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BioSpace News Archive
Browse BioSpace’s published news and press releases by year, month, and day.
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Drug Development
OLUMIANT® Significantly Improved Hair Regrowth to At Least 80% Scalp Coverage as Early as 24 Weeks Across First Completed Phase 3 Studies for Alopecia Areata
Eli Lilly and Company (NYSE: LLY) and Incyte (NASDAQ: INCY) announced today detailed results from two pivotal Phase 3 trials (BRAVE-AA1 and BRAVE-AA2), which found once-daily OLUMIANT
September 30, 2021
·
20 min read
Policy
Reata Pharmaceuticals Plans NDA Submission for Omaveloxolone in First Quarter of 2022 Following Completion of Pre-NDA Meeting with FDA
Reata Pharmaceuticals, Inc., a clinical-stage biopharmaceutical company, announced that it has completed its pre-New Drug Application meeting with the United States Food and Drug Administration for omaveloxolone for the treatment of patients with Friedreich’s ataxia and reaffirmed its plan to submit an NDA in the first quarter of 2022.
September 30, 2021
·
6 min read
Business
Nurix Therapeutics Expands its Board of Directors with the Addition of Two Industry Leaders
Nurix Therapeutics, Inc. today announced the appointments of Judith A. Reinsdorf and Paul M. Silva to its board of directors, effective October 1, 2021.
September 30, 2021
·
4 min read
Business
AngioDynamics Reports Fiscal 2022 First Quarter Financial Results; Updates Guidance
AngioDynamics, Inc. today announced financial results for the first quarter of fiscal year 2022, which ended August 31, 2021.
September 30, 2021
·
15 min read
Drug Development
InMed Pharmaceuticals Announces Commencement of Phase 2 Clinical Trial Investigating Cannabinol (CBN), a Rare Cannabinoid, in the Treatment of Epidermolysis Bullosa
InMed Pharmaceuticals Inc. today announced that it has commenced its Phase 2 clinical trial of INM-755 (cannabinol) cream in the treatment of Epidermolysis Bullosa (“EB”).
September 30, 2021
·
6 min read
Pharm Country
TG Therapeutics Submits Biologics License Application to the U.S. Food and Drug Administration for Ublituximab as a Treatment for Patients with Relapsing Forms of Multiple Sclerosis
TG Therapeutics, Inc. (NASDAQ: TGTX), today announced the submission of a Biologics License Application (BLA) to the U.S. Food and Drug Administration (FDA) requesting approval of ublituximab, the Company’s investigational glycoengineered anti-CD20 monoclonal antibody, as a treatment for patients with relapsing forms of multiple sclerosis (RMS).
September 30, 2021
·
7 min read
Braxia Scientific Reports Encouraging Results of Ketamine Study Showing Significant Reduction in Depressive Symptoms and Suicidality with Ketamine as a Solo Treatment
Braxia Scientific Corp. is pleased to report encouraging preliminary findings of a recent clinical study that suggests ketamine may be as effective as a standalone antidepressant, versus as an adjunctive therapy.
September 30, 2021
·
6 min read
Pharm Country
IntegriChain Experts to Speak at Medicaid Drug Rebate Program Conference
IntegriChain, delivering Life Sciences’ only comprehensive data and business process platform for market access, announced that four senior Medicaid rebate experts will present at Informa’s upcoming Medicaid Drug Rebate Program conference on validating Medicaid claims and readying for product launch.
September 30, 2021
·
4 min read
Business
HiberCell Appoints Jonathan Lanfear as Chief Operating Officer
HiberCell, a clinical stage biotechnology company developing therapeutics to treat cancer relapse and metastasis, announced the appointment of Jonathan Lanfear as chief operating officer with a focus on leading and driving HiberCell’s emerging global reach.
September 30, 2021
·
3 min read
Drug Development
New FINTEPLA® (Fenfluramine) Data Show Long-Term Seizure Frequency Reductions in Patients with Lennox-Gastaut Syndrome (LGS)
Zogenix (NASDAQ: ZGNX), a global biopharmaceutical company developing rare disease therapies, today announced data from an interim analysis of an on-going 12-month Phase 3 open-label extension (OLE) study (Study 1601; Part 2) showing that treatment with FINTEPLA® (fenfluramine) oral solution led to a clinically meaningful and sustained reduction in drop seizures in patients with Lennox-Gastaut syndrome (LGS) on antiseizure medications (ASMs)
September 30, 2021
·
7 min read
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