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Injectable cancer medication Keytruda Qlex Gains for FDA approval

The US Food and Drug Administration (FDA) has approved a new injected version of the Keytruda (Pembrolizumab) cancer drug that can be easier for many patients than the older intravenous version of the drug given by infusion.

The FDA approved the injected shape, Keytruda Qlex, for a wide variety of solid tumors that have been treated with the intravenous form of the drug, including certain malignant tumors in the lungs, breasts, colon, head and neck, digestive tract and reproductive system, the FDA said in a press release.

Keytruda’s safety and efficiency are similar, according to Merck.

With the injected version, “the main advantage is convenience and time,” explains Pavlos Msaouel, MD, PHD, associate professor at the University of Texas MD Anderson Cancer Center in Houston.

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