RecruitingPhase 1NCT04137900

Safety, Tolerability and Pharmacokinetics of a Monoclonal Antibody Specific to B-and T-Lymphocyte Attenuator (BTLA) as Monotherapy and in Combination With an Anti-PD1 Monoclonal Antibody for Injection in Subjects With Advanced Malignancies

A First-in-Human, Multicenter, Open-Label, Phase 1 Dose-Escalation and Cohort Expansion Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of TAB004 as Monotherapy and in Combination With Toripalimabin Subjects With Advanced Solid Malignancies Including Lymphoma


Sponsor

TopAlliance Biosciences

Enrollment

499 participants

Start Date

Oct 30, 2019

Study Type

INTERVENTIONAL

Conditions

Summary

The primary objective is to assess the safety and tolerability of TAB004 as monotherapy and in combination with toripalimab in subjects with selected advanced solid malignancies, including lymphoma, and to evaluate the recommended Phase 2 dose. The secondary objectives are to: 1) describe the pharmacokinetic (PK) profile of TAB004 monotherapy and in combination with toripalimab and to describe the PK profile of toripalimab when administered with TAB004, 2) evaluate antitumor activity of TAB004 monotherapy and in combination with toripalimab; and 3) determine the immunogenicity of TAB004 monotherapy and in combination with toripalimab and to determine the immunogenicity of toripalimab when administered with TAB004. The exploratory objectives are to: 1) evaluate pharmacodynamic effects of TAB004 on its target receptor BTLA, as well as effects on the immune system; 2) evaluate biomarkers that may correlate with activity of TAB004 as monotherapy and in combination with toripalimab; 3) evaluate the utility of BTLA ligand, herpesvirus-entry mediator (HVEM), and additional exploratory biomarkers that could aid in selection of appropriate subjects for TAB004 monotherapy and in combination with toripalimab.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new immunotherapy drug called TAB004, which targets a protein called BTLA (found on immune cells), alone and in combination with another immunotherapy (toripalimab, an anti-PD-1 drug), for people with advanced cancers that have not responded to other treatments. **You may be eligible if...** - You are 18 or older - You have advanced cancer (solid tumor or lymphoma) confirmed by biopsy that has progressed on prior treatment - Your general health is good (ECOG performance status 0 or 1) and life expectancy is at least 3 months - Your blood counts and organ function are within acceptable levels - You agree to use effective contraception during and for 90 days after treatment **You may NOT be eligible if...** - You have HIV, active hepatitis B or C - You have active autoimmune disease requiring ongoing systemic treatment - You have had an organ or bone marrow transplant - You have active brain metastases (cancer spread to the brain that is not stable or treated) - You are pregnant or breastfeeding - You received a live vaccine within 28 days before starting the study - You have a known history of tuberculosis Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGTAB004

Recombinant humanized IgG4κ monoclonal antibody specific to BTLA for injection

DRUGToripalimab

a human IgG4k monoclonal antibody that specifically binds to the programmed death 1 (PD-1)


Locations(24)

University of Alabama at Birmingham

Birmingham, Alabama, United States

University of Iowa Hospitals

Iowa City, Iowa, United States

University of California Irvine (UCI) Medical Center

Orange, California, United States

Boca Raton Clinical Research (BRCR)

Boca Raton, Florida, United States

UCLA Health Westwood Cancer Care

Los Angeles, California, United States

University of California San Francisco (UCSF) Medical Center-Mission Bay

San Francisco, California, United States

University of Wisconsin

Madison, Wisconsin, United States

Washington University

St Louis, Missouri, United States

Northwell Health

New Hyde Park, New York, United States

Carolina BioOncology Institute

Huntersville, North Carolina, United States

Thomas Jefferson University

Philadelphia, Pennsylvania, United States

University of Nebraska Medical Center

Omaha, Nebraska, United States

University of Maryland Medical Center

Baltimore, Maryland, United States

Karmanos Cancer Institute

Detroit, Michigan, United States

Sarah Cannon Research Institute

Nashville, Tennessee, United States

Massachusetts General Hospital

Boston, Massachusetts, United States

MD Anderson Cancer Center

Houston, Texas, United States

UC Health - University of Cincinnati Medical Center

Cincinnati, Ohio, United States

The Ohio State University Wexner Medical Center The James Cancer Hospital and Solove Research Institute

Columbus, Ohio, United States

New York Presbyterian / Weill Cornell Medical Center

New York, New York, United States

Winship Cancer Institute at Emory University

Atlanta, Georgia, United States

University of Arizona College of Medicine-Tucson

Tucson, Arizona, United States

University of Texas Southwestern Medical Center Harold C. Simmons Comprehensive Cancer Center

Dallas, Texas, United States

University of California at San Francisio

San Francisco, California, United States

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NCT04137900


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