Overview

A 6 Month Safety Extension Study of MBGS205

Status:
Completed
Trial end date:
2018-11-21
Target enrollment:
0
Participant gender:
Male
Summary
This is a 6 months, active treatment, extension study, open to subjects who have completed full 24 weeks in Study MBGS205 (A Phase IIb multicentre, double-blind, dose-ranging, randomised, placebo-controlled study evaluating safety and efficacy of BGS649 in male obese subjects with hypogonadotropic hypogonadism [HH]).The main purpose of Study MBGS206 is to evaluate long term safety and efficacy parameters in subjects after 12 months exposure with BGS649.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Mereo BioPharma
Criteria
Inclusion Criteria:

- Participating in Study MBGS205 and completion of the 24 week treatment period without
meeting any discontinuation criteria of Study MBGS205

- In opinion of the investigator has been compliant with the requirements of the Study
MBGS205 protocol.

Exclusion Criteria:

-Meeting any of the discontinuation criteria of initial Study MBGS205