CARsgen is working to transform outcomes for patients with solid tumors by advancing the potential of CAR T technologies
The BD Neopak Glass Prefillable Syringe platform is designed for the complex needs of biologics and combination products
The FDA has set a Prescription Drug User Fee Act (PDUFA) target action date of June 10, 2026
BFF provides bookable fermentation upscaling capacity, process expertise, and quality procedures for pilot campaigns, generating decision-grade data without companies needing to build their own facilities
Royalty Pharma to provide up to $500 million, including $75 million for Phase 2b funding
MH002, a rationally designed live microbial consortium, combines six well-characterized commensal strains to target disease-specific mechanisms
Vanda strongly disputes the FDA’s reasoning
The therapy is mutation-agnostic and aims to overcome limitations of existing EGFR-targeting drugs by concentrating degradation in tumors while sparing healthy tissue
Subscribe To Our Newsletter & Stay Updated