A Study in People With Advanced Cancer to Test How Well Different Doses of BI 770371 Alone or in Combination With Ezabenlimab Are Tolerated

NCT ID: NCT05327946

Last Updated: 2025-10-28

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE1
• Total Enrollment: 36 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-05-17
• Study Completion Date: 2026-09-30

Brief Summary

This study is open to adults with advanced cancer (solid tumours). People for whom previous treatment was not successful and for whom no other treatment options exist can join the study.

The purpose of this study is to find the highest dose of BI 770371 that people with advanced cancer can tolerate when taken alone or together with a medicine called ezabenlimab.

BI 770371 and ezabenlimab are antibodies that may help the immune system fight cancer (checkpoint inhibitors). In this study, BI 770371 is given to people for the first time.

Participants get BI 770371 alone or together with ezabenlimab as an infusion every 3 weeks.

It is planned that participants can stay in the study for up to 2 years, if they benefit from treatment and can tolerate it. During this time, they visit the study site regularly.

The doctors collect information on any health problems of the participants. The doctors also regularly monitor the size of the tumour.

Conditions

Solid Tumors

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Monotherapy dose escalation

Group Type: EXPERIMENTAL

BI 770371

Intervention Type: DRUG

BI 770371

Combination therapy dose escalation

Group Type: EXPERIMENTAL

BI 770371

Intervention Type: DRUG

BI 770371

ezabenlimab

Intervention Type: DRUG

ezabenlimab

Interventions

BI 770371

BI 770371

Intervention Type: DRUG

ezabenlimab

ezabenlimab

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Signed and dated written informed consent form (ICF) in accordance with International Council for Harmonisation-Good Clinical Practice (ICH-GCP) and local legislation prior to admission to the trial
• Patients ≥18 years of age and over the legal age of consent as required by local legislation at the time of signature of the ICF
• Presence of at least one measurable lesion according to Response Evaluation Criteria In Solid Tumours (RECIST) v1.1
• Eastern Cooperative Oncology Group (ECOG) Score: 0 to 1
• Life expectancy ≥3 months at the start of treatment in the opinion of the Investigator.
• Patients with a confirmed diagnosis of advanced, unresectable, and/or metastatic solid tumours (any type)
• Patients who have failed conventional treatment or for whom no therapy of proven efficacy exists or who are not eligible for established treatment options (including anti-Programmed Cell Death 1 (PD-1) or anti-Programmed Death-Ligand 1 (PD-L1) therapies, if relevant). Patients must have exhausted available treatment options known to prolong survival for their disease

Exclusion Criteria

• Major surgery (major according to the Investigator's assessment) performed within 12 weeks prior to randomisation or planned within 12 months after screening, e.g. hip replacement
• Presence of active invasive cancers other than the one treated in this trial within 5 years prior to screening, with the exception of appropriately treated basal-cell carcinoma of the skin, in situ carcinoma of the uterine cervix, or other local tumours considered cured by local treatment
• Untreated brain metastasis(es) that may be considered active. Patients with previously treated brain metastases may participate provided they are stable (i.e., without evidence of Progressive Disease (PD) by imaging for at least 4 weeks prior to the first dose of trial treatment, and any neurologic symptoms have returned to baseline), and there is no evidence of new or enlarging brain metastases
• Radiotherapy within 4 weeks prior to randomisation except as follows:

• Palliative radiotherapy to regions other than the chest is allowed if completed at least 2 weeks prior to randomisation
• Single dose palliative radiotherapy for symptomatic metastasis within 2 weeks prior to randomisation may be allowed but must be discussed with the Sponsor
• Patients who must or wish to continue the intake of restricted medications or any drug considered likely to interfere with the safe conduct of the trial
• History of pneumonitis within the last 5 years or Interstitial lung disease
• Known history of allergy to any trial drug, or any excipients of the trial drug(s)

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Boehringer Ingelheim

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Florida Cancer Specialists-Sarasota-61670

Sarasota, Florida, United States

John Theurer Cancer Center

Hackensack, New Jersey, United States

Centre Hospitalier de l'Universite de Montreal (CHUM)

Montreal, Quebec, Canada

National Cancer Center Hospital East

Chiba, Kashiwa, , Japan

National Cancer Center Hospital

Tokyo, Chuo-ku, , Japan

Countries

United States; Canada; Japan

Related Links

https://www.mystudywindow.com

Related Info

Other Identifiers

1501-0001

Identifier Type: -

Identifier Source: org_study_id