A Study of GSK2118436 in BRAF Mutant Metastatic Melanoma

Completed · Phase 2

Conditions studied: Melanoma

In brief

BRF113710 is a Phase II, single-arm, open-label study to assess the efficacy, safety, and tolerability of GSK2118436 administered twice daily as a single agent in subjects with BRAF mutant metastatic melanoma. Subjects will receive 150 mg of GSK2118436 twice daily and continue on treatment until disease progression, death, or unacceptable adverse event.

Key facts

Study ID

NCT01153763

Run by

GlaxoSmithKline

People needed

92

Starts

2010-08-09

Expected to finish

2016-06-01

Last updated by the study team

2017-09-27

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Must be at least 18 years of age
• Must have histologically confirmed cutaneous metastatic melanoma (Stage IV) that is BRAF mutation-positive (V600 E/K) as determined via central testing with a BRAF mutation assay.
• Is treatment naive or has received prior treatment for metastatic melanoma.
• Must have measurable disease according to Response Evaluation Criteria in Solid Tumors (RECIST 1.1).
• 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 Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1.
• Adequate organ function.

You may not qualify if…

• Previous treatment with a BRAF or MEK inhibitor.
• Cancer therapy (chemotherapy with delayed toxicity, radiation therapy, immunotherapy, biologic therapy, or major surgery) within the last 3 weeks; chemotherapy regimens without delayed toxicity within the last 2 weeks; or use of any investigational anti-cancer or other drug within 28 days or 5 half-lives, whichever is longer, preceding the first dose of GSK2118436.
• A history of known Human Immunodeficiency Virus (HIV), Hepatitis B Virus (HBV), or Hepatitis C Virus (HCV) infection.
• History or evidence of brain metastases on MRI or head CT if MRI is not able to be performed.
• History of other malignancy. Subjects who have been disease-free for 5 years, or subjects with a history of completely resected non-melanoma skin cancer or successfully treated in situ carcinoma are eligible.
• Certain cardiac abnormalities.

Where it is running

• GSK Investigational Site — Los Angeles, California, United States
• GSK Investigational Site — Los Angeles, California, United States
• GSK Investigational Site — San Francisco, California, United States
• GSK Investigational Site — Philadelphia, Pennsylvania, United States
• GSK Investigational Site — Nashville, Tennessee, United States
• GSK Investigational Site — Houston, Texas, United States
• GSK Investigational Site — Newcastle, New South Wales, Australia
• GSK Investigational Site — Westmead, New South Wales, Australia
• GSK Investigational Site — Nedlands, Western Australia, Australia
• GSK Investigational Site — Bordeaux, France
• GSK Investigational Site — Boulogne-Billancourt, France
• GSK Investigational Site — Lille, France
• GSK Investigational Site — Marseille, France
• GSK Investigational Site — Montpellier, France
• GSK Investigational Site — Paris, France
• GSK Investigational Site — Villejuif, France
• GSK Investigational Site — Essen, North Rhine-Westphalia, Germany
• GSK Investigational Site — Kiel, Schleswig-Holstein, Germany
• GSK Investigational Site — Lübeck, Schleswig-Holstein, Germany
• GSK Investigational Site — Berlin, Germany
• GSK Investigational Site — Naples, Campania, Italy
• GSK Investigational Site — Genoa, Liguria, Italy
• GSK Investigational Site — Padova, Veneto, Italy

Full record on ClinicalTrials.gov

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