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Clinical Trial Summary

This clinical trial is evaluating a drug called AC676 in participants with Relapsed/Refractory B-cell Malignancies. The main goals of the study are to: - Identify the recommended dose of AC676 that can be given safely to participants - Evaluate the safety profile of AC676 - Evaluate the pharmacokinetics of AC676 - Evaluate the effectiveness of AC676


Clinical Trial Description

AC676-001 is a Phase I, first-in-human, open-label, multi-center dose-escalation study of AC676 given as a single agent. AC676 is an investigational medicinal product that is an orally bioavailable BTK degrader for the treatment of B-cell malignancies. ;


Study Design


Related Conditions & MeSH terms

  • Neoplasms
  • Relapsed/Refractory B-cell Malignancies

NCT number NCT05780034
Study type Interventional
Source Accutar Biotechnology Inc
Contact Accutar Biotechnology
Phone 908-340-0879
Email medical@accutarbio.com
Status Recruiting
Phase Phase 1
Start date June 20, 2023
Completion date December 2025

See also
  Status Clinical Trial Phase
Completed NCT02457559 - Study to Assess the Long-term Safety and Efficacy of Tirabrutinib in Adults With Relapsed/Refractory B-cell Malignancies Phase 1
Not yet recruiting NCT04943016 - CD19 CAR T Cells in Children and Adults With Relapsed or Refractory CD19 Positive B Cell Malignancies Phase 1
Recruiting NCT04689308 - This is a Phase 1 Study of MH048 in Patients With Selected Relapsed/Refractory B-cell Malignancies Phase 1
Recruiting NCT04861779 - A Study of HSK29116 in Adults With Relapsed/Refractory B-cell Malignancies Phase 1