Dual weekly therapy delivers sustained growth gains in children with achondroplasia
Weekly navepegritide combination sustains growth through 78 weeks in achondroplasia. Read what the small COACH trial shows and cannot prove.
Weekly navepegritide combination sustains growth through 78 weeks in achondroplasia. Read what the small COACH trial shows and cannot prove.
Bezisterim improves motor, non-motor and inflammatory measures in a small Parkinson’s trial. Read what the data show and why doubts remain.
Aravax has secured United States Food and Drug Administration Fast Track designation for PVX108, an investigational peptide immunotherapy designed to retrain peanut-specific immune responses without containing whole peanut proteins or allergen extracts. The regulatory milestone increases the importance of Phase 2 results expected later in 2026.
LX2020 gains FDA RMAT status after early PKP2 heart data. Read what the designation changes and why the evidence remains preliminary.
ACR-2316 enters randomized expansion after early lung cancer responses. Read how Acrivon will compare two weekly doses across six tumor groups.
FDA clearance allows Bria-PROS+ to enter Phase 1/2a prostate cancer testing. Read how the off-the-shelf cellular immunotherapy works.
BP-205 Phase 1 data show a 25-hour half-life and support once-daily dosing as Harmony advances its orexin agonist into further clinical testing.
BEAM-302 enters pivotal AATD testing after early base-editing data. Read how the study could support an accelerated approval pathway.
Rhythm Pharmaceuticals reports an 11.6% BMI reduction with weekly RM-718 in a small hypothalamic obesity study. See what the data reveal.
Aravax wins FDA Fast Track status for PVX108 as Phase 2 peanut allergy data approach. Read what the designation changes for development.