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NCT06567600

Low-dose Gemcitabine and Cisplatin and PD-1/PD-L1 Antibody Therapy in Intrahepatic Cholangiocarcinoma

Not yet recruiting Phase 2 Last updated 22 August 2024
What this trial tests

Phase 2 trial testing Low-dose Gemcitabine and Cisplatin Chemotherapy plus PD-1/PD-L1Antibody in Intrahepatic Cholangiocarcinoma in 43 participants. Not yet recruiting.

Timeline
1 September 2024
Primary endpoint
31 December 2027
31 December 2028

Quick facts

Lead sponsorThird Affiliated Hospital, Sun Yat-Sen University
PhasePhase 2
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment43
Start date1 September 2024
Primary completion31 December 2027
Estimated completion31 December 2028
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Third Affiliated Hospital, Sun Yat-Sen University

Who can join

18 and older, any sex, with Intrahepatic Cholangiocarcinoma or Chemotherapy Effect. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In this phase 2 study, researchers aimed to evaluate the efficacy and safety of low-dose gemcitabine and cisplatin chemotherapy and the immune checkpoint inhibitor PD-1/PD-L1 antibody in patients with advanced and unresectable intrahepatic cholangiocarcinoma.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Intrahepatic Cholangiocarcinoma

Currently open trials in the same condition.

Other Third Affiliated Hospital, Sun Yat-Sen University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06567600.

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