Sanctioned for use with doxorubicin in cases that cannot be treated with radiation or surgery
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.
Lartruvo, a platelet-derived growth factor receptor-alpha blocking antibody, has been sanctioned for use with doxorubicin in cases that cannot be treated with radiation or surgery, the FDA said Wednesday in a news release.
The drug was evaluated in clinical trials involving 133 patients with soft tissue carcinomas. Average survival among patients who took Lartruvo and doxorubicin was 8.2 months, compared with 4.4 months among patients who took doxorubicin alone. Potential side effects identified during the studies included harm to a developing fetus, hypotension, fever, chills, nausea, fatigue, neutropenia, 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.
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