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Stem Cell Treatment Seen to Safely Aid Speech in ALS Patients in… – ALS News Today

Stem cells collected from a patients bone marrow and infused into the spinal fluid safely improved speaking abilities after 28 daysfor most of the 12 adults with amyotrophic lateral sclerosis (ALS) evaluated in a small study.

Its researchers recommend further investigation of this approach in treatingspeech difficultiesin ALS, a common and early symptom of this neurological disease that is known as dysarthria.

The study, Articulation recovery in ALS patients after lineage negative adjuvant cell therapy preliminary report, was published in the International Journal of Medical Sciences.

Current treatments for speech disorders in ALS, which is marked by the deterioration of nerve cells that control voluntary muscle movement (motor neurons), are medicines to ease muscle weakness, tongue twitching, and excess salivation, as well as speech therapy support.

Despite widespread use of these approaches, treatments that address speech problems in ALS are still limited.

The administration of stem cells isolated from a patient then used as a treatment in that same person (autologous) may help to trigger the release of neurological growth factors, called neurotrophic factors, provide support for motor neurons, and slow disease progression.

Researchers atPomeranian Medical University in Poland conducted an open-label, Phase 1 clinical trial (NCT02193893) in 12 ALS patients, four women and eight men, between the ages of 21 and 65.

Bone marrow was collected from each person, and stem cells then isolated to include only lineage-negative cells (LIN-). These are immature stem cells and progenitor cells that have not yet become functioning blood cells.

The LIN- cells were returned to each patient via an infusion into the cerebrospinal fluid (CSF, the liquid that surrounds the brain and spinal cord) of the lumbar vertebrae of the lower spine.

Before the procedure, and 28 days after, patients were evaluated for speech using the Frenchay Dysarthria Assessment (FDA), a standardized test that relies on a nine-point rating scale, measuring oral structure, function, and speech.

CSF was collected to measure levels of various neurotrophic factors and pro-inflammatory proteins, both before cell infusion and 28 days later.

Two particular factors nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF) were tested in patients blood on the day of the infusion, and three and seven days later, and again at three months.

Of note, neurotrophicfactors are signaling molecules that play an important role in the survival and growth of nerve cells.

Based on their FDA scores, patients were divided into two groups: group 1 was composed of eight patients who improved in five or more speech measures; the four patients in group 2 did not show such improvement.

Patients in group 1 were older (average age of 55.8), and had a shorter disease duration (average of 2.6 years), the researchers noted.

Compared to baseline (study start) measurements, seven out of the eight group 1 patients had marked improvements in phonation time the time a person can say a vowel. Lip performance was enhanced in six people in group 1, and palate functioning and voice loudness improved in five of these patients.

Improvements were found in about 54% of the analyzed speech functions among group 1 patients, and 35% of those in group 2.

It is noteworthy that tongue mobility was the only articulatory function that did not improve in all 12 patients, the researchers wrote.

No significant pre- and post-treatment differences were seen in pro-inflammatory proteins in the CSF of either group. However, one such protein, called C3, was almost two times higher in group 2 patients at the studys start.

At 28 days after the procedure, lower levels of the inflammation marker C-reactive protein in the CSF, particularly in group 1 patients, were found.

Baseline concentrations of the neurotrophic factor BDNF and ofplatelet-derived growth factor alpha (PDGF-AA) were higher in group 1 patients compared with group 2. At 28 days post-treatment, however, group 1 patients showed a significant decrease in concentrations of BDNF, PDGF-AA, andangiopoietin 2 (ANGP-2), and a downward trend in VEGF-A. No significant differences were found among those in group 2.

Growth factors are signaling molecules that, among other things, arecapable of stimulating cell proliferation and differentiation.

It remains unclear why, in parallel with the improvement of articulation, a statistically significant decrease in neurotrophins concentration was observed, the researchers wrote.

BDNF blood levels in both groups reached were highest two to three days after the infusion, then steadily decreased. The nerve growth factor (NGF) followed a similar pattern in group 2 patients. No difference in the levels of BDNF and NGF were found between these groups.

The outcomes of the LIN- cell application in ALS treatment of articulatory organs are promising, the researchers wrote, and proved to be both safe and feasible.

A short-lasting trophic effect of autologous LIN- administration could encourage repeated [cell] application in order to sustain their beneficial effects, however this approach needs further investigation, they added.

Steve holds a PhD in Biochemistry from the Faculty of Medicine at the University of Toronto, Canada. He worked as a medical scientist for 18 years, within both industry and academia, where his research focused on the discovery of new medicines to treat inflammatory disorders and infectious diseases. Steve recently stepped away from the lab and into science communications, where hes helping make medical science information more accessible for everyone.

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Ana holds a PhD in Immunology from the University of Lisbon and worked as a postdoctoral researcher at Instituto de Medicina Molecular (iMM) in Lisbon, Portugal. She graduated with a BSc in Genetics from the University of Newcastle and received a Masters in Biomolecular Archaeology from the University of Manchester, England. After leaving the lab to pursue a career in Science Communication, she served as the Director of Science Communication at iMM.

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Stem Cell Treatment Seen to Safely Aid Speech in ALS Patients in... - ALS News Today

Study Evaluates Diagnostic Value of the Karius Test for Pneumonia in Immunocompromised Patients – OncoZine

Immunocompromised patients are generally at high risk of Invasive Fungal Infections (IFI), potentially leading to diseases like pneumonia, an infection in the lungs which can be caused by a fungus, bacteria, or viral infection.

Pneumonia is a major cause of morbidity and mortality in these individuals and this may especially be the case in patients with hematological malignancies undergoing remission-induction chemotherapy for acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) and recipients of allogeneic hematopoietic stem cell transplants (HSCT).[1]

Although new treatment options have become available to treat patients with cancer and hematological malignancies, Invasive Fungal Infections remain a major concern due to the increased potential of morbidity and mortality in these patient populations.

The effects of novel anti-cancer agents Although a growing number of new immune-modulating drugs has shown to advance the treatment of patients with cancer, some of these agents have also attribute to the increase of risk for Invasive Fungal Infections. This increased risk may especially be seen in patients treated with tyrosine kinase inhibitors (TKI), in particular inhibitors of Bruton tyrosine kinase (BTK) mammalian target of rapamycin (mTOR) Janus kinase (JAK) and phosphatidylinositol 3 kinases (PI3K) delta.[1]

Inhibition of immune checkpoints, such as programmed cell death protein 1 (PD1) or cytotoxic T lymphocyte-associated protein 4 (CTLA4) may show a wide-ranging of mostly immune-related adverse events. Subsequent immunosuppression, primarily including corticosteroids, may, in turn, result in the development of opportunistic infections including fungi, requiring optimizing the management of immune-related adverse events.[1]

Diagnostic failure Immunocompromised patients can be infected by a broad range of potential pathogens. However, in many cases, diagnostic testing fails to identify a microbial etiology for lower respiratory illness even with bronchoalveolar lavage (BAL).

Studies have shown that culture methods, PCR, and antigen testing on BAL samples only yields a positive result of 30-67% of the time. In addition, Idiopathic Pulmonary Syndrome (IPS), a non-infectious pulmonary complication of transplants, can have many overlapping symptoms with infectious pneumonia. Treatment for IPS is the administration of steroids which can exacerbate infections. As a result, there is a major unmet medical need for better diagnostics to aid in the management of immunocompromised patients with pneumonia.

Clinical evaluation Karius, a life sciences company focused on generating genomic insights for infectious diseases, has developed a microbial cell-free plasma next-generation sequencing test for pathogen detection capable of detecting >1,000 organisms. The test is performed in a CLIA-certified/CAP-accredited laboratory with results typically provided within one day from sample receipt.

To understand the increased risk and to improve the timely diagnosis of pneumonia in immunocompromised adult patients, including those with hematological cancers, Karius, in collaboration withDuke Clinical Research Institute, has launched a multicenter, prospective study designed to evaluate the diagnostic value of the Karius Test.

The test developed by Karius is a non-invasive liquid biopsy, based on next-generation sequencing of microbial cell-free DNA that can rapidly detect over 1,000 bacteria, DNA viruses, fungi, and parasites. The test helps clinicians make rapid, treatment decisions and is currently being used by over 100 hospitals nationwide by mapping each patients microbial landscape from a single blood draw.

Diagnostic yield Given the medical need, the clinical evaluation will compare the diagnostic yield of the Karius Test to standard testing methods used to diagnose infectious causes of pneumonia in immunocompromised patients including those with hematological cancers.

Patients with suppressed immune systems are especially vulnerable to life-threatening pneumonia due to their decreased ability to fight infections. Standard methods to diagnose pneumonia can be invasive, time-consuming, often requiring weeks to months for a result, and in some cases inconclusive, failing to identify the pathogen causing the infection.

The PICKUP study (NCT04047719) will investigate the additive diagnostic value of the Karius Test in the diagnosis of pneumonia in these patients and its impact on clinical decision-making in this specific population. In addition, the Karius Test will be used to serially monitor pathogen levels during treatment to examine the association between microbial load and pneumonia progression.

The ability to diagnose invasive life-threatening infections in immunocompromised patients has been one of the most challenging areas in clinical infectious disease practice, noted Mickey Kertesz, Chief Executive Office of Karius.

We are enthusiastic to be collaborating with a number of leading cancer centers for this study and anticipate that the Karius Test will demonstrate a higher diagnostic yield than traditional invasive testing methods, Kertesz added

Unknown causative pathogen Often in pneumonia, the causative pathogen is unknown or can be challenging to diagnose despite extensive diagnostic testing, explained Stephen P. Bergin, M.D., Assistant Professor of Pulmonary and Critical Care Medicine at Duke University Health System and lead investigator for the PICKUP study.

Accurate and timely pathogen identification is particularly critical for immunocompromised patients who are susceptible to life-threatening infections from a much broader array of pathogens. We look forward to exploring the potential value of a non-invasive tool capable of rapidly diagnosing respiratory infections in this vulnerable population, Bergin concluded.

Overcoming limitations Previous studies have demonstrated the ability of the Karius Test to overcome many of these limitations to diagnose the cause of pneumonia and enable targeted treatment.

The PICKUP study will include approximately 200 patients from up to 10 centers in the United States, including Duke University Health, University of Pittsburgh Medical Center, Fred Hutchinson Cancer Research Center, The University of Texas MD Anderson Cancer Center, City of Hope, Tulane Cancer Center and Tulane Medical Center and The University of California, San Francisco Medical Center.

Clinical trials Pneumonia in the ImmunoCompromised Use of the Karius Test for the Detection of Undiagnosed Pathogens (PICKUP) NCT04047719

Reference [1] Mellinghoff SC, Panse J, Alakel N, et al. Primary prophylaxis of invasive fungal infections in patients with hematological malignancies: 2017 update of the recommendations of the Infectious Diseases Working Party (AGIHO) of the German Society for Haematology and Medical Oncology (DGHO). Ann Hematol. 2018;97(2):197-207. doi:10.1007/s00277-017-3196-2

Featured image: Karius laboratory. Photo courtesy: 2020 Karius. Used with permission.

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Study Evaluates Diagnostic Value of the Karius Test for Pneumonia in Immunocompromised Patients - OncoZine

Incyte/Morphosys take on CAR-Ts with $198,000 per year antibody – – pharmaphorum

Incyte and Morphosys Monjuvi antibody therapy has been approved for certain patients with lymphoma, as the companies hope to provide a more convenient alternative to expensive and cumbersome CAR-T therapy.

At the beginning of the year Incyte paid $750m to Morphosys for the CD-19 targeting antibody, which has been approved in combination with BMS Revlimid (lenalidomide) for adults with relapsed or refractory diffuse large B-cell lymphoma not otherwise specified.

The indication also covers DLBCL arising from low grade lymphoma and patients not eligible for autologous stem cell transplant.

Monjuvi (tafasitamab) targets the CD-19, a protein on the surface of B-cells that is also targeted by Amgens bispecific antibody Blincyto (blinatumomab) for acute lymphoblastic leukaemia (ALL), as well as two CAR-T therapies Novartis Kymriah (tisagenlecleucel) and Gileads Yescarta (axicabtagene ciloleucel) that are already approved for DLBCL and other B-cell cancers.

Under the agreement with Morphosys the companies will co-market the drugs in the US, while Incyte has exclusive rights outside the US.

The deal with Morphosys could see Incyte pay up to $1.1 billion should certain targets be achieved.

Xencor, which developed the drug before licensing it to Morphosys in 2010, will receive a $25 million milestone payment and a royalty on worldwide net sales.

Before any rebates or discounts Monjuvis wholesale price will average $16,500 per month in the first year of therapy, followed by an average of $13,000 per month in subsequent years because of a decrease in the required number of doses per cycle.

At around $198,000 for the first year this is pricey but may work out as less expensive than CAR-Ts from Novartis and Gilead, depending on how long patients stay on treatment.

CAR-Ts cost $373,000 in adult DLBCL for a single shot of the cell therapy.

CAR-Ts can be highly effective, producing a complete response in about a third of patients, but are made by harvesting a patients own cells and modifying them to fight cancer a lengthy process that might not appeal to all patients.

There are also dangerous side-effects with CAR-Ts, where doctors often have to manage cytokine storms where the immune system goes into overdrive and begins to attack a patients own body.

The FDA approval of Monjuvi was based on data from the MorphoSys-sponsored phase 2 L-MIND study, an open label, multicentre, single arm trial of Monjuvi in combination with lenalidomide as a treatment for adult patients with relapsed or refractory DLBCL.

Results from the study showed an overall response rate of 55%, including a complete response rate of 37% and a partial response rate of 18%.

Warnings and precautions for Monjuvi included infusion-related reactions, serious or severe myelosuppression (including neutropenia (50%), thrombocytopenia (18%), and anemia (7%)), infections (73%) and embryo-foetal toxicity. Neutropenia led to treatment discontinuation in 3.7% of patients.

This accelerated approval may depend on further confirmatory data from larger trials.

Updated to include pricing information

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Incyte/Morphosys take on CAR-Ts with $198,000 per year antibody - - pharmaphorum

Crowdfunding to the rescue for this cancer patient – Telangana Today

New Delhi: Cancer takes innumerable lives each year, and so does the unavailability of cancer treatment due to lack of funds. 33-year-old Nushafreen Palsetia, a software engineer based in Mumbai, was recently diagnosed with a very aggressive form of cancer. Despite a relapse, what helped was life-saving support pouring from over 1,700 donors.

Nushafreen was first diagnosed with Non-Hodgkin Lymphoma in April 2019. After a year of enduring aggressive treatment, she tried to get back to her normal life and work. Unfortunately, Non-Hodgkin Lymphoma, Diffuse Large B Cell Lymphoma (DLBCL), cancer relapsed in her liver in May 2020 which was an unexpected major shock, leaving her and all of her family overwhelmed.

Doctors planned to perform an autologous (her own stem cells) bone marrow transplant in India after the chemotherapy but further tests showed involvement of the bone marrow as well. Hence, her treating doctor recommended the modern CAR-T Cell therapy treatment, available only in the USA, UK, Israel, and a few European countries.

Nushafreens family found Israel as the most affordable option as compared to all other countries offering the treatment. They reached out to Sheba Medical Centre in Israel which estimated the medical expenses as 200,000 USD (approximately Rs 1.5 crore). The treatment will require Nushafreen to be hospitalized for a month or more for the response to treatment and immediate follow up.

As Nushafreens family couldnt afford the high medical expenses, an ImpactGuru crowdfunding campaign was initiated. In two weeks, Nushafreens ImpactGuru.com Page has raised over Rs 1 crore from 1750 donors. The platform raises money online for medical expenses via crowdfunding such as cancer, transplants, and accidents.

According to the co-founder and CEO of the healthcare crowdfunding platform, Piyush Jain, Crowdfunding is driven by a culture of generosity, it allows people to raise money quickly in a hassle free manner without any payback liability. This is a new record for our platform with a single patients family being able to raise more than Rs 1 crore. We hope Nushafreen recovers soon and more patients come forward to utilize our platform in their time of need to get the best available treatment for critical illnesses.

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Crowdfunding to the rescue for this cancer patient - Telangana Today

Global Stem Cell Reconstructive Market- Industry Analysis and Forecast (2020-2027)-by Sources, Cell Type, Application, End User and Region. – WOLE TV

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)-by Sources, Cell Type, Application, End User and Region. - WOLE TV

US Parkinsons disease treatment Market set to grow with massive rate by 2020 to 2025 – Galus Australis

Global Parkinsons disease treatment Market Research Report 2020: COVID-19 Outbreak Impact Analysis

The Parkinsons disease treatment market research report drafted by Brand Essence Market Research elucidates relevant market and competitive insights as well as regional and consumer information. In a nutshell, the research study covers every pivotal aspect of this business sphere that influences the existing trends, profitability position, market share, market size, regional valuation, and business expansion plans of key players in the Parkinsons disease treatment market.

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Global Parkinsons disease treatment Market: Global Size, Trends, Competitive, Historical & Forecast Analysis, 2018-2024. Scope of Global Parkinsons disease treatment Market Reports

Parkinsons disease is a neuro degenerative disorder in which parts of the brain become progressively damaged over many years. It is a type of movement disorder. It occurs when nerve tissue unable to produce a chemical named Dopamine which is used to send signals that help you move your body. Parkinsons disease usually developed for aged people i.e. above 60 years, but it can also start earlier. It is more common in men than in women. The cause of Parkinsons disease is unknown, but researchers think that both genetic and environmental factors are involved. Primary symptoms include tremors, Stiffness, Slowness, impaired balance, mild memory & Thinking problem and shuffling gait. Secondary symptoms include Anxiety, Depression, Fatigue, Low blood pressure, muscle cramp, Speech & communication problem, skin & Dental Problem and Dizziness, and Dementia. Risk of Parkinsons disease increases with age and the disease mainly affects person over 50 years of age.

The development of Parkinsons disease and the degree of destruction differ from person to person. Many people with Parkinsons disease live long productive lives, whereas others become disabled much more quickly. As symptoms worsen, it may become difficult to walk, talk, and complete simple tasks. Malnutrition and weight maintenance is common problem for people with Parkinsons disease. There is no test to diagnose Parkinsons disease with certainty. Treatment options include medication or surgical treatment. Combination of Levodopa with carbidopa is considered as a gold standard for symptomatic treatment of Parkinsons disease. Surgical treatment options include deep brain stimulation and Carbidopa/levodopa enteral suspension therapy but surgical therapy is effective only for patients who have previously responded to Levodopa therapy. Commercially available drugs for treatment of Parkinsons disease are Sinemet, Safinamide, Rotigotine, Ropinirole, Pramiprexol, Amantidine, Cycloset, Parlodel (Bromocriptine Mesylate), Rytary, Azilect, Northera, Stalevo, Comtess/Comtan and others. More than past decade, huge improvement has been made in the treatment of Parkinsons disease such as identification of new therapeutic targets through genetic research, understanding the common mutations that contribute to Parkinsons disease etc.

Global Parkinsons diseases Treatment Market report is segmented on the basis of Medication, Medical devices, End user, Distribution Channels and Geography. Based on Medication Global Parkinsons disease Treatment Market is classified into Dopamine Precursors, Peripheral Decarboxylase Inhibitors, COMT (Catechol-O-methyltransferase) Inhibitors, MAO (Monoamine Oxidase), Inhibitors and Others (anticholinergics, antihistaminics etc.)

On the basis of Medical Devices Global Parkinsons disease Treatment Market is classified into Deep Brain Stimulation (DBS) Devices, Carbidopa/Levodopa Enteral Suspension (Duopa) delivery devices and others. On the basis of End User Global Parkinsons disease Treatment Market is classified into Hospitals, Homecare setting, Clinics and Others. On the basis of Distribution Channel Global Parkinsons disease Drug Market is classified into Retail Pharmacies, Online Pharmacies, Hospital Pharmacies and Drug Stores.

The regions covered in Global Parkinsons diseases Treatment Market report are North America, Europe, Asia-Pacific and Rest of the World. On the basis of country level, Global Melanoma Drug Market sub divided in to U.S., Mexico, Canada, U.K., France, Germany, Italy, China, Japan, India, South East Asia, GCC, Africa, etc.

Key Players for Global Parkinsons disease treatment Market Reports

Global Parkinsons disease Treatment Market reports cover prominent players like Teva Pharmaceuticals, AstraZeneca, Novartis AG, Boehringer Ingelheim, GlaxoSmithKline Plc., Salix Pharmaceuticals, mpax Laboratories, Orion Corporation, Mylan N.V., Cipla Inc., Daiichi Sankyo, Apotex Inc, Impax Laboratories, Lundbeck, Sun Pharma, Wockhardt ,UCB, Valeant Pharmaceuticals Acadia, Abbvie, Zydus Cadilla, Strides, 1 A Pharma, Upsher-Smith, Intas, US World Meds, Dr. Reddys, Medtronic plc, Biotie Therapies Corp., Adamas Pharmaceuticals Inc., Akorn Inc., Astellas Pharma Inc., Desitin Arzneimittel GmbH, Endo International plc, Kyowa Hakko Kirin, Newron Pharmaceuticals and Merck.

Global Parkinsons disease treatment Market Dynamics

Global Parkinsons disease Treatment Market is mainly driven by growing prevalence of Parkinsons disease and government funding for research on Parkinsons disease. The increase in number of geriatric population and technological advancements such as combination therapies for prolong action of continuous dopaminergic stimulation drugs, gene therapy, neural transplantation are few other causes which are possible to boost the Parkinsons disease Treatment market. However some restraints like availability of alternative treatments is expected to hold back market and expiry of patents for several drugs such as Stalevo, Azilect, Rytary, Comtan etc. can cause the termination of Parkinsons disease Treatment market. High cost of treatment such as 14.4 Billion USD and lack of expertise for early diagnosis is likely to restrict the market growth.

Also lack of novel and successful therapies in the market to reduce the risk of mortality restraints for this market. The opportunities for Global Parkinsons disease Treatment market includes upcoming technologies like surface EMG (Electromyography) sensors, Pulse oximetry sensors, development in personalized medicine along with huge investment in anti-Parkinsons drugs research will boost the global Parkinsons disease Treatment market. Also development of novel drugs and combination therapy with less side effects and better survival rates is expected to increase the global Parkinsons disease Treatment market.

Global Parkinsons disease treatment Market Regional Analysis

Europe is likely to achieve the largest share of the global Parkinsons disease treatment market, which is expected to be followed by North America with a sizeable market share. High knowledge about the treatment, increase in expenditure for Research & Development, favorable medicinal reimbursement regulations and policies, the high occurrence of Parkinsons disease, the rapidly growing geriatric population and potential medical pipeline products are likely to contribute to the major share of Europe in Global Parkinsons disease treatment market. The global Parkinsons disease treatment market in the Asia Pacific is anticipated to develop at a profitable rate. The market share of the global Parkinsons disease treatment market is to be expected to grasp by China and Japan in the Asia Pacific, due to the large population of elderly people who are affected with Parkinsons disease.

Furthermore, increase in awareness of disease and government initiatives for improving health care facilities are expected to boost the regional market to a certain extent.

Key Benefits for Global Parkinsons disease treatment Market Reports

Global Parkinsons disease Treatment Market report covers in depth historical and forecast analysis. Global Parkinsons disease Treatment Market research report provides detail information about Market Introduction, Market Summary, Global market Revenue (Revenue USD), Global market sale (K Units), Global market Drivers, Market Restraints, Market opportunities, Competitive Analysis, Regional and Country Level. Global Parkinsons disease Treatment Market report helps to identify opportunities in market place. Global Parkinsons disease Treatment Market report covers extensive analysis of emerging trends and competitive landscape. Global Parkinsons disease treatment Market Segmentation

Global Parkinsons disease Treatment Market: By Medication Analysis

Dopamine Precursor Peripheral Decarboxylase Inhibitors COMT (Catechol-O-methyltransferase) Inhibitors MAO(monoamine oxidase) Inhibitors Others (anticholinergics, antihistaminics etc.) Global Parkinsons disease Treatment Market: By Medical Devices Analysis

Deep Brain Stimulation (DBS) Devices Carbidopa/Levodopa Enteral Suspension (Duopa) delivery devices Others Global Parkinsons disease Treatment Market: By End User Analysis

Hospitals Clinics Homecare setting Others Global Parkinsons disease Treatment Market: By Distribution Channel

Retail Pharmacies Online Pharmacies Hospital Pharmacies Drug Store Global Parkinsons disease Treatment Market: By Regional & Country Analysis

North America U.S. Mexico Canada Europe UK France Germany Italy Asia Pacific China Japan India Southeast Asia Latin America Brazil The Middle East and Africa GCC Africa Rest of Middle East and Africa

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Our industry professionals are working reluctantly to understand, assemble and timely deliver assessment on impact of COVID-19 disaster on many corporations and their clients to help them in taking excellent business decisions. We acknowledge everyone who is doing their part in this financial and healthcare crisis.

The Essential Content Covered in the GlobalParkinsons disease treatment Market Report:

* Top Key Company Profiles. * Main Business and Rival Information * SWOT Analysis and PESTEL Analysis * Production, Sales, Revenue, Price and Gross Margin * Market Share and Size

The report provides a 6-year forecast (2020-2026) assessed based on how the Parkinsons disease treatment market is predicted to grow in major regions like USA, Europe, Japan, China, India, Southeast Asia, South America, South Africa, Others.

Strategic Points Covered in TOC:

Chapter 1:Introduction, market driving force product scope, market risk, market overview, and market opportunities of the global Parkinsons disease treatment market.

Chapter 2:Evaluating the leading manufacturers of the global Parkinsons disease treatment market which consists of its revenue, sales, and price of the products.

Chapter 3: the competitive nature among key manufacturers, with market share, revenue, and sales.

Chapter 4:Presenting global Parkinsons disease treatment market by regions, market share and revenue and sales for the projected period.

Chapters 5, 6, 7, 8 and 9:To evaluate the market by segments, by countries and by manufacturers with revenue share and sales by key countries in these various regions.

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US Parkinsons disease treatment Market set to grow with massive rate by 2020 to 2025 - Galus Australis

Precision Cancer Therapies Market Size of Dynamics, Products, Application, Forecast Report 2019-2025 – The Daily Chronicle

Global Precision Cancer Therapies market- Report defines the vital growth factors, opportunities and market segment of top players during the forecast period from 2019 to 2025. The report Precision Cancer Therapies offers a complete market outlook and development rate during the past, present, and the forecast period, with concise study, Precision Cancer Therapies market effectively defines the market value, volume, price trend, and development opportunities. The comprehensive, versatile and up-to-date information on Precision Cancer Therapies market is provided in this report.

The latest research report on Precision Cancer Therapies market encompasses a detailed compilation of this industry, and a creditable overview of its segmentation. In short, the study incorporates a generic overview of the Precision Cancer Therapies market based on its current status and market size, in terms of volume and returns. The study also comprises a summary of important data considering the geographical terrain of the industry as well as the industry players that seem to have achieved a powerful status across the Precision Cancer Therapies market.

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The key players covered in this study Abbott Laboratories Bayer HealthCare GlaxoSmithKline OncoGenex Pharmaceuticals Hospira Boehringer Ingelheim AstraZeneca Aveo Pharmaceuticals

Market segment by Type, the product can be split into Hormone Therapy Immunotherapies Targeted Therapy Monoclonal Antibody Therapy Gene Therapy Market segment by Application, split into Hospitals Diagnostic Centers Oncology Clinics Research Institutes

Market segment by Regions/Countries, this report covers North America Europe China Japan Southeast Asia India Central & South America

The study objectives of this report are: To analyze global Precision Cancer Therapies status, future forecast, growth opportunity, key market and key players. To present the Precision Cancer Therapies development in North America, Europe, China, Japan, Southeast Asia, India and Central & South America. To strategically profile the key players and comprehensively analyze their development plan and strategies. To define, describe and forecast the market by type, market and key regions.

In this study, the years considered to estimate the market size of Precision Cancer Therapies are as follows: History Year: 2015-2019 Base Year: 2019 Estimated Year: 2020 Forecast Year 2020 to 2026 For the data information by region, company, type and application, 2019 is considered as the base year. Whenever data information was unavailable for the base year, the prior year has been considered.

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Complete Analysis of the Precision Cancer Therapies Market:

Comprehensive assessable analysis of the industry is provided for the period of 2019-2025 to help investors to capitalize on the essential market opportunities.

The key findings and recommendations highlight vital progressive industry trends in the global Precision Cancer Therapies market, thereby allowing players to improve effective long term policies

A complete analysis of the factors that drive market evolution is provided in the report.

To analyze opportunities in the market for stakeholders by categorizing the high-growth segments of the market

The numerous opportunities in the Precision Cancer Therapies market are also given.

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Furthermore, Global Precision Cancer Therapies Market following points are involved along with a detailed study of each point:

Generation of this Global Precision Cancer Therapies Industry is tested about applications, types, and regions with price analysis of players that are covered.

Revenue, sales are planned for this Precision Cancer Therapies market, including with various essentials along yet another facet is assessed in this section for foremost regions.

In continuation using earnings, this section studies consumption, and global Precision Cancer Therapies market. This area also sheds light on the variance between ingestion and distribution. Export and Precision Cancer Therapies significance data are provided in this part.

In this section, key players have been studied depending on product portfolio, their Precision Cancer Therapies market company profile, volume, price, price, and earnings.

Precision Cancer Therapies market analysis aside from business, the information, and supply, contact information from manufacturers, consumers and providers can also be presented. Additionally, a feasibility study to asset and SWOT analysis for endeavors have been contained.

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Precision Cancer Therapies Market Size of Dynamics, Products, Application, Forecast Report 2019-2025 - The Daily Chronicle

Cytovia Therapeutics Acquires Worldwide Rights to CytoImmune Therapeutics’ First-In-Class EGFR Dual-targeting CAR for NK Cell Treatment of…

August 03, 2020 08:03 ET | Source: Cytovia Therapeutics

NEW YORK and MONROVIA, Calif., Aug. 03, 2020 (GLOBE NEWSWIRE) -- Cytovia Therapeutics, Inc (Cytovia), an emerging biopharmaceutical company developing natural killer (NK) immunotherapies for cancer, today announces that it has acquired worldwide rights from CytoImmune Therapeutics for its novel EGFR Dual-targeting CAR to be used for NK cell therapy. Cytovia will conduct and finance all future development and will apply the EGFR Dual-targeting CAR to its iPSC CAR NK technology. CytoImmune will receive an upfront equity grant in Cytovia, future development milestones, and royalties.

Dr. Daniel Teper, Chairman and CEO of Cytovia added: We are honored to collaborate with Dr. Caligiuri, a pioneer in translating biological research on NK cells into impactful therapeutics. He has published solid data with intracranial injection of EGFR CAR NK cells to support their clinical development in glioblastoma. Additionally, EGFR is a clinically validated target which will allow us to expand the use of NK cellular therapy in multiple solid tumors.

Pre-clinical proof of concept data with intracranial administration of the EGFR Dual-targeting CAR-NK cells for the treatment of glioblastoma has been published in Nature Scientific Reports. The EGFR Dual-targeting CAR targets glioblastoma cells expressing EGFR wild-type and/or the mutant EGFR vIII. A single intracranial injection of EGFR CAR NK cells reduced the growth of glioblastoma and showed a statistically significant improvement in survival in animal models. The intracranial injection of the EGFR CAR NK cells remained localized in the brain without entering the systemic circulation or infiltrating extracranial organs or tissues, thus limiting toxicity.

Michael A. Caligiuri, MD, the scientific founder of CytoImmune, is joining the Cytovia Scientific Advisory Board. Dr Caligiuri is the Deana and Steve Campbell Physician in Chief Distinguished Chair and President of the City of Hope Cancer Center in Duarte, CA. Dr. Caligiuri is a world-renowned physician, scientist, builder, innovator, leader and visionary. He was elected a Member of the National Academy of Medicine for his work on NK cell biology and its clinical applications. He is a past President of the American Association for Cancer Research (AACR).

Dr Caligiuri commented: CAR NK cell therapy has the potential to transform cancer outcomes. We are excited to partner with Cytovia to rapidly bring EGFR Dual-targeting CAR NK cells, a next generation therapy, to patients with the ultimate goal of curing glioblastoma. Cytovias off-the-shelf iPSC CAR NK cell technology should increase the access to precision immunotherapy for many cancer patients.

ABOUT CAR NK CELL THERAPYChimeric Antigen Receptors (CAR) are fusion proteins that combine an extracellular antigen recognition domain with an intracellular co-stimulatory signaling domain. Natural Killer (NK) cells are modified genetically to allow insertion of a CAR. CAR NK cell therapy has demonstrated initial clinical relevance without the limitations of CAR-T, such as Cytokine Release Syndrome, neurotoxicity or Graft vs Host Disease (GVHD). Induced Pluripotent Stem Cells (iPSC) - derived CAR NKs are naturally allogeneic, available off-the-shelf and may be able to be administered on an outpatient basis. Recent developments with iPSC, an innovative technology, allow large quantities of homogeneous genetically modified CAR NK cells to be produced from a master cell bank, and thus hold promise to expand access of cell therapy for many patients.

ABOUT GLIOBLASTOMAGlioblastoma affects 290,000 new patients every year worldwide. Chemotherapy and radiotherapy lack specificity and provide limited efficacy along with high toxicity. The median overall survival from the time of diagnosis is only 14.6 months. Systemic and particularly intracranial or intratumoral immunotherapy, which can target localized and infiltrating cells, has shown initial promise in early clinical trials.

ABOUT CYTOVIA THERAPEUTICS, INC Cytovia Therapeutics Inc is an emerging biotechnology company that aims to accelerate patient access to transformational immunotherapies, addressing several of the most challenging unmet medical needs in cancer and severe acute infectious diseases. Cytovia focuses on Natural Killer (NK) cell biology and is leveraging multiple advanced patented technologies, including an induced pluripotent stem cell (iPSC) platform for CAR (Chimeric Antigen Receptors) NK cell therapy, next-generation precision gene-editing to enhance targeting of NK cells, and NK engager multi-functional antibodies. Our initial product portfolio focuses on both hematological malignancies such as multiple myeloma and solid tumors including hepatocellular carcinoma and glioblastoma. The company partners with the University of California San Francisco (UCSF), the New York Stem Cell Foundation (NYSCF) and the Hebrew University of Jerusalem. Learn more atwww.cytoviatx.com

ABOUT CYTOIMMUNE THERAPEUTICS CytoImmune Therapeutics (CytoImmune) is biotechnology company focused on the application of proprietary chimeric antigen receptors (CAR) for use in both off-the-shelf human natural killer (NK) cells and autologous cytotoxic effector T cells in the treatment of liquid and solid tumors. Our CoalesceNT platform harnesses the power of both a specific CAR and a different secretory bispecific antibody in a single construct to coordinate an immune response with CAR NK cells, cytolytic effector T cells, NK-T cells and g/d T cells. This combination of NK- and T-cell therapy expedites time-to-treatment and delivers a dynamic response that reflects both innate and adaptive immunity in an effort to reduce tumor evasion and the incidence of cancer recurrence.

Learn more at http://www.cytoimmune.com

Contact for media enquiries Sophie Badr Vice President, Corporate Affairs Sophie.badre@cytoviatx.com 1(929) 317 1565

Will Rossellini President will@cytoimmune.com 1(469) 222 2350

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Cytovia Therapeutics Acquires Worldwide Rights to CytoImmune Therapeutics' First-In-Class EGFR Dual-targeting CAR for NK Cell Treatment of...

Cell Proliferation Kit Market 2020-2026 analysis examined in new market research report with Focusing Key players like – BD Biosciences, GE…

The Global Cell Proliferation KitMarket

The globalCell Proliferation Kitmarket2020 mainly focuses on the market trend, market share, size and forecast. It is a brief and professional analysis on the current scenario of the Global Cell Proliferation Kitmarket.

The report on Cell Proliferation Kitmarket is a comprehensive study on global market analysis and insights. The report focuses on the emerging trends in the global and regional spaces on all the significant components, such as market capacity, cost, price, demand and supply, production, profit, and competitive landscape. The report analyzes past trends and future prospects in this report which makes it highly comprehensible for the analysis of the market. Moreover, the latest trends, product portfolio, demographics, geographical segmentation, and regulatory framework of the Cell Proliferation Kitmarket have also been included in the study.

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, Biological Industries, Thermo Fisher Scientific, Sigma-Aldrich (Merck), BD Biosciences, GE Healthcare, PerkinElmer, Millipoore (Merck), Bio-Rad, Biotium, Mindray Medical

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This research is a comprehensive way to understand the current landscape of the market, especially in 2020. Both top-down and bottom-up approaches are employed to estimate the complete market size. This will help all the market stakeholders to have a better understanding of the direction in which the market will be headed and future forecast.

For Product type segment the report listed main product type:

Colorimetric Detection Method Fluorescent Detection Method Other

For Application segment the report listed main types:

Clinical Industrial & Applied Science Stem Cell Research

Market research includes:

Market segmentation:

3 major segments covered by the report are as follows:

Research analysts have studied and analyzed the report on these 3 segments which cover the market share, revenues, growth rate along with the other factors that uplift the growth rate in Global Cell Proliferation Kitmarket. This study will lead in identifying the high growth areas as well as in identifying the growth factors which are helping in leading these segments.

Major importance has been given to the status of the key segments. The segmentation also includes the various End Users of this industry.

Regional analysis:

The report examines market on domestic and global level. Global prominent players and their market strategies are compiled in this report to understand the market strategies. The report forecasts the market size of segments with respect to countries in Americas (US, Canada, and Rest of Americas), Europe (UK, Germany, and Rest of Europe), APAC (China and Rest of APAC), MEA (KSA, UAE, and Rest of MEA), and ROW. The major takeaways in the report are product segment analysis, application segment analysis, regional segment analysis and data of the majorCell Proliferation KitMarketplayers from around the world.

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Cell Proliferation Kit Market 2020-2026 analysis examined in new market research report with Focusing Key players like - BD Biosciences, GE...

FDA hands MorphoSys and Incyte a quick OK on their potential blockbuster CAR-T alternative – Endpoints News

Nearly three years after okaying the CAR-Ts Yescarta and Kymriah, the FDA has approved a new CD19 therapy.

MorphoSys Monjuvi, or tafasitamab-cxix, was cleared Friday for use in refractory diffuse large B-cell lymphoma (DBLCL). The approval sets up both MorphoSys and their commercial partner Incyte to compete with Gilead and Novartis in the ultra-competitive indication, where similar trial results and far easier delivery could allow them to cut a fair share of the market.

The first approved indication is in second-line DBLCL, for patients ineligible for autologous stem cell transplant. Mizuhos Mara Goldstein estimated that market at around 6,000 US patients and said the drug had blockbuster potential, but she noted those patients have several other options available to them.

The initial market opportunity as a second-line treatment is meaningful, she wrote in a note to investors, though we are somewhat cautious on the ramp of the drug given the competitive landscape for this indication that includes seven drug regimens as well as treatment with CAR-T therapy.

SVB Leerinks Geoffrey Porges called the approval a best case scenario, noting it had been unclear whether the drug would be approved for second-line or third-line therapy. He estimated a potential patient population around 12,000.

Both analysts singled out Monjuvis duration in particular. The 21.7 months it showed at the top line readout is more than twice the 6 months to a year Roches antibody-drug Polivy, approved last year, has shown.

We believe the CAR-T like efficacy demonstrated by tafa, as well as its favorable safety profile should enable broad adoption in the 2L setting, Porges wrote in a note to investors, and expect the product to be preferred over Roches CD79 ADC Polivy.

Former MorphoSys CEO Simon Moroney positioned Monjuvi as an option for patients who cant handle the intense bodily stress of high-dose chemotherapy or stem cell transplant, or of CAR-T. In addition to the costly and lengthy process of extracting, treating and re-implanting T cells, CAR-T therapies also require patients to undergo conditioning regimens of intensive chemotherapy to clear out the bone marrow and essentially give a pocket for the new cells to take hold.

By contrast, Monjuvi is an anti-CD19 antibody that is given intravenously and requires no conditioning.

Our patients tend to be older median age in the trial is 72, Moroney told MedCity Newslast June, referring to participants in their pivotal Phase II study. They have comorbidities and are not eligible for CAR-T.

The FDA decision is an accelerated approval based on results from that Phase II study. Topline results released last year showed a 55% overall response rate and a 37% complete response rate. The latest data, released in May, showed a 59% response rate, a 39% complete response rate, and a median duration of response that had risen to 34.6 months nearly 3 years. The complete response rates were in line with the early CAR-T trials, and the FDA granted the drug priority review.

Both MorphoSys and Incyte have staked a lot on Monjuvi. MorphoSys raised $208 million in an IPO in 2018, funneling much of that cash into building out a US commercial operation in anticipation of their lead drugs approval. They tapped the US commercial lead for Merck KGaAs Bavencio, David Trexler, to lead that effort. And after Moroneys retirement, Jean-Paul Kress stepped in to lead a new stage for the company.

Incyte, meanwhile, spent $900 million earlier this year to join with Incyte on the commercial launch, hoping the CAR-T alternative could pour some oil into a sputtering R&D engine. Mizuhos Goldstein said the drug would help diversify Incytes revenue base, but its overall impact may be muted.

Monjuvi may not have enough impact in the near term to alter the fundamental picture for the company, she said of Incyte.

Goldstein also called the drug validation for Xencors platform. The California biotech originally developed the antibody. The approval triggered a $25 million milestone for them.

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FDA hands MorphoSys and Incyte a quick OK on their potential blockbuster CAR-T alternative - Endpoints News