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RECRUITING
NCT06276491
PHASE1

Phase 1, Safety and Tolerability Study of XmAb541 in Advanced Solid Tumors

Sponsor: Xencor, Inc.

View on ClinicalTrials.gov

Summary

The primary purpose of this study is to determine whether the investigational drug XmAb541 is safe and well tolerated, and to determine an optimal and safe dose(s) for further study. The study will also evaluate the effect of XmAb541 on tumor outcomes.

Official title: A Phase 1, First-in-Human, Dose Escalation and Expansion Study to Evaluate the Safety and Tolerability of XmAb541 in Advanced Solid Tumors

Key Details

Gender

All

Age Range

15 Years - Any

Study Type

INTERVENTIONAL

Enrollment

282

Start Date

2024-04-04

Completion Date

2028-12

Last Updated

2026-03-17

Healthy Volunteers

No

Interventions

BIOLOGICAL

XmAb541

Monoclonal bispecific antibody

Locations (16)

City of Hope

Duarte, California, United States

Stanford

Palo Alto, California, United States

University of California

San Francisco, California, United States

Moffitt Cancer Center

Tampa, Florida, United States

Winship Cancer Institute, Emory University

Atlanta, Georgia, United States

University of Chicago Medical Center

Chicago, Illinois, United States

Indian University Melvin and Bren Simon Comprehensive Cancer Center

Indianapolis, Indiana, United States

Karmanos Cancer Institute

Detroit, Michigan, United States

The John Theruer Cancer Center at Hackensack University Medical Center

Hackensack, New Jersey, United States

Icahn School of Medicine at Mount Sinai

New York, New York, United States

Montefiore Einstein Comprehensive Cancer Center

The Bronx, New York, United States

The Ohio State University

Columbus, Ohio, United States

OU Health Stephenson Cancer Center

Oklahoma City, Oklahoma, United States

UPMC Hillman Cancer Center

Pittsburgh, Pennsylvania, United States

SCRI Oncology Partners

Nashville, Tennessee, United States

University of Virginia

Charlottesville, Virginia, United States