Basal Cell Carcinoma Clinical Trial
Official title:
Observational Study of the Effectiveness and Safety of Vismodegib (Erivedge) in Patients Treated in Argentina
Verified date | February 2018 |
Source | Hoffmann-La Roche |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
This observational, noninterventional study is designed to further characterize the effectiveness and safety profile of vismodegib (Erivedge) in Argentine patients. Only patients with locally advanced basal cell carcinoma (laBCC) or metastatic basal cell carcinoma (mBCC) will be considered in the effectiveness analysis. Study duration is estimated to be approximately 12 months.
Status | Completed |
Enrollment | 75 |
Est. completion date | July 26, 2017 |
Est. primary completion date | July 26, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Argetine patients prescribed vismodegib according to standard of care and in line with Summary of Product Characteristics (SPC) and local labeling - Diagnosis of laBCC or mBCC for the effectiveness analysis Exclusion Criteria: - None specified |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Hoffmann-La Roche |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Response rate as assessed by the treating physician | Approximately 12 months | ||
Secondary | Duration of treatment | Approximately 12 months | ||
Secondary | Duration of response as assessed by the treating physician | Approximately 12 months | ||
Secondary | Incidence of adverse events | Approximately 12 months |
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