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Health Canada Approves Novartis’ KISQALI for High-Risk Early Breast Cancer

Jun 23, 2025
Health Canada has approved Novartis' KISQALI (ribociclib tablets) in combination with an aromatase inhibitor for the adjuvant treatment of adults with hormone receptor-positive (HR+),…
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Advarra Launches AI Council to Boost Innovation in Clinical Trials

Jun 20, 2025
Advarra announced the launch of the Council for Responsible Use of AI in Clinical Trials. The Council, which includes leaders from across the life sciences industry, will focus on…
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RyboDyn Joins Lilly Gateway Labs to Advance Immunotherapies Targeting Dark Proteome

Jun 20, 2025
RyboDyn, Inc., a biotechnology company pioneering first-in-class immunotherapies targeting the dark proteome, announced its selection to join Lilly Gateway Labs (LGL) in San Diego, an…
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Yeztugo Becomes First FDA-Approved HIV Prevention with 6-Month Protection

Jun 20, 2025
Gilead Sciences announced that the U.S. Food and Drug Administration (FDA) has approved Yeztugo (lenacapavir) as a pre-exposure prophylaxis (PrEP) to prevent sexually acquired HIV-1.…
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Actio Biosciences Raises $66M in Series B to Advance Genetics-Based Therapies

Jun 20, 2025
Actio Biosciences, a clinical-stage biotechnology company leveraging a novel approach to genetics and precision medicine to develop new therapeutics that target shared underlying…
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FNP-223 Receives FDA Fast Track Designation for Progressive Supranuclear Palsy

Jun 19, 2025
Ferrer has announced that its investigational therapy FNP-223, developed to treat progressive supranuclear palsy (PSP), has received Fast Track designation from the U.S. Food and Drug…
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J&J Seeks FDA Approval of STELARA for Pediatric Crohn’s Disease

Jun 19, 2025
Johnson & Johnson announced the submission of a supplemental Biologics License Application (sBLA) to the U.S. Food and Drug Administration (FDA) seeking to expand approval of…
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Draig Therapeutics Launches with $140M to Tackle Neuropsychiatric Disorders

Jun 19, 2025
Draig Therapeutics (“Draig”), a clinical-stage company aiming to transform the treatment of neuropsychiatric diseases, launches from stealth having raised a total of $140 million (£107…
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Dyne’s DYNE-101 Earns FDA Breakthrough Status, Eyes Accelerated DM1 Approval

Jun 18, 2025
Dyne Therapeutics, Inc. announced that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Therapy Designation to its investigational drug DYNE-101 for the treatment of…
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BioAegis Gets FDA Fast Track for ARDS Treatment with Gelsolin

Jun 18, 2025
BioAegis Therapeutics, a pioneering biotech company at the forefront of innovative therapies for inflammatory diseases, announces that the U.S. Food and Drug Administration (FDA) has…
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Industry Reports

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Press Releases

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New Era for Autoimmune T-Cell Engagers Takes Centre Stage…

From Innovation to Acquisition: CrossBridge Bio’s ADC…

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