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Phase 1b/2 to Evaluate the Safety, Tolerability, and Efficacy of TXN10128 in Combination With TOPO-I Inhibitor-based Therapies (Irinotecan or TROP2 ADC) in Advanced or Metastatic EGFR Mutated NSCLC (ENRISE)

2026年11月9日 更新者:Txinno Bioscience Inc.

A Multicenter, Open-label, Multi-cohort, Phase 1b/2 Study to Evaluate the Safety, Tolerability, and Efficacy of TXN10128 in Combination With Topoisomerase I Inhibitor-based Therapies (Irinotecan or TROP2 ADC) in Participants With Advanced or Metastatic Non-Small Cell Lung Cancer Harboring EGFR Mutations Following Progression on Prior Targeted Therapy

This is a multicenter, open-label, multi-cohort, Phase 1b/2 clinical study. This study evaluates TXN10128 in combination with either irinotecan (a topoisomerase I inhibitor) or a TROP2-directed antibody-drug conjugate (TROP2 ADC) in participants with advanced or metastatic NSCLC with confirmed EGFR mutations.

The study consists of three cohorts. It enrolls participants who have progressed after prior treatment with a third-generation EGFR tyrosine kinase inhibitor (TKI) and platinum-based doublet chemotherapy.

Part B enrolls participants who are currently receiving TROP2 ADC therapy or whose disease has progressed following such therapy (with no restriction on the number of prior lines).

In Part C, participants who are naïve to TROP2 ADC therapy and have received no more than three prior lines of systemic anticancer therapy will be enrolled. A safety run-in will first be conducted to confirm the safety of the combination with a TROP2 ADC. Based on the results, the Safety Review Committee (SRC) will select the recommended dose for expansion phase, which will follow Simon's two-stage design.

調査の概要

状態

募集

介入・治療

詳細な説明

Participants with advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) Harboring epidermal growth factor receptor (EGFR) mutations 3.1 Number of targeted participants Part A (Main Cohort): Approximately 45 participants (including a 10% dropout rate) Part B (Exploratory Cohort): Approximately 15 participants Part C (Expansion Cohort): about 44 participants (including a 10% dropout rate)

研究の種類

介入

入学 (推定)

104

段階

  • フェーズ2
  • フェーズ 1

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

  • 名前:Eun-Young Kwak, PhD
  • 電話番号:031 778 8688
  • メール:bella@txinno.com

研究場所

      • Gyeonggi-do、韓国
        • 募集
        • Ajou University Hospital
        • 主任研究者:
          • Taehwan Kim
      • Gyeonggi-do、韓国
        • 募集
        • Seoul University Bundang Hospital
        • 主任研究者:
          • Yu Jung Kim
      • Gyeonggi-do、韓国
        • まだ募集していません
        • The Catholic University of Korea, ST. Vincent's Hospital
        • 主任研究者:
          • ByungYong Shim
      • Incheon、韓国、21565
        • 募集
        • Gachon University Gil Medical Center
        • コンタクト:
          • Joo-Hwan Park, MD, PhD
        • 主任研究者:
          • Joo-Hwan Park, MD, PhD
      • Seoul、韓国
        • 募集
        • Severance Hospital
        • 主任研究者:
          • Hye Ryun Kim
      • Seoul、韓国
        • 募集
        • Korea University Guro Hospital
        • 主任研究者:
          • Eun Joo Kang
        • コンタクト:
          • 電話番号:8200000000
      • Seoul、韓国
        • まだ募集していません
        • Samsung Medical Center
        • コンタクト:
          • 電話番号:8200000000
        • 主任研究者:
          • JinSeok Ahn
      • Seoul、韓国
        • 募集
        • HanYang Univ. Hospital
        • 主任研究者:
          • Myung-Ju Ahn

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

19年歳以上 (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) Males and females aged 19 or older at the time of written informed consent. 2) Participants must have histologically or cytologically confirmed advanced or metastatic non-squamous NSCLC (Stage IIIB, IIIC, or IV per AJCC 8th edition) with an EGFR TKI-sensitizing mutation.

They must also meet the prior treatment requirements for each cohort.

* EGFR TKI-sensitizing mutations: mutations that are highly responsive to TKIs, such as exon 19 deletion or exon 21 L858R point mutation.

3) Participants who have experienced disease progression on or after prior third-generation EGFR TKI therapy, either during or after treatment, and who meet the following criteria

(1) Part A:

  • No prior treatment with a TROP2 ADC,

  • Have received no more than four* prior lines of anticancer therapy, including one platinum-based doublet chemotherapy regimen.

    (2) Part B: Prior treatment with a TROP2 ADC (3) Part C:

  • No prior treatment with a TROP2 ADC, and

  • Have received no more than three* prior lines of anticancer therapy, including one platinum-based doublet chemotherapy regimen

    *Counting of prior lines of anticancer therapy Neoadjuvant and adjuvant anticancer therapies are, in principle, not counted as prior lines. However, if disease recurrence or progression occurs within 6 months after completion of adjuvant therapy, such therapy will be counted as a prior line.

    4) Participants with documented evidence of an EGFR TKI-sensitizing mutation in the tumor, as confirmed by liquid biopsy or tissue biopsy performed prior to enrollment in this study, with the result* properly documented

    *EGFR mutation testing must be performed using a validated polymerase chain reaction (PCR) or next-generation sequencing (NGS) assay at an appropriately certified/accredited laboratory (e.g., a study specimen analysis facility or a laboratory holding a clinical laboratory standard accreditation).

    5) Participants with at least one measurable lesion per RECIST v1.1. If the participant has received prior radiotherapy, the measurable lesion must be located outside the prior radiation field unless there is clear evidence of progression of a lesion within the irradiated field.

    6) Participants who agree to provide either: a fresh tumor biopsy (core needle biopsy or excisional biopsy) obtained before the first dose of TXN10128 (C1D1), or an archival tumor specimen collected after the most recent prior anticancer therapy.

    7) Participants with an Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1.

    8) Participants with a life expectancy of at least 12 weeks. 9) Adequate hematologic and adequate major organ/cardiac function, as defined by the following laboratory results obtained within 7 days prior to the first dose of TXN10128 (C1D1):

    1. Adequate bone marrow function*: platelet count ≥100,000/mm³, hemoglobin (Hb) ≥10 g/dL, absolute neutrophil count (ANC) ≥1,500/mm³.

      * Hematologic parameters must be met without transfusion, granulocyte colony-stimulating factor (G-CSF), or other hematopoietic growth factor support within 1 week prior to the relevant laboratory assessment.

    2. Adequate hepatic function: aspartate aminotransferase (AST)/alanine aminotransferase (ALT) ≤2.5×upper limit of normal (ULN) (≤5×ULN in the presence of liver metastases or hepatocellular carcinoma); total bilirubin (TBL) ≤1.5×ULN (<3×ULN in participants with Gilbert's syndrome).

    3. Adequate renal function: creatinine clearance (CrCl) ≥50 mL/min*. * CrCl = [140 - age (years)] × weight (kg) (× 0.85 for female participants) / [serum creatinine (mg/dL) × 72]

    4. Adequate coagulation function: international normalized ratio (INR)/prothrombin time (PT)/activated partial thromboplastin time (aPTT) ≤1.5×ULN.

    5. Systolic blood pressure≤160 mmHg, diastolic blood pressure≤100 mmHg

    6. QTcF interval*: Mean QTcF value from triplicate ECGs ≤480 msec *In cases where QTc assessment is difficult due to structural abnormalities of the cardiac conduction system, such as right bundle branch block (RBBB) or left bundle branch block (LBBB), a specific formula may be applied in consultation with the sponsor. Once selected, the same method must be used consistently for subsequent assessments of QTc changes.

    10) Recovery from adverse events (AEs) of prior therapy to Grade ≤1 (except for alopecia or stable CTCAE Grade 2 peripheral neuropathy).

    11) For participants of reproductive potential, agreement to practice adequate abstinence and contraception, and agreement not to donate ova or sperm. Males and females of childbearing potential must agree to use one of the following medically acceptable methods of contraception from the last dose of TXN10128 through 28 weeks after the last dose.

  • Hormonal contraceptives (oral, injectable, or implantable

  • Intrauterine device (IUD) or intrauterine system (IUS);

  • Sterilization procedures or surgery (e.g., hysterectomy, bilateral oophorectomy, or bilateral salpingectomy);

  • Vasectomized partner;

  • Male participants must use a condom during sexual intercourse with a female partner of childbearing potential or a pregnant partner during the period of IP administration and for 4 months after the last dose. Sexual abstinence:

Complete abstinence from sexual intercourse is also acceptable when, in the investigator's judgment, the participant's age, occupation, lifestyle, or sexual orientation assures contraception. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or post-ovulation methods), abstinence, and withdrawal are not considered acceptable methods of contraception.

12) Participants who are willing and able to comply with the procedures required by this clinical study protocol, including hospitalization, procedures and interventions, tumor biopsy (core needle biopsy or excisional biopsy), and laboratory tests, and who have voluntarily provided written informed consent.

Exclusion Criteria:

  • 1) Participants with any of the following concurrent medical conditions:

    1. Symptoms of spinal cord compression
    2. Active central nervous system (CNS) metastases

However, at the investigator's discretion, participants may be enrolled if they meet any of the following:

- Neurologically stable CNS metastases that have either been off corticosteroids for at least 4 weeks prior to the first dose of TXN10128 or have been maintained on a stable dose of corticosteroids [hydrocortisone ≤30 mg/day, dexamethasone ≤2 mg/day, or prednisone ≤10 mg/day (or equivalent)].

- At least 2 weeks have elapsed since the completion of brain radiotherapy. (3) Pathologically confirmed leptomeningeal metastases (4) Clinically significant coagulation disorders, including disseminated intravascular coagulation (DIC).) (5) Participants with histologically mixed small cell lung cancer (SCLC) and NSCLC.

(6) Uncontrolled diarrhea of Grade ≥2 per NCI-CTCAE version 6.0 2) Participants with any of the following medical history:

  1. Clinically significant (e.g., active) cardiovascular disease within 24 weeks prior to the first dose of TXN10128 (C1D1):

    - History of long QT syndrome;

    • Stroke, Myocardial Infarction;
    • Unstable angina or significant cardiac arrhythmia requiring pharmacologic treatment;
    • Congestive heart failure (New York Heart Association [NYHA] Classification ≥Class 3).
  2. Prior allogeneic hematopoietic stem cell transplantation, or prior autologous or allogeneic CAR-T cell therapy, or solid organ transplantation.

  3. Known positive status for human immunodeficiency virus (HIV) infection.

  4. Active hepatitis B or C infection (however, participants may be eligible if HBV DNA or HCV RNA is controlled to below the institutional lower limit of detection).

  5. Active infection requiring intravenous antibiotic therapy within 2 weeks prior to study enrollment.

  6. Active interstitial lung disease (ILD) requiring steroid or immunosuppressive therapy, or a history of ILD, or suspected ILD findings on screening imaging assessment.

  7. Pulmonary disease including pneumonia or pulmonary fibrosis, or severe impairment of pulmonary function resulting therefrom.

  8. History of another primary malignancy within 2 years prior to screening (however, participants with a history within 2 years of basal cell or squamous cell carcinoma of the skin, superficial bladder cancer, papillary thyroid carcinoma, or carcinoma in situ at other sites may be eligible if successfully treated and without recurrence, based on the investigator's medical judgment).

  9. Inability to take oral medications, gastrointestinal disorders causing malabsorption syndrome, or uncontrolled inflammatory gastrointestinal (GI) disease (e.g., intestinal paralysis, intestinal obstruction, Crohn's disease, ulcerative colitis).

  10. Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedures.

  11. Participants who experienced a Grade ≥3 immune-related adverse event (irAE) with prior immunotherapy, excluding clinically non-significant laboratory abnormalities.

  12. Active autoimmune disease requiring systemic therapy within the past 2 years (i.e., use of disease-modifying agents, corticosteroids, or immunosuppressive drugs). Chronic systemic steroid therapy (at doses exceeding 10 mg/day prednisone equivalent) or any other form of immunosuppressive therapy within 2 weeks (14 days) prior to the first dose of TXN10128 is not permitted. However, replacement therapies such as thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency are not considered forms of systemic therapy and are permitted.

3) Participants who have received any of the following treatments:

  1. Prior treatment with an IP targeting ENPP1 inhibitors or STING agonists.

  2. Use of the following anticancer therapies within the specified timeframes prior to the first dose of TXN10128 (C1D1):

    - Cytotoxic chemotherapy, targeted therapy, or hormonal therapy within 2 weeks; however, nitrosourea or mitomycin administered within 6 weeks prior to the first dose;

    - Prior antibody or protein-based immunotherapy, or IP within 4 weeks;

    • Radiotherapy administered to a wide field, including the spine and pelvis, within 4 weeks; however, limited-field radiation administered for symptom palliation within 2 weeks.
  3. Major surgery within 4 weeks prior to the first dose of TXN10128 (C1D1) (placement of a central venous catheter is not considered major surgery).

  4. Administration of live vaccines, live-attenuated vaccines, or mRNA vaccines, within 4 weeks prior to the first dose of TXN10128 (C1D1).

  5. Participants who are receiving strong CYP3A4 inhibitors/inducers (e.g., ketoconazole, rifampin, carbamazepine) within 2 weeks prior to the first dose of the IP, or who require continuation of such agents during the study period.

4) Participants with a history of hypersensitivity to the combination anticancer therapy, any of its components, or agents of similar class, including anaphylaxis/anaphylactoid reactions and angioedema, or who have any other contraindications to treatment.

5) Pregnant or lactating women. 6) Participants who, in the opinion of the investigator, are not suitable for study participation [Part A, B] 7) Participants who are homozygous (UGT1A1*6/*6, UGT1A1*28/*28) or compound heterozygous (UGT1A1*6/*28) for UGT1A1*6 or UGT1A1*28.

8) Participants who are receiving atazanavir sulfate.

[Part C] 9) Clinically significant corneal disease that may affect treatment or assessment, as judged by the investigator.

10) Participants who, at screening, are receiving strong inhibitors (e.g., cyclosporine, verapamil) or inducers of major drug transporters (P-gp, OATP1B1/1B3, BCRP, MRP1, MATE2-K), and who require continuation of such agents during the study period.

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:非ランダム化
  • 介入モデル:並列代入
  • 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
他の:Part A

TXN10128 in combination with irinotecan in participants who had not previously received a TROP2 ADC.

oral ENPP1 inhibitor

他の:Part B

TXN10128 in combination with irinotecan in participants who had previously received a TROP2 ADC.

oral ENPP1 inhibitor

他の:Part C

TXN10128 in combination with TROP2 ADC in participants who had not previously received a TROP2 ADC.

oral ENPP1 inhibitor

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
Progression Free Survival
時間枠:From enrollment until disease progression or the end of the study; tumor assessments every 8 weeks through Week 24 and every 12 weeks thereafter.

By central independent reviewer

From enrollment until disease progression or the end of the study; tumor assessments every 8 weeks through Week 24 and every 12 weeks thereafter.

二次結果の測定

結果測定
メジャーの説明
時間枠
objective Response Rate
時間枠:From enrollment until disease progression or the end of the study; tumor assessments every 8 weeks through Week 24 and every 12 weeks thereafter.

By central independent reviewer

From enrollment until disease progression or the end of the study; tumor assessments every 8 weeks through Week 24 and every 12 weeks thereafter.
Disease Control Rate
時間枠:From enrollment until disease progression or the end of the study; tumor assessments every 8 weeks through Week 24 and every 12 weeks thereafter.

By central independent reviewer

From enrollment until disease progression or the end of the study; tumor assessments every 8 weeks through Week 24 and every 12 weeks thereafter.

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。

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出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

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 (実際)

2026年10月8日

一次修了 (推定)

2028年9月30日

研究の完了 (推定)

2029年3月31日

試験登録日

最初に提出

2026年10月26日

QC基準を満たした最初の提出物

2026年11月9日

最初の投稿 (実際)

2026年11月12日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月12日

QC基準を満たした最後の更新が送信されました

2026年11月9日

最終確認日

2026年10月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

未定

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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