Patient Guide: Effectiveness and Safety of Dabrafenib in Combination With Trametinib as Adjuvant Treatment for Chinese Patients With Stage III BRAF V600 Mutation-positive Melanoma After Complete Resection

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 9 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04666272
Status: ACTIVE_NOT_RECRUITING
Condition: Melanoma
Phase: Not Specified

Where You Can Participate

This study is available at 9 locations across the country.

Top locations include:
  • • Fuzhou, Fujian
  • • Zhengzhou, Henan
  • • Wuhan, Hubei
  • • And 6 more locations

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Effectiveness and Safety of Dabrafenib in Combination With Trametinib as Adjuvant Treatment for Chinese Patients With Stage III BRAF V600 Mutation-positive Melanoma After Complete Resection - Join Clinical Trial NCTNCT04666272

How to Join This Clinical Trial - NCTNCT04666272

Learn how to participate in this Not Specified trial studying an investigational therapy for Melanoma. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Melanoma
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04666272 - 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 9 locations. Find a study site near you:

Clinical Research Site

Fuzhou, Fujian 350014 - China

Status: Contact for availability

Clinical Research Site

Zhengzhou, Henan 410100 - China

Status: Contact for availability

Clinical Research Site

Wuhan, Hubei 430022 - China

Status: Contact for availability

Clinical Research Site

Changsha, Hunan 410013 - China

Status: Contact for availability

Clinical Research Site

Nanjing, Jiangsu 210008 - China

Status: Contact for availability

Clinical Research Site

Changchun, Jilin 130021 - China

Status: Contact for availability

Clinical Research Site

Kunming, Yunnan 650106 - China

Status: Contact for availability

Clinical Research Site

Hangzhou, Zhejiang 310022 - China

Status: Contact for availability

Clinical Research Site

Beijing, 100036 - China

Status: Contact for availability

How to Enroll in This Study

To learn more about participating in this Not Specified clinical trial for Melanoma:

  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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