WEDNESDAY, Oct. 19, 2016 (HealthDay News) -- Lartruvo (olaratumab) has been approved by the U.S. Food and Drug Administration to treat adults with certain soft-tissue sarcomas, cancers that develop in areas such as the muscles, fat, blood vessels and tendons.
Lartruvo has been sanctioned for use with the chemotherapy drug doxorubicin in cases that cannot be treated with radiation or surgery, the FDA said Wednesday in a news release.
More than 12,000 new cases of soft-tissue sarcoma are projected to be diagnosed this year and nearly 5,000 people are likely to die from the disease, the agency said, citing estimates from the U.S. National Cancer Institute.
Lartruvo is designed to block cell receptors that fuel tumor growth, the FDA said. The drug was evaluated in clinical trials involving 133 people with soft-tissue sarcomas. Average overall survival among people who took Lartruvo and doxorubicin was 26.5 months, compared with 14.7 months among people who took doxorubicin alone.
Potential side effects identified during the studies included harm to a developing fetus, low blood pressure, fever, chills, nausea, fatigue, low white blood cell count and musculoskeletal pain.
Lartruvo's maker, Indianapolis-based Eli Lilly and Company, is conducting a larger study to further evaluate the drug's effectiveness among numerous types of soft-tissue sarcoma, the agency said.
To learn more, visit the Food and Drug Administration.
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