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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

調査の概要

詳細な説明

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.

研究の種類

介入

入学 (推定)

76

段階

  • 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

研究場所

    • Beijing Municipality
      • Beijing、Beijing Municipality、中国、100142
        • 募集
        • Beijing Cancer Hospital
        • コンタクト:
      • Beijing、Beijing Municipality、中国、100176
        • まだ募集していません
        • Beijing Youcare Kechuang Pharmaceutical Technology Co., Ltd.
        • コンタクト:

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: 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.

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: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.

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
時間枠
Incidence of Dose-Limiting Toxicity (DLT)
時間枠:DLT assessment: 28 days post-first dose
DLT assessment: 28 days post-first dose
Treatment-Emergent Adverse Events (TEAEs)
時間枠: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)
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Cmax
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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)
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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)
時間枠: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)
時間枠: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
時間枠: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
時間枠: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

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3月10日

一次修了 (推定)

2027年12月8日

研究の完了 (推定)

2030年12月7日

試験登録日

最初に提出

2026年5月27日

QC基準を満たした最初の提出物

2026年6月1日

最初の投稿 (実際)

2026年6月8日

学習記録の更新

投稿された最後の更新 (実際)

2026年8月21日

QC基準を満たした最後の更新が送信されました

2026年8月19日

最終確認日

2026年8月1日

詳しくは

本研究に関する用語

追加の関連 MeSH 用語

その他の研究ID番号

  • CLSP-YKYY031-Z01

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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