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2026
Pharma News, 2026
FDA Approves Eton's Desmoda Oral Solution for Central Diabetes Insipidus
The FDA has approved Desmoda (desmopressin acetate) oral solution by Eton Pharmaceuticals for managing central diabetes insipidus in adults and children.
Asahi Kasei Acquires Aicuris Anti-infective Cures for $920.7 Million
Asahi Kasei is acquiring Aicuris Anti-infective Cures for $920.7m to expand its specialty pharma platform into severe infectious diseases and boost R&D.
FDA Unveils Ultra-Rare Therapy Pathway & Fast-Tracks New Lung Cancer Drug
The FDA released draft guidance for an ultra-rare disease therapy pathway, the Plausible Mechanism Framework, and fast-tracked lung cancer drug Hernexeos.
Quotient & Ipsen Extend Partnership for Ultra-Rare FOP Disease Therapy
Quotient Sciences and Ipsen extend their commercial partnership to produce Sohonos for FOP, enhancing HPAPI capabilities at the Boothwyn, PA facility.
India's Single-Dose Dengue Vaccine Candidate Advancing to Phase 3 Trials
Panacea Biotec's single-dose dengue vaccine candidate, DengiAll, advances to Phase III trials, offering hope for India's first domestic dengue prevention.
IQVIA to Acquire Charles River Drug Discovery Assets to Expand R&D Pipeline
IQVIA Holdings agrees to acquire selected drug discovery assets from Charles River Laboratories to expand its end-to-end R&D and early-stage capabilities.
New Promising Drug PXS-5505 for Invasive Lobular Breast Cancer Tested
EPFL researchers have developed new preclinical models and successfully tested PXS-5505, a promising new drug targeting invasive lobular breast carcinoma.
EMA Backs Orphan Drug Status for Soligenix’s SGX945 in Behçet's Disease
Soligenix receives a positive EMA COMP opinion for SGX945 orphan drug designation to treat Behçet's Disease, advancing its novel dusquetide therapy.
Agentic AI & The Human Element: Building Trustworthy Clinical Trial Automation
Explore how agentic AI can automate and improve clinical trial setups while emphasizing the critical need for human oversight and strong governance protocols.
HotSpot Therapeutics to Present IRF5 Data at 15th European Lupus Meeting
HotSpot Therapeutics will present preclinical data from its IRF5 small molecule inhibitor program at the 15th European Lupus Meeting in Lisbon, Portugal.
FDA Accepts Beren Therapeutics' NDA for Niemann-Pick Disease Treatment
The FDA has accepted Beren Therapeutics' NDA for adrabetadex, a potential disease-modifying treatment for infantile-onset Niemann-Pick disease type C.
Gibson Oncology Starts Phase 2 Trial of LMP744 for Recurrent Glioblastoma
Gibson Oncology enters Phase 2 clinical trials with LMP744 to treat first-time recurrent glioblastoma, targeting topoisomerase 1 and cMYC oncogene inhibition.
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