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OncoMatch/Clinical Trials/NCT05422690

The Purpose of This Research Study is to See if Combining Gemcitabine, Cisplatin and Durvalumab Chemotherapy Treatments With a Direct Tumor Therapy Yittrium-90 (Y-90) Will Work Better Together to Shrink Tumors and Control Cancer

Is NCT05422690 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Induction Chemotherapy Triplet Therapy and Consolidation Doublet Therapy: for intrahepatic cholangiocarcinoma.

Phase 2RecruitingInova Health Care ServicesNCT05422690Data as of Jun 2026

Treatment: Induction Chemotherapy Triplet Therapy · Consolidation Doublet Therapy:The purpose of this research is to see if combining gemcitabine, cisplatin and Durvalumab chemotherapy treatments with a direct tumor therapy called Yittrium-90, will work better together to shrink the tumor and control cancer.

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Extracted eligibility criteria

Treatments studied

Other

Induction Chemotherapy Triplet TherapyConsolidation Doublet Therapy:

Cancer type

Cholangiocarcinoma

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Cannot have received: chemotherapy

Exception: adjuvant therapy with capecitabine

Previous treatment with chemotherapy, intra-arterial or radiotherapy for iCCA is exclusionary, with the exception of adjuvant therapy with capecitabine which is allowed.

Cannot have received: intra-arterial therapy

Previous treatment with chemotherapy, intra-arterial or radiotherapy for iCCA is exclusionary, with the exception of adjuvant therapy with capecitabine which is allowed.

Cannot have received: radiotherapy

Previous treatment with chemotherapy, intra-arterial or radiotherapy for iCCA is exclusionary, with the exception of adjuvant therapy with capecitabine which is allowed.

Lab requirements

Liver function

Noncirrhotic liver required; Child-Pugh score must be less than 5; Child-Pugh B7 or greater cirrhosis excluded; Serum albumin < 3 g/dL excluded; Serum bilirubin > 2 mg/dL excluded; AST or ALT > 5x ULN excluded

Noncirrhotic liver ... Child-Pugh score must be less than 5 ... Serum albumin < 3 g/dL ... Serum bilirubin > 2 mg/dL ... AST or ALT > 5x ULN

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Keary Janet · Fairfax, Virginia

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT05422690 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior chemotherapy, intra-arterial therapy, radiotherapy disqualifies patients from enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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