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NCT07221656Not yet recruiting

Evaluation of Prolonged Asparaginase Activity Levels After Calaspargase Pegol Administration

Source: ClinicalTrials.gov · Last updated 2 Apr 2026

Brief summary (registry, in English)

This study evaluates the median duration of therapeutic serum asparaginase activity (SAA) levels after administration of calaspargase pegol (Cal-PEG) and the potential association between peak SAA levels and duration of therapeutic levels with toxicity in pediatric patients with acute lymphoblastic leukemia or lymphoma.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
20 (estimated)
First submitted
24 Oct 2025
Start date
1 Feb 2027
Primary completion date
31 Dec 2028
Lead sponsor
Mayo Clinic
NCT number
NCT07221656

What you commit to

  • Study type: Observational
  • Planned participants: 20
  • From 1 Feb 2027 to the primary completion date, 31 Dec 2028
  • 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.

Age

  • Age \> 21 years

Other

  • Patients who are actively enrolled on Children's Oncology Group (COG) trial AALL1732 in an inotuzumab containing arm
  • Pregnancy

Who the study is looking for

  • Acute lymphoblastic leukemia/lymphoma being treated by the pediatric hematology team
  • Receiving calaspargase as part of treatment for malignancy

Age in the registry: - to 21 years · 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 StatesUnknown status

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