luveltamab tazevibulin (STRO-002) - Sutro Biopharma
Sutro Biopharma Announces Initiation of the Registration-enabling REFRαME-P1 Trial with Luvelta for Pediatric Patients with CBF/GLIS AML (GlobeNewswire) - Nov 1, 2024 - "Sutro Biopharma, Inc...announced that REFRαME-P1, the registration-directed study of luveltamab tazevibulin (luvelta) for pediatric patients with CBFA2T3::GLIS2 (CBF/GLIS; RAM phenotype) acute myeloid leukemia (AML), has been initiated and is open for enrollment." 
Trial status • Acute Myelogenous Leukemia
https://www.globenewswire.com/news-release/2024/11/01/2973317/0/en/Sutro-Biopharma-Announces-Initiation-of-the-Registration-enabling-REFR%CE%B1ME-P1-Trial-with-Luvelta-for-Pediatric-Patients-with-CBF-GLIS-AML.html
 
Nov 1, 2024
 
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