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Loxo,Bayer gets U.S approval for cancer drug Larotrectinib

Loxo,Bayer gets U.S approval for cancer drug Larotrectinib

New Delhi: A Loxo Oncology Inc drug larotrectinib shown to be effective against a wide variety of cancers driven by a single, rare genetic mutation has won U.S. approval, the Food and Drug Administration announced on Monday.

The drug, larotrectinib, will be sold under the brand name Vitrakvi and priced at $32,800 per month, in partnership with Bayer AG. It will be Loxo’s first commercial medicine.

Kevin O’Leary, Bayer’s vice president of pricing and contracting, said Bayer and Loxo will assist patients financially and offer a value-based program, refunding both out-of-pocket and insurer payments for patients who do not see a clinical benefit within the first three months of treatment.

The mutation, known as TRK fusion, occurs in no more than 3,000 Americans each year, or less than 1 per cent of patients with solid tumour cancers, according to Bayer.

The FDA said it approved Vitrakvi for adults and pediatric patients who have advanced solid tumour cancers with the gene mutation that has progressed after other treatments.

In a 122-patient clinical trial, larotrectinib significantly reduced tumours in 81 per cent of those with 24 different types of cancer, including lung, pancreatic, breast, thyroid, colon and soft tissue sarcomas. Researchers reported an extremely mild side effect profile for the medicine.

“Today’s approval marks another step in an important shift toward treating cancers based on their tumour genetics rather than their site of origin in the body,” FDA Commissioner Scott Gottlieb said in a statement.

Merck & Co’s Keytruda last year became the first cancer drug to win approval for a so-called tumour-agnostic use, though that remains a small market for the big-selling drug.

Currently, most cancer patients are not routinely tested for tumour mutations, making it difficult to find those who will benefit from the drug. O’Leary said in a phone interview that Bayer is talking with payers about expanding testing.

Oppenheimer has forecast annual larotrectinib sales of more than $1 billion by 2024.

Loxo is also developing a drug, LOXO-292, that targets another rare gene fusion mutation known as RET, seen in thyroid, lung and other cancers. Loxo and Bayer have a follow-up TRK drug in development known as LOXO-195.

Similar drugs being developed by Roche and others are expected to fuel increased demand for advanced genetic testing of tumours in order to identify the patients likely to benefit from the treatments.

The U.S. government earlier this year said the Medicare program for Americans aged 65 and older will cover so-called next-generation sequencing, which looks for hundreds of mutations across all solid tumours, for advanced cancer patients.

Also Read: Loxo-Bayer cancer drug gets priority review from FDA

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Source: Reuters
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