A Study to Test Different Doses of BI 765063 Alone and in Combination With BI 754091 in Japanese Patients With Different Types of Advanced Cancer (Solid Tumors)

NCT04653142 | Completed Phase 1

• 1 other identifier: 1443-0004
• Study Type: interventional
• Target: 18
• Locations: 1 country
• Sites: 4

Brief Summary

This study is open to Japanese adults with advanced cancer (solid tumors). This is a study in people for whom previous treatment was not successful and for whom no standard therapy exists. The purpose of this study is to find the highest dose of BI 765063 that people can tolerate when taken alone or together with a medicine called BI 754091. BI 765063 and BI 754091 are antibodies that may help the immune system fight cancer (checkpoint inhibitors). Participants get BI 765063 alone or together with BI 754091 as infusion every 3 weeks. Participants can stay in the study as long as they benefit from treatment and can tolerate it. The doctors check the health of the participants and note any health problems that could have been caused by BI 765063 or BI 754091.

Conditions

Solid Tumors

Outcome Measures

Primary Outcomes (4)

• Maximum Tolerated Dose (MTD) of BI 765063, Part A

  up to 3 weeks

• Maximum Tolerated Dose (MTD) of BI 765063, Part B

  up to 3 weeks

• Number of patients with dose limiting toxicity (DLT) in the MTD evaluation period, Part A

  up to 3 weeks

• Number of patients with dose limiting toxicity (DLT) in the MTD evaluation period, Part B

  up to 3 weeks

Secondary Outcomes (10)

• Number of patients with DLTs, Part A

  3 weeks per treatment cycle

• Number of patients with DLTs, Part B

  3 weeks per treatment cycle

• Percentage of patients with drug related Adverse Events (AE), Part A

  3 weeks per treatment cycle

• Percentage of patients with drug related Adverse Events (AE), Part B

  3 weeks per treatment cycle

• Cmax (maximum concentration) for BI 765063, Part A

  up to 3 weeks

Study Arms (1)

BI 765063 (Part A) and BI 765063 + BI 754091 (Part B)

EXPERIMENTAL

Drug: BI 765063; Drug: BI 754091

Interventions

BI 765063 DRUG

BI 765063

BI 765063 (Part A) and BI 765063 + BI 754091 (Part B)

BI 754091 DRUG

BI 754091

BI 765063 (Part A) and BI 765063 + BI 754091 (Part B)

Eligibility Criteria

• Age: 20 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Signed and dated the written informed consent form (ICF) prior to any trial-specific procedures
• Male or female aged ≥ 20 years (no upper limit of age) at the time of ICF signature
• Patients who were born in Japan, and have lived outside Japan \<10 years
• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 at the screening visit
• Life expectancy of at least 3 months
• Patients with at least one Signal Regulatory Protein-alpha (SIRPα) V1 allele will be selected, i.e. homozygous V1/V1 or heterozygous V1/V2; SIRPα polymorphism will be assessed in blood sampling (patient DNA); V1 allele is understood to include V1 and V1-like alleles
• Patients with histologically or cytologically documented advanced/metastatic primary or recurrent solid tumors who failed or are not eligible to standard therapy

You may not qualify if:

• Patients without at least one SIRPα V1 allele, i.e. SIRPα V2/V2 individuals
• Previous treatment with study medications in this trial
• Patients with symptomatic/active central nervous system (CNS) metastases. Patients with previously treated brain metastases are eligible, if there is no evidence of progression for at least 28 days before the first study drug administration without requirement for treatment with corticosteroids, as ascertained by clinical examination and brain imaging magnetic resonance imaging (MRI) or computed tomography (CT)) during the screening period
• Any tumor location necessitating an urgent therapeutic intervention (e.g., palliative care, surgery or radiation therapy, such as spinal cord compression, other compressive mass, uncontrolled painful lesion, bone fracture)
• Presence of active invasive cancers other than the one treated in this trial within 5 years prior to screening, except appropriately treated basal cell carcinoma of the skin, or in situ carcinoma of uterine cervix, or other local tumors considered cured by local treatment
• Patients with active autoimmune disease or a documented history of autoimmune disease, that requires systemic treatment, i.e. corticosteroids or immunosuppressive drugs, except patients with vitiligo, resolved childhood asthma/atopy, alopecia, or any chronic skin condition that does not require systemic therapy, patients with autoimmune-related hypothyroidism on a stable dose of thyroid replacement hormone and/or controlled Type 1 diabetes mellitus on a stable insulin regimen may be eligible
• Patients who has experienced severe infusion related reaction (IRR) to monoclonal antibody (mAb) (Grade ≥ 3 NCI CTCAE v5.0)

Sponsors & Collaborators

• Boehringer Ingelheim: lead

Study Sites (4)

National Cancer Center Hospital East

Chiba, Kashiwa, 277-8577, Japan

Location

Shikoku Cancer Center

Ehime, Matsuyama, 791-0280, Japan

Location

Osaka International Cancer Institute

Osaka, Osaka, 541-8567, Japan

Location

National Cancer Center Hospital

Tokyo, Chuo-ku, 104-0045, Japan

Location

Related Links

• Related Info

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SEQUENTIAL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Model Details: After the completion of dose escalation with BI 765063 in Part A, Part B will commence and successive dose groups of patients will receive escalating doses of BI 765063 in combination with a fixed dose of BI 754091.

Study Record Dates

• First Submitted: November 27, 2020
• First Posted: December 4, 2020
• Study Start: December 15, 2020
• Primary Completion: April 20, 2022
• Study Completion: April 20, 2022
• Last Updated: May 10, 2022

Record last verified: 2022-05

Data Sharing

• IPD Sharing: Will not share

Locations

JP (4)