CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 40 enrolled
Drug / intervention
tucatinib +6 moredrug
Likely dose
tucatinib 150 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/NCT04430738
NCT04430738Phase 2Active

A Phase 1b/2 Dose Escalation and Expansion Study of Tucatinib in Combination With Trastuzumab and Oxaliplatin-based Chemotherapy or Pembrolizumab-containing Combinations for HER2+ Gastrointestinal Cancers

Seagen, a wholly owned subsidiary of Pfizer·interventional·Posted Jun 12, 2020·Updated Feb 24, 2026

In Brief

A Phase 2 clinical trial evaluating tucatinib, trastuzumab, and 5 other interventions for Colorectal Carcinoma and 5 related conditions. Active but no longer recruiting, targeting 40 participants across 27 sites in 2 countries.

Detailed Summary

This trial studies tucatinib to find out if it is safe when given with trastuzumab and other anti-cancer drugs (pembrolizumab, FOLFOX, and CAPOX). It will look at what side effects happen when participants take this combination of drugs. A side effect is anything the drug does other than treating cancer. It will also look at whether tucatinib works with these drugs to treat certain types of cancer. The participants in this trial have HER2-positive (HER2+) cancer in their gut, stomach, intestines, or gallbladder (gastrointestinal cancer).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesJapan, United States
Collaborators--

Timeline

Phase 2Active
2021202220232024202520262027
First PostedJun 12, 2020
Enrollment StartSep 15, 2020
Primary CompletionJul 31, 2024
Study CompletionDec 31, 2026
TodayJul 2, 2026
Enrollment to primary: 3.9 yearsPosted 6.1 years ago

Interventions

tucatinibdrug

For Cohort 1A, 150 mg will be administered twice daily by mouth (orally) from Cycle 1 Day 8 onwards. For all other cohorts, 300 mg (or intermediate dose) will be given orally twice daily starting on Cycle 1 Day 1.

trastuzumabdrug

Cohorts 1A and 1B: a 6 mg/kg loading dose will be given into the vein (IV; intravenously) on Cycle 1 Day 1, followed by a dose of 4 mg/kg IV every 2 weeks starting on Cycle 2 Day 1. Cohorts 1C, 1D, 1E, 1F, 1G, 2A, and 2B: an 8 mg/kg loading dose will be administered IV on Cycle 1 Day 1, followed by a dose of 6 mg/kg IV every 3 weeks thereafter.

oxaliplatindrug

85 mg/m\^2 given IV every 2 weeks for cohorts using FOLFOX. For cohorts using CAPOX regimen, 130 mg/m\^2 given every 3 weeks.

leucovorindrug

200 (mFOLFOX7) or 400 (mFOLFOX6) mg/m\^2 given IV every 2 weeks. Part of FOLFOX regimen.

fluorouracildrug

400 mg/m\^2 (IV bolus after leucovorin) and/or 2400 mg/m\^2 (continuous infusion over 46 hours). Part of FOLFOX regimen.

capecitabinedrug

1000 mg/m\^2 is taken twice per day orally on Days 1-14 of each 3 week cycle. Part of CAPOX regimen.

pembrolizumabdrug

400 mg given by IV on day 1 of cycle 1, then every 6 weeks.