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Study of CMAB807 Post-change in Manufacturing Site and Prolia in Healthy Volunteers

NCT06361355 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 128

Last updated 2024-11-07

No results posted yet for this study

Summary

This is a randomized, double-blinded, parallel-controlled Phase I study of CMAB807 administered by subcutaneous injection. This study will characterize the pharmacokinetic, pharmacodynamics, safety and immunogenicity of CMAB807 Post-change in Manufacturing Site, versus Prolia #Denosumab# in healthy male subjects after a single dose

Conditions

  • Healthy Volunteers

Interventions

BIOLOGICAL

Post-change CMAB807

for subcutaneous injection only

BIOLOGICAL

Prolia

for subcutaneous injection only

Sponsors & Collaborators

  • Taizhou Mabtech Pharmaceutical Co.,Ltd

    lead INDUSTRY

Principal Investigators

  • Hu Wei, Doctor · The Second Hospital of Anhui University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-11-02
Primary Completion
2024-06-03
Completion
2024-07-05

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06361355 on ClinicalTrials.gov