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A Study to Determine Number of Patients Who Develop High Ammonia Levels After Receiving Recombinant Erwinia Asparaginase
RECRUITINGSponsored by Mayo Clinic
Actively Recruiting
SponsorMayo Clinic
Started2023-11-02
Est. completion2026-12-01
Eligibility
Age1 Year+
Healthy vol.Accepted
Locations1 site
View on ClinicalTrials.gov →
NCT06600659
Summary
This study evaluates the incidence of symptomatic hyperammonemia (high ammonia levels) in patients being treated with recombinant Erwinia asparaginase.
Eligibility
Age: 1 Year+Healthy volunteers accepted
Inclusion Criteria: * Followed by pediatric hematology/oncology * Receiving recombinant Erwinia asparaginase for treatment of malignancy Exclusion Criteria: * Patients \< 1 year of age * Patients who have previously received recombinant Erwinia asparaginase within the past two weeks
Conditions3
Acute Lymphobkastic LeukemiaCancerHematopoietic and Lymphatic System Neoplasm
Locations1 site
Mayo Clinic in Rochester
Rochester, Minnesota, 55905
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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
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Actively Recruiting
SponsorMayo Clinic
Started2023-11-02
Est. completion2026-12-01
Eligibility
Age1 Year+
Healthy vol.Accepted
Locations1 site
View on ClinicalTrials.gov →
NCT06600659