drugset / Trial / NCT03045302
Assessment of BIM23B065, Given as Repeated Subcutaneous Injection in Subjects With Acromegaly
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |