CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 11 enrolled
Drug / intervention
Pembrolizumab (MK-3475) +2 morebiological
Likely dose
Pembrolizumab (MK-3475) 200 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03111732
NCT03111732Phase 2Completed

A Phase 2 Study of Pembrolizumab, a Monoclonal Antibody Against PD-1, in Combination With Capecitabine and Oxaliplatin (CAPOX) in Subjects With Advanced Biliary Tract Carcinoma (BTC)

National Cancer Institute (NCI)·interventional·Posted Apr 13, 2017·Updated Dec 3, 2021

In Brief

A Phase 2 clinical trial evaluating Pembrolizumab (MK-3475), Oxaliplatin, and 1 other intervention for Biliary Tract Neoplasms and 4 related conditions. Completed, enrolled 11 participants across 1 site.

Detailed Summary

Background: Biliary tract cancers are rare but they are serious. Researchers want to see if a certain drug helps the immune system fight cancer cells. The drug is called pembrolizumab. It may work even better with two chemotherapy drugs that are widely used to treat gastrointestinal cancers. Objective: To study if pembrolizumab given with capecitabine and oxaliplatin (CAPOX) increases the time it takes for a person's biliary tract cancer to get worse. Eligibility: People age 18 and older with previously treated biliary tract cancer that has spread to other parts of the body Design: Participants will be screened with tests as part of their regular cancer care. Each study cycle is 3 weeks. For 6 cycles, participants will: Get pembrolizumab and oxaliplatin on day 1 of each cycle. They will be given in an intravenous (IV) catheter. Take capecitabine by mouth for 2 weeks then have 1 week without it. Participants will complete a patient diary. Starting with cycle 7, participants will get only pembrolizumab. They will get it once every 3 weeks. On day 1 of every cycle, participants will have: Physical exam Review of symptoms and how well they do normal activities Blood tests Every 9 weeks, they will have a scan. Participants may have tumor samples taken. Participants will have a final visit about 1 month after they stop the study drug. After that, they will be contacted by phone or email yearly.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
201820192020202120222023202420252026
First PostedApr 13, 2017
Enrollment StartJun 14, 2017
Primary CompletionJul 22, 2020
Study CompletionNov 8, 2021
TodayJul 2, 2026
Enrollment to primary: 3.1 yearsPosted 9.2 years ago

Interventions

Pembrolizumab (MK-3475)biological

200 mg will be administered as an IV infusion on Day 1 of each 21 day cycle

Oxaliplatindrug

130mg/m(2) IV Infusion will be administered as an IV infusion on Day 1 of cycles 1-6

Capecitabinedrug

750 mg/m(2) will be administered orally twice a day on Days 1-14 of cycles 1-6