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Subcutaneously Administered CAMPATH in CD52 Expressing Hematologic Malignancies

Hematologic Malignancies Clinical Trial

Official title:
A Phase I Study of Subcutaneously Administered CAMPATH in CD52 Expressing Hematologic Malignancies

Clinical Trial Summary

This phase I study will involve escalating doses of CAMPATH until the goal dose for the cohort is tolerated. The CAMPATH goal dose will be administered to the patient subcutaneously (SQ) 3 times per week for up to 12 weeks.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00113048
Study type Interventional
Source Sanofi
Contact
Status Terminated
Phase Phase 1
Start date December 2003
Completion date September 2005
View Details
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