Trial Condition(s):

Advanced solid tumor, Head and neck squamous cell carcinoma

Phase 1 study of BAY1905254 - An early clinical research study to evaluate a new drug called Bapotulimab (BAY1905254) in the expansion cohort in combination with Pembrolizumab in Head and Neck cancer that has returned or is discovered to be metastatic and is expressing PDL1.

Bayer Identifier:

18789

ClinicalTrials.gov Identifier:

NCT03666273

EudraCT Number:

2018-000990-63

Recruitment Complete

Trial Purpose

This study is being done to learn more about a new drug called Bapotulimab given in combination with Pembrolizumab. The purpose of this study is to learn if this new combination of drugs is safe for the participants, how it affects the body and to try to find the best dose of the new drug to give to participants and to obtain a preliminary assessment of the tumor response efficacy in the recurrent or metastatic Head and Neck Cancer.

Inclusion Criteria
- Male or female patients aged ≥ 18 years.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1.
- Patients must have measurable disease (at least one unidimensional measurable lesion by Computed tomography [CT] or Magnetic resonance imaging [MRI]) per Response evaluation criteria in solid tumors (RECIST) 1.1, and following histologically confirmed, advanced or metastatic solid tumors:
-- Dose escalation: All solid tumor types with a likelihood of sensitivity to immunotherapy, as judged by the investigator.
-- Expansion of Bapotulimab in combination with pembrolizumab in Head and neck squamous cell carcinoma (HNSCC): recurrent or metastatic head and neck squamous cell carcinoma IO-naïve PDL1+/ CPS≥1(PD-L1: Programmed death ligand 1; CPS: Combined positive score).
- Provision of archival tumor tissue at screening is mandatory for all patients in dose escalation.
- For dose escalation, patients: must have received standard therapy or have no standard therapy available or patients have actively refused any treatment which would be regarded standard. Or in the opinion of investigator have been considered ineligible for a particular form of standard therapy on medical grounds.
- Adequate bone marrow, liver and renal function.
- Adequate cardiac function, measured by echocardiography.

Main
Exclusion Criteria
- History of severe immune related adverse effects from prior immunotherapy (CTCAE v.5.0 Grade 4; CTCAE v.5.0 Grade 3 requiring treatment > 4 weeks), except hypothyroidism clinically stable on hormone replacement treatment and controlled type 1 diabetes.
- Severe (CTCAE v.5.0 Grade ≥ 3) infections within 4 weeks before the first study drug administration, including but not limited to hospitalization for complications of infection, bacteremia, or severe pneumonia. Clinically active infections (CTCAE v.5.0 > Grade 1) within 2 weeks before the first study drug administration.
- Previous or active myocarditis/myositis in history (independent of cause)
- Active or history of autoimmune disease.
- Known human immunodeficiency virus (HIV) infection.
- Active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection.
- Treatment with systemic immunosuppressant medications within 2 weeks before the first study drug administration.
- Ongoing or previous anti-cancer treatment or any immunostimulatory treatment including but not limited to interferons (IFNs), interleukin (IL)-2 and agonists for members of the tumor necrosis factor (TNF) receptor superfamily (e.g. 4-1BB) within 4 weeks before the first study drug administration.
- For dose expansion cohort of Bapotulimab in combination with pembrolizumab in HNSCC: has progressive disease (PD) within six (6) months of completion of curatively intended systemic treatment for locoregionally advanced HNSCC.

Trial Summary

Enrollment Goal
120
Trial Dates
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Phase
1
Could I receive a placebo?
No
Products
BAY1905254
Accepts Healthy Volunteers
No

Where to Participate

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Locations
Status
LocationsStatus
Locations

Yale University School of Medicine

New Haven, United States, 06510

Status
Active, not recruiting
 
Locations

South Texas Accelerated Research Therapeutics, LLC

San Antonio, United States, 78229

Status
Completed
 
Locations

University of Texas MD Anderson Cancer Center

Houston, United States, 77030

Status
Active, not recruiting
 
Locations

Henry Ford Health System

Detroit, United States, 48202

Status
Active, not recruiting
 
Locations

University of Chicago Hospitals

Chicago, United States, 60637

Status
Completed
 
Locations

Ohio State University

Columbus, United States, 43210

Status
Active, not recruiting
 
Locations

University of Arizona Cancer Center

Tucson, United States, 85724

Status
Completed
 
Locations

University Hospitals Cleveland Medical Center

Cleveland, United States, 44106

Status
Active, not recruiting
 

Trial Design