BRAF-/MEK-Inhibition With Dabrafenib and Trametinib in Melanoma Patients

NCT03944356 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 232

Last updated 2025-03-12

No results posted yet for this study

Summary

Adjuvant therapy with dabrafenib plus trametinib in melanoma was approved in 2018 by the EMA (EUropean Medicines Agency).

The purpose of this non-interventional study is to assess the usage of adjuvant dabrafenib and trametinib in clinical practice, where the patient population may differ from study population.

Conditions

Interventions

DRUG

Dabrafenib and Trametinib

Dabrafenib and trametinib treatment under routine conditions according to the applying SmPC.

Sponsors & Collaborators

  • EuMelaReg gGmbH

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-07-01
Primary Completion
2023-12-31
Completion
2024-10-08

Countries

  • Germany

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03944356 on ClinicalTrials.gov