Fate Therapeutics Gets FDA Clearance for FT839 Autoimmune CAR-T Therapy
Fate Therapeutics receives FDA clearance for FT839 autoimmune CAR-T therapy, a dual-targeted allogeneic cell product designed to treat rheumatoid...
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Fate Therapeutics receives FDA clearance for FT839 autoimmune CAR-T therapy, a dual-targeted allogeneic cell product designed to treat rheumatoid...
Nature Medicine's RWE trial emulation framework is reshaping FDA approval pathways. Here's what sponsors running traditional RCTs need to...
SAT-3247 showed muscle fat reduction in DMD adults at six months, with participants displaying improved upper limb function and...
Setmelanotide Phase 3 Trial achieves 19.8 percentage-point BMI reduction in hypothalamic obesity, published in NEJM following FDA approval.
Caidya and Simbec-Orion's June 2026 merger creates real site-level friction: dual CTMS logins, monitoring model gaps, and budget renegotiations...
FDA accepts Arcutis ZORYVE for atopic dermatitis in 3-month-old infants, expanding treatment options for the youngest patients with the...
ARMR Sciences' fentanyl vaccine entered Phase 1 in January 2026 with 40 participants. The science is credible. The path...
Theriva's VCN-01 Phase 2a trial in Spain aims to test more frequent dosing in metastatic pancreatic cancer and evaluate...
Givinostat extended ambulation to median age 17.3 years in DMD patients, with quantitative MRI data showing preserved muscle tissue...
FDA confirms single Phase 3 trial sufficient for ATH434 NDA in Multiple System Atrophy, backed by Phase 2 evidence.