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TANGENT (SNX-301-020)

A Phase III, Multicentre, Randomised, Double-Blind Study to Assess the Safety and Efficacy of Emactuzumab vs. Placebo in Subjects with Tenosynovial Giant Cell Tumour.
  • Ouvert à Paris depuis le : 14/02/2025
  • Public cible : Adult
  • Phase : Phase III

Description de l'essai

The primary efficacy objective of this study is to estimate the treatment effect of emactuzumab by ORR by 6 months from initiation of therapy in the blinded phase compared to placebo.;ORR according to RECIST v1.1 by 6 months from initiation of therapy based on independent, blinded central review
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