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Het effect van ochtend- versus avonddoseren van sunitinib op de medicijnspiegels in het bloed.


- candidate number13140
- NTR NumberNTR3526
- ISRCTNISRCTN wordt niet meer aangevraagd.
- Date ISRCTN created
- date ISRCTN requested
- Date Registered NTR12-jul-2012
- Secondary IDs12-138 METC ErasmusMC
- Public TitleHet effect van ochtend- versus avonddoseren van sunitinib op de medicijnspiegels in het bloed.
- Scientific TitleEffects of morning versus evening dosing on the pharmacokinetics and pharmacodynamics of sunitinib (Sutent).
- ACRONYM
- hypothesisThere is a difference in activity of CYP3A4, and therefor probably also in pharmacokinetics of sunitinib during the day.
- Healt Condition(s) or Problem(s) studiedAdvanced clear cell renal cell carcinoma,, Advanced p-NET, Metastatic GIST, Sunitinib
- Inclusion criteria1. Age ≥ 18 years;
2. Histological or cytological confirmed diagnosis of advanced clear‐cell renal cell carcinoma, GIST or pancreatic neuro‐endocrine tumor, treated with sunitinib;
3. WHO performance score ≤ 1 at study entry;
4. Any stable dose of sunitinib at study entry, defined as no dose change within 3 weeks prior to pharmacokinetics;
5. Adequate hematological functions (ANC > 1.0 x 109/L, platelets > 100 x 109/L);
6. Adequate liver and renal function defined as bilirubin concentration ≤ 2 x ULN, AST and ALT ≤ 2.5 x ULN, serum creatinin concentration ≤ 2 x ULN;
7. Written informed consent;
8. For patients with reproductive potential a reliable method of contraception (excluding oral contraceptives) must be used.
- Exclusion criteria1. Pregnant or child nursing patients;
2. Serious illness or medical unstable condition requiring treatment, symptomatic CNS metastasis or history of psychiatric disorder that would prohibit the understanding and giving of informed consent;
3. Major surgery within 2 weeks prior to start of the protocol;
4. Use of CYP3A4 inhibiting or inducing medication;
5. Patients who are unable to collect blood from;
6. Patients with known allergy to sunitinib or midazolam;
7. Patients unwilling or unable to give written informed consent.
- mec approval receivedyes
- multicenter trialno
- randomisedyes
- masking/blindingNone
- controlNot applicable
- groupParallel
- Type2 or more arms, non-randomized
- Studytypeobservational
- planned startdate 10-jul-2012
- planned closingdate1-jul-2014
- Target number of participants18
- Interventions1. Blood withdrawal for pharmacokinetics of sunitinib and midazolam;
2. Administration of midazolam;
3. Urine sample collection.
- Primary outcomeDifference in pharmacokinetics of sunitinib in morning intake compared to evening intake.
- Secondary outcome1. To investigate whether daily variation in CYP3A4 activity exists in humans based on midazolam and 4‐hydroxycholesterol pharmacokinetics and urine 4‐OHcholesterol;
2. To investigate if evening dosing of sunitinib affects the side effects of this drug;
3. To investigate the influence of single‐nucleotide polymorphisms in PK genes on the exposure to sunitinib (based on the MEC02.1002 protocol).
- Timepoints2 courses of sunitinib treatment.
- Trial web siteN/A
- statusopen: patient inclusion
- CONTACT FOR PUBLIC QUERIESMD PhD Ron H.J. Mathijssen
- CONTACT for SCIENTIFIC QUERIESMD PhD Ron H.J. Mathijssen
- Sponsor/Initiator Erasmus Medical Center, Department of Medical Oncology
- Funding
(Source(s) of Monetary or Material Support)
Erasmus Medical Center, Department of Medical Oncology
- PublicationsN/A
- Brief summarySince metabolism of sunitinib is dependant of different cytochrome P450 enzymes, including CYP3A4, which in cell-lines and rodents show a circadian rhythm in expression, it is very likely that pharmacokinetics of sunitinib is time dependant. The activity of CYP3A4 probably drops in night time. Higher concentrations of sunitinib and its active metabolite may be reached when sunitinib is taken in the evening. Patients participating in this cross-over study will be followed, during two courses of sunitinib. In one of both courses, they will take sunitinib at 08.00 AM, and during the other course at 18.00 PM. During both courses, they will behospiatlized during 24 hours for pharmacokinetic measurements of sunitinib. To investigate the circadian rhythm of CYP3A4, patients will be administered a low dose of midazolam. Pharmacokinetics of midazolam and 1OH-midazolam will be measured. In addition, also the endogenous marker 4beta-hydroxycholesterol will be studied as an extra test to study CYP3A4 dynamics. After completing these two courses, patients are free to decide at wich time they will continue sunitinib intake.
- Main changes (audit trail)05-Apr-2013: Several changes due to an amendment - NM
Name of the trial: "Effect of dosing time on the pharmacokinetics and pharmacodynamics of sunitinib"
Hypothesis: dosing-time of sunitinib may alter the pharmacokinetics.
Summary: Since metabolism of sunitinib is dependant of different cytochrome P450 enzymes, including CYP3A4, which in cell-lines and rodents show a circadian rhythm in expression, it is very likely that pharmacokinetics of sunitinib is time dependant. Exposure to sunitinib may therefore be influenced by dosing-time.
Patients participating in this cross-over study will be followed, during three courses of sunitinib. In one of three courses, they will take sunitinib at 08.00, one course at 18.00, and one course at 13.00 . During all three courses, they will behospiatlized during 24 hours for pharmacokinetic measurements of sunitinib.
To investigate the circadian rhythm of CYP3A4, patients will be administered a low dose of midazolam. Pharmacokinetics of midazolam and 1OH-midazolam will be measured. In addition, also the endogenous marker 4beta-hydroxycholesterol will be studied as an extra test to study CYP3A4 dynamics.
After completing these three courses, patients are free to decide at wich time they will continue sunitinib intake.
- RECORD12-jul-2012 - 5-apr-2013


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