← Back to Clinical Trials
Recruiting Phase 2 NCT01344200

CELECOXIB Plasma and Cerebral Spinal Fluid Pharmacokinetics in Children

◆ AI Clinical Summary
Plain-language summary for patients

Trial Parameters

Condition Pharmacokinetics of Celecoxib in Children
Sponsor Children's Hospital of Eastern Ontario
Study Type INTERVENTIONAL
Phase Phase 2
Enrollment 65
Sex ALL
Min Age 2 Years
Max Age 12 Years
Start Date 2024-01-29
Completion 2026-01-31
Interventions
CelecoxibPlacebo

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

Brief Summary

Celecoxib is effective for reducing postoperative pain in adults. Children use celecoxib more rapidly than adults and require higher doses. Celecoxib is partially metabolized in the liver by a certain enzyme. A person's genetic variation of this enzyme can influence how well their body uses Celecoxib. Furthermore, Celecoxib down-regulates P-glycoprotein (P-gp), a drug efflux transporter located at the blood brain barrier responsible for central nervous system (CNS) extrusion of ondansetron and possibly fentanyl; therefore celecoxib may augment the CNS effects of these drugs. Understanding the blood and cerebrospinal fluid (CSF) profile of celecoxib in children and the influence of genetics on metabolism would help to develop appropriate celecoxib dosing in children for various treatment options.

Eligibility Criteria

Inclusion Criteria: Children aged 2-12 years, undergoing Maintenance phase chemotherapy for hematological malignancies and lymphomas (i.e. acute lymphoblastic leukemia \[ALL\] and lymphoblastic lymphomas \[LLy\] at CHEO. At this point, all patients would have achieved remission an average of 6 months earlier. Exclusion Criteria: 1. Age \< 2yrs and \>12yrs old 2. Children with non-hematologic malignancies 3. AML 4. Children undergoing a bone marrow aspiration (BMA) only 5. Serum creatinine \> 2 X UNL (upper normal limit) within 30 days 6. Abnormal liver function; alanine aminotransferase (ALT) \> 2 X UNL, Aspartate aminotransferase (AST) \> 2 X UNL, total \& direct bilirubin \> 2 X UNL within 30 days 7. History of peptic ulcer disease 8. Allergy to celecoxib or NSAIDs (note: sulpha allergy does not exclude celecoxib) 9. Recent (within 7 days) celecoxib ingestion 10. Patients receiving CYP2C9 inhibitors fluconazole, amiodarone, oxandrolone 11. Patients receiving CYP2C9 inducers rifampin

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology
}