FDA approves Vitrakvi for cancers with certain genetic trait

November 28, 2018

(HealthDay)—Vitrakvi (larotrectinib) has been approved by the U.S. Food and Drug Administration to treat adult and pediatric patients whose cancers have a specific genetic feature.

The approval marks the second drug sanctioned to treat any type of cancer with a certain genetic feature, rather than the drug targeting a cancer that originated in a specific part of the body, the agency said in a news release. Vitrakvi targets that have a neurotrophic receptor tyrosine kinase (NTRK) gene fusion without a known acquired resistance mutation.

The type of mutation targeted by the drug is rare, but can occur in many places in the body. The drug was evaluated in involving 55 children and adults with a targeted form of cancer. Of the 75 percent of recipients who responded to the drug, 73 percent of responses lasted at least six months and 39 percent lasted a year or more, the FDA said.

The drug's most common side effects included fatigue, nausea, cough, constipation, diarrhea, dizziness, and vomiting. Pregnant or breastfeeding women should not take Vitrakvi, which could harm a developing fetus or newborn baby, the agency said.

Explore further: New drug approved for all cancers with genetic marker

More information: More information

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