drugset / Trial / NCT02280434
Phase 1 Study Accessing the Safety and Tolerability of CBP-307
Phase 1
Completed
64 enrolled
Connect Biopharm LLC
Nucleus Network Ltd · collabTigermed Consulting Co., Ltd · collab
RandomizedParallel-groupQuadruple-blindTreatment
Summary
This study will evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of CBP-307 following oral single and multiple escalating dose administration in healthy subjects.
Timeline
- Start
- 2014-11
- Primary completion
- 2015-08
- Completion
- 2015-08
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | CBP-307 | Unknown | 0.1 mg | Oral |
| Comparator | CBP-307 | Unknown | 0.15 mg | Oral |
| Comparator | CBP-307 | Unknown | 0.25 mg | Oral |
| Comparator | CBP-307 | Unknown | 0.5 mg | Oral |
| Comparator | CBP-307 | Unknown | 2.5 mg | Oral |