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Phase I Clinical Trial of YKYY031 for Injection in Patients With Advanced Solid Tumors (YKYY031,tumors)

Phase I Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Antitumor Activity of YKYY031 for Injection in Patients With Advanced Solid Tumors

Phase I study of YKYY031 for injection in patients with advanced solid tumors

研究概览

详细说明

This is a open-label, dose-escalation and dose-expansion Phase 1 clinical study to evaluate the pharmacokinetic (PK) profile, safety, tolerability, and preliminary antitumor activity of YKYY031 Injection in subjects with advanced solid tumors who have failed standard therapy and have no effective treatment options, including but not limited to colorectal cancer and pancreatic cancer.

研究类型

介入性

注册 (估计的)

76

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Beijing Municipality
      • Beijing、Beijing Municipality、中国、100142
        • 招聘中
        • Beijing Cancer Hospital
        • 接触:
      • Beijing、Beijing Municipality、中国、100176
        • 尚未招聘
        • Beijing Youcare Kechuang Pharmaceutical Technology Co., Ltd.
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion criteria: Participants meeting all the following criteria may be enrolled

  1. Male or female patients aged 18 to 75 years old at the time of signing the informed consent form.
  2. Histologically or cytologically confirmed advanced or metastatic solid tumors that have failed standard therapy and have no effective treatment options, including but not limited to colorectal cancer, pancreatic cancer, etc.

    For colorectal cancer (CRC) patients, prior receipt of at least second-line standard therapy failure and no effective treatment options; adjuvant/neoadjuvant chemotherapy failure during or within 6 months after the last treatment is considered first-line failure.

    For pancreatic cancer patients, prior receipt of at least first-line standard therapy failure and no effective treatment options; adjuvant/neoadjuvant chemotherapy failure during or within 6 months after the last treatment is considered first-line failure.

  3. Patients must have human leukocyte antigen (HLA) subtype HLA-A*11:01.
  4. Patients must test positive for at least one of the tumor-specific antigens (TSA) targeted by YKYY031, including KRAS G12D, KRAS G12C, KRAS G12V, KRAS G13D, KRAS G12R, KRAS G12S, PIK3CA E542K, TP53 R248Q, PIK3CA E545K, BRAF V600E, PIK3CA H1047L, FBXW7 R465C.
  5. Eastern Cooperative Oncology Group (ECOG) performance status score: 0-1.
  6. Expected survival duration ≥ 3 months.
  7. At least one measurable lesion (non-nodal lesions with longest diameter ≥10 mm, nodal lesions with shortest diameter ≥15 mm) according to RECIST V1.1.
  8. Major organ function is good, meeting the following requirements:

    Hemoglobin ≥90 g/L, absolute neutrophil count ≥1.5×10⁹/L, platelet count ≥80×10⁹/L within 14 days prior to the first dose, without the use of hematopoietic growth factors, blood transfusions, blood products, albumin, or blood products.

    Total bilirubin ≤1.5× upper limit of normal (ULN); if liver metastasis or Gilbert's syndrome is present, total bilirubin ≤3×ULN.

    Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≤3×ULN; if liver metastasis is present, ALT or AST ≤5×ULN.

    Serum creatinine ≤1.5×ULN or creatinine clearance ≥50 mL/min (calculated using the Cockcroft-Gault formula).

    Prothrombin time ≤1.5×ULN (unless using warfarin anticoagulation). International normalized ratio (INR) ≤1.5×ULN (unless using warfarin anticoagulation).

    Left ventricular ejection fraction (LVEF) ≥50% as assessed by cardiac Doppler ultrasound/MUGA.

  9. Participants with childbearing potential or male participants must have no plans for conception, egg donation, or sperm donation from the date of signing the informed consent form until 6 months after the last study treatment, and must agree to use effective contraception (including one or more non-pharmacological contraceptive measures) or safety measures during this period.
  10. Agree to comply with all requirements and procedures of the clinical trial and voluntarily sign the informed consent form.

Exclusion Criteria:

Participants meeting any of the following criteria will be excluded

  1. Allergy to the investigational product (including any excipients). History of severe allergy to any drug, food, or vaccine, such as anaphylactic shock, angioneurotic edema, allergic dyspnea, anaphylactoid purpura, thrombocytopenic purpura, Arthus reaction, etc.
  2. History of other malignancies, except for cured skin basal cell carcinoma, skin squamous cell carcinoma, superficial bladder cancer, cervical carcinoma in situ, etc., that have not recurred within 5 years prior to screening, as judged by the investigator to be eligible for enrollment.
  3. Symptomatic central nervous system metastasis or meningeal metastasis, or other evidence indicating uncontrolled central nervous system metastasis or meningeal metastasis, as judged by the investigator to be unsuitable for enrollment. Patients with stable brain metastases (no imaging progression within 4 weeks, and not requiring corticosteroid treatment for at least 4 weeks before the first dose of the study drug) may be enrolled.
  4. Significant clinically significant cardiovascular diseases, including but not limited to:

    1. Congestive heart failure (New York Heart Association [NYHA] class > II)
    2. Myocardial infarction, unstable angina, severe pericardial disease, severe myocardial disease within the past 6 months
    3. Need for treatment of valvular regurgitation or stenosis
    4. Any supraventricular or ventricular arrhythmia requiring treatment or intervention; uncontrolled malignant arrhythmia; complete left bundle branch block, second- or third-degree atrioventricular block
    5. QT interval (QTcF) >450 ms in males, >470 ms in females
    6. Uncontrolled hypertension (defined as systolic blood pressure ≥160 mmHg or diastolic blood pressure ≥100 mmHg despite treatment with two or three antihypertensive agents)
  5. Any active autoimmune disease or history of autoimmune disease, including but not limited to immunologically related neurological diseases, multiple sclerosis, autoimmune (demyelinating) neuropathy, Guillain-Barré syndrome, myasthenia gravis, systemic lupus erythematosus, connective tissue disease, scleroderma, autoimmune hepatitis, toxic epidermal necrolysis, or Stevens-Johnson syndrome (except for type 1 diabetes mellitus on a stable dose of insulin, hypothyroidism on stable hormone replacement therapy, etc.).
  6. Any uncontrolled clinical disease (e.g., respiratory, circulatory, neurological, hematological, genitourinary, endocrine system diseases) or psychiatric disease (e.g., depression, schizophrenia) or other major illness, as judged by the investigator to interfere with providing informed consent, interpretation of trial results, participation in the trial posing risks to the participant, or otherwise affecting the achievement of trial objectives, including uncontrolled pleural effusion, pericardial effusion, or ascites as judged by the investigator.
  7. Known history of interstitial pneumonia or high suspicion of interstitial pneumonia; or presence of pulmonary abnormalities that may interfere with the detection or management of suspected drug-related pulmonary toxicity during the trial.
  8. Any abnormality at the injection site that, as judged by the investigator, would hinder observation of local reactions at the injection site.
  9. Presence of contraindications to intramuscular injection.
  10. Received any antitumor therapy (including chemotherapy, targeted therapy, immunotherapy, etc.) or participated in another drug or device clinical trial within 4 weeks or 5 half-lives (whichever is shorter) prior to the first dose; received traditional Chinese medicine or patent Chinese medicine with clear antitumor indications within 2 weeks prior to the first dose.
  11. Previous antitumor treatment-related adverse events that have not recovered to ≤ grade 1 according to CTCAE, except for toxicities judged by the investigator to have no safety risk, such as alopecia, grade 2 peripheral neurotoxicity, hypothyroidism stabilized by hormone replacement therapy, etc.
  12. Prior organ transplantation or allogeneic hematopoietic stem cell transplantation.
  13. Use of corticosteroids (>10 mg/day prednisone or equivalent other glucocorticoids) or other immunosuppressants for systemic treatment within 14 days prior to the first dose of the vaccine. Inhaled or topical steroids and adrenal hormone replacement at doses ≤10 mg/day prednisone are allowed in the absence of active autoimmune disease.
  14. Received live/attenuated live/inactivated vaccines within 4 weeks prior to the first dose of the vaccine.
  15. Prior receipt of a therapeutic tumor vaccine targeting the same antigen.
  16. Bleeding disorders (e.g., coagulation factor deficiency, coagulation dysfunction [as judged by the investigator to be unsuitable for enrollment]), or a history of significant bruising or bleeding after injection or blood draw.
  17. Blood donation or significant blood loss (>450 mL) within 3 months prior to screening, or planned blood or blood component donation during the study period.
  18. Major surgery within 4 weeks prior to screening (minor procedures such as catheter placement and biopsy required by the protocol are not exclusionary), or unresolved effects of surgery or trauma within 14 days prior to enrollment.
  19. History of substance abuse or known medical, psychological, or social conditions, such as alcoholism or drug addiction.
  20. Positive human immunodeficiency virus antibody test result, active syphilis (defined as positive syphilis antibody test and positive reagin test), active hepatitis B (defined as hepatitis B virus [HBV] DNA ≥2000 IU/mL), or active hepatitis C (defined as hepatitis C virus [HCV] RNA test positive).
  21. Active tuberculosis (TB) (patients suspected of having active TB require further consultation with the infectious disease department for definitive diagnosis) or history of active TB; or severe acute or chronic infection requiring systemic treatment.
  22. Pregnant or breastfeeding women.
  23. Any other condition deemed by the investigator to make the participant unsuitable for participation in this trial.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:YKYY031 for injection
intramuscular, a single intramuscular injection of the corresponding dose of YKYY031 for injection
Eligible participants selected through screening will be sequentially assigned to dose groups A1 to A6 (in ascending order of dose) according to their enrollment sequence. Each participant will receive a single intramuscular injection of the corresponding dose of YKYY031 for injection.
Based on the results of the dose-escalation trial, 1-2 dose groups will be selected for the dose-expansion trial of YKYY031 for injection as monotherapy or in combination with other drugs. Eligible participants will be sequentially assigned to dose groups B1 to B2 (in ascending order of dose) according to their enrollment sequence. Each participant will receive a single intramuscular injection of the corresponding dose of YKYY031 for injection.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Incidence of Dose-Limiting Toxicity (DLT)
大体时间:DLT assessment: 28 days post-first dose
DLT assessment: 28 days post-first dose
Treatment-Emergent Adverse Events (TEAEs)
大体时间:Safety assessments: from first dose until the 28 days after the last dose
Safety assessments: from first dose until the 28 days after the last dose
Serious Adverse Events (SAEs)
大体时间:Safety assessments: from first dose until the 28 days after the last dose
Safety assessments: from first dose until the 28 days after the last dose

次要结果测量

结果测量
措施说明
大体时间
Cmax
大体时间:Pre-dose to end of treatment + 28 days (sampling at Day1, Day8, Day15, Day22, Day28, then once every three weeks, assessed up to 2 years)
Peak plasma concentration
Pre-dose to end of treatment + 28 days (sampling at Day1, Day8, Day15, Day22, Day28, then once every three weeks, assessed up to 2 years)
AUC
大体时间:Pre-dose to end of treatment + 28 days (sampling at Day1, Day8, Day15, Day22, Day28, then once every three weeks, assessed up to 2 years)
Area under the plasma concentration versus time curve
Pre-dose to end of treatment + 28 days (sampling at Day1, Day8, Day15, Day22, Day28, then once every three weeks, assessed up to 2 years)
Objective Response Rate (ORR) per RECIST v1.1
大体时间:Every 8 weeks from first dose until disease progression or death (assessed up to 2 years)
Every 8 weeks from first dose until disease progression or death (assessed up to 2 years)
Disease Control Rate (DCR) per RECIST v1.1
大体时间:Every 8 weeks from first dose until disease progression or death (assessed up to 2 years)
Every 8 weeks from first dose until disease progression or death (assessed up to 2 years)
Duration of Response (DOR) per RECIST v1.1
大体时间:From first documented Complete response (CR) / Partial response (PR) to first documented Disease progression (PD) or death (assessed up to 2 years)
From first documented Complete response (CR) / Partial response (PR) to first documented Disease progression (PD) or death (assessed up to 2 years)
Progression-Free Survival (PFS) per RECIST v1.1
大体时间:From first dose to first documented PD or death (assessed up to 2 years)
From first dose to first documented PD or death (assessed up to 2 years)
Overall Survival (OS)
大体时间:From first dose to death from any cause (assessed up to 2 years)
From first dose to death from any cause (assessed up to 2 years)
Immune Objective Response Rate (iORR) per iRECIST
大体时间:Every 8 weeks from first dose until disease progression or death (assessed up to 2 years)
Every 8 weeks from first dose until disease progression or death (assessed up to 2 years)
Immune Disease Control Rate (iDCR) per iRECIST
大体时间:Every 8 weeks from first dose until disease progression or death (assessed up to 2 years)
Every 8 weeks from first dose until disease progression or death (assessed up to 2 years)
Immune Duration of Response (iDOR) per iRECIST
大体时间:From first documented immune CR/PR to first documented immune progression or death (assessed up to 2 years)
From first documented immune CR/PR to first documented immune progression or death (assessed up to 2 years)
Immune Progression-Free Survival (iPFS) per iRECIST
大体时间:From first dose to first documented immune progression or death (assessed up to 2 years)
From first dose to first documented immune progression or death (assessed up to 2 years)
Incidence of anti-drug antibodies (immunogenicity)
大体时间:Pre-dose to end of treatment + 28 days (ssampling at Day1, Day8, Day15, Day22, Day28, then once every three weeks, treatment end/early withdrawal visit, safety follow-up if applicable, assessed up to 2 years)
Pre-dose to end of treatment + 28 days (ssampling at Day1, Day8, Day15, Day22, Day28, then once every three weeks, treatment end/early withdrawal visit, safety follow-up if applicable, assessed up to 2 years)
Antigen-specific T cell levels in PBMC (ELISpot-IFN-γ)
大体时间:Pre-dose to end of treatment + 28 days (sampling at Day1, Day8, Day15, Day22, Day28, then once every three weeks, treatment end/early withdrawal visit, safety follow-up if applicable, assessed up to 2 years)
Pre-dose to end of treatment + 28 days (sampling at Day1, Day8, Day15, Day22, Day28, then once every three weeks, treatment end/early withdrawal visit, safety follow-up if applicable, assessed up to 2 years)
Immune cell subset changes
大体时间:Pre-dose to end of treatment + 28 days (sampling at Day1, Day8, Day15, Day22, Day28, then once every three weeks, treatment end/early withdrawal visit, safety follow-up if applicable, assessed up to 2 years)
Pre-dose to end of treatment + 28 days (sampling at Day1, Day8, Day15, Day22, Day28, then once every three weeks, treatment end/early withdrawal visit, safety follow-up if applicable, assessed up to 2 years)
ctDNA
大体时间:Screening, Day28, then once every three weeks post-Day22, optional tumor tissue sampling as clinically indicated
Biomarkers
Screening, Day28, then once every three weeks post-Day22, optional tumor tissue sampling as clinically indicated

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年3月10日

初级完成 (估计的)

2027年12月8日

研究完成 (估计的)

2030年12月7日

研究注册日期

首次提交

2026年5月27日

首先提交符合 QC 标准的

2026年6月1日

首次发布 (实际的)

2026年6月8日

研究记录更新

最后更新发布 (实际的)

2026年8月21日

上次提交的符合 QC 标准的更新

2026年8月19日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • CLSP-YKYY031-Z01

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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