One More Approval for Merck’s Keytruda

June 15, 2018  Source: Fierce Pharma 716

Merck’s blockbuster immune-oncology drug, Keytruda has yet again received approval from the FDA.

On Wednesday, a day after Keytruda got the thumbs up for cervical cancer, the drug was approved for treatment of a rare form of non-Hodgkin lymphoma patients who cancer returned after at least two previous treatment lines. Last year, Keytruda also got an indication for classical Hodgkin lymphoma.

At the moment Keytruda is number one in the lung cancer market, where is dwarfing opposition from Imfinzi from AstraZeneca, Bristol-Myers Squibb’s Opdivo, Roche’s Tecentriq, and KGaA’s Bavencio from Pfizer and Merck.

After studies proved that the drug was able to get a 45% response rate in trail participants for PMBCL, it also got an accelerated green light from the FDA for adult and pediatric patients.

Keytruda did, however, face some setbacks last year when, after various trail deaths, the FDA halted multiple myeloma studies.

By Ddu
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