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BioMendics to Present on Epidermolysis Bullosa Simplex at the 7th Annual Dermatology Drug Development Summit for Inflammatory Skin Diseases

BioMendics LLC, a pharmaceutical company developing new medicines to improve the lives of patients living with rare skin diseases, today announced its participation in the 7th Annual Dermatology Drug Development Summit for Inflammatory Skin Diseases, taking place from October 31 - November 2 in Boston, Massachusetts.
Karen Mcguire Dermatology Drug Development Summit Stanford Medicine Orphan Drug Designation Rare Pediatric Disease Stabilize Intermediate Filaments
Source: yahoo.com

Tenaya Therapeutics Announces FDA Clearance to Begin Clinical Testing of TN-401 Gene Therapy for the Treatment of PKP2-Associated Arrhythmogenic Right Ventricular Cardiomyopathy

PKP2 Mutations Are the Leading Cause of ARVC, a Dangerous Condition Linked to Sudden Cardiac Arrest in Young People Estimated to Affect 70,000 People in the US TN-401 Preclinical Studies Demonstrated...
Julie Seidel Whit Tingley Wendy Ryan Exchange Commission Globenewswire Inc Clinical Program

Research shows Northern Nevada locals in favor of expanding smoke-free laws to include casinos and bars

A research project was recently published by the Journal of Hospital Management and Health Policy, indicating that 60 percent of Washoe County residents (and 74 percent of Washoe County non-smokers) would favor a law prohibiting smoking in all casinos in Washoe County.
University Of Nevada United States Washoe County Johnny Hartman Katiem Snider Emily Wood

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Intellia Therapeutics Receives Priority Medicines (PRIME) Designation From the European Medicines Agency for NTLA-2002, an Investigational In Vivo CRISPR Genome Editing Treatment for Hereditary Angioedema

CAMBRIDGE, Mass., Oct. 13, 2023 -- Intellia Therapeutics, Inc. , a leading clinical-stage genome editing company focused on developing potentially curative therapeutics leveraging CRISPR-based...
United Kingdom Alina Li John Leonard Matt Crenson Ian Karp Exchange Commission

Takeda's Dengue Vaccine Recommended by World Health Organization Advisory Group for Introduction in High Dengue Burden and Transmission Areas in Children Ages Six to 16 Years

Experts Reviewed Data from QDENGA’s Clinical Program Across 19 Phase 1, 2 and 3 Trials with More Than 28,000 ParticipantsWHO Will Consider the SAGE Recommendation and Provide Final Guidance on the Use of QDENGA in Public Vaccination Programs in the Coming MonthsDengue Poses a Significant and Growing Public Health Bu...
Sri Lanka United States Dominican Republic Maiko Miura Gary Dubin Strategic Advisory Group Of Experts

Takedas Dengue Vaccine Recommended by World Health Organization Advisory Group for Introduction in High Dengue Burden and Transmission Areas in Children Ages Six to 16 Years

Takeda TSE4502NYSETAK today announced that the World Health Organizations WHO Strategic Advisory Group of Experts SAGE on Immunization shared recommendations for use of QDENGA Dengue Tetravalent Vaccine Live Attenuated TAK003.
Dominican Republic United States Sri Lanka Gary Dubin Maiko Miura World Health Organization

Kymera Therapeutics Receives U.S. FDA Fast Track Designation for KT-333, a First-in-Class, Investigational STAT3 Degrader for the Treatment of Relapsed/Refractory Cutaneous T-Cell Lymphoma and Relapsed/Refractory Peripheral T-Cell Lymphoma

KT-333 Phase 1 oncology trial ongoing with an update including initial evaluation of its clinical antitumor activity in patients expected in the fourth quarter of 2023 Fast Track designation can...
United States Todd Cooper Jared Gollob Justine Koenigsberg Exchange Commission Clinical Program

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