CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 44 enrolled / 44 target
Drug / intervention
Dabrafenib Mesylate +1 moredrug
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/NCT04439292
NCT04439292Phase 2ActiveUpdate Overdue (0.3/mo)Completion was 31mo ago

MATCH Treatment Subprotocol H: Phase II Study of Dabrafenib and Trametinib in Patients With Tumors With BRAF V600E or V600K Mutations (Excluding Melanoma, Thyroid Cancer, Colorectal Adenocarcinoma, and Non-Small Cell Lung Cancer)

National Cancer Institute (NCI)·interventional·Posted Jun 19, 2020·Updated Jun 12, 2026

In Brief

A Phase 2 clinical trial evaluating Dabrafenib Mesylate and Trametinib Dimethyl Sulfoxide for Advanced Lymphoma and 5 related conditions. Active but no longer recruiting, targeting 44 participants across 1 site.

Signals

Enrollment appears stalled

Detailed Summary

This phase II MATCH treatment trial identifies the effects of trametinib and dabrafenib in patients whose cancer has genetic changes called BRAF V600 mutations. Dabrafenib may stop the growth of cancer by blocking BRAF proteins which may be needed for cell growth. Trametinib may stop the growth of cancer cells by blocking MEK proteins which, in addition to BRAF proteins, may also be needed for cell growth. Researchers hope to learn if giving trametinib with dabrafenib will shrink this type of cancer or stop its growth.

Study Details

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

Timeline

Phase 2Active
201620172018201920202021202220232024202520262027
First PostedJun 19, 2020
Enrollment StartJan 4, 2016
Primary CompletionNov 27, 2023
Study CompletionDec 31, 2026
TodayJul 2, 2026
Enrollment to primary: 7.9 yearsPosted 6.0 years ago

Arms & Interventions

Treatment (dabrafenib, trametinib)experimental

Patients receive dabrafenib mesylate PO BID and trametinib dimethyl sulfoxide PO QD on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.

Drug: Dabrafenib MesylateDrug: Trametinib Dimethyl Sulfoxide

Interventions

Dabrafenib Mesylatedrug

Given PO

Trametinib Dimethyl Sulfoxidedrug

Given PO