A randomised, double blind, placebo controlled, multi center, parallel group, dose finding, pivotal, phase IIb/III study to evaluate the efficacy, safety and tolerability of intravenous BYM338 at 52 weeks on physical function, muscle....

Project Details

Short titleR:KBD A randomised, double bli
StatusFinished
Effective start/end date12/09/14 → 20/07/16

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