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FDA Approves Evkeeza for Youngest Children with Rare Genetic Cholesterol Disorder

Sep 29, 2025
Regeneron Pharmaceuticals announced that the U.S. Food and Drug Administration (FDA) has approved Evkeeza (evinacumab-dgnb) for treating children aged 1 to under 5 years with homozygous…
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Er-Kim and Sentynl Therapeutics Partner to Expand Access to Rare Disease Treatments in EMEA and…

Sep 26, 2025
Er-Kim, an international pharmaceutical company focused on commercializing novel therapies across the EMEA region, has entered into a distribution agreement with Sentynl Therapeutics,…
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Biostar Pharma’s Utidelone Receives Third Orphan Drug Designation from FDA for Pancreatic Cancer

Sep 26, 2025
Biostar Pharma, the U.S. subsidiary of Beijing Biostar Biopharmaceutical, announced that its core drug candidate, Utidelone, has been granted Orphan Drug Designation (ODD) by the U.S.…
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Eli Lilly Expands Innovation Network with New Gateway Labs Site in San Diego

Sep 26, 2025
Eli Lilly and Company has officially opened its newest Lilly Gateway Labs (LGL) location in San Diego, California, marking an expansion of its shared innovation hubs that support…
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Lonza’s Synaffix Partners with Qurient to Develop Dual-Payload ADC

Sep 26, 2025
Synaffix B.V., a Lonza company focused on advancing clinical-stage antibody-drug conjugate (ADC) technologies, has entered into a licensing agreement with South Korea–based…
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Basilea Secures BARDA Contract for Phase 3 Oral Antibiotic Development

Sep 26, 2025
Basilea Pharmaceutica Ltd, a commercial-stage biopharmaceutical company based in Allschwil, Switzerland, announced that it has been awarded a contract by the U.S. Biomedical Advanced…
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Harmony Biosciences Shares Phase 3 RECONNECT Data on ZYN002 for Fragile X Syndrome

Sep 26, 2025
Harmony Biosciences Holdings, Inc. has released topline results from its Phase 3 RECONNECT Study evaluating ZYN002, a transdermal cannabidiol gel, in patients with Fragile X syndrome…
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FDA Approves Inluriyo for Advanced ER+, HER2-, ESR1-Mutated Breast Cancer

Sep 26, 2025
The U.S. Food and Drug Administration (FDA) has approved Inluriyo (imlunestrant, 200 mg tablets), a new oral treatment from Eli Lilly and Company, for adults with estrogen…
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European Commission Approves Eli Lilly’s Kisunla for Early Alzheimer’s Disease

Sep 26, 2025
Eli Lilly and Company announced that the European Commission has granted marketing authorization for Kisunla (donanemab) to treat adults with early symptomatic Alzheimer’s disease (AD),…
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Cellectar Biosciences Partners with Evestia Clinical for Phase 1b Trial of CLR 125 in…

Sep 25, 2025
Cellectar Biosciences, a late-stage clinical biopharmaceutical company specializing in cancer drug development, has entered into an agreement with Evestia Clinical to provide full…
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Industry Reports

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Press Releases

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