One of your patients might be eligible to enroll in a clinical trial currently recruiting people with breast cancer.

In 2021, the FDA criticised MSD for relying on an early endpoint to seek approval for Keytruda in early-stage TNBC.

Roche RHHBY announced that the FDA has approved the subcutaneous (SC) formulation of the blockbuster immunotherapy drug ...

Merck’s Keytruda plus Padcev receives European approval for first-line treatment of unresectable or metastatic urothelial carcinoma in adults: Rahway, New Jersey Wednesday, Sept ...

In stage 4, a tumor that began in the liver has spread to either nearby lymph nodes and/or distant lymph nodes and organs.Liver cancer is relatively rare, with under 42,000 cases being diagnosed each ...

Study findings were mixed regarding the postsurgical combination of Keytruda and chemotherapy with or without radiation among ...

Positive opinion granted for KEYTRUDA plus chemotherapy for the first-line treatment of adult patients with primary advanced or recurrent endometrial carcinoma who are candidates for systemic therapy, ...

Iovance's FDA-approved cell therapy for melanoma and the financial uncertainties affect its stock and long-term viability.

At WCLC, five-year survival data to be presented on Libtayo (PD-1 inhibitor) first-line monotherapy in advanced non-small cell lung cancerAt ...

At 10 years, more than one-third (34.0%) of patients with advanced melanoma were alive after treatment with KEYTRUDA, ...

Gilead Sciences, Inc. (Nasdaq: GILD) will present new data from the company’s broad lung cancer clinical development program during the IASLC 2024 World Conference on Lung Cancer hosted by the ...

Detailed results from the TROPION-Lung01 Phase III trial showed a clinically meaningful trend toward improving overall survival (OS) with datopotamab ...