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NCT05653180
IBI310 in Combination With Sintilimab in Patients With Advanced Biliary Tract Cancer
Conditions: Advanced Biliary Tract Cancer
Sex: All
Ages: 18 Years – N/A
Phase: PHASE1, PHASE2
Enrollment: 20
Sponsor: Innovent Biologics (Suzhou) Co. Ltd.
Location: China
Summary
This research study is designed to establish whether the combination of IBI310 & Sintilimab has efficacy in patients with advanced BTC
Eligibility Criteria
Inclusion Criteria:The subject must sign the written informed consent form, and can comply with the visits and related procedures specified in the protocol.Aged ≥18 years.Patients with unresectable or relapsed or metastatic advanced Biliary tract cancer,and diagnosed by histology/cytology (except carcinoma of ampulla).Had progressed after receiving at least first-line systemic treatment (if a patient has progressed within 6 months after receiving systemic treatment during adjuvant chemotherapy or concurrent radiochemotherapy, she will be deemed to have received first-line treatment).Patients who have never received any anti-PD-1, anti-PD-L1/L2 antibody, anti-CTLA-4 antibody, or other immunotherapy.The subject must have at least one measurable lesion as the target lesion (according to RECIST V1.1).
A measurable lesion in the radiation field from previous radiotherapy or local treatment, can also be chosen as the target lesion if confirmed progression.Exclusion Criteria:Diagnosis of other malignant tumors within 5 years before the first administration, excluding radically cured skin basal cell carcinoma, skin squamous cell carcinoma, radically resected carcinoma in situ and/or thyroid papillary carcinoma.Patients who have previously received organ or bone marrow transplantation.Patients with acute or chronic active hepatitis B or C infection, hepatitis B virus (HBV) DNA> 2000 IU/ml or 104 copies/ml; hepatitis C virus (HCV) antibody positive and HCV-RNA >103 copies/ml;.
Patients with acute or chronic active hepatitis B or C infection who have received nucleotide antiviral therapy and are below the above standards can be selected.Uncontrollable hypertension, systolic blood pressure ≥150 mmHg or diastolic blood pressure ≥100 mmHg after best medical treatment, history of hypertensive crisis or hypertensive encephalopathy.Pleural effusion, ascites, and pericardial effusion with clinical symptoms or requiring drainage , patients who only shows with a few pleural effusion, ascites, and pericardial effusion by imaging and with no clinical symptoms can be selected.
Source: ClinicalTrials.gov (NCT05653180). StuddyBuddy aggregates publicly available trial information.