drugset / Trial / NCT07776132

Pharmacokinetic Characteristics, Safety, and Immunogenicity of HLX29 Compared With HLX11

NCT07776132 ↗

Phase 1 Not yet recruiting 60 enrolled Shanghai Henlius Biotech
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a randomized, double-blind, parallel-controlled study to compare the PK profile of HLX29 and HLX11 and evaluate their safety, tolerability, and immunogenicity after a single intravenous dose in healthy male adult participants.

Timeline

Start
2026-11-05
Primary completion
2027-01-31
Completion
2027-03-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator HLX11 Monoclonal antibody — Intravenous
Subject HLX29 Unknown — Intravenous

Indications

No indication recorded.