Enhertu recently received Breakthrough Therapy Designation, accelerating development and review for this critical patient population
Iza-bren met both dual primary endpoints, delivering statistically significant and clinically meaningful improvements in progression-free survival
Arcellx develops innovative immunotherapies for cancer and other incurable diseases
Iberdomide has the potential to be the first approved CELMoD agent
The FDA’s regulatory decision is expected in Q2 2026 under the Prescription Drug User Fee Act (PDUFA)
This marks the second indication for which gumokimab has gained NDA review acceptance
Improvements were also seen in complete response rates, duration of response, and time to next treatment
The partnership will launch a Phase 1b cohort within Boehringer’s ongoing Beamion-BCGC1 trial
The therapy is mutation-agnostic and aims to overcome limitations of existing EGFR-targeting drugs by concentrating degradation in tumors while sparing healthy tissue
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