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News of Pralsetinib

On September 4, 2020, the U.S. Food and Drug Administration (FDA) approved Pralsetinib (trade name: Gavreto) for the treatment of adult patients with metastatic RET gene fusion-positive non-small cell lung cancer.

On December 1, 2020, Genentech announced that the U.S. Food and Drug Administration (FDA) had approved Pralsetinib (trade name: Gavreto) for the treatment of patients with advanced or metastatic RET gene mutation-positive and RET gene fusion-positive thyroid cancer.

On August 9, 2023, the U.S. Food and Drug Administration (FDA) approved Pralsetinib (trade name: Gavreto) for the routine treatment of RET gene fusion-positive non-small cell lung cancer.

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Lucius Pharmaceuticals (Lao) LTD. (Lucius Pharmaceuticals), with its manufacturing campus in Laos located in the capital city of Vientiane in 2020, officially begins its great journey to make effective and affordable medicines available to people in need around the world...More

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