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Merz, Kvvit Partner to Develop INBRIJA in Greater China

May 27, 2026
Merz Therapeutics GmbH and Jiangxi Kvvit Pharmaceutical Co. Ltd. have entered into an exclusive licensing and collaboration agreement to develop and commercialize INBRIJA® (levodopa…
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Insilico, HLFM Partner on AI Longevity Models

May 27, 2026
Insilico Medicine and Human Life Foundation Models, Inc. (HLFM) have entered into a multi-million-dollar collaboration to develop what the companies describe as the biotechnology…
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FDA Grants Fast Track to Elunetirom for Bipolar Depression

May 27, 2026
Autobahn Therapeutics announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation to elunetirom, the company’s lead investigational therapy for the…
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Lilly Reports Positive Early Results for VERVE-102

May 27, 2026
Eli Lilly and Company reported positive interim results from the Phase 1b Heart-2 clinical study of VERVE-102, an investigational gene-editing therapy designed to lower low-density…
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EMA Panel Backs BRAFTOVI for Metastatic Colorectal Cancer

May 26, 2026
Pierre Fabre Laboratories announced that the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) has issued a positive opinion recommending approval of…
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Advancing Respiratory Medicine Following ATS – What Now?

May 26, 2026
The energy coming out of this year’s ATS meeting was unmistakable: respiratory medicine is entering a new era of scientific ambition, cross‑industry collaboration, and patient‑centred…
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FDA Approves First Hepatitis Delta Treatment in United States

May 25, 2026
Gilead Sciences announced that the U.S. Food and Drug Administration (FDA) has granted accelerated approval to Hepcludex® (bulevirtide-gmod) 8.5 mg for the treatment of adults living…
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CHMP Supports MAVIRET Approval for Acute Hepatitis C

May 25, 2026
AbbVie announced that the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion recommending approval of MAVIRET®…
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FDA Approves Datroway for Advanced Triple-Negative Breast Cancer

May 25, 2026
AstraZeneca and Daiichi Sankyo announced that the U.S. Food and Drug Administration (FDA) has approved Datroway (datopotamab deruxtecan) for adults with unresectable or metastatic…
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EMA Fast-Tracks Regeneron Gene Therapy for Rare Hearing Loss

May 22, 2026
Regeneron Pharmaceuticals said the European Medicines Agency (EMA) has accepted for review under its Accelerated Assessment pathway the Marketing Authorization Application (MAA) for…
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Industry Reports

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Press Releases

Advancing Respiratory Medicine Following ATS – What Now?

World ADC San Diego Unveils Preliminary Agenda for 17th…

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IQ MPS Leaders to Share Industry Progress on Advancing In…

4th ADC Linker & Conjugation Summit Announces 2026…

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