drugset / Trial / NCT05738993

A Double-Blind, Comparative, Randomized Clinical Study of the Pharmacokinetics, Safety, and Immunogenicity of a Single Intravenous Infusion of BCD-178 or Perjeta® in Healthy Volunteers

NCT05738993

Phase 1 Unknown 100 enrolled Biocad
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a double-blind, comparative, randomized phase I study comparing pharmacokinetics, safety and immunogenicity profiles of a biosimilar pertuzumab (BCD-178) and Perjeta after a single intravenous infusion in healthy male volunteers

Timeline

Start
2022-08-08
Primary completion
2023-04-30
Completion
2024-01-31

Drugs

EvaluationDrugModalityDoseRoute
Subject BCD-178 Unknown 420 mg Intravenous
Comparator Pertuzumab Monoclonal antibody 420 mg Intravenous

Indications