A Treatment-Option Protocol to Provide Brentuximab Vedotin to Eligible Patients Completing Studies SGN35-005 or C25001
Trial ID or NCT#
Status
Purpose
The purpose of this study is to provide the option of brentuximab vedotin treatment to eligible patients in studies SGN35-005 and C25001
Official Title
An Open-label, Treatment-option Protocol of Brentuximab Vedotin in Patients With Relapsed or Refractory Hodgkin Lymphoma, Systemic Anaplastic Large Cell Lymphoma, or CD30-positive Cutaneous T-cell Lymphoma
Eligibility Criteria
- * Participated in either the SGN35-005 or C25001 clinical study and experienced progression. Patients who received brentuximab vedotin in C25001 must have had an objective response at the time of discontinuation.* Completed any previous treatment with radiation, chemotherapy, biologics and/or investigational agents at least 4 weeks prior to the first dose of brentuximab vedotin
- * History of another primary malignancy that has not been in remission for at least 3 years* Known cerebral/meningeal disease* Peripheral neuropathy of grade 2 or greater* Females who are pregnant or breastfeeding
Investigator(s)
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Contact
CCTO
650-498-7061
View on ClinicalTrials.gov