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Validation of dried blood spot sampling in therapeutic drug monitoring of nilotinib

Validation of dried blood spot sampling in therapeutic drug monitoring of nilotinib - Dried Blood Spot Nilotinib

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON37855
Enrollment
40
Registered
2012-12-10
Start date
2013-02-04
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Myelogenous Leukemia

Interventions

None listed

Sponsors

Vrije Universiteit Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients with CML who are treated with nilotinib.

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
Difference between specimens across blood sampling methods, and between duplicate specimens for the same blood sampling method will be determined.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)