drugset / Trial / NCT03172208

Caplacizumab Single and Multiple Dose Study in Healthy Japanese and White Subjects.

NCT03172208

Phase 1 Completed 60 enrolled Ablynx, a Sanofi company
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

EvaluationDrugModalityDoseRoute
Subject Caplacizumab Protein / enzyme biologic Intravenous

Indications

No indication recorded.