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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)

9 de novembro de 2026 atualizado por: 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.

Visão geral do estudo

Status

Recrutamento

Intervenção / Tratamento

Descrição detalhada

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)

Tipo de estudo

Intervencional

Inscrição (Estimado)

104

Estágio

  • Fase 2
  • Fase 1

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

  • Nome: Eun-Young Kwak, PhD
  • Número de telefone: 031 778 8688
  • E-mail: bella@txinno.com

Locais de estudo

      • Gyeonggi-do, Coréia do Sul
        • Recrutamento
        • Ajou University Hospital
        • Investigador principal:
          • Taehwan Kim
      • Gyeonggi-do, Coréia do Sul
        • Recrutamento
        • Seoul University Bundang Hospital
        • Investigador principal:
          • Yu Jung Kim
      • Gyeonggi-do, Coréia do Sul
        • Ainda não está recrutando
        • The Catholic University of Korea, ST. Vincent's Hospital
        • Investigador principal:
          • ByungYong Shim
      • Incheon, Coréia do Sul, 21565
        • Recrutamento
        • Gachon University Gil Medical Center
        • Contato:
          • Joo-Hwan Park, MD, PhD
        • Investigador principal:
          • Joo-Hwan Park, MD, PhD
      • Seoul, Coréia do Sul
        • Recrutamento
        • Severance Hospital
        • Investigador principal:
          • Hye Ryun Kim
      • Seoul, Coréia do Sul
        • Recrutamento
        • Korea University Guro Hospital
        • Investigador principal:
          • Eun Joo Kang
        • Contato:
          • Número de telefone: 8200000000
      • Seoul, Coréia do Sul
        • Ainda não está recrutando
        • Samsung Medical Center
        • Contato:
          • Número de telefone: 8200000000
        • Investigador principal:
          • JinSeok Ahn
      • Seoul, Coréia do Sul
        • Recrutamento
        • HanYang Univ. Hospital
        • Investigador principal:
          • Myung-Ju Ahn

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

19 anos e mais velhos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

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.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Não randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Outro: Part A

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

oral ENPP1 inhibitor

Outro: Part B

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

oral ENPP1 inhibitor

Outro: Part C

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

oral ENPP1 inhibitor

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Progression Free Survival
Prazo: 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.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
objective Response Rate
Prazo: 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
Prazo: 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.

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Publicações e links úteis

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Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

8 de outubro de 2026

Conclusão Primária (Estimado)

30 de setembro de 2028

Conclusão do estudo (Estimado)

31 de março de 2029

Datas de inscrição no estudo

Enviado pela primeira vez

26 de outubro de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

9 de novembro de 2026

Primeira postagem (Real)

12 de novembro de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

12 de novembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

9 de novembro de 2026

Última verificação

1 de outubro de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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