drugset / Trial / NCT03172208
Caplacizumab Single and Multiple Dose Study in Healthy Japanese and White Subjects.
RandomizedParallel-groupTriple-blindOther
Summary
Primary objective: To assess the safety and tolerability of single ascending intravenous (i.v.) doses, a single subcutaneous (s.c.) dose of caplacizumab (Part I), and multiple s.c. doses of caplacizumab (Part II) in Japanese subjects. Secondary objectives: * To compare the pharmacokinetic (PK) and pharmacodynamic (PD) profiles (total vWF:Ag concentration levels \[vWF:Ag\], coagulation factor VIII \[FVIII:C\], and ristocetin cofactor activity \[RICO\]) after single i.v. or s.c. administration of caplacizumab in Japanese and White subjects. * To evaluate the immunogenicity of caplacizumab (anti-drug antibodies \[ADA\]) in Japanese subjects.
Timeline
- Start
- 2017-06-05
- Primary completion
- 2017-10-19
- Completion
- 2017-10-19
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Caplacizumab | Protein / enzyme biologic | — | Intravenous |
Indications
No indication recorded.