CI

At a glance

ClinicalIndex Comparison Record
Phase 3Active· 153 enrolled / 153 target
Drug / intervention
Dabrafenib +3 moredrug
Likely dose
Dabrafenib 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/NCT04940052
NCT04940052Phase 3ActiveUpdate Overdue (2.8/mo)Completion was 17mo ago

A Randomized, Double-blind, Placebo-controlled Phase III Study to Evaluate the Efficacy and Safety of Dabrafenib Plus Trametinib in Previously Treated Patients With Locally Advanced or Metastatic, Radio-active Iodine Refractory BRAFV600E Mutation-positive Differentiated Thyroid Cancer (DTC)

Novartis Pharmaceuticals·interventional·Posted Jun 25, 2021·Updated Jun 26, 2026

In Brief

A Phase 3 clinical trial evaluating Dabrafenib, Trametinib, and 2 other interventions for Differentiated Thyroid Cancer (DTC). Active but no longer recruiting, targeting 153 participants across 41 sites in 11 countries.

Signals

Enrollment appears stalled

Detailed Summary

The purpose of this study is to assess the efficacy and safety of dabrafenib in combination with trametinib for treating adult patients with locally advanced or metastatic Differentiated Thyroid Cancer (DTC) harboring the BRAFV600E mutation, who are refractory to radioactive iodine (RAI) therapy and have experienced disease progression following one or two prior VEGFR-targeted treatments.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesArgentina, Brazil, Canada, China, India, Malaysia, South Korea, Taiwan, Turkey (Türkiye), United States, Vietnam
Collaborators--

Timeline

Phase 3Active
202220232024202520262027
First PostedJun 25, 2021
Enrollment StartNov 15, 2021
Primary CompletionJan 22, 2025
Study CompletionMay 25, 2027
TodayJul 2, 2026
Enrollment to primary: 3.2 yearsPosted 5.0 years ago

Arms & Interventions

Dabrafenib plus Trametinibexperimental

Eligible participants will receive Dabrafenib 150 mg twice a day (BID) and Trametinib 2 mg once a day (QD) until disease progression as per RECIST 1.1 as confirmed by blinded independent review committee (BIRC), unacceptable toxicity, pregnancy, loss of clinical benefit as determined by the investigator, withdrawal of consent, lost to follow-up, death, or study termination by the sponsor.

Drug: DabrafenibDrug: Trametinib
Dabrafenib Placebo plus Trametinib Placeboplacebo_comparator

Eligible participants will receive matching placebo for Dabrafenib 150 mg twice a day (BID) and matching placebo for Trametinib 2 mg once a day (QD) until disease progression as per RECIST 1.1 as confirmed by blinded independent review committee (BIRC), unacceptable toxicity, pregnancy, loss of clinical benefit as determined by the investigator, withdrawal of consent, lost to follow-up, death, or study termination by the sponsor.

Drug: Trametinib PlaceboDrug: Dabrafenib placebo

Interventions

Dabrafenibdrug

Dabrafenib 150 mg capsule administered orally twice a day (BID)

Trametinibdrug

Trametinib 2 mg tablet administered once a day (QD)

Trametinib Placebodrug

matching placebo tablet for Trametinib 2 mg will be administered orally once a day (QD)

Dabrafenib placebodrug

matching placebo capsule for Dabrafenib 150 mg will be administered orally twice a day (BID)