Drug Discovery & DDS– category –
-
C4 Therapeutics Grants Stock Options to New Employees Under Nasdaq Rule, Bolstering TPD Talent Acquisition
C4 Therapeutics, Inc. USA Overview C4 Therapeutics (C4T) announced it has granted stock options to newly hired employees under Nasdaq Listing Rule 5635(c)(4). This inducement grant is a critical component of the company's strategy to adv... -
BioMarin to Present Corporate Strategy and Pipeline at Canaccord Genuity Annual Growth Conference
BioMarin Pharmaceutical Inc. (Investor Relations) USA Overview BioMarin Pharmaceutical announced its participation in the Canaccord Genuity 46th Annual Growth Conference in Boston on August 12, 2026. This investor-focused event provides ... -
C4 Therapeutics Enters New Partnership with Roche for Degrader-Antibody Conjugate (DAC) Development, Reports Strong Q2
C4 Therapeutics, Inc. USA Overview C4 Therapeutics (C4T) reported robust financial results for Q2 2026 and announced a new collaboration agreement with Roche to advance research into degrader-antibody conjugate (DAC) modalities. This str... -
Generate Biomedicines Advances Novel AI-Designed Candidate GB-4362 to Clinical Development, Pushing Tolerability Limits
Generate:Biomedicines (Blog Posts) USA Overview Generate:Biomedicines announced the advancement of its novel candidate drug, GB-4362, designed using its generative biology platform, into clinical development. This milestone exemplifies t... -
Merck’s sBLA for ENFLONSIA™ Accepted by FDA for Expanded RSV Prophylaxis in High-Risk Infants Under Two for Second Season
Merck.com (News releases) USA Overview Merck announced that the U.S. FDA has accepted its supplemental Biologics License Application (sBLA) for ENFLONSIA™ (clesrovimab-cfor) to expand its Respiratory Syncytial Virus (RSV) lower respirato... -
Merck Achieves Robust Q2 2026 Performance, Upgrades Full-Year Guidance, and Empatran Secures FDA Breakthrough Therapy Designation for Lupus
Merck USA Overview Merck reported strong second-quarter 2026 financial results and consequently upgraded its full-year guidance, bolstered by the U.S. FDA's Breakthrough Therapy Designation for Empatran in July. Empatran, developed for l... -
Researchers Uncover Key Cellular Uptake Pathway for Antisense Therapies, Paving Way for Enhanced Efficacy
ecancer Global Overview Researchers have made a significant discovery, identifying the crucial intracellular uptake pathway for antisense oligonucleotides (ASOs), a therapeutic approach to halt aberrant protein production in various dise... -
AI Generative Biology Transforms Drug Discovery: Multiple AI-Designed Drugs Enter Clinics, One in Late-Stage Development
SynBioBeta USA Overview AI-driven generative biology is rapidly transitioning from laboratory promise to human clinical trials, fundamentally reshaping the drug discovery paradigm. At the AI4 2026 conference, biotech leaders highlighted ... -
Exosome Therapeutics Advancing in Neurodegenerative and Oncology Fields, Eyeing Blood-Brain Barrier Penetration
BioInformant Global Overview Exosome therapeutics are showing significant promise in 2026, particularly for neurodegenerative diseases due to their unique ability to cross the blood-brain barrier, with clinical development also progressi... -
FDA Grants Accelerated Approval to BMS’s CELMoD Zenbexus in Quadruple Therapy for Relapsed/Refractory Multiple Myeloma
Drugs.com, FDA.gov USA Overview The U.S. FDA has granted accelerated approval to Bristol Myers Squibb's cereblon E3 ligase modulating agent (CELMoD) Zenbexus (iberdomide) in combination with daratumumab, hyaluronidase-fihj, and dexametha...
