CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 35 enrolled / 35 target
Drug / intervention
Pertuzumab +5 morebiological
Likely dose
Not stated in 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/NCT06136897
NCT06136897Phase 2ActiveUpdate Overdue (0.3/mo)Completion was 55mo ago

MATCH Treatment Subprotocol J: Trastuzumab and Pertuzumab (HP) in Patients With Non-Breast, Non-Gastric/GEJ, and Non-Colorectal Cancers With HER2 Amplification

National Cancer Institute (NCI)·interventional·Posted Nov 18, 2023·Updated Jun 26, 2026

In Brief

A Phase 2 clinical trial evaluating Biopsy Procedure, Biospecimen Collection, and 4 other interventions for Malignant Solid Neoplasm. Active but no longer recruiting, targeting 35 participants across 1 site.

Signals

Enrollment appears stalled

Detailed Summary

This phase II MATCH treatment trial tests how well trastuzumab and pertuzumab work in treating patients with HER2-amplified non-breast, non-gastric/gastroesophageal junction, and non-colorectal cancers. Pertuzumab and trastuzumab are monoclonal antibodies and forms of targeted therapy that attach to a receptor protein called HER2. HER2 is found on some cancer cells. When pertuzumab or trastuzumab attach to HER2, the signals that tell the cells to grow are blocked and the tumor cell may be marked for destruction by the body's immune system. Trastuzumab is approved for the treatment of certain types of HER2-amplified cancers such as breast and gastric cancers. Research has shown that treatment with two anti-HER2 therapies in combination may be more effective at treating HER2-positive patients than giving one anti-HER2 therapy alone. Giving trastuzumab and pertuzumab in combination may be effective at treating patients with HER2-amplified cancers that aren't breast, gastric, or colorectal.

Study Details

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

Timeline

Phase 2Active
20172018201920202021202220232024202520262027
First PostedNov 18, 2023
Enrollment StartMar 23, 2017
Primary CompletionNov 3, 2021
Study CompletionJan 15, 2027
TodayJul 2, 2026
Enrollment to primary: 4.6 yearsPosted 2.6 years ago

Arms & Interventions

Treatment (pertuzumab, trastuzumab)experimental

Patients receive pertuzumab IV over 30-60 minutes and trastuzumab IV over 30 minutes on day 1 of each cycle. Cycles repeat every 3 weeks in the absence of disease progression or unacceptable toxicity. Patients also undergo radiologic evaluation throughout the trial, ECHO at screening and end of treatment, and biopsy and collection of blood samples on trial and at end of treatment.

Procedure: Biopsy ProcedureProcedure: Biospecimen CollectionProcedure: Echocardiography TestBiological: PertuzumabProcedure: Radiologic ExaminationBiological: Trastuzumab

Interventions

Biopsy Procedureprocedure

Undergo biopsy

Biospecimen Collectionprocedure

Undergo collection of blood samples

Echocardiography Testprocedure

Undergo ECHO

Pertuzumabbiological

Given IV

Radiologic Examinationprocedure

Undergo radiologic evaluation

Trastuzumabbiological

Given IV