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Clinical Trial Summary

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.


Clinical Trial Description

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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02468674
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 2
Start date July 22, 2015
Completion date December 3, 2018

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