TATE and Pembrolizumab for Colorectal and Lung Cancers

This study is looking at a treatment combination of TATE (Trans-arterial Tirapazamine Embolization) and pembrolizumab (a checkpoint inhibitor, which helps your immune system fight cancer) for people with metastatic colorectal cancer (mCRC) or non-small cell lung cancer (NSCLC) that has spread to the liver. You might be eligible if your cancer has specific characteristics, like not having certain mutations (changes in your genes) such as EGFR or AKT. For mCRC, the study will compare this new combination to standard treatments like TAS-102 or regorafenib, focusing on how long people live (Overall Survival). For NSCLC, everyone will receive TATE and pembrolizumab, and researchers will measure how much the tumors shrink (Overall Response Rate).

Study design
This is an open-label study, meaning you and your doctors will know which treatment you are receiving. It aims to enroll 110 participants.
What's involved
Pembrolizumab is given intravenously (IV) every 3 or 6 weeks for up to 2 years or until your cancer progresses. If you are in the mCRC arm, you might take TAS-102 or regorafenib pills on a specific schedule.
Compensation
Not stated in the trial record.
Follow-up
Overall survival for mCRC will be measured at 24 months. Overall response rate for NSCLC will be measured within 24 months.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT04701476

TATE and Pembrolizumab (MK3475) in mCRC and NSCLC

Recruiting
PHASE2Ages 18+InterventionalTreatment
Teclison Ltd.
~110 participants
Updated 2026-04-16 on ClinicalTrials.gov
What's tested:TATE and pembrolizumabTAS-102 pillRegorafenib Pill

At a glance

Recruiting sites
3 of 3 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Overall Survival for the mCRC cohort
Measured over 24 months
+1 more outcome measured
Colorectal Cancer; Lung Cancer
3 sites across 2 states
Taiwan2
California1
  • Ray Lee · STUDY_DIRECTOR · Teclison Limited

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Eligibility criteria

Inclusion

Liver metastatic MSS-mCRC or NSCLC without EGFR or AKT mutations
mCRC progressed on at least two lines of standard chemotherapy; or
NSCLC progressed on chemotherapy and an immune checkpoint inhibitor
Measurable disease
ECOG 0-1
At least 4 weeks from prior chemotherapy and free from chemo-related toxicity
Adequate organ function

Exclusion

Prior organ transplantation
Liver metastasis more than 50%
Oxygen saturation less than 92% in room air
Prior autoimmune disorder
CNS metastasis
Major GI bleeding in the last 2 months
  • Overall Survival for the mCRC cohort24 months

    From the first day of treatment to death

  • Overall Response Rate (ORR) for the NSCLC cohortwithin 24 months

    Per RECIST 1.1 criteria