Pharmacogenomics Effects on High-Dose Methotrexate Clearance in Patients With Diffuse Large B-Cel… (NCT06031194) | Clinical Trial Compass
CompletedNot Applicable
Pharmacogenomics Effects on High-Dose Methotrexate Clearance in Patients With Diffuse Large B-Cell Lymphoma
United States20 participantsStarted 2023-05-10
Plain-language summary
This study evaluates pharmacogenomic effects on high-dose methotrexate clearance in patients with diffuse large B-cell lymphoma.
Who can participate
Age range18 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* \* Adult (age ≥ 18 years at diagnosis)
* Diagnosis of DLBCL or PCNSL
* Planned to undergo treatment with HDMTX (≥ 3 g/m\^2) at the James Cancer Hospital.
Note: patients with CKD are eligible to participate regardless of eGFR provided the treating physician is planning a dose of HDMTX of at least 3 g/ m\^2.
* Ability to provide informed consent.
Exclusion Criteria:
* \* Patients with a "currently active" second malignancy that, in the opinion of the principal investigator, will interfere with patient participation, or confound data interpretation
* Pregnancy (positive serum or urine pregnancy test), lactating or breast feeding
* Prisoners or incarcerated patients
* Total bilirubin \> 5 mg/dL
What they're measuring
1
SNPs (single nucleotide polymorphisms) associated with delayed MTX clearance
Timeframe: Up to 24 weeks
Trial details
NCT IDNCT06031194
SponsorOhio State University Comprehensive Cancer Center