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Phase 3 N=423 Randomized Quadruple-blind Treatment

A Study Comparing Trametinib and Dabrafenib Combination Therapy to Dabrafenib Monotherapy in Subjects With BRAF-mutant Melanoma

Melanoma

Enrolled (actual)
423
Serious AEs
42.7%
Results posted
Aug 2014
Primary outcome: Primary: Progression-Free Survival (PFS) as Assessed by the Investigator — 10.2; 8.8 Months

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Dabrafenib (Drug); Trametinib (Drug); Trametinib placebo (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Novartis Pharmaceuticals
Primary completion
Aug 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Progression-Free Survival (PFS) as Assessed by the Investigator
10.2; 8.8
SECONDARY
Overall Survival (OS)
25.8; 18.7
SECONDARY
Objective Response Rate (ORR) as Assessed by the Investigator
146; 113
SECONDARY
Duration of Response (DoR)
12.9; 10.2
SECONDARY
Trametinib Pharmacokinetic Concentrations
9.9209; 0.0000; 19.0382; 0.0261; 16.7496; 0.0000
SECONDARY
Dabrafenib and Dabrafenib Metabolites (Hydroxy-, Carboxy- and Desmethyl-Dabrafenib) Concentrations
92.1; 64.4; 1309.6; 1362.3; 458.9; 539.7
SECONDARY
Number of Participants With Adverse Events and Serious Adverse Events
203; 205; 24; 100; 80; 8

Summary

This was a two-arm, double-blinded, randomized, Phase III study comparing dabrafenib and trametinib combination therapy to dabrafenib administered with a placebo (dabrafenib monotherapy). Subjects with histologically confirmed cutaneous melanoma that is either Stage IIIC (unresectable) or Stage IV, and BRAF V600E/K mutation positive were screened for eligibility. Subjects who had prior systemic anti-cancer treatment in the advanced or metastatic setting were not eligible although prior systemic treatment in the adjuvant setting was allowed. Subjects were stratified according to the baseline lactate dehydrogenase level and BRAF genotype.

Eligibility Criteria

Inclusion Criteria

  • Histologically confirmed cutaneous melanoma that is either Stage IIIC (unresectable) or Stage IV (metastatic), and determined to be BRAF V600E/K mutation-positive using the bioMerieux (bMx) investigational use only (IUO) THxID BRAF Assay (IDE: G120011). The assay will be conducted by a central reference laboratory. Subjects with ocular or mucosal melanoma are not eligible.
  • The subject must have a radiologically measurable tumor
  • The subject is able to carry out daily life activities without significant difficulty (ECOG performance status score of 0 or 1).
  • Able to swallow and retain oral medication
  • Sexually active subjects must use acceptable methods of contraception during the course of the study
  • Adequate organ system function and blood counts

Exclusion Criteria

  • Prior treatment with a BRAF or a MEK inhibitor
  • Prior systemic anti-cancer treatment for Stage IIIC (unresectable) or Stage IV (metastatic) melanoma. Prior systemic treatment in the adjuvant setting is allowed. (Note: Ipilimumab treatment must end at least 8 weeks prior to randomization.)
  • The subject has received major surgery or certain tyes of cancer therapy with 21 days of starting treatment
  • Current use of prohibited medication listed in the protocol
  • Left ventricular ejection fraction less than the lower limit of normal
  • Uncontrolled blood pressurl
  • History or current evidence of retinal vein occlusion or central serous retinopathy
  • Brain metastases unless previously treated with surgery or stereotactic radiosurgery and the disease has been stable for at least 12 weeks
  • The subject is pregnant or nursing
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01584648). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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