Dabrafenib Plus Trametinib vs Vemurafenib Alone in Unresectable or Metastatic BRAF V600E/K Cutaneous Melanoma



Status:Active, not recruiting
Conditions:Skin Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:11/10/2018
Start Date:June 4, 2012
End Date:March 18, 2019

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A Phase III, Randomised, Open-label Study Comparing the Combination of the BRAF Inhibitor, Dabrafenib and the MEK Inhibitor, Trametinib to the BRAF Inhibitor Vemurafenib in Subjects With Unresectable (Stage IIIc) or Metastatic (Stage IV) BRAF V600E/K Mutation Positive Cutaneous Melanoma

This is a two-arm, open-label, randomised, Phase III study comparing dabrafenib (GSK2118436)
and trametinib (GSK1120212) combination therapy to vemurafenib. Subjects with histologically
confirmed cutaneous melanoma that is either stage IIIc (unresectable) or stage IV, and BRAF
V600E/K mutation positive will be screened for eligibility. Subjects who have had prior
systemic anti-cancer treatment in the advanced or metastatic setting will not be eligible
although prior systemic treatment in the adjuvant setting will be allowed. Approximately 694
subjects will be randomised 1:1 (combination therapy:vemurafenib). The primary endpoint is
overall survival (OS) for subjects receiving the combination therapy compared with those
receiving vemurafenib.


Inclusion Criteria:

- >= 18 years of age

- Stage IIIc or Stage IV BRAF V600E/K cutaneous melanoma

- Measurable disease according to RECIST 1.1

- Women of childbearing potential with negative serum pregnancy test prior to
randomisation

- Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1

- Adequate baseline organ function

Exclusion Criteria:

- Any prior use of a BRAF or MEK inhibitor

- Prior systemic anti-cancer treatment in the advanced or metastatic setting; prior
systemic treatment in the adjuvant setting is allowed

- History of another malignancy (except subjects who have been disease free for 3 years
or with a history of completely resected non-melanoma skin cancer)

- Known HIV, HBV, HCV infection (except chronic or cleared HBV and HCV infection which
will be allowed)

- Brain metastases (except if all known lesions were previously treated with surgery or
stereotactic radiosurgery and lesions, if still present, are confirmed stable for >=
12 weeks prior to randomisation or if no longer present are confirmed no evidence of
disease for >= 12 weeks, and are asymptomatic with no corticosteroid requirements for
>= 4 weeks prior to randomisation, and no enzyme inducing anticonvulsants for >= 4
weeks prior to randomisation

- History or evidence of cardiovascular risk (LVEF < LLN; QTcB >= 480 msec; blood
pressure or systolic >=140 mmHg or diastolic >= 90 mmHg which cannot be controlled by
anti-hypertensive therapy)

- History or current evidence/risk of retinal vein occlusion (RVO) or central serous
retinopathy (CSR)
We found this trial at
34
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Ann Arbor, Michigan 48109
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Atlanta, Georgia 30322
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Aurora, Colorado 80010
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Bend, Oregon 97701
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Beverly Hills, California 90211
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Birmingham, Alabama 35209
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Burlington, Vermont 05401
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Capital Federal, Buenos Aires
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Chapel Hill, North Carolina 27599
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Charleston, South Carolina 29407
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Charlotte, North Carolina 28277
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Charlottesville, Virginia 22904
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Cincinnati, Ohio 45229
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Cincinnati, OH
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Columbus, Ohio 43205
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Dallas, Texas 75216
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Dallas, TX
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Durham, North Carolina 27710
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Durham, NC
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Fridley, Minnesota 55432
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Gilbert, Arizona 85234
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Gilbert, AZ
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Greenville, South Carolina 29605
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Hackensack, New Jersey 07601
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Iowa City, Iowa 52240
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Jacksonville, Florida 32216
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Las Vegas, Nevada 89135
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Las Vegas, NV
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Miami Beach, Florida 33140
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Milwaukee, Wisconsin 53209
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Nashville, Tennessee 37205
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New Brunswick, New Jersey 08901
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230 Park Avenue, 21st Floor
New York, New York 10169
1-888-669-6682)
Novartis Novartis, which was created in 1996 by the merger of the Swiss companies Ciba-Geigy...
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Orlando, Florida 32806
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Portland, Oregon 97228
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Saint Louis, Missouri 63128
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Salt Lake City, Utah 84103
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San Francisco, California 94121
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Vallejo, California 94589
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Vallejo, CA
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