journal

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

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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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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