drugset / Trial / NCT03045302

Assessment of BIM23B065, Given as Repeated Subcutaneous Injection in Subjects With Acromegaly

NCT03045302 ↗

Phase 2 Terminated 4 enrolled Ipsen
NaSingle-groupOpen-labelTreatment

Summary

The purpose of the protocol is evaluate the safety, the pharmacodynamics and the pharmacokinetic of repeated administration of BIM23B065 in subjects with acromegaly.

Timeline

Start
2017-01-26
Primary completion
2017-05-17
Completion
2017-06-02

Outcome

Outcome not reported

Stopped (Business): “Early termination is a sponsor decision. No new safety signal or serious adverse event has been observed.”

Drugs

EvaluationDrugModalityDoseRoute
Subject BIM23B065 Unknown 0.4 mg Subcutaneous
Subject BIM23B065 Unknown 0.6 mg Subcutaneous
Subject BIM23B065 Unknown 0.8 mg Subcutaneous
Subject BIM23B065 Unknown 1 mg Subcutaneous

Indications