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A Phase IIa Study Evaluating Injectable ALK-N001 in Patients With Advanced Gastrointestinal Tumors

13 de septiembre de 2026 actualizado por: Zhejiang Anglikang Pharmaceutical Co., Ltd.

An Open-label, Multicenter Phase IIa Study to Evaluate the Efficacy and Safety of Injectable ALK-N001 in Patients With Advanced Gastrointestinal Tumors

This open-label, multicenter Phase IIa study is to evaluate the efficacy and safety of injectable ALK-N001 in patients with advanced gastrointestinal tumors, with the primary objective to assess its preliminary efficacy.

Descripción general del estudio

Estado

Aún no reclutando

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Estimado)

174

Fase

  • Fase 2

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  1. Voluntarily sign informed consent, understand the study and be willing and able to comply with all study procedures.
  2. Age ≥18 years (male or female) at the time of signing informed consent.
  3. Histologically or cytologically confirmed locally advanced or metastatic esophageal squamous cell carcinoma, colorectal adenocarcinoma, or other gastrointestinal tumors.
  4. Disease progression or intolerance after prior standard-of-care (SoC) treatment:

    1. Cohort1 (ESCC): Not eligible for curative surgery/radiochemotherapy; progressed or intolerant after at least 1st-line platinum-based chemotherapy plus PD-(L)1 inhibitor. If immunotherapy is declined/ineligible, progressed after ≥2 lines of systemic therapy.
    2. Cohort2 (CRC): Received standard systemic therapy for metastatic colorectal cancer and experienced progression or intolerance. Must have received fluoropyrimidine, oxaliplatin and irinotecan-based chemotherapy (±bevacizumab/cetuximab), unless contraindicated. For MSI-H/dMMR tumors, prior PD-(L)1 inhibitor is required.
    3. Cohort3 (Other GI tumors): Not curable by surgery; disease progression/intolerance after standard-of-care therapy, or no available effective treatment.
  5. At least one measurable lesion per RECIST V1.1 (lesions in prior radiation field generally not measurable unless clear progression).
  6. ECOG performance status 0 or 1.
  7. Expected survival ≥3 months.
  8. Adequate organ function:

    • Bone marrow (no transfusion/growth factors within prior 14 days): ANC ≥1.5×10⁹/L; PLT ≥90×10⁹/L; Hb ≥90 g/L
    • Liver: TBIL ≤1.5×ULN; ALT ≤3×ULN (≤5×ULN for liver metastasis); AST ≤3×ULN (≤5×ULN for liver metastasis); ALB ≥35 g/L
    • Renal: Cr ≤1.5×ULN; if Cr>1.5×ULN, CrCl ≥50 mL/min (Cockcroft-Gault formula)
    • Coagulation: APTT ≤1.5×ULN; INR ≤1.5×ULN
  9. Women of childbearing potential must have negative pregnancy test at screening and agree to effective contraception or abstinence from consent until 6 months after last dose. Male participants must use effective contraception or abstinence from consent until 6 months after last dose; no sperm donation.

Exclusion Criteria:

  • 1. Received chemotherapy, radiotherapy (palliative local radiotherapy within prior 2 weeks), biotherapy, targeted therapy, immunotherapy, TIL or other anti-tumor therapies within 4 weeks before first dose.

    1. Anti-endocrine therapy within 2 weeks or 5 half-lives; oral CDK4/6i, small molecule targeted agents, anti-tumor Chinese medicine.
    2. CAR-T, CAR-NK or tumor vaccine within prior 3 months.
    3. Live vaccine within 2 weeks; non-live vaccine within 4 weeks before first dose.
    4. Investigational drug within 4 weeks or 5 half-lives before first dose (whichever shorter).

      2. Use of strong CYP3A4 inducer/inhibitor within 7 days before first dose or planned during study.

      3. Prior treatment with DXD-containing ADC or PDC. 4. Active infection at screening requiring systemic anti-infective therapy within 2 weeks prior to first dose.

      5. Known BRAF mutation or NTRK fusion positive colorectal cancer (Cohort2). 6. Unstable or progressive CNS/leptomeningeal metastases (stable brain metastases ≥1 month, no new/enlarging lesions and off steroids ≥4 weeks may enroll).

      7. Clinically uncontrolled third-space effusion requiring therapeutic paracentesis/drainage within prior 14 days.

      8. Prior or current interstitial lung disease (ILD), non-infectious pneumonitis requiring steroids, suspected ILD or severely impaired pulmonary function.

      9. Severe GI disease including chronic inflammatory bowel disease, bowel obstruction or chronic diarrhea.

      10. Esophageal stent placement, tracheal stent or esophageal stricture (Cohort1).

      11. Severe cardiovascular disease:

    1. Clinically significant cardiac arrhythmias or 2nd/3rd degree AV block requiring intervention.
    2. Acute coronary syndrome, heart failure, stroke or grade ≥3 cardiovascular event within 6 months.
    3. NYHA Class ≥II heart failure (exception: stable NYHA II, LVEF≥50%, no exacerbation ≥6 months after optimized medical treatment, confirmed by cardiologist).
    4. Uncontrolled hypertension: SBP≥150 mmHg and/or DBP≥100 mmHg. 12. History of GI perforation/fistula within 6 months before first dose, or tumor invading adjacent organs (great vessel/trachea) with high risk of bleeding/fistula.

      13. History of severe thromboembolism within prior 6 months; known inherited/acquired thrombophilia.

      14. Other malignancy within past 5 years (exception: cured cervical carcinoma in situ, cutaneous squamous cell carcinoma, basal cell carcinoma, papillary thyroid carcinoma).

      15. Prior allogeneic hematopoietic stem cell or solid organ transplantation. 16. Prior anti-tumor adverse events not recovered to ≤ Grade1 (NCI-CTCAE v6.0, alopecia and investigator-assessed non-risk toxicities excluded) or not meeting eligibility lab criteria.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: No aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Cohort 1 (ESCC), Dose A (37.5 mg/m²)
Participants with advanced esophageal squamous cell carcinoma (ESCC) receive injectable ALK-N001 at 37.5 mg/m² intravenously every 2 weeks (Q2W) per 28-day cycle. Enrollment and dose expansion may be adjusted by the Safety Review Committee (SRC) based on accumulated safety, PK, PD and preliminary anti-tumor data. Treatment continues until intolerable toxicity, progressive disease, or other discontinuation criteria.
Injectable ALK-N001 is administered intravenously every 2 weeks (Q2W; 28-day treatment cycle). Two predefined dose levels are available: 37.5 mg/m² (Dose A) and 50 mg/m² (Dose B). Enrollment or suspension of dose groups may be determined by the Safety Review Committee (SRC) based on safety, PK, PD and preliminary anti-tumor activity data.
Otros nombres:
  • QHL-1618
Experimental: Cohort 1 (ESCC), Dose B (50 mg/m²)
Participants with advanced esophageal squamous cell carcinoma (ESCC) receive injectable ALK-N001 at 50 mg/m² intravenously every 2 weeks (Q2W) per 28-day cycle. Enrollment and dose expansion may be adjusted by the Safety Review Committee (SRC) based on accumulated safety, PK, PD and preliminary anti-tumor data. Treatment continues until intolerable toxicity, progressive disease, or other discontinuation criteria.
Injectable ALK-N001 is administered intravenously every 2 weeks (Q2W; 28-day treatment cycle). Two predefined dose levels are available: 37.5 mg/m² (Dose A) and 50 mg/m² (Dose B). Enrollment or suspension of dose groups may be determined by the Safety Review Committee (SRC) based on safety, PK, PD and preliminary anti-tumor activity data.
Otros nombres:
  • QHL-1618
Experimental: Cohort 2 (CRC), Dose A (37.5 mg/m²)
Participants with advanced colorectal carcinoma (CRC) receive injectable ALK-N001 at 37.5 mg/m² intravenously every 2 weeks (Q2W) per 28-day cycle. Enrollment and dose expansion may be adjusted by the Safety Review Committee (SRC) based on accumulated safety, PK, PD and preliminary anti-tumor data. Treatment continues until intolerable toxicity, progressive disease, or other discontinuation criteria.
Injectable ALK-N001 is administered intravenously every 2 weeks (Q2W; 28-day treatment cycle). Two predefined dose levels are available: 37.5 mg/m² (Dose A) and 50 mg/m² (Dose B). Enrollment or suspension of dose groups may be determined by the Safety Review Committee (SRC) based on safety, PK, PD and preliminary anti-tumor activity data.
Otros nombres:
  • QHL-1618
Experimental: Cohort 2 (CRC), Dose B (50 mg/m²)
Participants with advanced colorectal carcinoma (CRC) receive injectable ALK-N001 at 50 mg/m² intravenously every 2 weeks (Q2W) per 28-day cycle. Enrollment and dose expansion may be adjusted by the Safety Review Committee (SRC) based on accumulated safety, PK, PD and preliminary anti-tumor data. Treatment continues until intolerable toxicity, progressive disease, or other discontinuation criteria.
Injectable ALK-N001 is administered intravenously every 2 weeks (Q2W; 28-day treatment cycle). Two predefined dose levels are available: 37.5 mg/m² (Dose A) and 50 mg/m² (Dose B). Enrollment or suspension of dose groups may be determined by the Safety Review Committee (SRC) based on safety, PK, PD and preliminary anti-tumor activity data.
Otros nombres:
  • QHL-1618
Experimental: Cohort 3 (Other GI Tumors), Dose A (37.5 mg/m²)
Participants with advanced other gastrointestinal tumors receive injectable ALK-N001 at 37.5 mg/m² intravenously every 2 weeks (Q2W) per 28-day cycle. Cohort 3 is exploratory and will be activated only if meaningful anti-tumor signals are observed in concurrent ALK-N001 trials. SRC may adjust enrollment based on safety, PK, PD and efficacy data. Treatment continues until intolerable toxicity, progressive disease, or other discontinuation criteria.
Injectable ALK-N001 is administered intravenously every 2 weeks (Q2W; 28-day treatment cycle). Two predefined dose levels are available: 37.5 mg/m² (Dose A) and 50 mg/m² (Dose B). Enrollment or suspension of dose groups may be determined by the Safety Review Committee (SRC) based on safety, PK, PD and preliminary anti-tumor activity data.
Otros nombres:
  • QHL-1618
Experimental: Cohort 3 (Other GI Tumors), Dose B (50 mg/m²)
Participants with advanced other gastrointestinal tumors receive injectable ALK-N001 at 50 mg/m² intravenously every 2 weeks (Q2W) per 28-day cycle. Cohort 3 is exploratory and will be activated only if meaningful anti-tumor signals are observed in concurrent ALK-N001 trials. SRC may adjust enrollment based on safety, PK, PD and efficacy data. Treatment continues until intolerable toxicity, progressive disease, or other discontinuation criteria.
Injectable ALK-N001 is administered intravenously every 2 weeks (Q2W; 28-day treatment cycle). Two predefined dose levels are available: 37.5 mg/m² (Dose A) and 50 mg/m² (Dose B). Enrollment or suspension of dose groups may be determined by the Safety Review Committee (SRC) based on safety, PK, PD and preliminary anti-tumor activity data.
Otros nombres:
  • QHL-1618

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Objective Response Rate (ORR), assessed per Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1
Periodo de tiempo: Up to approximately 24 months from the first dose.
ORR is defined as the proportion of participants with confirmed complete response (CR) or partial response (PR) as evaluated by RECIST V1.1.
Up to approximately 24 months from the first dose.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Duration of Response (DOR)
Periodo de tiempo: Up to approximately 24 months from the first dose.
Description: DOR is defined as the time from the first documentation of CR/PR until the first documented progressive disease (PD) or death from any cause.
Up to approximately 24 months from the first dose.
Disease Control Rate (DCR)
Periodo de tiempo: Up to approximately 24 months from the first dose.

DCR is the proportion of participants achieving CR, PR, or stable disease (SD) per RECIST V1.1.

Time Frame: Up to approximately 24 months from the first dose.

Up to approximately 24 months from the first dose.
Progression-Free Survival (PFS)
Periodo de tiempo: Up to approximately 24 months from the first dose.
PFS is the time from study enrollment to documented PD or death from any cause. 6-,12-,24-month PFS rates will be calculated.
Up to approximately 24 months from the first dose.
Overall Survival (OS)
Periodo de tiempo: Up to approximately 24 months from the first dose.
OS is defined as the time from enrollment to death from any cause. 12-,24-month OS rates will be calculated.
Up to approximately 24 months from the first dose.
Safety (Adverse Events and Serious Adverse Events)
Periodo de tiempo: From informed consent until 28±7 days after last dose.
Incidence, severity and relatedness of AEs and SAEs; laboratory tests, 12-lead ECG, vital signs, physical examination and ECOG performance status.
From informed consent until 28±7 days after last dose.
Population Pharmacokinetics (PopPK) of total DXD and free DXD
Periodo de tiempo: From first dose up to end of treatment.
Characterize PopPK profiles of total DXD and free DXD.
From first dose up to end of treatment.
Exposure-Response (E-R) relationship of total DXD and free DXD
Periodo de tiempo: From first dose up to approximately 24 months after first dose.
E-R relationship between total/free DXD exposure and efficacy, safety and biomarkers.
From first dose up to approximately 24 months after first dose.

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Expression level of Legumain in tumor tissue
Periodo de tiempo: Screening (mandatory baseline sample collection); optional sampling at disease progression; analysis up to approximately 24 months after the first dose.
Tumor tissue samples (fresh biopsy or archived paraffin-embedded tissue) will be collected from all participants at screening (mandatory) and at disease progression (optional) for central laboratory Legumain testing. Previous genetic or protein testing reports will be collected if available. Evaluate the correlation between tumor Legumain expression and anti-tumor efficacy.
Screening (mandatory baseline sample collection); optional sampling at disease progression; analysis up to approximately 24 months after the first dose.

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de septiembre de 2026

Finalización primaria (Estimado)

1 de diciembre de 2027

Finalización del estudio (Estimado)

1 de abril de 2028

Fechas de registro del estudio

Enviado por primera vez

13 de septiembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

13 de septiembre de 2026

Publicado por primera vez (Actual)

17 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

17 de septiembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

13 de septiembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • ALK-N001-003

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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