Clinical TrialsPetosemtamab, a unique bispecific antibody, shows an impressive 67% overall response rate in Phase 2 trials for head and neck squamous cell carcinoma.
Market PotentialPetosemtamab is trending favorably towards best-in-class status, offering greater commercial advantages in treating HPV+ patients in a large market with high unmet needs.
Regulatory ProgressThe FDA has not requested additional clinical data for Zenocutuzumab, indicating a smooth approval process and no expected material impact on product launch.