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Oragenics Partners with Receptor.AI to Expand Neurological Drug Pipeline Using AI-Powered Discovery

Oct 8, 2025
Oragenics, a clinical-stage biotech company focused on brain-targeted therapeutics, has announced a strategic collaboration with Receptor.AI, a drug profiling company leveraging…
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Affinia Therapeutics Secures $40 Million to Advance First-in-Class Gene Therapy for Rare Heart…

Oct 8, 2025
Affinia Therapeutics has announced the close of a $40 million Series C financing round to advance development of its lead gene therapy candidate, AFTX-201, for the treatment of BAG3…
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Datroway Becomes First Therapy to Improve Survival Over Chemotherapy in Hard-to-Treat…

Oct 7, 2025
AstraZeneca and Daiichi Sankyo have announced breakthrough results from the Phase III TROPION-Breast02 trial, showing that their antibody drug conjugate Datroway (datopotamab…
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Chiesi Group and Arbor Biotechnologies Partner to Advance Gene Editing Therapies for Rare Liver…

Oct 7, 2025
Chiesi Group and Arbor Biotechnologies have announced an exclusive global collaboration and licensing agreement to advance the development of innovative gene editing therapies for rare…
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FDA Lifts Clinical Hold on Neurizon Therapeutics’ ALS Drug NUZ-001, Clearing Path for Phase 2/3…

Oct 7, 2025
Neurizon Therapeutics Limited has announced that the U.S. Food and Drug Administration (FDA) has lifted the clinical hold on its lead investigational therapy, NUZ-001, a key step…
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FDA Approves Roche’s Tecentriq and Lurbinectedin Combo as First Maintenance Therapy for Advanced…

Oct 6, 2025
Roche has announced that the U.S. Food and Drug Administration (FDA) has approved the combination of Tecentriq® (atezolizumab) and Tecentriq Hybreza® (atezolizumab and…
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FDA Grants Fast Track Designation to Bristol Myers Squibb’s Alzheimer’s Antibody BMS-986446

Oct 3, 2025
Bristol Myers Squibb announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track Designation to BMS-986446, a promising anti-microtubule binding region-tau…
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FDA Grants Breakthrough Therapy Designation to Taysha’s Gene Therapy for Rett Syndrome

Oct 3, 2025
Taysha Gene Therapies announced that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Therapy designation to TSHA-102, its intrathecally delivered AAV9 gene therapy…
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Halozyme to Acquire Elektrofi in $750M Biologics Delivery Deal

Oct 3, 2025
Halozyme Therapeutics has announced a definitive agreement to acquire Elektrofi, a biopharmaceutical company known for its breakthrough ultra-high concentration biologics delivery…
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Takeda Ends Cell Therapy Program Amid Strategic Refocus

Oct 3, 2025
Takeda Pharmaceutical Company has announced it will discontinue its cell therapy research and development efforts as part of a broader strategic portfolio prioritization. The company…
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Industry Reports

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Press Releases

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