drugset / Trial / NCT00581191
Study Evaluating the Safety and Tolerability of Single Ascending Dose (SAD) SLV-351 in Healthy Subjects
Phase 1
Terminated
72 enrolled
Wyeth is now a wholly owned subsidiary of Pfizer
Solvay Pharmaceuticals · collab
RandomizedSingle-groupTriple-blindTreatment
Summary
Safety and tolerability of single oral doses in healthy subjects.
Timeline
- Start
- 2008-01
- Primary completion
- 2008-03
- Completion
- 2008-03
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | SLV-351 | Unknown | 0.5 mg | Oral |
| Subject | SLV-351 | Unknown | 1 mg | Oral |
| Subject | SLV-351 | Unknown | 2.5 mg | Oral |
| Subject | SLV-351 | Unknown | 5 mg | Oral |
| Subject | SLV-351 | Unknown | 10 mg | Oral |
| Subject | SLV-351 | Unknown | 15 mg | Oral |
| Subject | SLV-351 | Unknown | 20 mg | Oral |
| Subject | SLV-351 | Unknown | 30 mg | Oral |
Indications
No indication recorded.