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BioSpace News Archive
Browse BioSpace’s published news and press releases by year, month, and day.
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Bio NC
IQVIA Recognized as a Leader in BPO Solutions for Pharmaceutical Sales and Marketing
IQVIA recognized in IDC MarketScape™ for its data and analytics capabilities and growing suite of software platforms.
December 1, 2021
·
3 min read
Biotech Bay
Allogene Therapeutics Announces Conference Call to Review ALPHA, ALPHA2 and UNIVERSAL Phase 1 Data Presented at the 2021 American Society of Hematology Annual Meeting
Conference Call and Webcast Scheduled for Monday, December 13, 2021 at 1:30 PM PT/4:30 PM ET.
December 1, 2021
·
2 min read
New Nomenclature Redefines Fatty Liver Disease Therapy, says Chinese Medical Journal Study
Excess fat accumulation in the liver is detrimental to health and can lead to liver cancer. Given the link between this condition and alcohol consumption, the presence of fatty livers in individuals who don’t consume large amounts of alcohol was termed “non-alcoholic fatty liver disease” or NAFLD in the 1980s.
December 1, 2021
·
2 min read
Business
Notable and CicloMed Initiate Phase 1B/2A Clinical Trial of Fosciclopirox in Acute Myelogenous Leukemia Under Co-Development Agreement
Notable Labs, Inc., a clinical-stage predictive precision therapeutics company and CicloMed LLC, a developmental-stage pharmaceutical company have initiated a Phase 1B/2A clinical trial of fosciclopirox in patients with refractory acute myelogenous leukemia under the terms of a co-development agreement.
December 1, 2021
·
4 min read
Pharm Country
BD Issues 2021 Global Inclusion, Diversity and Equity Report
Progress Builds Strong Foundation for Bold 2030+ ESG Goals to Advance the World of Health for All.
December 1, 2021
·
4 min read
Pharm Country
U.S. FDA Accepts for Priority Review the Supplemental Biologics License Application for Merck’s VAXNEUVANCE™ (Pneumococcal 15-valent Conjugate Vaccine) for Use in Infants and Children
Merck (NYSE: MRK), known as MSD outside the United States and Canada, today announced the U.S. Food and Drug Administration (FDA) has accepted for Priority Review a supplemental Biologics License Application (sBLA) for VAXNEUVANCE.
December 1, 2021
·
6 min read
Genetown
Curie Therapeutics Raises $75 Million Financing to Further its Mission of Transforming Cancer Care with Precision Radiopharmaceuticals
Curie Therapeutics Inc today announced a Series A investment of $75 million by its founding syndicate to continue the development of its multimodal pipeline of precision radiopharmaceuticals to a broad range of high unmet need solid tumors.
December 1, 2021
·
5 min read
Business
Sage Therapeutics and Biogen Announce Positive, One-Year Zuranolone 50 mg Data in the Ongoing Open-Label SHORELINE Study in Patients with MDD
In the zuranolone 50 mg cohort, the majority of patients who responded to an initial 14-day course received only one two-week course of treatment during the study and nearly 80% received only one or two treatment courses in total.
December 1, 2021
·
16 min read
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