Deze pagina is automatisch vertaald en de nauwkeurigheid van de vertaling kan niet worden gegarandeerd. Raadpleeg de Engelse versie voor een brontekst.

A Single-arm, Multicenter Clinical Study of Iparomlimab and Toripalimab in Combination With Bevacizumab and Chemotherapy as First-line Treatment for Advanced Biliary Tract Cancer

10 september 2026 bijgewerkt door: Xianglin Yuan

A Study of Iparomlimab and Toripalimab in Combination With Bevacizumab and Chemotherapy as First-line Treatment for Advanced Biliary Tract Cancer

This is a single-arm, multicenter clinical study designed to evaluate the efficacy and safety of Iparomlimab and Toripalimab (QL1706) in combination with bevacizumab and chemotherapy as first-line treatment for patients with advanced biliary tract cancer

Studie Overzicht

Studietype

Ingrijpend

Inschrijving (Geschat)

32

Fase

  • Fase 4

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • Hubei
      • Wuhan, Hubei, China
        • Werving
        • Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
        • Contact:

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

Inclusion Criteria:

  • Informed Consent: Patients voluntarily join this study and sign the informed consent form.
  • Age: 18 to 75 years old, male or female.
  • Histologically or cytologically confirmed, unresectable locally advanced or metastatic biliary tract cancer (BTC), including cholangiocarcinoma (intrahepatic and extrahepatic) and gallbladder carcinoma.
  • No prior systemic anti-tumor therapy for locally advanced or metastatic BTC.
  • At least one measurable lesion according to RECIST v1.1 that is suitable for accurate repeated measurement. Lesions previously irradiated or brain metastases are not eligible as target lesions.
  • Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 or 1.
  • Adequate organ function
  • For HBsAg positive subjects: HBV DNA must be < 2000 IU/mL (or < 10⁴ copies/mL), and effective antiviral therapy (e.g., Entecavir, Tenofovir, TAF, or Tenofovir Amibufenamide) must be administered throughout the study.

Subjects with a history of HCV infection but negative HCV RNA PCR results may be considered uninfected.

  • Female subjects of childbearing potential must have a negative urine or serum pregnancy test (if urine test is not definitively negative, a serum test is required).
  • Willingness to use highly effective contraceptive measures during the study and for 3 months after the last dose.
  • Willing and able to comply with scheduled visits, treatment plans, laboratory tests, and other requirements of the study.

Exclusion Criteria:

  • Histologically or cytologically confirmed small cell carcinoma, neuroendocrine tumors, lymphoma, sarcoma, colloid carcinoma, adenosquamous carcinoma, squamous cell carcinoma, mucinous intraductal papillary neoplasm, mucinous cystic neoplasms, or other rare pathological types of biliary tract tumors.
  • Brain Metastases: History of brain metastases or presence of active brain metastases.
  • Vascular Invasion & Bleeding Risk: Imaging at screening shows tumor invasion or encasement (>180 degrees) of major blood vessels; or the tumor presents with significant necrosis or cavitation, and the investigator judges that enrollment poses a high risk of bleeding.
  • Cardiac Disease: Uncontrolled cardiac clinical symptoms or diseases, including but not limited to:

    1. Cardiac insufficiency classified as Class II or higher according to the New York Heart Association (NYHA) criteria, or Left Ventricular Ejection Fraction (LVEF) < 50% on echocardiography;
    2. Unstable angina pectoris;
    3. Myocardial infarction within 1 year prior to study entry;
    4. Clinically significant supraventricular or ventricular arrhythmias requiring treatment or intervention;
    5. QTc interval > 450 ms (male) or > 470 ms (female) (QTc calculated using the Fridericia formula; if abnormal, repeat ECG three times at 2-minute intervals and use the average value).
  • Autoimmune Disease: Active autoimmune disease or a history of autoimmune disease likely to recur (including but not limited to autoimmune hepatitis, interstitial pneumonia, uveitis, enteritis, hypophysitis, vasculitis, nephritis, hyperthyroidism, or hypothyroidism [patients controlled solely by hormone replacement therapy are not excluded]).
  • Esophageal/Gastric Varices: History of esophageal or gastric variceal bleeding due to portal hypertension within 6 months prior to the first dose; known severe varices on endoscopy within 3 months prior to the first dose; or evidence of portal hypertension (including splenomegaly on imaging) with high bleeding risk assessed by the investigator (including moderate-to-severe esophageal/gastric varices with bleeding risk, local active gastrointestinal ulcers, and persistent positive fecal occult blood tests). Endoscopy is required to exclude patients with "red color signs." Patients with a history of "red color signs" are excluded.
  • Hemorrhage: Any life-threatening bleeding event within 3 months prior to the first dose, including events requiring blood transfusion, surgery, local therapy, or continuous medication.
  • Systemic Immunosuppression: Use of systemic corticosteroids or other immunosuppressive therapies for active autoimmune diseases within the past 2 years. Note: Replacement therapy (e.g., thyroxine, insulin, or physiological corticosteroid replacement for adrenal or pituitary insufficiency) is not considered systemic treatment.
  • Inflammatory Bowel Disease: Active or prior history of inflammatory bowel disease (e.g., Crohn's disease, ulcerative colitis) or chronic diarrhea.
  • Transplantation: History of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation.
  • Pneumonitis/ILD: Previous or current history of non-infectious pneumonitis/interstitial lung disease requiring systemic glucocorticoid therapy.

Surgery: Major surgical procedure or severe trauma within 30 days prior to the first dose, or planned major surgery within 30 days after the first dose (as determined by the investigator); minor local surgery within 3 days prior to the first dose (excluding peripherally inserted central catheter [PICC] line placement and implantable venous port insertion).

  • Infection: Severe active infection judged by the investigator.
  • Pregnancy: Pregnant women or those planning to become pregnant during the study period.
  • Prior Trials: Participation in another drug clinical trial within 12 months prior to enrollment.
  • Other: Other conditions deemed unsuitable for enrollment by the investigator.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: QL1706 plus bevacizumab and chemotherapy
Iparomlimab/Toripalimab (QL1706) 5 mg/kg IV Q3W (D1); Bevacizumab 7.5 mg/kg IV Q3W (D1); Gemcitabine 1000 mg/m² IV Q3W (D1, D8); Cisplatin 25 mg/m² IV Q3W (D1, D8)
Bevacizumab: 7.5 mg/kg, IV, Q3W, Day 1.
Gemcitabine: 1000 mg/m², IV, Q3W, Days 1 and 8
Cisplatin: 25 mg/m², IV, Q3W, Days 1 and 8
Iparomlimab and Toripalimab (QL1706): 5mg/kg, intravenous (IV), once every 3 weeks (Q3W), Day 1.
Andere namen:
  • QL1706

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
6-month progression-free survival rate
Tijdsspanne: From date of enrollment to 6 months
The primary endpoint was the 6-month progression-free survival rate
From date of enrollment to 6 months

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Median Progression-Free Survival
Tijdsspanne: Up to approximately 24 months
Defined as the time from enrollment to disease progression or death from any cause, whichever occurs first.
Up to approximately 24 months
Objective Response Rate (ORR)
Tijdsspanne: Up to approximately 24 months
Defined as the proportion of participants with a best overall response of Complete Response (CR) or Partial Response (PR) according to RECIST 1.1.
Up to approximately 24 months
Disease Control Rate (DCR)
Tijdsspanne: Up to approximately 24 months
Proportion of participants achieving a best overall response of CR, PR, or Stable Disease (SD) per RECIST 1.1
Up to approximately 24 months
Duration of Response (DOR)
Tijdsspanne: Up to approximately 24 months
Time from the first documented CR or PR to the first documented disease progression or death from any cause.
Up to approximately 24 months
Overall Survival (OS)
Tijdsspanne: Up to approximately 36 months
Time from enrollment to death from any cause.
Up to approximately 36 months

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

10 juni 2026

Primaire voltooiing (Geschat)

1 juli 2028

Studie voltooiing (Geschat)

31 december 2028

Studieregistratiedata

Eerst ingediend

24 mei 2026

Eerst ingediend dat voldeed aan de QC-criteria

24 mei 2026

Eerst geplaatst (Werkelijk)

1 juni 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

15 september 2026

Laatste update ingediend die voldeed aan QC-criteria

10 september 2026

Laatst geverifieerd

1 mei 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

Abonneren