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

NCT02439411 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 135

Last updated 2019-12-02

No results posted yet for this study

Summary

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

Conditions

  • Malignant Melanoma Stage IV
  • Malignant Melanoma Stage IIIc

Interventions

DRUG

Trametinib

Sponsors & Collaborators

  • GlaxoSmithKline

    collaborator INDUSTRY
  • Grupo Español Multidisciplinar de Melanoma

    lead OTHER

Principal Investigators

  • Salvador Martín Algarra, M.D., Ph.D. · Clinica Universidad de Navarra

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-03-03
Primary Completion
2016-09-30
Completion
2016-09-30

Countries

  • Spain

Study Locations

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Entities

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 NCT02439411 on ClinicalTrials.gov