このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

Study of IBI3028 in Participants With Locally Advanced, Unresectable, or Metastatic Solid Tumors

A Phase 1, Multi-Center, Open-Label Study Evaluating IBI3028 Treatment in Participants With Locally Advanced, Unresectable, or Metastatic Solid Tumors

This is a phase 1 multi-center, open-label study evaluating IBI3028 Treatment in participants with locally advanced, unresectable, or metastatic solid tumors

調査の概要

研究の種類

介入

入学 (推定)

493

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

    • Tianjin Municipality
      • Tianjin、Tianjin Municipality、中国、300060
        • 募集
        • Tianjin Medical University Cancer Institute and Hospital
        • 主任研究者:
          • Yi Hu
        • 主任研究者:
          • Jihui Hao
        • 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

  1. Be able to understand and sign written informed consent to participate in this study, including all assessments and procedures specified in this protocol;
  2. Male or female participants aged 18 years or older;
  3. Have histologically or cytologically confirmed unresectable locally advanced or metastatic solid tumors;
  4. Have at least one evaluable lesion (dose escalation) or measurable lesion (dose expansion) as per RECIST v1.1 within 28 days prior to the first dose of IBI3028;
  5. ECOG PS(Eastern Cooperative Oncology Group Performance Status)score of 0-1;
  6. Anticipated life expectancy of ≥ 12 weeks;
  7. Adequate bone marrow and organ function as evidenced by :

    1. Hematological function: ANC(Absolute neutrophil count) ≥ 1.5 × 10 9 /L; platelet count (PLT) ≥ 90 × 10 9 /L; hemoglobin ≥ 9.0 g/dL, and without receiving granulocyte-colony stimulating factor (G-CSF), granulocyte-macrophage colony stimulating factor (GM-CSF), thrombopoietin (TPO), interleukin-11, or other leukocyte/platelet stimulating growth factors (including red blood cell and platelet transfusions) within at least 7 days before the first dose of the study drug;
    2. Hepatic function: total bilirubin ≤ 1.5 × ULN (Upper Limit of Normal) (≤ 3 × ULN for participants with Gilbert's syndrome); AST(Aspartate Aminotransferase) and ALT (Alanine Aminotransferase)≤ 2.5 × ULN in the absence of liver metastases (≤ 5 × ULN if liver metastases are present); albumin ≥ 2.8 g/dL;
    3. Renal function: creatinine clearance ≥ 30 mL/min (using Cockcroft-Gault formula); urine protein < 2+ or 24-h total urine protein < 1 g;
    4. Cardiac function: Left ventricular ejection fraction (LVEF) ≥ 50%, no clinically significant pericardial effusion as determined by ECHO or MUGA(Multigated Acquisition), and no clinically significant ECG result;
    5. Coagulation function: International normalized ratio (INR) ≤ 1.5; activated partial thromboplastin time (aPTT) ≤ 1.5 × ULN (participants receiving anticoagulant therapy with coagulation function within the range above are allowed);
    6. Pulmonary function: With at least the lowest level of pulmonary reserve, defined as Grade ≤ 1 dyspnea and blood oxygen saturation ≥ 95% in non-oxygen breathing state;
  8. Participants (both male and female participants) who will be not of childbearing potential or who agree to use at least 1 highly effective method of contraception during the study (from start of screening or within 2 weeks prior to first dose, whichever occurs first, and continue until 7 months for females and 4 months for males after the last dose of study drug).

Exclusion Criteria

  1. Participation in any other interventional clinical study other than an observational (non-interventional) study or during the follow-up period of an interventional study;
  2. Prior anti-tumor therapy:

    Participants who have received cytotoxic therapy within 3 weeks or 5 half-lives (whichever is shorter) prior to the first administration of study intervention ; Participants who have received PD-1/PD-L1 therapy within 4 weeks prior to the first administration of study drug; Participants who have received treatment with small molecule targeted therapy within 14 days or 5 half-lives (whichever is shorter) prior to the first dose of the study drug; Palliative radiation therapy within 2 weeks or radical radiation therapy within 4 weeks prior to the first dose of study drug; Participants who had received adoptive cell therapy within 8 weeks prior to the first administration of study intervention.

  3. Have received live vaccines within 4 weeks or tumor vaccines within 3 months prior to the first administration of the study drug, or plan to receive any live vaccines during the study;
  4. Use of strong cytochrome P450 3A4 (CYP3A4) enzyme inhibitors within 2 weeks or 5 half-lives (whichever is shorter) prior to the first dose of study drug;
  5. Adverse reactions caused by previous anti-tumor treatments that have not resolved to Grade 0 or 1 or baseline level according to NCI CTCAE v5.0 before the first dose of the study drug (except for alopecia, fatigue, pigmentation, and other conditions with no safety implications per the Investigator's clinical judgement);
  6. Known allergies, hypersensitivity, or intolerance to IBI3028 or its excipients (refer to the Investigator's Brochure);
  7. Have undergone major surgery (craniotomy, thoracotomy, or laparotomy, and other surgeries according to Investigators' opinion, excluding needle biopsy) within 4 weeks prior to the first dose of the investigational product, or are expected to undergo major surgery during the study, or have severe unhealed wounds, ulcers, etc.;
  8. Known symptomatic central nervous system (CNS) metastases. Participants with asymptomatic CNS metastases (ie, no neurologic syndrome and metastases ≤1.5 cm in diameter) or stable disease after treatment as judged by the investigator may be considered if: they have no metastases in the midbrain, pons, cerebellum, meninges, medulla oblongata, or spinal cord; stable status for at least 4 weeks prior to the first dose of study drug (≤1.5 mg/day dexamethasone or equivalent and baseline anticonvulsants are allowed), and have no new or enlarging CNS metastases as clearly demonstrated by clinical evidence; Note : CNS lesions are not considered target lesions.
  9. Uncontrolled disease or condition, including:

    1. Uncontrolled infection requiring systemic antibiotics, antivirals, or antifungals prior to the first dose of the study drug;
    2. With known human immunodeficiency virus (HIV) infection, or HIV positive (HIV 1/2 Ab positive), for participants outside mainland China, participants with positive HIV antibody test at screening are eligible to participate in the study under the premise of undetectable viral load, or well-controlled under antiretroviral therapy (defined as CD4+ T cell count ≥ 350 cells/μL and no history of AIDS-defining opportunistic infection within 12 months before the first dose);
    3. Acute or chronic active hepatitis B (HBsAg positive and/or HBcAb positive, and HBV DNA titer ≥ 10 4 copies/mL or ≥ 2000 IU/mL) or hepatitis C (HCV Ab positive, and HCV RNA > 10 3 copies/mL or above the lower limit of detection);
    4. Active tuberculosis infection, or still receiving anti-tuberculosis treatment, or receiving anti-tuberculosis treatment within 1 year before the first dose of the study drug;
    5. Uncontrolled myocarditis or symptomatic congestive heart failure Class II-IV (New York Heart Association ,NYHA), symptomatic or uncontrolled arrhythmia, QTc interval > 480 ms, or personal or family history of congenital long/short QT syndrome;
    6. Uncontrolled hypertension with SBP ≥ 160 mmHg or DBP ≥ 100 mmHg measured on 2 follow-up visits despite adequate standard treatment;
    7. Current gastrointestinal tract (muscle-derived tube from the oral cavity to the anus, including oral cavity, pharynx, esophagus, stomach, duodenum, jejunum, ileum, cecum, appendix, colon, rectum, and anus) or endotracheal stent implantation;
    8. Significant malnutrition, such as malnutrition requiring parenteral nutrition;
    9. Spinal cord compression that has not been radically cured by surgery and/or radiotherapy;
    10. Ascites, pleural effusion, or pericardial effusion that is symptomatic and requires intervention prior to the first dose of study intervention (participants who do not require treatment or who recover steadily without intervention are eligible).
  10. With a history of pneumonia requiring corticosteroid treatment, or a history of clinically significant lung diseases (such as interstitial lung disease, non-infectious pneumonitis, or uncontrolled lung diseases such as pulmonary fibrosis, severe radiation pneumonitis, and acute lung injury), or suspected of having these diseases by imaging during the screening period;
  11. Any history of arterial thromboembolic events within 6 months prior to the first dose of the study drug, including myocardial infarction, unstable angina, cerebrovascular stroke, or transient ischemic attack;
  12. Esophageal or gastric varices requiring immediate intervention (e.g., ligature or sclerotherapy) or at high risk of bleeding according to the opinion of the investigator or a gastroenterologist or hepatologist. Participants with evidence of portal hypertension (including imaging findings of hypersplenism) or a history of esophageal and gastric variceal bleeding must undergo endoscopic evaluation within 3 months prior to the first dose of the study drug;
  13. Any history of life-threatening hemorrhage or hemorrhage requiring blood transfusion, endoscopy, or surgery within 3 months prior to the first dose of the investigational product ;
  14. Unhealed gastrointestinal obstruction, perforation, or fistula. At risk of gastrointestinal obstruction or perforation (including but not limited to: acute diverticulitis, abdominal abscess, etc.), history of extensive bowel resection (segmental colectomy or extensive bowel resection accompanied with chronic diarrhea), active inflammatory bowel disease, or Grade ≥ 2 chronic diarrhea;
  15. History of immunodeficiency diseases, including congenital or acquired immunodeficiency diseases;
  16. History of allogeneic organ transplantation or allogeneic bone marrow transplantation, or autologous hematopoietic stem cell transplantation within 3 months prior to the first dose of the investigational drug, except for corneal transplantation;
  17. History of other malignancy within 2 years before the first dose of study drug(s), with the following exceptions:

    1. Malignancy (other than in situ) treated with curative therapy with no known active disease present for ≥ 2 years prior to the first dose of study drug and at low risk of recurrence according to the physician's opinion;
    2. Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of residual or recurrent disease;
    3. Adequately treated carcinoma in situ without evidence of residual or recurrent disease;
    4. Prostate intraepithelial neoplasia without evidence of prostate cancer;
    5. Adequately treated urothelial papillary non-invasive carcinoma.
  18. Presence of any indwelling tubes or drains (such as percutaneous nephrostomy tubes, indwelling Foley catheters, biliary drainage tubes, or peritoneal/pericardial catheters); Note: Thoracic catheters or dedicated central venous access catheters such as Port-A-Cath or Hickman catheters are allowed.
  19. Other acute or chronic diseases or laboratory abnormalities, which may increase the risk of participating in the study or receiving the investigational product, interfere with the interpretation of study results, and make the participant unsuitable for participating in the study based on the investigator's judgment;
  20. Neurological, mental, or social conditions that affect the compliance with trial requirements, significantly increase the risk of AEs, or affect the participants' signing of written informed consent (IC);
  21. Females who are pregnant, have a positive pregnancy test result, or are breastfeeding;
  22. Not fit to participate in this study at the discretion of 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:順次割り当て
  • 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:Drug: IBI3028
IBI3028 will be dosed until disease progression, toxicity intolerance, starting of new systemic anti-cancer treatment, withdrawal of consent, occurrence of other reasons for discontinuing study therapy, or treatment duration reaching the maximum of 24 months, whichever occurs first.
Recombinant anti-EGFR(Epidermal growth factor receptor) and c-Met antibodies-dual-payload conjugate 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
メジャーの説明
時間枠
身体検査結果に臨床的に重大な変化があった被験者の数
時間枠:最長3年
研究者によって報告された臨床的に重大な異常な身体検査所見。
最長3年
心電図に臨床的に重大な変化が見られた被験者の数
時間枠:最長3年
研究者によって報告された臨床的に重要な異常な心電図所見。
最長3年
バイタルサインに臨床的に有意な変化がある被験者の数
時間枠:最大3年
体温、脈拍、呼吸速度、安静時のパルスオキシメトリーによる酸素飽和度、血圧を含むバイタルサイン
最大3年
用量制限毒性(DLT)
時間枠:最大21日
MTDおよび/またはRP2Dを確立するための毒性(DLT)を制限します。
最大21日
実験室パラメーターに臨床的に有意な変化がある被験者の数
時間枠:最大3年
調査員によって報告された臨床的に有意な異常な検査室パラメーターの調査結果。
最大3年
Numbers of subjects with adverse events
時間枠:Up to 3 years
Defined as any untoward medical occurrence, whether or not there is a causal relationship with the study drug, in a clinical study subject from the time informed consent form is signed
Up to 3 years
Numbers of subjects with serious adverse events
時間枠:Up to 3 years
Defined as any serious untoward medical occurrence, whether or not there is a causal relationship with the study drug, in a clinical study subject from the time informed consent form is signed
Up to 3 years
Number of AEs(adverse events) leading to dose interruption
時間枠:Up to 3 years
AEs(adverse events) leading to dose interruption reported by the investigator
Up to 3 years
Number of AEs leading to dose delay
時間枠:Up to 3 years
AEs leading to dose delay reported by the investigator
Up to 3 years
Number of AEs leading to dose reduction
時間枠:Up to 3 years
AEs leading to dose reduction reported by the investigator
Up to 3 years
Number of AEs leading to permanent discontinuation
時間枠:Up to 3 years
AEs leading to permanent discontinuation reported by the investigator
Up to 3 years
Objective response rate (ORR) in dose expansion
時間枠:Up to 3 years
Objective response rate (ORR) as evaluated per the RECIST v1.1 criteria.
Up to 3 years

二次結果の測定

結果測定
メジャーの説明
時間枠
Area under the curve (AUC)
時間枠:Up to 3 years
Area under the curve (AUC) of single and multiple doses of IBI3028
Up to 3 years
Maximum concentration (Cmax)
時間枠:Up to 3 years
Maximum concentration (Cmax) of single and multiple doses of IBI3028
Up to 3 years
Time to maximum concentration (Tmax)
時間枠:Up to 3 years
Time to maximum concentration (Tmax) of single and multiple doses of IBI3028
Up to 3 years
Clearance (CL)
時間枠:Up to 3 years
Clearance (CL) of single and multiple doses of IBI3028
Up to 3 years
Apparent volume of distribution (V)
時間枠:Up to 3 years
apparent volume of distribution (V) of single and multiple doses of IBI3028
Up to 3 years
Half-life (t1/2)
時間枠:Up to 3 years
Half-life (t1/2) of IBI3020 to the last administration of IBI3028
Up to 3 years
Anti-drug antibody (ADA)
時間枠:Up to 3 years
Incidence and characterization of anti-drug antibody (ADA)
Up to 3 years
Neutralizing antibody (NAb)
時間枠:Up to 3 years
Incidence and characterization of neutralizing antibody (NAb)
Up to 3 years
Objective response rate (ORR)
時間枠:Up to 3 years
Objective response rate (ORR) as evaluated per the RECIST v1.1 criteria
Up to 3 years
Duration of response (DoR)
時間枠:Up to 3 years
Duration of response (DoR) as evaluated per the RECIST v1.1 criteria
Up to 3 years
Disease control rate (DCR)
時間枠:Up to 3 years
Disease control rate (DCR) as evaluated per the RECIST v1.1 criteria
Up to 3 years
Time to response (TTR)
時間枠:Up to 3 years
Time to response (TTR) as evaluated per the RECIST v1.1 criteria
Up to 3 years
Progression-free survival (PFS)
時間枠:Up to 3 years
progression-free survival (PFS) as evaluated per the RECIST v1.1 criteria
Up to 3 years
Overall survival (OS)
時間枠:Up to 3 years
OS is defined as the time from the date of first dose of study drug until the date of death from any cause.
Up to 3 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3月31日

一次修了 (推定)

2027年6月30日

研究の完了 (推定)

2028年6月30日

試験登録日

最初に提出

2026年4月27日

QC基準を満たした最初の提出物

2026年5月11日

最初の投稿 (実際)

2026年5月15日

学習記録の更新

投稿された最後の更新 (実際)

2026年5月15日

QC基準を満たした最後の更新が送信されました

2026年5月11日

最終確認日

2026年5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。

大腸がんの臨床試験

  • Novartis Pharmaceuticals
    終了しました
    メラノーマ | 高度なEGFR変異体非小さな細胞肺cancer(NSCLC) | KRAS G12変異NSCLC | 食道扁平上皮がん(SCC) | ヘッド/ネックSCC | 進行した胃腸間質腫瘍(GIST) | 進行したNRAS/BRAFT WT皮膚黒色腫
    アメリカ, 台湾, オランダ, カナダ, スペイン, シンガポール, イタリア, 日本, 韓国
  • Jonsson Comprehensive Cancer Center
    National Cancer Institute (NCI); Highlight Therapeutics
    積極的、募集していない
    平滑筋肉腫 | 悪性末梢神経鞘腫瘍 | 滑膜肉腫 | 未分化多形肉腫 | 骨の未分化高悪性度多形肉腫 | 粘液線維肉腫 | II期の体幹および四肢の軟部肉腫 AJCC v8 | III期の体幹および四肢の軟部肉腫 AJCC v8 | IIIA 期の体幹および四肢の軟部肉腫 AJCC v8 | IIIB 期の体幹および四肢の軟部肉腫 AJCC v8 | 切除可能な軟部肉腫 | 多形性横紋筋肉腫 | 切除可能な脱分化型脂肪肉腫 | 切除可能な未分化多形肉腫 | 軟部組織線維肉腫 | 紡錘細胞肉腫 | ステージ I 後腹膜肉腫 AJCC (American Joint Committee on Cancer) v8 | 体幹および四肢の I 期軟部肉腫 AJCC v8 | ステージ... およびその他の条件
    アメリカ

Drug: IBI3028の臨床試験

購読する