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Phase I/IIa Clinical Trial of IMC001 in Patients With Advanced Epithelial Solid Tumors. (IMC001 EpCAM)

8 giugno 2026 aggiornato da: Suzhou Immunofoco Biotechnology Co., Ltd

Phase I/IIa Clinical Trial Evaluating the Safety and Efficacy of IMC001 in Patients With Advanced Epithelial Solid Tumors.

This is an open -label phase I /IIa study designed to evaluate the safety and efficacy of IMC001 in patients with advanced epithelial solid tumors. The study comprises two parts: a phase I dose-escalation phase and a phase IIa phase to further explore and validate efficacy .In the Phase I dose-escalation phase of this study, approximately 7-15 subjects with advanced epithelial solid tumors will be recruited to evaluate the safety and tolerability of autologous IMC001 treatment . In the expansion phase, at least two dose groups will be selected , each recruiting 5-10 subjects. Combined with the subjects from the escalation phase, each dose group will be expanded to approximately 10 subjects to determine the recommended RP2D dose for progression to Phase IIa . DLT ( digestive tract aging) assessment will be performed on subjects in each cohort within 28 days of IMC001 infusion . the RP2D is determined , approximately 6-20 subjects will be initially enrolled at this dose for each selected tumor type to further explore the efficacy and safety of autologous IMC001 for this indication. Subsequently, the protocol may be revised based on statistical hypotheses and regulatory requirements to continue enrolling subjects in the selected tumor types to further validate the efficacy and safety in specific tumor types.the date on which the last participant completes a two-year follow-up visit, is lost to follow up, withdraws informed consent, or dies (whichever occurs first) . It is important to note that for long-term follow-up programs such as ADA, RCL, and VIS (up to 15 years), which require protocol-based follow-up, these follow-ups will be conducted continuously according to protocol and regulatory requirements. However, the actual study participation time for each participant will vary depending on screening requirements, response to treatment, long-term follow-up arrangements, and survival status .

Panoramica dello studio

Stato

Iscrizione su invito

Tipo di studio

Interventistico

Iscrizione (Stimato)

30

Fase

  • Fase 2
  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

      • Beijing, Cina
        • Beijing Cancer Hospital

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  1. to provide a signed and dated informed consent form before conducting any research-related procedures , and willing and able to comply with all research procedures.
  2. Applicants must be 18 years of age or older and 75 years of age or younger; both male and female applicants are welcome .
  3. Subjects with histologically or cytologically confirmed locally advanced/metastatic epithelial solid tumors , including but not limited to subjects with advanced gastric cancer/gastroesophageal junction adenocarcinoma, triple-negative breast cancer, biliary tract tumors, ovarian cancer, colorectal cancer, pancreatic cancer, gastrointestinal and pancreatic neuroendocrine tumors, etc.
  4. Disease progression or intolerance to standard systemic therapy , including:

    • Gastric cancer and gastroesophageal junction adenocarcinoma that have failed or are intolerant of at least two lines of standard systemic therapy. If first-line three-drug combination therapy has failed or is intolerant, enrollment may be made after thorough investigator evaluation.
    • Triple-negative breast cancer: Subjects with unresectable locally advanced or metastatic triple-negative breast cancer who have failed at least two lines of standard systemic therapy. All subjects must have previously received taxane therapy, regardless of the stage of disease at the time of treatment.
    • Other subjects with epithelial solid tumors who have failed or are intolerant of standard treatment.
  5. Tumor tissue samples (primary or metastatic, archived or newly collected) from the expected subjects, tested by the central laboratory, are EpCAM histologically positive (defined as tumor cell positivity ≥10% and staining intensity ≥1+).
  6. The expected survival period of the subjects is ≥12 weeks .
  7. According to RECIST 1.1 criteria, there should be at least one stably measurable target lesion (where the largest lesion should be ≤4). In the 3×10⁵ CAR -T cells/kg dose group, subjects with evaluable lesions (unmeasurable lesions) can be admitted.
  8. ECOG performance status score 0-1 .
  9. The subject has adequate organ and bone marrow function. Laboratory screening must meet the following criteria: all laboratory test results should be within the stable ranges outlined below, and there should be no ongoing supportive treatment. If any laboratory test result is abnormal according to the following criteria, a repeat test may be performed within one week. If the test results still do not meet the following criteria, the subject's screening has failed.

    1. Blood tests [No intensive blood transfusions (≥2 times within 1 week), platelet transfusions, or cell growth factor injections (excluding recombinant erythropoietin)) within 7 days prior to the test]: Neutrophil count (ANC) ≥1.5×10⁹ / L; Platelet count (PLT) ≥100 × 10⁹ / L; Hemoglobin content (Hb) ≥9.0g / dL; Lymphocyte count ( ALC ) ≥0.5× 10⁹ /L ;
    2. Liver function: alanine aminotransferase (ALT) ≤ 2.5 × ULN, aspartate aminotransferase (AST) ≤ 2.5 × ULN, serum total bilirubin (TB) ≤ 2 × ULN; for subjects with liver metastases, AST and ALT < 5 × ULN ;
    3. Kidney function: Serum creatinine ≤1.5×ULN; if serum creatinine >1.5×ULN, creatinine clearance rate >50mL/min is required (according to the Cockcroft-Gault formula); qualitative urine protein ≤1+; if qualitative urine protein ≥2+, a 24-hour urine protein quantification test is required (if the 24-hour urine protein quantification test is <1g, it is acceptable).
    4. Amylase and lipase ≤1.5×ULN; alkaline phosphatase (ALP) ≤2.5×ULN, and for subjects with bone metastases, ALP <5×ULN ;
    5. Coagulation function: Activated partial thromboplastin time ≤ 1.5 ULN, prothrombin time ≤ 1.5 × ULN ;
  10. All toxicities resulting from prior antitumor therapy were reduced to grade 0-1 (according to NCI CTCAE version 5.0) or to a level acceptable to the inclusion criteria. Other toxicities, such as alopecia and vitiligo, which the investigators deemed not to pose a safety risk to the subjects, were excluded .

Reproductive status: Female subjects of reproductive age or male subjects whose sexual partners are women of reproductive age, who are willing to use medically approved and highly effective contraceptive methods, such as intrauterine devices or condoms, from the time they sign the informed consent form until 12 months after cell infusion (women of reproductive age include premenopausal women and women within 24 months after menopause) .

Exclusion Criteria:

  1. Pregnant and breastfeeding women .
  2. Positive for human immunodeficiency virus (HIV) antibodies; hepatitis B virus infection ( if the subject is positive for hepatitis B surface antigen, regardless of whether the core antibody is negative or positive, they can also be enrolled if the viral DNA load is negative, and prophylactic antiviral treatment should be considered ); acute or chronic active hepatitis C (positive for HCV antibodies); positive for syphilis antibodies; Epstein-Barr virus (EBV) infection ( positive for IgM or known EBV infection ); cytomegalovirus (CMV) infection (positive for IgM); positive for human T-lymphotropic virus (HTLV). The results of the above pathogen tests are subject to the results of the central laboratory .
  3. Severe infections that are in an active phase or poorly controlled clinically .
  4. The patients had uncontrollable pleural effusion, pericardial effusion, and ascites before enrollment .
  5. Extensive or diffuse lung metastases , extensive or diffuse liver metastases , extensive or diffuse bone metastases .
  6. Subjects with intestinal obstruction or obstructive jaundice who are deemed unsuitable for participation in this trial by the researchers .
  7. Blood oxygen saturation ≤95% without oxygen supplementation .
  8. Patients with other serious lung diseases that may limit their participation in this study, such as pulmonary embolism, chronic obstructive pulmonary disease, symptomatic or poorly controlled interstitial lung disease, or clinically significant abnormalities in pulmonary function tests .
  9. Subjects with a known history or current hepatic encephalopathy requiring treatment; subjects with a current or history of central nervous system disorders, such as seizures, cerebral ischemia/hemorrhagic disease, dementia, cerebellar disease, or any autoimmune disease involving the central nervous system .
  10. Central nervous system metastasis or meningeal metastasis .
  11. Currently, patients have unstable heart disease requiring treatment or heart disease that cannot be controlled by treatment, or hypertension that is poorly controlled according to investigators (defined as systolic blood pressure ≥160 mmHg and/or diastolic blood pressure >100 mmHg after standard antihypertensive drug treatment); or diabetes that is poorly controlled despite standard treatment (fasting blood glucose ≥10.2 mmol/L) .
  12. If any of the following cardiac clinical symptoms or conditions exist within 6 months prior to cell infusion:

    1. Left ventricular ejection fraction (LVEF) < 50%;
    2. History of myocardial infarction within the past year; or unstable angina; or percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG); or use of a pacemaker;
    3. Resting electrocardiogram examination: QTc F > 450ms (male) or QTc F > 470ms (female);
    4. An electrocardiogram at rest reveals clinically significant abnormalities (such as abnormalities in heart rate, conduction, or morphological characteristics) or complete left bundle branch block or third-degree atrioventricular block or a PR interval >250 ms.
  13. Evidence of a significant coagulation disorder or other obvious risk of bleeding, including:

    1. Abnormal coagulation function that is clinically significant;
    2. History of intracranial hemorrhage or spinal cord hemorrhage;
    3. Patients with tumor lesions invading major blood vessels and posing a significant risk of bleeding;
    4. Subjects who currently have unstable or active ulcers or active gastrointestinal bleeding;
    5. An embolic event occurred within 6 months prior to cell reinfusion;
    6. Within one month prior to cell reinfusion, there has been clinically significant hemoptysis or obvious bleeding from tumor lesions;
    7. Had a major trauma or major surgery within one month prior to enrollment;
    8. The presence of any bleeding disorder, such as hemophilia, von Willebrand disease, etc.;
    9. The patient has received anticoagulation therapy (excluding low molecular weight heparin) for therapeutic purposes within 2 weeks prior to cell reinfusion.
    10. Subjects are receiving routine anticoagulation therapy (such as warfarin or heparin). Subjects require long-term antiplatelet therapy (aspirin >300 mg/day; clopidogrel >75 mg/day); dipyridamole, ticlopidine, or cilostazol, etc.
  14. The patient has received systemic steroids equivalent to >15 mg/day of prednisone for more than 3 days within 2 weeks prior to apheresis, excluding inhaled steroids .
  15. Subjects requiring systemic therapy with corticosteroids or other immunosuppressive drugs during treatment. Subjects with any active autoimmune disease, or a history of autoimmune disease with anticipated relapse (including but not limited to: systemic lupus erythematosus, rheumatoid arthritis, psoriasis, multiple sclerosis, inflammatory bowel disease, and asthma requiring medical intervention with bronchodilators). Exceptions include: type 1 diabetes; skin diseases not requiring systemic treatment (e.g., vitiligo, psoriasis); alopecia; hypothyroidism requiring only hormone replacement therapy; asthma that was completely remitted in childhood and requires no intervention in adulthood; or other conditions not expected to relapse in the absence of external triggers .
  16. Subjects with a prior or concurrent history of other malignant tumors, except in the following circumstances:

    1. Basal cell or squamous cell carcinoma that has undergone adequate treatment (sufficient wound healing is required before enrollment in the study).
    2. Cervical cancer or breast cancer in situ, cured and with no signs of recurrence for at least 3 years prior to the study;
    3. The primary malignant tumor has been completely removed and has been in complete remission for ≥5 years ; d ) The concurrent malignant tumor was an epithelial tumor that expressed EpCAM .
  17. Subjects who have previously received other gene therapies, including but not limited to CAR-T therapy and TCR-T therapy .
  18. The following treatments or medications were received before cell reinfusion: chemotherapy, targeted therapy, biotherapy, endocrine therapy, immunotherapy, or other anti-tumor treatments (excluding treatments that meet the protocol requirements before reinfusion, such as lymph node pretreatment and bridging therapy); less than 28 days or less than 5 half-lives since the first infusion treatment in this study (whichever is shorter); or traditional Chinese medicine treatment with anti-tumor indications received within 2 weeks before cell reinfusion .
  19. of severe allergies, such as anaphylactic shock .
  20. Subjects with severe mental disorders .
  21. Subjects who develop new cardiac arrhythmias, including but not limited to arrhythmias that cannot be controlled by medication; hypotension requiring vasopressors; or bacterial, fungal, or viral infections requiring intravenous antibiotics. Subjects receiving antibiotics to prevent infection may continue to participate in the trial at the investigator's discretion .
  22. The patient had participated in other interventional clinical studies and used investigational drugs within one month prior to the planned infusion of IMC001 .
  23. Subjects who received a live attenuated vaccine within 4 weeks prior to the planned single-donor administration or who are scheduled to receive a live attenuated vaccine during the study.
  24. Subjects with any other concurrent serious and /or uncontrolled medical conditions that the investigators deem unsuitable for participation in this trial.

Researchers assessed that participants were unable or unwilling to comply with the requirements of the research protocol .

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Each subject will be infused once with autologous CAR-T cell injection targeting EpCAM
In the Phase I dose-escalation phase of this study, approximately 7-15 subjects with advanced epithelial solid tumors will be recruited to evaluate the safety and tolerability of autologous IMC001 treatment. DLT (digestive-thickness assessment) will be performed on subjects in each cohort within 28 days after IMC001 infusion; the definition of DLT is detailed below. The expansion phase will select at least two dose groups, each recruiting 5-10 subjects (in conjunction with the escalation phase, expanding each dose group to approximately 10 subjects), to determine the recommended RP2D dose for progression to Phase IIa.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Observe dose limiting toxicity (DLTs) of IMC001 within 28 days after administration according to the DLT definition in the protocol
Lasso di tempo: Within 28 days after administration of IMC001
White blood cells (10 ^ 9/L), red blood cells (10 ^ 12/L), platelet count (10 ^ 9/L), hemoglobin (g/L), treatment-related lymphohistiocytosis (HLH)/hemophagocytic lymphohistiocytosis (HPS), cytokine release syndrome (CRS), immune cell therapy related neurotoxicity syndrome (ICANS)
Within 28 days after administration of IMC001
After treatment with IMC001, the recommended Phase II dose (RP2D) is determined based on dose limiting toxicity (DLT) and clinical response, including potential side effects
Lasso di tempo: Complete the incremental and expansion phases for all dose groups, and have the Safety Monitoring Committee (SMC) further evaluate safety and initial efficacy, and determine the recommended dose for entering Phase IIa (RP2D).
According to the results of the Safety Monitoring Committee (SMC) meeting, 2-3 dose levels will be selected for expansion, with an additional 5 to 10 subjects (excluding dose escalation subjects) to further evaluate safety and initial efficacy, and determine the recommended dose for entering Phase IIa (RP2D).
Complete the incremental and expansion phases for all dose groups, and have the Safety Monitoring Committee (SMC) further evaluate safety and initial efficacy, and determine the recommended dose for entering Phase IIa (RP2D).
Evaluate the objective response rate (ORR) of tumors based on RECIST 1.1
Lasso di tempo: According to the study protocol, periodic imaging assessments will be conducted at scheduled visits until the confirmed PD, 2 years (96 weeks) after infusion, loss to follow-up, withdrawal of informed consent, or death (whichever occurs first)
According to RECIST 1.1, the number of people who have achieved complete remission (CR) and partial remission (PR) is evaluated
According to the study protocol, periodic imaging assessments will be conducted at scheduled visits until the confirmed PD, 2 years (96 weeks) after infusion, loss to follow-up, withdrawal of informed consent, or death (whichever occurs first)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Pharmacokinetic evaluation (regarding Cmax)
Lasso di tempo: From IMC001 infusion until 96 weeks.
Maximum concentration of CAR-T cells in peripheral blood after administration (CAR+cells/μL blood)
From IMC001 infusion until 96 weeks.
Pharmacokinetic evaluation (regarding Tmax)
Lasso di tempo: From IMC001 infusion until 96 weeks.
Time to reach maximum concentration (Days)
From IMC001 infusion until 96 weeks.
Pharmacokinetic evaluation (approximately AUC0-28d)
Lasso di tempo: From IMC001 infusion to 28 days after infusion
The area under the CAR-T concentration time curve within 28 days after IMC001 infusion
From IMC001 infusion to 28 days after infusion
Pharmacodynamic evaluation
Lasso di tempo: Collect data from IMC001 infusion (day -1, day 0, day 1, day 3, day 7, day 9, day 14, day 21, day 28) until disease progression or peak monitoring occurs, if CAR copy number, death, or other cause is not detected for two consecutive episodes (whichever o
The concentration levels of CAR-T related serum cytokines such as CRP, IL-6, and INF - γ at each time point
Collect data from IMC001 infusion (day -1, day 0, day 1, day 3, day 7, day 9, day 14, day 21, day 28) until disease progression or peak monitoring occurs, if CAR copy number, death, or other cause is not detected for two consecutive episodes (whichever o

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
Replicative lentivirus (RCL)
Lasso di tempo: Baseline, 16 weeks, 48 weeks, until subject loss to follow-up, death, withdrawal of informed consent, cell transfusion for 2 years (96 weeks) or termination of the trial (whichever occurs first), with a maximum monitoring period of 15 years.
Detecting the presence of replication type lentivirus (RCL) in peripheral blood
Baseline, 16 weeks, 48 weeks, until subject loss to follow-up, death, withdrawal of informed consent, cell transfusion for 2 years (96 weeks) or termination of the trial (whichever occurs first), with a maximum monitoring period of 15 years.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

5 marzo 2026

Completamento primario (Stimato)

31 dicembre 2027

Completamento dello studio (Stimato)

31 dicembre 2027

Date di iscrizione allo studio

Primo inviato

20 gennaio 2026

Primo inviato che soddisfa i criteri di controllo qualità

8 giugno 2026

Primo Inserito (Effettivo)

12 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

12 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

8 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • IMC001-RT02

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

prodotto fabbricato ed esportato dagli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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