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A Study of Dose Escalation of ES502 in Patients With Advanced Pancreatic Cancer

10 giugno 2026 aggiornato da: BAIYONG SHEN, Ruijin Hospital

A Dose-escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, Immunogenicity, and Preliminary Antitumor Activity of ES502 Injection in Patients With Advanced Pancreatic Cancer

ESSIGHT-HJG-ES502-01 is a dose-escalation study of ES502 in patients with advanced pancreatic cancer. The study will enroll patients with advanced, RAS G12V positive pancreatic cancer who have no effective treatment options available (HLA genotyping required).

Panoramica dello studio

Stato

Reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

The study will adopt the standard "3+3" design., with a first-in-human (FIH) dose of 20 μg administered once every four weeks (Q4W). Subsequent dosing frequency will be adjusted based on pharmacodynamics and pharmacokinetics data. The primary objectives of this study are to evaluate the safety and tolerability of ES502 and to determine its maximum tolerated dose (MTD). The secondary objectives are to evaluate its antitumor activity, pharmacokinetics (PK), and pharmacodynamics (PD).

Tipo di studio

Interventistico

Iscrizione (Stimato)

24

Fase

  • Prima fase 1

Contatti e Sedi

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

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, Cina, 200025
        • Reclutamento
        • Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
        • Investigatore principale:
          • Baiyong Shen
        • Contatto:

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:

-

To be enrolled in this study, participants must meet all of the following inclusion criteria:

  1. Age ≥18 years, regardless of gender;
  2. Available fresh or archived tumor tissue samples (within the past 5 years) for testing at screening;
  3. Individuals with histologically or cytologically confirmed advanced solid tumors for whom no standard therapy exists, who are refractory to standard therapy, or who are deemed unsuitable for standard therapy by the investigator. Tumor types include but are not limited to: pancreatic cancer, colorectal cancer, non-small cell lung cancer, intrahepatic cholangiocarcinoma, gallbladder cancer, ovarian cancer, endometrial cancer, and intestinal cancer;
  4. RAS G12V mutation (KRAS/NRAS/HRAS) and positivity for HLA-DPB1*03:01, *14:01, *25:01, or *104:01;
  5. Individuals with at least one measurable lesion (defined per RECIST v1.1 as a lesion with the longest diameter ≥10 mm, or a lymph node with a short axis of ≥15 mm); lesions that have undergone radiotherapy or other local therapies are not considered target lesions unless they demonstrate clear progression;
  6. ECOG score: 0-1;
  7. Expected survival greater than 3 months;
  8. Adequate hematological and organ function, as evidenced by the following laboratory tests (the individual must not have received a blood transfusion, long-acting EPO or long-acting G-CSF within 14 days before study treatment, or not have received short-acting EPO or short-acting G-CSF within 7 days before study treatment): 1) hematology: absolute neutrophil count (ANC) ≥1.5 × 10⁹/L, platelet count (PLT) ≥100 × 10⁹/L, hemoglobin (Hb) ≥90 g/L; 2) liver function test: both aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤3.0 × upper limit of normal (ULN), total bilirubin (TBIL) ≤1.5 × ULN. Exceptions: liver metastasis, AST and/or ALT ≤5 × ULN; Gilbert's syndrome, TBIL ≤3 × ULN; pancreatic head cancer or biliary obstruction, TBIL ≤3 × ULN; 3) kidney function test: creatinine clearance (CrCL) ≥50 mL/min (by Cockcroft-Gault formula); 4) coagulation function test: activated partial thromboplastin time (APTT) ≤1.5 × ULN and international normalized ratio (INR) or prothrombin time (PT) ≤1.5 × ULN; 5) echocardiography: left ventricular ejection fraction (LVEF) ≥50%; eligibility for enrollment of individuals with out-of-range laboratory results should be determined at the investigator's discretion.
  9. Women of childbearing potential who agree to use at least one medically recognized method for contraception (e.g., intrauterine device, contraceptive pills, or condoms) during the study treatment and for 1 year after the last treatment, and have a negative pregnancy test result at screening;
  10. Prior antitumor treatment-related adverse events (AEs) (per NCI-CTCAE v6.0) have resolve to ≤ Grade 1 at screening, except for alopecia, Grade 2 hypothyroidism, and non-clinically significant or asymptomatic laboratory abnormalities;
  11. Individuals who fully understand the informed consent information, agree to participate in this clinical study, and voluntarily sign the Informed Consent Form (ICF).

Exclusion Criteria:

-

To be enrolled in this study, participants must not meet any of the following exclusion criteria:

To be enrolled in this study, participants must not meet any of the following exclusion criteria:

  1. Individuals with the following tumors:

    • Malignant tumors other than those under investigation in this study (except for cured thyroid cancer, skin basal cell carcinoma, or cervical carcinoma in situ) within the past 5 years;
    • Meningeal metastases;
    • Brain metastases, except for individuals who have received systematic and radical therapy (radiotherapy or surgery) for brain metastases, demonstrated radiologically stable disease for at least 4 weeks, discontinued systemic corticosteroids for more than 2 weeks, and remain asymptomatic.
  2. Individuals with the following conditions:

    • Received prior targeted therapy targeting RAS-G12V within 4 weeks before the first dose, or within 5 half-lives of the therapeutic agent, whichever is longer;
    • Participation in other clinical studies involving an investigational product within 4 weeks before the first dose;
    • Use of systemic antitumor therapy (including but not limited to chemotherapy, radiotherapy, biotherapy, immunotherapy, and cell therapy) within 4 weeks or 5 half-lives (whichever is shorter) before the first dose;
    • Receipt of major surgery without complete recovery within 4 weeks before the first dose, or planning to undergo major surgery during the study;
    • Receipt of systemic immunosuppressants or systemic corticosteroids within 1 week before the first dose;
    • Receipt of live-attenuated vaccines within 4 weeks before the first dose, or planning to receive such vaccines during the study;
    • Planning to receive any other systemic antitumor therapy (chemotherapy, radiotherapy, biotherapy, immunotherapy, cell therapy, etc.) during the study;
  3. Symptomatic ascites, pleural effusion or pericardial effusion requiring drainage at screening, or history of drainage for serous effusion within 4 weeks before the first dose;
  4. History of clinically significant cardiovascular disorders at screening, including but not limited to congestive heart failure (NYHA Class ≥ II), unstable angina, myocardial infarction, stroke or transient ischemic attack (TIA), severe arrhythmias (including but not limited to atrial fibrillation or paroxysmal supraventricular tachycardia, complete left bundle branch block or third-degree atrioventricular block with clinical significance and requiring clinical intervention), or poorly controlled hypertension (systolic blood pressure ≥160 mmHg and/or diastolic blood pressure ≥100 mmHg) within 6 months before enrollment;
  5. QT interval corrected by Fridericia's formula (QTcF) ≥470 ms;
  6. History of severe infection within 4 weeks before the first dose; active infection requiring therapeutic intravenous antibiotics within 2 weeks before the first dose. Use of prophylactic antibiotics is not an exclusion criterion;
  7. Active autoimmune diseases, or any conditions requiring systemic corticosteroids or immunosuppressants (prednisone at ≥20 mg/day or an equivalent dose) at screening;
  8. History or evidence of clinically unstable or poorly controlled disorders (including but not limited to cardiac, pulmonary, renal, hepatic, metabolic or hematological disorders) at screening;
  9. History of severe allergy or known hypersensitivity to the investigational product or its components;
  10. Organ transplantation, allogeneic stem cell transplantation or renal replacement therapy in the past or at screening;
  11. Pulmonary embolism, pulmonary fibrosis, interstitial lung disease or acute lung disease in the past or at screening;
  12. Positivity for Treponema pallidum antibody, positivity for human immunodeficiency virus (HIV) antibody, or active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection at screening. Definition of active HBV infection: positivity for hepatitis B surface antigen (HBsAg), and HBV DNA above the ULN; definition of active HCV infection: positivity for hepatitis C antibody, and HCV RNA above the ULN. Such conditions unsuitable for enrollment as judged by the investigator;
  13. Other circumstances inappropriate for participation in this study as considered by the investigator.

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: Dose escalation cohort
A dose-escalation study will be conducted following the standard 3+3 design, with doses of 20, 60, 180, and 540 μg. A total of 10-24 subjects are planned to be enrolled. Depending on the subject's conditions (including but not limited to safety results, pharmacokinetic and pharmacodynamic data, etc.), and under the premise of ensuring subject safety, the investigator and/or ethics committee may decide to increase the dose or add new dose groups.
Bispecific soluble HLA-DP restricted RASG12V specific T-cell receptor fused to anti-CD3 with Fc

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
To evaluate the safety and tolerability of ES502 in subjects with advanced solid tumors
Lasso di tempo: 2 years
DLT, and incidence and severity of adverse effects.
2 years
To determine the maximum tolerated dose (MTD)
Lasso di tempo: 2 years
2 years

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Preliminary antitumor activity
Lasso di tempo: 2 years
Objective response rate (ORR),%
2 years
Preliminary antitumor activity
Lasso di tempo: 2 years
Disease control rate (DCR),%
2 years
Preliminary antitumor activity
Lasso di tempo: 2 years
Duration of response (DOR), in week, in month
2 years
Preliminary antitumor activity
Lasso di tempo: 2 years
Progression-free survival (PFS) ,in month
2 years
Preliminary antitumor activity
Lasso di tempo: 2 years
Overall survival (OS), in month
2 years
To evaluate the immunogenicity of ES502 in subjects with advanced solid tumors
Lasso di tempo: 2 years
Immunogenicity: Seropositivity rates of anti-drug antibodies (ADAs) and neutralizing antibodies (NAbs)
2 years
Pharmacokinetic (PK)
Lasso di tempo: 2 years
Maximum plasma concentration (Cmax), ng/mL
2 years
Pharmacokinetic (PK)
Lasso di tempo: 2 years
Half-life (t1/2) in minutes
2 years
Pharmacokinetic (PK)
Lasso di tempo: 2 years
Time to Cmax (Tmax) in hours
2 years
Pharmacokinetic (PK)
Lasso di tempo: 2 years
Area under the plasma concentration-time curve (AUC0-∞), ng·h/mL
2 years
Pharmacokinetic (PK)
Lasso di tempo: 2 years
Mean residence time (MRT) in hours
2 years
Pharmacokinetic (PK)
Lasso di tempo: 2 years
Plasma clearance (CL),mL/min
2 years
Pharmacokinetic (PK)
Lasso di tempo: 2 years
Volume of distribution (Vd),L/kg
2 years

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
Pharmacodynamic (PD)
Lasso di tempo: 2 years
Changes in peripheral blood T cells (CD3+ T cells, CD4+ T cells, and CD8+ T cells),cells/μL
2 years
Pharmacodynamic (PD)
Lasso di tempo: 2 years
Changes in peripheral blood cytokines (IFN-γ, TNF-α, IL-2, IL-6, IL-10, CXCL9, CXCL10, CXCL11, and MCP-1),pg/mL
2 years
Pharmacodynamic (PD)
Lasso di tempo: 2 years
RAS G12V mutation frequency,%
2 years
Pharmacodynamic (PD)
Lasso di tempo: 2 years
Expression levels of HLA-DP, PD-L1, CD3, CD4 and CD8 ,MFI
2 years
Pharmacodynamic (PD)
Lasso di tempo: 2 years
Allele combination status of HLA-DPA1 and HLA-DPB1 (DPA1 composed of 01:03, 02:01, or 02:02; DPB1 composed of 03:01, 14:01, 25:01, or 104:01).
2 years
Immunogenicity
Lasso di tempo: 2 years
Anti-drug antibodies (ADAs), ng/mL
2 years
Immunogenicity
Lasso di tempo: 2 years
Neutralizing antibodies (NAbs),%
2 years

Collaboratori e investigatori

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

Sponsor

Investigatori

  • Direttore dello studio: Baiyong Shen, Ruijin Hospital

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)

18 maggio 2026

Completamento primario (Stimato)

1 dicembre 2028

Completamento dello studio (Stimato)

1 giugno 2029

Date di iscrizione allo studio

Primo inviato

5 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

10 giugno 2026

Primo Inserito (Effettivo)

16 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

16 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

10 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

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

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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