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An Open-Label, Multicenter, Phase IB/II Clinical Study of HRS-7172 in Combination With Antitumor Therapy in Participants With Solid Tumors

2026年9月2日 更新者:Jiangsu HengRui Medicine Co., Ltd.

An Open-Label, Multicenter, Phase IB/II Clinical Study of the Safety, Tolerability, and Efficacy of HRS-7172 in Combination With Antitumor Therapy in Participants With Solid Tumors

This is a Phase IB/II clinical trial designed to evaluate HRS-7172 in combination with antitumor drugs in participants with advanced pancreatic cancer harboring RAS mutations or amplifications.

The study process includes a screening period (from signed informed consent to first dose), a treatment period (from first dose to last dose), and a follow-up period (safety and survival follow-up after last dose). A Safety Monitoring Committee (SMC), composed of the principal investigator and sponsor representatives, will be established during the study to review the safety and efficacy data generated. The SMC will make decisions on study-related matters, including but not limited to combination regimen dose exploration, combination regimen selection, efficacy expansion cohort selection, expansion initiation timing, and recommended dose for expansion (RDE).

This study aims to evaluate the safety, tolerability, and efficacy of HRS-7172 in combination with other antitumor therapies in participants with advanced or metastatic pancreatic cancer harboring RAS mutations or amplifications.

調査の概要

研究の種類

介入

入学 (推定)

140

段階

  • フェーズ2
  • 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

研究連絡先のバックアップ

研究場所

    • Shanghai Municipality
      • Shanghai、Shanghai Municipality、中国、200032
        • Fudan University Shanghai Cancer Center
        • 主任研究者:
          • Xianjun Yu

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. Capable of giving informed consent, have signed and dated the IRB/EC-approved informed consent form, and are willing and able to comply with scheduled visits, examination requirements, and other study procedures.
  2. Aged 18 to 70 years (inclusive) at the time of signing the informed consent form, regardless of sex.
  3. ECOG performance status of 0 or 1.
  4. Locally advanced or metastatic pancreatic cancer confirmed by histology and cytology, with RAS mutation/amplification detected by tissue or blood genetic testing.
  5. Participants who have received at most one prior line of standard therapy.
  6. Life expectancy ≥ 12 weeks.
  7. At least one measurable lesion as defined by RECIST v1.1.
  8. Participants must provide formalin-fixed, paraffin-embedded tumor tissue blocks or unstained tumor specimens.
  9. Adequate organ and bone marrow function.
  10. Female participants of childbearing potential must agree to use contraception and refrain from donating eggs from the time of signing the informed consent form until 6 months after the last dose of the study drug; serum human chorionic gonadotropin (HCG) test must be negative within 7 days prior to the first dose, and must not be breastfeeding. Male participants whose partners are women of childbearing potential must agree to use contraception and refrain from donating sperm from the time of signing the informed consent form until 5 months after the last dose of the study drug.

Exclusion Criteria:

  1. Participants with untreated or active central nervous system (CNS) metastases or leptomeningeal metastases (including history thereof).
  2. Concurrent other malignancies ≤ 3 years prior to the first dose, with the following exceptions: adequately treated carcinoma in situ of the cervix, basal cell or squamous cell skin carcinoma, localized prostate cancer after radical surgery, ductal carcinoma in situ after radical surgery, and papillary thyroid carcinoma after radical surgery (hormonal therapy for non-metastatic prostate cancer or breast cancer is permitted).
  3. Participants with uncontrollable tumor-related pain as determined by the investigator. Participants requiring analgesic therapy must have a stable analgesic regimen at study entry; symptomatic lesions eligible for palliative radiotherapy should have completed treatment before study entry.
  4. Severe cardiovascular or cerebrovascular diseases.
  5. Gastrointestinal diseases affecting drug administration/absorption, including but not limited to dysphagia, malabsorption syndrome, refractory nausea, vomiting, diarrhea, Crohn's disease, and ulcerative colitis; intestinal obstruction or related symptoms and signs within 6 months prior to the start of study treatment, unless surgically treated with complete resolution; clinically significant acute or chronic pancreatitis; other gastrointestinal conditions deemed unsuitable for enrollment by the investigator.
  6. Clinically significant bleeding events (including but not limited to hematemesis, melena, hematochezia, etc., excluding hemorrhoidal bleeding or isolated fecal occult blood positive) within 6 months prior to the start of study treatment, or a definite bleeding tendency, high bleeding risk, coagulation disorder, or thrombotic tendency.
  7. Clinically symptomatic moderate or severe ascites (i.e., requiring therapeutic paracentesis or drainage within 2 weeks prior to the start of study treatment; participants with only small-volume ascites on imaging without clinical symptoms may be enrolled); uncontrolled or moderate or greater pleural effusion or pericardial effusion.
  8. Severe infection within 4 weeks prior to the start of study treatment, including but not limited to bacteremia, severe pneumonia, or other serious infectious complications requiring hospitalization; active infection of CTCAE ≥ Grade 2 requiring systemic antibiotic therapy within 2 weeks prior to the first dose; excluding participants receiving prophylactic antibiotic therapy (e.g., for prevention of urinary tract infection).
  9. History of immunodeficiency, including HIV positive; active hepatitis B (positive HBsAg at screening with HBV DNA quantification ≥ 1000 copies/mL or 500 IU/mL) or hepatitis C (anti-HCV positive with HCV RNA positive).
  10. Active pulmonary tuberculosis infection within 1 year prior to enrollment as determined by history or imaging, or a history of active pulmonary tuberculosis infection more than 1 year ago without standard treatment.
  11. Adverse reactions from prior antitumor therapy that have not recovered to CTCAE ≤ Grade 1 (except alopecia, Grade 2 peripheral neurotoxicity, laboratory values meeting enrollment criteria, or other conditions determined by the investigator not to affect study drug treatment).
  12. Systemic antitumor therapy (including chemotherapy, biological therapy, targeted therapy, immunotherapy, radical radiotherapy, etc.) within 4 weeks prior to the start of study treatment.
  13. Major organ surgery (excluding needle biopsy), significant trauma within 4 weeks prior to the first dose of study drug, or planned elective surgery during the study; minor traumatic procedures (biopsy, endoscopy, and drainage) within 7 days prior to the first dose.
  14. Receipt of live attenuated vaccines within 28 days prior to the first dose of study drug, or anticipated need for live attenuated vaccines during the study treatment period.
  15. Pregnant or lactating women, or female participants planning to become pregnant during the study period or within 7 months after the last dose of study drug.
  16. History of severe allergic reactions to any component of any study drug to be received, or to other monoclonal antibodies.
  17. Participants judged by the investigator to have other factors that may affect study results or lead to premature study termination, such as alcoholism, drug abuse, other serious diseases (including mental illness) requiring concomitant treatment, severely abnormal laboratory values, family or social factors, and other circumstances that may affect participant safety or the collection of study data.

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:ランダム化
  • 介入モデル:並列代入
  • 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:Treatment group A-low dose: HRS-7172 + AG + SHR-1316
HRS-7172 + AG + SHR-1316; low dose
実験的:Treatment group A-high dose: HRS-7172 + AG + SHR-1316
HRS-7172 + AG + SHR-1316; high dose
HRS-7172 + AG + SHR-1316; low/high dose
実験的:Treatment group A1: HRS-7172 + AG
HRS-7172 + AG; low/high dose
実験的:Treatment group A2: HRS-7172 + AG + SHR-1316
HRS-7172 + AG + SHR-1316; high dose
HRS-7172 + AG + SHR-1316; low/high dose
実験的:Treatment group B-low dose: HRS-717 + HRS-4642+SHR-1316
HRS-717 + HRS-4642+SHR-1316; low dose
HRS-717 + HRS-4642+SHR-1316; high dose
HRS-717 + HRS-4642+SHR-1316; low/high dose
実験的:Treatment group B-high dose: HRS-717 + HRS-4642+SHR-1316
HRS-717 + HRS-4642+SHR-1316; low dose
HRS-717 + HRS-4642+SHR-1316; high dose
HRS-717 + HRS-4642+SHR-1316; low/high dose
実験的:Treatment group B1: HRS-717 + HRS-4642
HRS-717 + HRS-4642; low/high dose
実験的:Treatment group B2: HRS-717 + HRS-4642+SHR-1316
HRS-717 + HRS-4642+SHR-1316; low dose
HRS-717 + HRS-4642+SHR-1316; high dose
HRS-717 + HRS-4642+SHR-1316; low/high dose

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
RDE in advanced pancreatic cancer with RAS mutation or amplification
時間枠:From the signing of the informed consent form to the end of the safety follow-up. Estimated to be 2 years
From the signing of the informed consent form to the end of the safety follow-up. Estimated to be 2 years
Incidence and severity of adverse events (AEs) (per NCI-CTCAE V6.0 criteria)
時間枠:From the signing of the informed consent form to the end of the safety follow-up. Estimated to be 2 years
From the signing of the informed consent form to the end of the safety follow-up. Estimated to be 2 years
ORR assessed by the investigator
時間枠:From the signing of the informed consent form to the end of the safety follow-up. Estimated to be 2 years
From the signing of the informed consent form to the end of the safety follow-up. Estimated to be 2 years

二次結果の測定

結果測定
時間枠
Objective Response Rate (ORR) as assessed by the investigator
時間枠:From signing of the informed consent form to the end of the safety follow-up. Estimated to be 2 years
From signing of the informed consent form to the end of the safety follow-up. Estimated to be 2 years
Disease Control Rate (DCR) as assessed by the investigator
時間枠:From signing of the informed consent form to the end of the safety follow-up. Estimated to be 2 years
From signing of the informed consent form to the end of the safety follow-up. Estimated to be 2 years
Duration of Response (DoR) as assessed by the investigator
時間枠:From signing of the informed consent form to the end of the safety follow-up. Estimated to be 2 years
From signing of the informed consent form to the end of the safety follow-up. Estimated to be 2 years
Progression-Free Survival (PFS) as assessed by the investigator
時間枠:From signing of the informed consent form to the end of the safety follow-up. Estimated to be 2 years
From signing of the informed consent form to the end of the safety follow-up. Estimated to be 2 years
Overall Survival (OS)
時間枠:From signing of the informed consent form to the end of the safety follow-up. Estimated to be 2 years
From signing of the informed consent form to the end of the safety follow-up. Estimated to be 2 years
Anti-Drug Antibodies (ADA)
時間枠:From pre-dose on C1D1 to 30 days after the last dose. Estimated to be 2 years
From pre-dose on C1D1 to 30 days after the last dose. Estimated to be 2 years
Incidence and severity of AEs
時間枠:From the participant's signing of the informed consent form to the end of the safety follow-up period. Estimated to be 2 years
From the participant's signing of the informed consent form to the end of the safety follow-up period. Estimated to be 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 (推定)

2026年9月1日

一次修了 (推定)

2028年12月31日

研究の完了 (推定)

2029年12月31日

試験登録日

最初に提出

2026年9月2日

QC基準を満たした最初の提出物

2026年9月2日

最初の投稿 (実際)

2026年9月8日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月8日

QC基準を満たした最後の更新が送信されました

2026年9月2日

最終確認日

2026年9月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

未定

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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