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Clinical Trial Summary

The objective of this study is to evaluate the safety, efficacy, pharmacokinetics, and immunogenicity of MRG004A in patients with Tissue Factor positive advanced or metastatic solid tumors.


Clinical Trial Description

This study consists of two parts. Part A is a dose escalation study to determine the maximum tolerated dose (MTD) and recommended phase II dose (RP2D) of MRG004A. Part B is a disease specific multi-cohort dose expansion study to further assess the efficacy and safety of MRG004A at confirmed RP2D. ;


Study Design


Related Conditions & MeSH terms

  • Advanced or Metastatic Solid Tumors
  • Neoplasms

NCT number NCT04843709
Study type Interventional
Source Shanghai Miracogen Inc.
Contact Jenny Li
Phone 650-237-9339
Email clinicaltrials@miracogen.com.cn
Status Recruiting
Phase Phase 1/Phase 2
Start date July 26, 2021
Completion date June 2025

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