Sarcopenia Clinical Trial
Official title:
A 24 Week Off Drug Extension, Parallel Group, Study Assessing Durability of Effect on Skeletal Muscle Strength and Function Following a 6-month Double-blind, Placebo Controlled Study Evaluating Bimagrumab in Older Adults With Sarcopenia (InvestiGAIT Extension)
This extension study was a 24-week off-drug follow-up of the core CBYM338E2202 (NCT ) study and the main objective was to determine the long-term durability of bimagrumab (BYM338) effect after a 6-month treatment period.
Two populations were defined as below:
- Population I: Patients enrolled prior to the protocol amendment 1, who received
bimagrumab 70 mg, 210 mg or 700 mg in the core study, were randomly assigned to two
subgroups within each of three treatment arms to either receive bimagrumab at the same
dose level or placebo. Patients receiving placebo in the core study continued receiving
placebo in the extension study.
- Population II: Patients enrolled after protocol amendment 1, who received bimagrumab 700
mg or placebo in the core study, did not receive study medication in the extension study
and were followed-up per schedule defined in this protocol amendment.
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