A Study of RO5185426 in Patients With Metastatic Melanoma
Status: | Completed |
---|---|
Conditions: | Skin Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/21/2016 |
Start Date: | December 2010 |
End Date: | October 2011 |
A SINGLE ARM, OPEN LABEL, EXPANDED ACCESS STUDY OF RG7204 IN PREVIOUSLY TREATED PATIENTS WITH METASTATIC MELANOMA
This is an open-label, non-comparative, multicenter, expanded access study of RO5185426 in
patients who have received prior systemic therapy for metastatic melanoma and who have no
other satisfactory treatment options.
patients who have received prior systemic therapy for metastatic melanoma and who have no
other satisfactory treatment options.
Inclusion Criteria:
- Histologically confirmed metastatic melanoma with documented BRAF V600E mutation,
determined by the cobas BRAF V600 mutation test
- Patients with clinical evidence of disease progression during or after at least one
prior systemic therapy for metastatic melanoma
- Patients with either measurable or non-measurable disease
- Adequate recovery from most recent systemic or local treatment for metastatic
melanoma
- Adequate organ function
- For women of childbearing potential, agreement to the use of two acceptable methods
of contraception, including one barrier method, during the study and for 6 months
after discontinuation of RO5185426
- For men with female partners of childbearing potential, agreement to use a latex
condom, and to advise their female partner to use an additional method of
contraception during the study and for 6 months after discontinuation of RO5185426
- Negative serum or urine pregnancy test within 7 days of commencement of treatment in
premenopausal women. Women who are either surgically sterile or have been
post-menopausal for at least 1 year are eligible to participate in this study
- Agreement not to donate blood or blood products during the study and for at least 6
months after discontinuation of RO5185426; for male patients, agreement not to donate
sperm during the study and for at least 6 months after discontinuation of RO5185426
Exclusion Criteria:
- Evidence of symptomatic CNS lesions as determined by investigator
- Patients with a previous malignancy within the past 2 years are excluded except for
patients with basal or squamous cell carcinoma (SCC) of the skin or carcinoma in-situ
of the cervix. Isolated elevation in PSA in absence of radiographic evidence of
metastatic prostate cancer is allowed
- Pregnant or breast-feeding
- Concurrent anti-tumor therapy
- Any of the following within 6 months prior to study drug administration: myocardial
infarction, severe/unstable angina, symptomatic congestive heart failure,
cerebrovascular accident or transient ischemic attack, pulmonary embolism,
hypertension not adequately controlled by current medications
- Uncontrolled medical illness
We found this trial at
23
sites
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