
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.
On December 1, 2020, South San Francisco, California – Genentech, a member of the Roche Group, annou···【more】
Recommended:622026-15-01
On August 9, 2023, the U.S. Food and Drug Administration (FDA) approved pralsetinib (trade name: Gav···【more】
Recommended:492026-15-01
On December 1, 2020, South San Francisco, California – Genentech, a member of the Roche Group, announced that the U.S. Food and Drug Administration (FDA) has approved Gavreto™ (pra···【more】
Article source:Lucius LaosRelease date:2026-01-15Recommended:62
On August 9, 2023, the U.S. Food and Drug Administration (FDA) approved pralsetinib (trade name: Gavreto, developed by Genentech) for regular use in adult patients with metastatic ···【more】
Article source:Lucius LaosRelease date:2026-01-15Recommended:49

Lucius Pharmaceutical Co., Ltd., was established in 2020 in Vientiane, the capital of Laos. It aims to offer safe, effective, and affordable medicines globally. With a factory spanning 25,000 square meters, the company manufactures 200+ generic drugs in diverse therapeutic fields.
Address:No.26 Thongmang village, Xaythany district, Vientiane Capital, Laos
E-mail:laoslucius@gmail.com
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