Last updated on February 2018

Therapy Optimisation for the Treatment of Hairy Cell Leukemia

Brief description of study

The trial will test the effectiveness and toxicity of subcutaneous treatment with one cycle of cladribine in patients with hairy cell leukemia requiring treatment.

They have to be untreated so far or may be pretreated with alpha-interferon.

Detailed Study Description

Evaluation of remission status will take place 4 months after treatment. In addition, it will be tested whether patients with non-optimal response will have a benefit from a second cycle of cladribine.

Non-optimal response is: patients with detectable residual disease; achievement of partial remission or detectable residual infiltration in the bone marrow.

Clinical Study Identifier: NCT02131753

Contact Investigators or Research Sites near you

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Helmut Oettle, PhD

Community based hemato-oncology medical office
Friedrichshafen, Germany
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Recruitment Status: Open

Brief Description Eligibility Contact Research Team

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