Current Headlines
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New Treatment For Acute Myeloid Leukemia
11/25/2025
Biomedical research that began at the School of Medicine has yielded a much-needed new treatment for patients with the deadliest blood cancer, acute myeloid leukemia.
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Drug Discovery Center Integrates AI For Big Impact
11/24/2025
The UNC Eshelman School of Pharmacy is home to a scientific force driving the future of translational medicine — the Center for Integrative Chemical Biology and Drug Discovery. This center seamlessly blends chemistry, biology and computational science to discover new therapeutic agents and targets.
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Tonix Pharmaceuticals Announces FDA IND Clearance For Phase 2 Study Of TNX-102 SL For The Treatment Of Major Depressive Disorder
11/24/2025
Tonix Pharmaceuticals Holding Corp. (Nasdaq: TNXP) (“Tonix” or the “Company”), a fully-integrated commercial biotechnology company, today announced the U.S. Food and Drug Administration (FDA) has cleared the Investigational New Drug (IND) application to support clinical development of TNX-102 SL (cyclobenzaprine HCl sublingual tablets) 5.6 mg for the treatment of major depressive disorder (MDD) in adults.
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HKeyBio Launches The HKEY-AIDMD 3.0--A Next-Generation Platform To Crack The Toughest Challenge In Autoimmune And Allergy Drug Development: Multi-Target Combination Strategy Optimization
11/24/2025
HKeyBio, a global leading CRO specializing in preclinical and translational research for autoimmune and allergic disease drug development, has officially launched the upgraded HKEY-AIDMD 3.0 platform.
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Otsuka Pharmaceutical Submits New Drug Application To U.S. FDA For Centanafadine For The Treatment Of ADHD In Children, Adolescents, And Adults
11/24/2025
Otsuka Pharmaceutical Development & Commercialization, Inc. and Otsuka Pharmaceutical Co., Ltd. (Otsuka) today announce the filing of a New Drug Application (NDA) with the U.S. Food and Drug Administration (FDA) for centanafadine, once daily extended release capsules, a novel norepinephrine, dopamine, and serotonin reuptake inhibitor (NDSRI), for the treatment of attention-deficit hyperactivity disorder (ADHD) in children, adolescents, and adults.
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BioCorteX Announces Strategic Partnership With CD Biopharma Of China
11/24/2025
BioCorteX, the UK-based pioneering tech bio company, said Wednesday that it had entered into a strategic collaboration with Chinese biotech company CD Biopharma to accelerate the development of next-generation precision immunotherapy-based drugs that fight solid tumors such as lung and breast cancer.
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Avenzo Therapeutics Granted Fast Track Designation For AVZO-103, A Potential Best-In-Class Nectin4/TROP2 Bispecific Antibody-Drug Conjugate, For The Treatment Of Patients With Urothelial Cancer Previously Treated With Enfortumab Vedotin
11/24/2025
Avenzo Therapeutics, Inc. (“Avenzo”), a clinical-stage biotechnology company developing next-generation oncology therapies, today announced the U.S. Food and Drug Administration (FDA) granted Fast Track designation to AVZO-103, a potential best-in-class Nectin4/TROP2 bispecific antibody-drug conjugate (BsADC).
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Biodlink And Lepu Biopharma Celebrate Successful Launch Of The World's First EGFR-Targeting ADC Drug, Marking A Major Milestone In Mutual Collaboration In Biologics CMC
11/21/2025
On November 20, 2025, BioDlink (Stock Code: 1875.HK), a leading biologics CDMO, together with Lepu Biopharma (2157.HK), announced the successful market launch of MEIYOUHENG®(Becotatug Vedotin injection) , the world's first EGFR-targeting antibody-drug conjugate (ADC).
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FDA Approves First Cancer Drug Based On Broad Institute Science
11/20/2025
The US Food and Drug Administration has approved the first cancer drug based on discoveries from Broad Institute scientists. The drug, sevabertinib, was developed by Bayer Healthcare Pharmaceuticals in close collaboration with the Broad, and is the first FDA-approved medicine from the long-standing Broad-Bayer oncology research alliance.
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SCYNEXIS Completes Transfer Of BREXAFEMME® New Drug Application To GSK
11/19/2025
SCYNEXIS, Inc. (NASDAQ: SCYX), a biotechnology company pioneering innovative medicines to overcome and prevent difficult-to-treat and drug-resistant infections, today announced that it has completed the transfer of the BREXAFEMME (ibrexafungerp) New Drug Application (NDA) to GSK.