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Study identifier: NCT07299955 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Phase 1 Comparative Study to Evaluate Pharmacokinetics, Immunogenicity, Safety and Tolerability of Bmab3000 and Herceptin Hylecta® After a Single 600 mg SC Injection in Healthy Male Volunteers

Condition: Healthy Male Participants  ·  Sponsor: Biocon Biologics UK PLC

PhasePhase 1
Planned participants150
Who can joinMale, 18 Years to 65 Years
Healthy volunteersYes

About this study

This phase I study is to compare the pharmacokinetics (PK), immunogenicity, safety, and tolerability of Bmab3000 (test) and Herceptin Hylecta (reference) after a single subcutaneous (s.c.) dose in healthy male volunteers.

This description comes directly from the study's public registry record.

Talk to the study team

Dr Gursharan Singh, MBBS, PhD  ·  9650628534  ·  gursharan.singh@biocon.com

Rajesh CN  ·  +919725466994  ·  rajesh.cn@biocon.com

Always discuss trial participation with your own doctor first.

Locations (1)

New Zealand Clinical Research (NZCR)Christchurch, Main Building: 264 Antigua Street,, New ZealandRecruiting

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Source record: clinicaltrials.gov/study/NCT07299955