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Phase 3 N=250 Randomized Treatment

A Study Comparing GSK2118436 to Dacarbazine (DTIC) in Previously Untreated Subjects With BRAF Mutation Positive Advanced (Stage III) or Metastatic (Stage IV) Melanoma

Cancer

Enrolled (actual)
250
Serious AEs
30.7%
Results posted
May 2014
Primary outcome: Primary: Progression-free Survival (PFS) as Assessed by the Investigator — 6.9; 2.7 Months — p=<0.0001

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
GSK2118436 (Drug); Dacarbazine (DTIC) (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
GlaxoSmithKline
Primary completion
Dec 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
Progression-free Survival (PFS) as Assessed by the Investigator
6.9; 2.7 <0.0001 sig
PRIMARY
Progression-free Survival (PFS) as Assessed by an Independent Radiologist: Randomized Phase
6.7; 2.9
SECONDARY
Overall Survival
20.0; 15.6
SECONDARY
Number of Participants With a Best Overall Response of Confirmed Complete Response (CR) or Confirmed Partial Response (PR) as Assessed by the Investigator: Randomized Phase
26; 4; 86; 11
SECONDARY
Number of Participants With a Best Overall Response of Confirmed CR or PR as Assessed by an Independent Radiologist: Randomized Phase
6; 1; 87; 3
SECONDARY
Duration of Response as Assessed by the Investigator: Randomized Phase
9.2; 8.2
SECONDARY
Duration of Response as Assessed by an Independent Radiologist: Randomized Phase
5.5; NA
SECONDARY
Progression-free Survival (PFS2) as Assessed by the Investigator: Crossover Phase
4.3
SECONDARY
Number of Participants With a Best Overall Response of Confirmed Complete Response (CR) or Confirmed Partial Response (PR) as Assessed by the Investigator: Crossover Phase
0; 12
SECONDARY
Duration of Response as Assessed by the Investigator: Crossover Phase
4.4
SECONDARY
Number of Participants With Non-melanoma Skin Lesions: Randomized Phase
14; 0; 24; 0
SECONDARY
Agreement Rate for V600E Mutation Validation of the BRAF Mutation Assay
96.70; 90.00; 95.00; 94.90

Summary

BRF113683 is a Phase III, randomized, open-label study comparing the efficacy, safety, and tolerability of GSK2118436 to dacarbazine (DTIC), in subjects with BRAF mutant advanced (Stage III) or metastatic (Stage IV) melanoma. Subjects will be randomized to receive 150 mg of GSK2118436 twice daily or 1000 mg/m2 DTIC every 3 weeks and continue on treatment until disease progression, death, or unacceptable adverse event. Subjects who progress on DTIC will be allowed to crossover to an optional extension arm of the study to receive GSK2118436.

Eligibility Criteria

Inclusion Criteria

  • Adults at least 18 years of age
  • Has advanced (unresectable Stage III) or metastatic (Stage IV) melanoma that is BRAF mutation positive (V600E)
  • Is treatment naive for advanced (unresectable) or metastatic melanoma, with the exception of Interleukin 2 (IL-2) which is allowed.
  • Has measurable disease according to RECIST 1.1 criteria.
  • Women of child-bearing potential must have a negative pregnancy test within 14 days prior to the first dose of study treatment.
  • Women with reproductive potential must be willing to practice acceptable methods of birth control during the study and for up to 4 weeks after the last dose of study medication.
  • Men with reproductive potential must be willing to practice acceptable methods of birth control during the study and for up to 16 weeks after the last dose of study medication.
  • Must have adequate organ function.
  • Must have Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1.

Exclusion Criteria

  • Currently receiving cancer therapy (chemotherapy, radiation therapy, immunotherapy, biologic therapy or surgery).
  • Evidence of active central nervous system (CNS) disease.
  • Previous treatment for metastatic melanoma, including treatment with BRAF or MEK inhibitor.
  • A history of other malignancy. Subjects who have been disease-free for 5 years or subjects with a history of complete resected non-melanoma skin cancer or successfully treated in situ carcinoma are eligible.
  • History of Human Immunodeficiency Virus (HIV) infection.
  • Certain cardiac abnormalities
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01227889). 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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