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临床试验/NCT06077500
NCT06077500
进行中(未招募)
1 期

DAREONᵀᴹ-8: A Phase I, Open-label, Dose Escalation and Expansion Trial of Repeated Intravenous Infusions of BI 764532 Combined With Standard of Care (Platinium, Etoposide, and Anti-PD-L1) in Patients With Extensive-stage Small Cell Lung Carcinoma

Boehringer Ingelheim35 个研究点 分布在 8 个国家目标入组 46 人2024年2月14日

概览

阶段
1 期
干预措施
BI 764532
疾病 / 适应症
Small Cell Lung Carcinoma (SCLC)
发起方
Boehringer Ingelheim
入组人数
46
试验地点
35
主要终点
Part A - Dose escalation: Occurrence of dose limiting toxicities (DLTs) in the maximum tolerated dose (MTD) evaluation period
状态
进行中(未招募)
最后更新
18天前

概览

简要总结

This study is open to adults with extensive stage small cell lung cancer. The study is in people with advanced cancer that are eligible for standard of care including chemotherapy and anti-PD-L1 (Programmed Cell Death Ligand 1) immunotherapy.

The purpose of this study is to find out the highest dose of BI 764532 (also called obrixtamig) that people can tolerate when taken together with standard of care. BI 764532 is an antibody-like molecule that may help the immune system fight cancer. Participants get BI 764532 and different standard treatments as infusions into a vein.

If there is benefit for the participants and if they can tolerate it, the treatment is given for the entire duration of the study. During this time, participants visit the study site regularly. The visits also depend on the response to the treatment. At the study visits, the doctors check the health of the participants, take necessary laboratory tests, and note any health problems that could have been caused by the study treatment.

注册库
clinicaltrials.gov
开始日期
2024年2月14日
结束日期
2027年4月1日
最后更新
18天前
研究类型
Interventional
研究设计
Sequential
性别
All

研究者

责任方
Sponsor

入排标准

入选标准

  • Male or female participants ≥18 years old and at least at the legal age of consent in countries where it is greater than 18 years at the time of signature of the informed consent form (ICF)
  • Signed and dated written informed consent in accordance with International Council for Harmonisation-Good Clinical Practice (ICH-GCP) and local legislation prior to admission to the trial
  • Histologically or cytologically confirmed extensive-stage small cell lung carcinoma (ES-SCLC)
  • Availability of archival tumour tissue
  • Patients must be eligible for platinum+etoposide+anti-Programmed Cell Death Ligand 1 (PD-L1) regimen as first line standard of care (SoC) treatment:
  • In Part A, patients must be eligible to receive carboplatin + etoposide + atezolizumab
  • In Part B, patients must be eligible to receive etoposide, carboplatin or cisplatin, and atezolizumab or durvalumab
  • No prior systemic treatment for ES-SCLC
  • Prior systematic anti-cancer treatment for limited-stage small cell lung cancer (SCLC) must have been complete at least 6 months prior to the diagnosis of ES-SCLC
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-1 Further inclusion criteria apply.

排除标准

  • Previous treatment in this trial
  • Treatment with a systemic anti-cancer therapy or investigational drug within 28 days or 5 half-lives (whichever is longer) of the first administration of trial medication
  • Presence of leptomeningeal carcinomatosis
  • Previous treatment with Delta-like ligand 3 (DLL3)-targeting T cell engagers and cell therapies
  • Patients who have been treated with extensive field radiotherapy including whole brain irradiation within 2 weeks prior to first administration of BI 764532
  • Persistent toxicity from previous treatments that has not resolved to ≤ Common Terminology Criteria for Adverse Events (CTCAE) Grade 1 (except for alopecia, asthenia/fatigue, CTCAE Grade 2 neuropathy, or Grade 2 endocrinopathies controlled by replacement therapy)
  • Major surgery (major according to the investigator's assessment) within 28 days prior to first administration of BI 764532 or planned during treatment period, e.g. hip replacement
  • Any documented active or suspected malignancy or history of malignancy within 5 years prior to Screening (other than the target indication), except for appropriately treated basal cell carcinoma of the skin or in situ carcinoma of uterine cervix Further exclusion criteria apply.

研究组 & 干预措施

Part A - Dose escalation: BI 764532 very low dose + carboplatin + etoposide + atezolizumab

干预措施: BI 764532

Part A - Dose escalation: BI 764532 medium dose + carboplatin + etoposide + atezolizumab

干预措施: BI 764532

Part A - Dose escalation: BI 764532 high dose + carboplatin + etoposide + atezolizumab

干预措施: BI 764532

Part A - Dose escalation: BI 764532 low dose + carboplatin + etoposide + atezolizumab

干预措施: BI 764532

Part B - Dose expansion: BI 764532 + carboplatin + etoposide + atezolizumab

干预措施: BI 764532

Part B - Dose expansion: BI 764532 + carboplatin + etoposide + durvalumab

干预措施: BI 764532

Part B - Dose expansion: BI 764532 + cisplatin + etoposide + durvalumab

干预措施: BI 764532

Part B - Dose expansion: BI 764532 + carboplatin + etoposide + durvalumab

干预措施: Carboplatin

Part B - Dose expansion: BI 764532 + cisplatin + etoposide + durvalumab

干预措施: Etoposide

Part B - Dose expansion: BI 764532 + carboplatin + etoposide + durvalumab

干预措施: Etoposide

Part B - Dose expansion: BI 764532 + carboplatin + etoposide + durvalumab

干预措施: Durvalumab

Part B - Dose expansion: BI 764532 + cisplatin + etoposide + durvalumab

干预措施: Cisplatin

Part B - Dose expansion: BI 764532 + cisplatin + etoposide + durvalumab

干预措施: Durvalumab

Part A - Dose escalation: BI 764532 very low dose + carboplatin + etoposide + atezolizumab

干预措施: Carboplatin

Part A - Dose escalation: BI 764532 very low dose + carboplatin + etoposide + atezolizumab

干预措施: Etoposide

Part A - Dose escalation: BI 764532 very low dose + carboplatin + etoposide + atezolizumab

干预措施: Atezolizumab

Part A - Dose escalation: BI 764532 low dose + carboplatin + etoposide + atezolizumab

干预措施: Carboplatin

Part A - Dose escalation: BI 764532 low dose + carboplatin + etoposide + atezolizumab

干预措施: Etoposide

Part A - Dose escalation: BI 764532 medium dose + carboplatin + etoposide + atezolizumab

干预措施: Etoposide

Part A - Dose escalation: BI 764532 medium dose + carboplatin + etoposide + atezolizumab

干预措施: Atezolizumab

Part A - Dose escalation: BI 764532 high dose + carboplatin + etoposide + atezolizumab

干预措施: Atezolizumab

Part A - Dose escalation: BI 764532 high dose + carboplatin + etoposide + atezolizumab

干预措施: Carboplatin

Part A - Dose escalation: BI 764532 high dose + carboplatin + etoposide + atezolizumab

干预措施: Etoposide

Part B - Dose expansion: BI 764532 + carboplatin + etoposide + atezolizumab

干预措施: Etoposide

Part B - Dose expansion: BI 764532 + carboplatin + etoposide + atezolizumab

干预措施: Atezolizumab

Part A - Dose escalation: BI 764532 low dose + carboplatin + etoposide + atezolizumab

干预措施: Atezolizumab

Part A - Dose escalation: BI 764532 medium dose + carboplatin + etoposide + atezolizumab

干预措施: Carboplatin

Part B - Dose expansion: BI 764532 + carboplatin + etoposide + atezolizumab

干预措施: Carboplatin

结局指标

主要结局

Part A - Dose escalation: Occurrence of dose limiting toxicities (DLTs) in the maximum tolerated dose (MTD) evaluation period

时间窗: up to 6 weeks

Part B - Dose expansion: Occurrence of dose limiting toxicities (DLTs) during the on-treatment period

时间窗: up to 23 months

次要结局

  • Part A - Dose escalation: Occurrence of dose limiting toxicities (DLTs) during the on-treatment period(up to 23 months)
  • Part A - Dose escalation: Occurrence of adverse events (AEs) during the on-treatment period(up to 23 months)
  • Part B - Dose expansion: Objective response (OR)(up to 23 months)
  • Part B - Dose expansion: Duration of response (DoR)(up to 23 months)

研究点 (35)

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