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NCT06600659Recruiting

A Study to Determine Number of Patients Who Develop High Ammonia Levels After Receiving Recombinant Erwinia Asparaginase

A Pilot Study to Establish Incidence and Characteristics of Patients at Risk for Symptomatic Hyperammonemia Secondary to Recombinant Erwinia Asparaginase

Source: ClinicalTrials.gov · Last updated 6 Feb 2026

Brief summary (registry, in English)

This study evaluates the incidence of symptomatic hyperammonemia (high ammonia levels) in patients being treated with recombinant Erwinia asparaginase.

Status (registry)
Recruiting
Study type
Observational
Enrollment
10 (estimated)
First submitted
12 Sept 2024
Start date
2 Nov 2023
Primary completion date
1 Dec 2026
Lead sponsor
Mayo Clinic
NCT number
NCT06600659

What you commit to

  • Study type: Observational
  • Planned participants: 10
  • From 2 Nov 2023 to the primary completion date, 1 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who have previously received recombinant Erwinia asparaginase within the past two weeks

Age

  • Patients \< 1 year of age

Who the study is looking for

  • Followed by pediatric hematology/oncology
  • Receiving recombinant Erwinia asparaginase for treatment of malignancy

Age in the registry: 1 year to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Mayo Clinic in Rochester
Coordinator of this site? Confirm its status
RochesterUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.