Patient Guide: Study of 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

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 41 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04940052
Status: ACTIVE_NOT_RECRUITING
Condition: Differentiated Thyroid Cancer
Phase: PHASE3

Where You Can Participate

This study is available at 41 locations across the country.

Top locations include:
  • • Chicago, Illinois
  • • Boston, Massachusetts
  • • Caba, Buenos Aires
  • • And 38 more locations

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Study of 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 - Join Clinical Trial NCTNCT04940052

How to Join This Clinical Trial - NCTNCT04940052

Learn how to participate in this PHASE3 trial studying an investigational therapy for Differentiated Thyroid Cancer. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Differentiated Thyroid Cancer. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Differentiated Thyroid Cancer
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04940052 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 41 locations. Find a study site near you:

Clinical Research Site

Chicago, Illinois 60611 - United States

Status: Contact for availability

Clinical Research Site

Boston, Massachusetts 02114 - United States

Status: Contact for availability

Clinical Research Site

Caba, Buenos Aires C1417DTB - Argentina

Status: Contact for availability

Clinical Research Site

Rio De Janiero, RJ 20231-050 - Brazil

Status: Contact for availability

Clinical Research Site

Blumenau, Santa Catarina 89015-200 - Brazil

Status: Contact for availability

Clinical Research Site

Sao Paulo, SP 01246-000 - Brazil

Status: Contact for availability

Clinical Research Site

Edmonton, Alberta T6G 1Z2 - Canada

Status: Contact for availability

Clinical Research Site

London, Ontario N6A 5W9 - Canada

Status: Contact for availability

Clinical Research Site

Fuzhou, Fujian 350014 - China

Status: Contact for availability

Clinical Research Site

Zhengzhou, Henan 450008 - China

Status: Contact for availability

And 31 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Differentiated Thyroid Cancer:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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