Merck receives positive EU CHMP opinion for Keytruda as adjuvant treatment for cell lung cancer
Opinion granted based on positive disease-free survival results from the Phase 3 KEYNOTE-091 trial
Opinion granted based on positive disease-free survival results from the Phase 3 KEYNOTE-091 trial
The Government of India continues to prioritise initiatives aimed at enhancing the accessibility and equity of health services
KEYTRUDA is the first immunotherapy approved in the EU for the first-line treatment of this patient population
With India supplying around 60% of the world's vaccine needs and 20-22% of generic exports, the country is dedicated to providing affordable, high-quality drugs and contribute to global accessibility
Combating the prevalent stigma against TB in the society, India has been committed to providing, enabling and patient-centric support to all, individuals suffering from TB
There is a pressing need for continuous improvement and innovation in food safety systems to keep pace with emerging food trends and habits
If approved, KEYTRUDA would be the first immunotherapy for the first-line treatment of HER2-positive advanced gastric or GEJ cancer in tumors expressing PD-L1 (CPS ?1) in the EU
Based on a subgroup analysis by PD-L1 expression from KEYNOTE-811, Merck is working with the US FDA to update the current indication for KEYTRUDA in HER2-positive gastric or GEJ adenocarcinoma
In Phase 3 CCTG IND.227/KEYNOTE-483 trial, KEYTRUDA plus chemotherapy also demonstrated statistically significant improvements in PFS and ORR compared to chemotherapy alone
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