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Distribution NIlotinib in semen in men treated for chronic Myeloid leukAemia

Recruiting
Conditions
CM
Registration Number
NL-OMON26150
Lead Sponsor
VU University Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
10
Inclusion Criteria

•male patients

•aged >18 years

Exclusion Criteria

•Refractory CML with persistent leucocytosis

•Sterilisation

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Percentage of nilotinib present in seminal fluid in relation to the plasma concentration.
Secondary Outcome Measures
NameTimeMethod
Calculated maximal concentration nilotinib absorbed by the partner, using the volume of distribution of the tyrosine kinase inhibitors and the percentage in seminal fluid found in this study.
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