drugset / Trial / NCT03599063
Singe Dose, First in Human Study of PF- 06946860 in Healthy Adult Subjects
RandomizedSequentialTriple-blindBasic science
Summary
The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics of PF-06946860 in healthy adult subjects following single ascending doses This is the first clinical study of PF-06946860.
Timeline
- Start
- 2018-07-30
- Primary completion
- 2019-09-18
- Completion
- 2019-09-18
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | ponsegromab | Monoclonal antibody | 0.1 mg | Subcutaneous |
| Subject | ponsegromab | Monoclonal antibody | 0.3 mg | Subcutaneous |
| Subject | ponsegromab | Monoclonal antibody | 1 mg | Subcutaneous |
| Subject | ponsegromab | Monoclonal antibody | 3 mg | Subcutaneous |
| Subject | ponsegromab | Monoclonal antibody | 10 mg | Subcutaneous |
| Subject | ponsegromab | Monoclonal antibody | 30 mg | Subcutaneous |
| Subject | ponsegromab | Monoclonal antibody | 100 mg | Subcutaneous |
Indications
No indication recorded.