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A Study of AC676 for the Treatment of Relapsed/Refractory B-Cell Malignancies

Phase 1
Recruiting
Conditions
Relapsed/Refractory B-cell Malignancies
Interventions
Registration Number
NCT05780034
Lead Sponsor
Accutar Biotechnology Inc
Brief 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

Detailed 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.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  1. Adult male and female patients, at least 18 years-of-age at the time of signature of the informed consent form (ICF).
  2. Patients with histologically confirmed relapsed/refractory Chronic Lymphocytic Leukemia (CLL), Small Lymphocytic Lymphoma (SLL), Mantle Cell Lymphoma (MCL), Follicular Lymphoma (FL), non-GCB Diffuse Large B-cell Lymphoma (DLBCL), Marginal Zone Lymphoma (MZL), or Waldenström Macroglobulinemia (WM).
  3. Must have received at least 2 prior systemic therapies or have no other therapies to provide significant clinical benefit in the opinion of the Investigator or who are not amenable (intolerability, patient choice) to standard therapies.
Exclusion Criteria

Patients who meet any of the following criteria will be excluded from study entry:

  1. Treatment with any of the following:

    • Small molecule anti-cancer drugs within 5 half-lives or 2 days (whichever is longer, not to exceed 14 days).
    • Systemic chemotherapy within 14 days.
    • Radiation therapy within 14 days
    • Biologics (Antibodies) treatment within 28 days,
    • Radioimmunoconjugates or toxin conjugates within 12 weeks.
    • Prior Chimeric antigen receptor (CAR) T cell therapy (and prior use of immunoglobulin replacement therapy to treat associated adverse events) within 3 months. For patients with DLBCL, no prior CAR- T therapy is allowed.
    • Autologous or allogenic stem cell transplant within 100 days and must not have ongoing graft-versus-host disease (GVHD) and no ongoing therapy to treat GVHD.
  2. History of central nervous system lymphoma/leukemia in remission for less than 2 years.

  3. Medical history of active bleeding within 2 months prior to study entry, or susceptible to bleeding by the judgement of investigator.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
AC676 Dose EscalationAC676Participants will receive an assigned dose of AC676 in a 28-days cycle.
Primary Outcome Measures
NameTimeMethod
Incidence of dose limiting toxicities (DLTs) from AC676 monotherapyFrom cycle 1 day 1 to Cycle 1 day 28. Cycles are 28 days.
Incidence of treatment-emergent adverse events (TEAEs) and clinically significant Grade 3 or higher laboratory abnormalities using CTCAE v5.0 criteria.Approximately 18 months
Maximum tolerated dose (MTD) and/or recommended Phase II dose (RP2D)Approximately 18 months
Secondary Outcome Measures
NameTimeMethod
Pharmacokinetic Analysis: maximum plasma concentration (Cmax)Up to approximately 20 weeks
Pharmacokinetic Analysis: time to maximum plasma concentration (tmax)Up to approximately 20 weeks
Objective Response Rate (ORR) in patients receiving AC676Approximately 18 months
Time to Response (TTR) in patients receiving AC676Approximately 18 months
Progression Free Survival rate (PFS) in patients receiving AC676Approximately 18 months
Disease Control Rate (DCR) in patients receiving AC676Approximately 18 months
Duration of Response (DOR) in patients receiving AC676Approximately 18 months
Pharmacokinetic Analysis: area under the plasma concentration-time curve over the dosing interval (AUC(0-inf))Up to approximately 20 weeks
Pharmacokinetic Analysis: terminal elimination half-life (t1/2)Up to approximately 20 weeks
Pharmacokinetic Analysis: area under the plasma concentration-time curve from over the dosing interval (AUC(0-tau))Up to approximately 20 weeks

Trial Locations

Locations (7)

University of Texas Southwestern Medical Center

🇺🇸

Dallas, Texas, United States

Swedish Cancer Institute

🇺🇸

Seattle, Washington, United States

Colorado Blood Cancer Institute

🇺🇸

Denver, Colorado, United States

The Ohio State University - The James Cancer Hospital and Solove Research Institute

🇺🇸

Columbus, Ohio, United States

Tennessee Oncology

🇺🇸

Nashville, Tennessee, United States

Florida Cancer Specialists

🇺🇸

Sarasota, Florida, United States

Oregon Health & Science University

🇺🇸

Portland, Oregon, United States

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