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BioSpace News Archive
Browse BioSpace’s published news and press releases by year, month, and day.
255 Results
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Drug Development
Astellas Wins FDA Approval for Hot Flash Treatment in Menopausal Women
Veozah, an oral once-daily medication, is the first FDA-approved NK3 receptor antagonist for hot flashes, a common symptom of menopause that can affect health and quality of life.
May 15, 2023
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2 min read
·
Tristan Manalac
Business
AstraZeneca Expands ADC Portfolio with $600M Deal with LaNova
The company’s second antibody-drug conjugate deal of 2023, with Shanghai-based LaNova Medicines, adds a potential first-in-class GPRC5D-directed ADC for multiple myeloma.
May 15, 2023
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2 min read
·
Kate Goodwin
Drug Development
Lilly-Backed Nido Biosciences Launches with $109M to Target Neurological Diseases
The precision neuroscience startup has notched $109 million in seed, Series A and B financing as it looks to further develop a Phase I candidate to treat a rare X-linked neuromuscular disorder.
May 15, 2023
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1 min read
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Lisa Munger
Drug Development
ReCode–a New Contestant in the mRNA Race
ReCode plans to use its SORT LNP genetic medicines delivery technology to treat CF and PCD patients who don’t respond to current treatments.
May 15, 2023
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3 min read
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Rosemary Scott
Beckman Coulter Unveils Next Generation Immunoassay Analyzer Enabling Elite Laboratory Performance with No Daily Maintenance
Beckman Coulter, a clinical diagnostics leader, unveiled the DxI 9000 Access Immunoassay Analyzer, the most productive immunoassay analyzer per footprint.
May 15, 2023
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6 min read
Drug Development
Phase 3 Study of DFP-10917 in the R/R AML Patients Shall Be Done with the 1st Interim Analysis for NDA Approval.
150 patients have been enrolled at the multi-clinical centers in US to the Phase 3 randomized trial of DFP-10917 vs non-intensive reinduction or intensive reinduction in the 2nd, 3rd, or 4th salvage of AML and the 1st interim analysis of this study shall be done for NDA approval to the FDA in US soon after confirmation of the superiority of DFP-10917 arm.
May 15, 2023
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1 min read
Drug Development
Biophytis has Filed with the EMA for Authorization to Initiate SARA-31 Phase 3 Study in Sarcopenia
Biophytis SA announced that it has submitted the application for Clinical Trial Authorization to initiate SARA-31, the first phase 3 study in sarcopenia, on the European portal of the EMA.
May 15, 2023
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5 min read
Business
RaySearch expands collaboration with BEBIG Medical
RaySearch Laboratories AB is pleased to announce that the strategic partnership with BEBIG Medical, which began in 2018, has been extended through a memorandum of the agreement.
May 15, 2023
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2 min read
BioNxt Receives Approval for European Clinical Study of Transdermal Rotigotine Patch for Parkinson’s Disease
BioNxt Solutions Inc. is pleased to report that it has received government approval for to proceed with its comparative drug absorption study for the Company’s transdermal Rotigotine patch for the treatment of Parkinson’s disease.
May 15, 2023
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4 min read
Business
Alvotech Issues Annual Equality Report Covering 2022
Alvotech, a global biotech company specializing in the development and manufacture of biosimilar medicines for patients worldwide, announced the release of its second annual Equality Report covering 2022.
May 15, 2023
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8 min read
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