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Making The Impossible Possible: A Conversation With Martine Rothblatt – Forbes

Posted: Published on October 30th, 2020

In this riveting Whats Ahead conversation youll hear how Martine Rothblatt, creator of SiriusXM, left the communications field entirely to hunt for a cure for a rare, mortal disease with which her daughter was diagnosed. The pressure was intense, as patients usually died within two to three years of diagnosis. Continue reading

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Hypertensive Emergency Medications Market Shares, Strategies and Forecast Worldwide, 2018-2028 – The Cloud Tribune

Posted: Published on October 30th, 2020

Fact.MR, in a recently published market study, highlights the important factors that are expected to shape the growth of the Hypertensive Emergency Medications market over the forecast period(2018-2028).The current trends, market drivers, opportunities, and restraints are thoroughly evaluated to provide a clear understanding of the current market landscape and the course theHypertensive Emergency Medicationsmarketis likely to take over the upcoming decade. The COVID-19 (Coronavirus) outbreak has led to both advantages and disadvantages for companies in the Hypertensive Emergency Medications market. With the help of our recently published report, market players can adopt innovative strategies to overcome the challenges that lie ahead of the COVID-19 lockdown period. Continue reading

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Cerevel Therapeutics Announces First Patients Dosed in all Phase 3 Trials of Tavapadon for the Treatment of Parkinson’s Disease – BioSpace

Posted: Published on October 30th, 2020

Company developing investigational treatment for both newly diagnosed patients and those with a more advanced form of the disease in need of adjunctive therapy BOSTON, Oct. 30, 2020 (GLOBE NEWSWIRE) -- Cerevel Therapeutics (NASDAQ:CERE), a company dedicated to unraveling the mysteries of the brain to treat neuroscience diseases, today announced that the first participants have been dosed in all three of the clinical trials in their Phase 3 program evaluating tavapadon in patients with Parkinsons disease. Continue reading

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Vanderbilt University anti-inflammatory therapy licensed to Amytrx is now in clinical trials for eczema treatment – Vanderbilt University News

Posted: Published on October 30th, 2020

A cell-penetrating, anti-inflammatory peptide developed byJacek Hawiger, Louise B. McGavock Chair and Distinguished Professor of Medicine, and licensed to biopharmaceutical companyAmytrx, has been approved by the FDA for testing as a potential therapeutic for mild to moderate eczema. The peptide, known as AMTX-100, has been in clinical trials since March Continue reading

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LEO Pharma announces positive results of Phase 2b dose-finding study with delgocitinib cream in adult patients with mild-to-severe chronic hand eczema…

Posted: Published on October 30th, 2020

Details Category: Small Molecules Published on Friday, 30 October 2020 15:20 Hits: 102 Results were presented during the Late-Breaking News session of the European Academy of Dermatology and Venereology (EADV) Virtual 2020 BALLERUP, Denmark & MADISON, NJ, USA I October 29, 2020 I LEO Pharma A/S, a global leader in medical dermatology, today announced positive results of a Phase 2b dose-finding study with delgocitinib cream, an investigational topical pan-Janus kinase (JAK)-inhibitor, during the Late Breaking News session of the European Academy of Dermatology and Venereology (EADV) Virtual 2020.1 Delgocitinib inhibits activation of the JAK-STAT pathway, which plays a key role in the immune system in driving the pathophysiology of chronic inflammatory skin diseases.2,3 The cream formulation of delgocitinib is an investigational therapy under clinical development and has not been approved by any regulatory authority. The primary endpoint for the randomized, double-blind, vehicle-controlled, multi-center Phase 2b dose-finding trial was the proportion of adult patients with mild-to-severe CHE who achieved an Investigators Global Assessment (IGA)-CHE score of 0 (clear) or 1 (almost clear) with a 2 point improvement from baseline, at week 16.1 A key secondary endpoint was change in Hand Eczema Severity Index (HECSI) from baseline to week 16.1 The results presented today showed that delgocitinib cream demonstrated a statistically significant dose-response relationship for these endpoints compared to vehicle.1 Across all treatment groups, the majority of adverse events were non-serious, mild or moderate in severity and not considered treatment related.1 In addition, none of the three serious adverse events were considered treatment related,1 and the most frequently reported adverse events were nasopharyngitis, eczema and headache.1 "There is a significant unmet need for additional treatments for long-term control of CHE, which can cause considerable social and employment burden for both individuals and society, said Prof Continue reading

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Dermatologist recommended tips to take care of your babys skin during the winter season – TheHealthSite

Posted: Published on October 30th, 2020

Babies have sensitive skin and are more prone to skin problems. Here are some tips by Dr. Sirisha Singh, Dermatologist to help you take care of your babys skin during the winter weather Continue reading

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Muscular Dystrophy: Types, Symptoms, and Diagnosis

Posted: Published on October 28th, 2020

What is muscular dystrophy? Muscular dystrophy is a group of inherited diseases that damage and weaken your muscles over time Continue reading

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Catabasis Pharmaceuticals Announces Top-Line Results for the Phase 3 PolarisDMD Trial of Edasalonexent in Duchenne Muscular Dystrophy – BioSpace

Posted: Published on October 28th, 2020

Oct. 26, 2020 21:00 UTC -- PolarisDMD Trial Did Not Achieve Primary or Secondary Endpoints -- BOSTON--(BUSINESS WIRE)-- Catabasis Pharmaceuticals, Inc., Inc. (NASDAQ:CATB), a clinical-stage biopharmaceutical company, today announced that the Phase 3 PolarisDMD trial of edasalonexent in Duchenne muscular dystrophy (DMD) did not meet the primary endpoint, which was a change from baseline in the North Star Ambulatory Assessment (NSAA) over one year of edasalonexent compared to placebo Continue reading

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Muscular Dystrophy Association Launches MOVR Visualization and Reporting Platform to Improve Patient Care and Accelerate Drug Discovery – PRNewswire

Posted: Published on October 28th, 2020

NEW YORK, Oct. 28, 2020 /PRNewswire/ --The Muscular Dystrophy Association (MDA) announced today the launch of the neuroMuscular ObserVational Research (MOVR) Visualization and Reporting Platform (VRP). The new platform represents a monumental leap in advancing neuromuscular disease research and improving patient care. Continue reading

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Catabasis Rocked by DMD Trial Failure, Will Scrap Study and Explore Strategic Options – BioSpace

Posted: Published on October 28th, 2020

Shares of Catabasis Pharmaceuticals have plunged more than 64% in premarket trading following Mondays announcement the companys last-stage Duchenne muscular dystrophy treatment failed to meet the trials primary and secondary endpoints. The company will scrap the program and explore strategic options. On Monday, Boston-based Catabasis said its Phase III PolarisDMD trial of edasalonexent in Duchenne muscular dystrophy (DMD) did not meet the primary endpoint, which was a change from baseline in the North Star Ambulatory Assessment (NSAA) over one year of edasalonexent in comparison to placebo Continue reading

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