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A Study of BL-B01D1 Combined With Glecirasib in Patients With KRAS G12C-Mutated Locally Advanced or Metastatic Non-Small Cell Lung Cancer

2026年9月14日 更新者:Sichuan Baili Pharmaceutical Co., Ltd.

A Phase II Clinical Study to Evaluate the Efficacy and Safety of BL-B01D1 for Injection Combined With Glecirasib in Patients With KRAS G12C-Mutated Locally Advanced or Metastatic Non-Small Cell Lung Cancer

This Phase II study is a clinical study to explore the efficacy and safety of BL-B01D1 for injection in combination with glecirasib in the treatment of patients with locally advanced or metastatic non-small cell lung cancer with KRAS G12C mutation confirmed by histopathology and/or cytology.

調査の概要

状態

まだ募集していません

条件

介入・治療

研究の種類

介入

入学 (推定)

36

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

    • Guangdong
      • Guangzhou、Guangdong、中国
        • Sun Yat-sen University Cancer Center
        • コンタクト:
          • Likun Chen

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年~75年 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  1. Voluntarily sign the informed consent form and comply with protocol requirements;
  2. No restriction on gender;
  3. Age ≥18 years and ≤75 years;
  4. Expected survival time ≥3 months;
  5. Patients with locally advanced or metastatic non-small cell lung cancer;
  6. Agree to provide archived tumor tissue specimens from the primary or metastatic lesion within 2 years, or fresh tissue samples;
  7. Must have at least one measurable lesion as defined by RECIST v1.1;
  8. ECOG performance status score ≤1;
  9. Toxicity from prior antitumor therapy has recovered to ≤Grade 1 as defined by NCI-CTCAE v6.0;
  10. No severe cardiac dysfunction, with left ventricular ejection fraction ≥50%;
  11. Organ function levels must meet the requirements;
  12. Coagulation function: international normalized ratio ≤1.5, and activated partial thromboplastin time ≤1.5×ULN;
  13. Urine protein ≤1+ or <1000 mg/24 h;
  14. For premenopausal women of childbearing potential, a pregnancy test must be performed within 7 days before starting treatment; serum pregnancy testing must exclude pregnancy, and the patient must be non-lactating; all enrolled patients (regardless of male or female) should use adequate barrier contraception throughout the entire treatment period and for 7 months after treatment completion.

Exclusion Criteria:

  1. Prior treatment with drugs targeting KRAS G12C;
  2. Prior use of ADC drugs with small-molecule toxins as topoisomerase I inhibitors;
  3. Coexisting other known oncogenic driver gene mutations that can be targeted therapeutically;
  4. Prior history of intestinal disease or major gastric surgery;
  5. Participation in any other clinical trial within 4 weeks before the first administration of this trial;
  6. History of severe heart disease or cerebrovascular disease;
  7. Receipt of radical radiotherapy, major surgery, extensive radiotherapy, etc., within 4 weeks before randomization in the study;
  8. Unstable thrombotic events requiring therapeutic intervention within 6 months before screening;
  9. QTc interval prolongation, complete left bundle branch block, third-degree atrioventricular block, frequent and uncontrollable arrhythmias;
  10. History of interstitial lung disease/interstitial pneumonia treated with steroids, etc.;
  11. Concurrent pulmonary disease leading to clinically severe impairment of respiratory function;
  12. Severe infection occurring within 4 weeks before randomization in the study;
  13. Patients at risk of active autoimmune disease, or patients with a history of autoimmune disease;
  14. Diagnosis of active malignancy within 5 years before randomization in the study;
  15. Positive human immunodeficiency virus antibody, active tuberculosis, active syphilis, active hepatitis B virus infection, or hepatitis C virus infection;
  16. Hypertension poorly controlled with two antihypertensive drugs;
  17. Patients with poorly controlled blood glucose;
  18. Presence of a large amount of serous cavity effusion, or serous cavity effusion with obvious symptoms caused by the serous cavity effusion, etc.;
  19. Active central nervous system metastasis;
  20. Imaging examination suggesting that the tumor has invaded or encased the abdomen, chest, etc.;
  21. Severe and unhealed wounds, ulcers, or fractures within 4 weeks before signing informed consent;
  22. Trial participants with clinically obvious bleeding or a clear bleeding tendency within 4 weeks before signing informed consent;
  23. History of allogeneic stem cell, bone marrow, or organ transplantation;
  24. Patients with a history of allergy to recombinant humanized antibodies or allergy to any excipient component of BL-B01D1;
  25. History of severe neurological or psychiatric disease;
  26. History of autologous or allogeneic stem cell transplantation;
  27. Pregnant or breastfeeding women;
  28. Trial participants planning to receive vaccination or who received a live vaccine within 28 days before randomization in the study;
  29. Other circumstances in which the investigator considers it inappropriate to participate in this clinical trial.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:BL-B01D1 + Glecirasib

Participants receive BL-B01D1 + Glecirasib in the first cycle (3 weeks). Participants with clinical benefit could receive additional treatment for more cycles. The administration will be terminated because of disease progression or intolerable toxicity occurring or other reasons.

Administration by intravenous infusion for a cycle of 3 weeks.

他の名前:
  • BMS-986507
  • Iza-Bren
  • Izalontamab Brengitecan

Oral administration at a fixed daily dose for a cycle of 3 weeks.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Objective Response Rate (ORR)
時間枠:Up to approximately 24 months

Objective response rate (ORR) is defined as the number of CR and PR in the treatment and control groups divided by the number of that group in the full analysis set (FAS).

Up to approximately 24 months

二次結果の測定

結果測定
メジャーの説明
時間枠
Disease Control Rate (DCR)
時間枠:Up to approximately 24 months

Disease Control Rate (DCR) : Percentage of all randomized subjects who rated the best overall response (BOR) as complete response (CR), partial response (PR), and disease stabilization (SD) according to RECIST 1.1 criteria.

Up to approximately 24 months
Duration of Response (DOR)
時間枠:Up to approximately 24 months

Duration of Response (DOR) : defined as the period from the date when tumor response is first recorded to the date when objective tumor progression is first recorded or the date of death.

Up to approximately 24 months
Treatment Emergent Adverse Event (TEAE)
時間枠:Up to approximately 24 months

TEAE is defined as any unfavorable and unintended change in the structure, function, or chemistry of the body temporally emerging, or any worsening (i.e., any clinically significant adverse change in frequency and/or intensity) of a pre-existing condition during the treatment of BL-B01D1. The type, frequency and severity of TEAE will be evaluated during the treatment of BL-B01D1.

Up to approximately 24 months
Progression-free survival (PFS)
時間枠:Up to approximately 24 months

Progression-free survival (PFS) as assessed by BICR is defined as the time between the date subjects were randomized and the first observation of disease progression (based on BICR's image-based assessment) or death.

Up to approximately 24 months

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

協力者

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年9月1日

一次修了 (推定)

2028年12月1日

研究の完了 (推定)

2028年12月1日

試験登録日

最初に提出

2026年9月14日

QC基準を満たした最初の提出物

2026年9月14日

最初の投稿 (実際)

2026年9月18日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月18日

QC基準を満たした最後の更新が送信されました

2026年9月14日

最終確認日

2026年9月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • BL-B01D1-219

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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