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FDA Approves Sirolimus Protein-Bound Particles for PEComa

On Novemeber 23, 2021, the U.S. Food and Drug Administration (FDA) approved sirolimus protein-bound particles for injectable suspension (albumin-bound) for intravenous use for the treatment of adult patients with locally advanced unresectable or metastatic malignant perivascular epithelioid cell tumor (PEComa).

Read Aadi Bioscience, Inc.'s announcement.

Posted 11/23/2021