Johnson & Johnson's Rybrevant Faspro was approved as a treatment for people with lung cancer by the Food and Drug Administration.
Rybrevant Faspro was approved across all indications for subcutaneous administration for patients with epidermal growth factor receptor-mutated non-small cell lung cancer, J&J said Wednesday.
The approval is based on the results of a Phase 3 trial, which met both co-primary pharmacokinetic endpoints.
Patients treated showed longer duration of response, improved progression-free survival and longer overall survival.
Rybrevant Faspro enables a simpler, shorter administration time for a first-line combination regime when combined with Lazcluze.
Rybrevant is approved in the U.S. across four indications in that specific type of lung cancer.
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