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US FDA approves Mirati’s lung cancer drug

Mirati was seeking approval for the drug for treating patients with advanced lung cancer who have stopped responding to other therapies

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The US Food and Drug Administration (FDA) recently approved Mirati Therapeutics’s lung cancer drug Adagrasib, according to the health regulator’s website.

Mirati was seeking approval for the drug for treating patients with advanced lung cancer who have stopped responding to other therapies.

Adagrasib, the oral drug, is designed to target a mutated form of a gene known as KRAS that occurs in about 13 per cent of Non-Small Cell Lung Cancers (NSCLC), the most common form of the disease, and less frequently, in some other solid tumours.

Another KRAS inhibitor, Amgen’s Lumakras is already available to treat patients suffering from advanced lung cancer as a second-line therapy, after an initial therapy fails or stops working.

Third-quarter sales of Lumakras, which was approved last year, totalled $75 million.

Earlier this month, Mirati presented early data from studies of adagrasib in combination with Merck & Co’s immunotherapy Keytruda as an initial treatment for metastatic NSCLC.

The results showed the combination helped about half of trial participants. However, Mirati said it would first conduct a pivotal trial only in patients with lower levels of the protein targeted by Keytruda, with a high bar of proving superiority over standard of care.

Edits by EP News Bureau

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