About this trial

This study evaluates the impact of calaspargase pegol (Cal-PEG) on the coagulation system in pediatric patients with acute lymphoblastic leukemia/lymphoma (ALL).

Eligibility criteria

Qualifiers

Age 2-21.5 years

Confirmed diagnosis of acute lymphoblastic leukemia/lymphoma

Planned treatment with Cal-PEG

Informed consent obtained from parents or guardians

Disqualifiers

Pre-existing coagulation disorders

Known hypersensitivity to asparaginase products

Liver failure

Any acute or chronic disease that is known to affect coagulation testing (e.g. nephrotic syndrome)

Trial design

Treatments tested in this trial

  • Non-Interventional Study

Treatment groups

15 Participants
are divided into 1 treatment group

Locations

1
Mayo Clinic in Rochester55905, RochesterMinnesota, United States

Sponsors and collaborators

Mayo Clinic

Lead sponsor