ClinicalTrials.Veeva

Menu

Retrospective Analysis of Dabrafenib +/- Trametinib Compassionate Use Experience in Spain (DEIS)

G

Grupo Español Multidisciplinar de Melanoma

Status

Completed

Conditions

Malignant Melanoma Stage IIIc
Malignant Melanoma Stage IV

Treatments

Drug: Trametinib

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT02439411
GEM1401

Details and patient eligibility

About

The purpose of this study is to analyze whether Dabrafenib +/- Trametinib are effective in overall survival, response rates and toxicity in both programs.

Enrollment

135 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who have received at least one dose of dabrafenib or combination with trametinib as part of a compassionate use for the treatment of metastatic melanoma, with deadline the start of treatment the April 30, 2014.

Exclusion criteria

  • Patients with a history not available.

Trial design

135 participants in 2 patient groups

Dabrafenib
Dabrafenib plus Trametinib
Description:
Patients treated with Dabrafenib plus Trametinib
Treatment:
Drug: Trametinib

Trial contacts and locations

29

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems