A Study of Dose Escalation of ES502 in Patients With Advanced Pancreatic Cancer
2026年6月10日 更新者: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).
調査の概要
詳細な説明
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).
研究の種類
介入
入学 (推定)
24
段階
- 初期フェーズ 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:Chenlei Wen
- 電話番号:+86-13761638756
- メール:wcl12161@rjh.com.cn
研究連絡先のバックアップ
- 名前:Baiyong Shen
- 電話番号:+86-(021)-64370045-678801
- メール:shenby@shsmu.edu.cn
研究場所
-
-
Shanghai Municipality
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Shanghai、Shanghai Municipality、中国、200025
- 募集
- Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
-
主任研究者:
- Baiyong Shen
-
コンタクト:
- Chenlei Wen
- 電話番号:+86-13761638756
- メール:wcl12161@rjh.com.cn
-
-
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
- 大人
- 高齢者
健康ボランティアの受け入れ
いいえ
説明
Inclusion Criteria:
-
To be enrolled in this study, participants must meet all of the following inclusion criteria:
- Age ≥18 years, regardless of gender;
- Available fresh or archived tumor tissue samples (within the past 5 years) for testing at screening;
- 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;
- RAS G12V mutation (KRAS/NRAS/HRAS) and positivity for HLA-DPB1*03:01, *14:01, *25:01, or *104:01;
- 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;
- ECOG score: 0-1;
- Expected survival greater than 3 months;
- 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.
- 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;
- 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;
- 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:
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.
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;
- 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;
- 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;
- QT interval corrected by Fridericia's formula (QTcF) ≥470 ms;
- 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;
- Active autoimmune diseases, or any conditions requiring systemic corticosteroids or immunosuppressants (prednisone at ≥20 mg/day or an equivalent dose) at screening;
- 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;
- History of severe allergy or known hypersensitivity to the investigational product or its components;
- Organ transplantation, allogeneic stem cell transplantation or renal replacement therapy in the past or at screening;
- Pulmonary embolism, pulmonary fibrosis, interstitial lung disease or acute lung disease in the past or at screening;
- 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;
- Other circumstances inappropriate for participation in this study as considered by the investigator.
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:なし
- 介入モデル:単一グループの割り当て
- 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 |
|---|---|
|
実験的: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.
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Bispecific soluble HLA-DP restricted RASG12V specific T-cell receptor fused to anti-CD3 with Fc
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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 |
|---|---|---|
|
To evaluate the safety and tolerability of ES502 in subjects with advanced solid tumors
時間枠:2 years
|
DLT, and incidence and severity of adverse effects.
|
2 years
|
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To determine the maximum tolerated dose (MTD)
時間枠:2 years
|
2 years
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Preliminary antitumor activity
時間枠:2 years
|
Objective response rate (ORR),%
|
2 years
|
|
Preliminary antitumor activity
時間枠:2 years
|
Disease control rate (DCR),%
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2 years
|
|
Preliminary antitumor activity
時間枠:2 years
|
Duration of response (DOR), in week, in month
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2 years
|
|
Preliminary antitumor activity
時間枠:2 years
|
Progression-free survival (PFS) ,in month
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2 years
|
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Preliminary antitumor activity
時間枠:2 years
|
Overall survival (OS), in month
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2 years
|
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To evaluate the immunogenicity of ES502 in subjects with advanced solid tumors
時間枠:2 years
|
Immunogenicity: Seropositivity rates of anti-drug antibodies (ADAs) and neutralizing antibodies (NAbs)
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2 years
|
|
Pharmacokinetic (PK)
時間枠:2 years
|
Maximum plasma concentration (Cmax), ng/mL
|
2 years
|
|
Pharmacokinetic (PK)
時間枠:2 years
|
Half-life (t1/2) in minutes
|
2 years
|
|
Pharmacokinetic (PK)
時間枠:2 years
|
Time to Cmax (Tmax) in hours
|
2 years
|
|
Pharmacokinetic (PK)
時間枠:2 years
|
Area under the plasma concentration-time curve (AUC0-∞), ng·h/mL
|
2 years
|
|
Pharmacokinetic (PK)
時間枠:2 years
|
Mean residence time (MRT) in hours
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2 years
|
|
Pharmacokinetic (PK)
時間枠:2 years
|
Plasma clearance (CL),mL/min
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2 years
|
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Pharmacokinetic (PK)
時間枠:2 years
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Volume of distribution (Vd),L/kg
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2 years
|
その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Pharmacodynamic (PD)
時間枠:2 years
|
Changes in peripheral blood T cells (CD3+ T cells, CD4+ T cells, and CD8+ T cells),cells/μL
|
2 years
|
|
Pharmacodynamic (PD)
時間枠: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)
時間枠:2 years
|
RAS G12V mutation frequency,%
|
2 years
|
|
Pharmacodynamic (PD)
時間枠:2 years
|
Expression levels of HLA-DP, PD-L1, CD3, CD4 and CD8 ,MFI
|
2 years
|
|
Pharmacodynamic (PD)
時間枠: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).
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2 years
|
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Immunogenicity
時間枠:2 years
|
Anti-drug antibodies (ADAs), ng/mL
|
2 years
|
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Immunogenicity
時間枠:2 years
|
Neutralizing antibodies (NAbs),%
|
2 years
|
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。
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5月18日
一次修了 (推定)
2028年12月1日
研究の完了 (推定)
2029年6月1日
試験登録日
最初に提出
2026年6月5日
QC基準を満たした最初の提出物
2026年6月10日
最初の投稿 (実際)
2026年6月16日
学習記録の更新
投稿された最後の更新 (実際)
2026年6月16日
QC基準を満たした最後の更新が送信されました
2026年6月10日
最終確認日
2026年6月1日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
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