A Study Evaluating Different Doses of BI 765049 When Given Alone and When Given With Ezabenlimab to Patients With Advanced Solid Tumors Expressing the Protein B7-H6 on the Cell Surface

Phase 1

Completed

• Conditions: Colorectal Neoplasms, Carcinoma, Non-Small-Cell Lung, Pancreatic Neoplasms, Carcinoma, Hepatocellular, Head and Neck Neoplasms, Gastrointestinal Neoplasms
• Interventions: Drug: BI 765049; Drug: ezabenlimab

• Registration Number: NCT04752215
• Lead Sponsor: Boehringer Ingelheim

Brief Summary

This study is open to adults with advanced solid tumors whose previous cancer treatment was not successful. People can participate if their tumor has the B7-H6 marker or if they have colorectal cancer.

The study tests 2 medicines called BI 765049 and ezabenlimab (BI 754091). Both medicines may help the immune system fight cancer.

The purpose of this study is to find out the highest dose of BI 765049 alone and in combination with ezabenlimab the participants can tolerate. In this study, BI 765049 is given to people for the first time.

Participants can stay in the study for up to 3 years, if they benefit from treatment and can tolerate it. During this time, they get BI 765049 alone or in combination with ezabenlimab as infusion into a vein every 3 weeks.

The doctors check the health of the participants and note any health problems that could have been caused by BI 765049 or ezabenlimab. The doctors also regularly monitor the size of the tumor.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2021-02-11
• Study First Submitted QC: 2021-02-11
• Study First Posted: 2021-02-12
• Study Start: 2021-05-18
• Primary Completion: 2024-11-19
• Study Completion: 2024-11-19
• Status Verified: 2025-01
• Last Update Submitted: 2025-01-09
• Last Update Posted: 2025-01-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 67

Inclusion Criteria

• Signed and dated, written informed consent form (ICF) (ICF1 for B7-H6 testing for all patients except those with advanced or metastatic colorectal cancer (CRC); and ICF2 for all patients) describing the study in accordance with International Council on Harmonisation Good Clinical Practice (ICH-GCP) and local legislation prior to any trial-specific procedures, sampling, or analyses.
• Patient must be ≥18 years of age at the time of signature on the ICFs (ICF1 and ICF2).
• Patients with a histologically or cytologically confirmed diagnosis of an advanced, unresectable, and/or metastatic colorectal carcinoma (CRC), non-small cell lung cancer (NSCLC), hepatocellular carcinoma (HCC), head and neck squamous cell carcinoma (HNSCC), gastric carcinoma, and pancreatic carcinoma. At least 1 patient in each back-fill slot must be a non-CRC patient (i.e., NSCLC, HCC, HNSCC, gastric carcinoma, or pancreatic carcinoma).
• Patients with disease progression despite conventional treatment, intolerant to or not a candidate for conventional treatment, or with a tumor for which no conventional treatment exists.
• All patients must agree to the collection of tumor samples (as slides from archival diagnostic samples or fresh tumor biopsies) for confirmation of B7-H6 expression either at Screening visit 02 (for CRC patients) or Screening visit 01 (for all other patients). To qualify for a back-fill slot or recommended dose expansion (RDE) cohort, the patient must agree to the collection of mandatory pre-treatment and on-treatment fresh tumor biopsies.
• Patient diagnosed with advanced or metastatic CRC or patient with confirmed B7-H6 expression on tumor tissue sample (archived or fresh tumor biopsy) based on central pathology review.
• Patients with an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
• Patient must have at least one evaluable target lesion outside of the central nervous system (CNS) as defined per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 separate from any lesion(s) identified for tumor biopsy. Tumor lesions that have been irradiated at least ≥28 days before the start of treatment, and have subsequently had documented progression, may be chosen as target lesions only in the absence of measurable lesions that have not been irradiated.
• Further inclusion criteria apply

Read More

Exclusion Criteria

• Patient with a history of a major surgery within 28 days prior to first dose of BI 765049 (major according to the Investigator's and/or Medical Monitor's assessment).

• Patient with a history of a previous or concomitant malignancies. Patient with a malignancy considered effectively treated and cured by 'local treatment' within the last 2 years and that is distinct from the one treated in this trial will be allowed.

• Patient with known leptomeningeal disease or spinal cord compression due to disease.

• Patient requiring anticoagulant treatment which cannot be safely interrupted, if medically needed for a study procedure (e.g., biopsy) based on the opinion of the Investigator.

• History of systemic antimicrobials required for an infection within 7 days of first dose BI 765049.

• Patient with any of the following laboratory evidence of hepatitis virus infection. Test results obtained in routine diagnostics are acceptable for screening if done within 14 days before the ICF2 date:

  • Positive results of hepatitis B surface (HBs) antigen
  • Presence of hepatitis B core (HBc) antibody together with hepatitis B virus (HBV)-DNA
  • Presence of hepatitis C-RNA

• Patient with known human immunodeficiency virus (HIV) infection.

• Patient previous treatment history:

  • Treatment with a systemic anti-cancer therapy or investigational drug within 21 days or 5 half-lives (whichever is shorter) of the first administration of BI 765049.
  • Treatment with extensive field radiotherapy including whole brain irradiation within 14 days prior to first administration of BI 765049.

• Further exclusion criteria apply

Read More

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
BI 765049 single treatment group	BI 765049	BI 765049
BI 765049 + ezabenlimab combination treatment group	BI 765049	BI 765049 + ezabenlimab
BI 765049 + ezabenlimab combination treatment group	ezabenlimab	BI 765049 + ezabenlimab

Primary Outcome Measures

Name	Time	Method
Number of patients with dose limiting toxicities (DLTs) in the maximum tolerated dose (MTD) evaluation period	Up to 3 weeks
Maximum tolerated dose (MTD) in any studied regimen	Up to 3 weeks	defined as the highest dose with less than 25 percent (%) risk of the true dose limiting toxicity (DLT) rate being equal to or above 33 percent (%) during the MTD evaluation period

Secondary Outcome Measures

Name	Time	Method
Area under the concentration-time curve of BI 765049 over a uniform dosing interval τ (AUCτ)	Up to 36 months
Maximum measured concentration of BI 765049 (Cmax)	Up to 36 months
Objective response based on Response Evaluation Criteria in Solid Tumors (RECIST v1.1) in patients with measurable disease	Up to 36 months

Trial Locations

Locations (14)

MD Anderson Cancer Center Orlando; 🇺🇸 Orlando, Florida, United States

University of Alabama at Birmingham; 🇺🇸 Birmingham, Alabama, United States

Valkyrie Clinical Trials; 🇺🇸 Los Angeles, California, United States

University of California Irvine; 🇺🇸 Orange, California, United States

HealthONE; 🇺🇸 Denver, Colorado, United States

Florida Cancer Specialists-Sarasota-61670; 🇺🇸 Sarasota, Florida, United States

Northwestern University; 🇺🇸 Chicago, Illinois, United States

Norton Healthcare - Norton Cancer Institute - Louisville; 🇺🇸 Louisville, Kentucky, United States

New York University Langone Medical Center; 🇺🇸 New York, New York, United States

Stephenson Cancer Center; 🇺🇸 Oklahoma City, Oklahoma, United States

Tennessee Oncology, PLLC-Nashville-52568; 🇺🇸 Nashville, Tennessee, United States

Mary Crowley Cancer Research Center; 🇺🇸 Dallas, Texas, United States

Baylor University Medical Center; 🇺🇸 Dallas, Texas, United States

Princess Margaret Cancer Centre; 🇨🇦 Toronto, Canada