Foresee Pharmaceuticals Co., Ltd. (6576.TWO) (“Foresee”) announced today that the 505(b)(2) New Drug Application (NDA) for FP-001 LMIS 50mg, or CAMCEVI™ 42MG, a ready-to-use 6-month depot formulation of leuprolide mesylate, has been accepted for review by the U.S. Food and Drug Administration (FDA). In its Day-74 letter, the FDA stated tha
October 8, 2020
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