A Study of Erwinaze Administered Intravenously in Patients Who Had an Allergy to Frontline Asparaginase Therapy



Status:Completed
Conditions:Blood Cancer, Lymphoma
Therapuetic Areas:Oncology
Healthy:No
Age Range:1 - 30
Updated:7/16/2013
Start Date:July 2012
End Date:December 2013
Contact:Colleen Gramkowski
Email:colleen.gramkowski@jazzpharma.com
Phone:215-867-4919

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Phase II, An Open Label, Single Arm, Multi-Center Pharmacokinetic Study of Intravenous Erwinaze (Asparaginase Erwinia Chrysanthemi)Following Allergy to Native E. Coli Asparaginase (Elspar or Kidrolase), Pegaspargase (Oncaspar) or Calaspargase Pegol (EZN-2285) in Children, Adolescents and Young Adults With Acute Lymphoblastic Leukemia (ALL) or Lymphoblastic Lymphoma.


This study will utilize Erwinaze via intravenous administration in patients between the
ages of 1 and 30 who have experienced an allergy to their frontline therapy. The study will
determine the proportion of patients with 2 day nadir serum asparaginase activity levels
that are >0.1 IU/mL during the first 2 weeks of treatment with 3 times per week IV dosing.


Inclusion Criteria:

- Diagnosis of Acute Lymphoblastic Leukemia (ALL) or Lymphoblastic Lymphoma,

- Ages >/= 1 and
- Undergoing asparaginase treatment for ALL or lymphoblastic lymphoma

- Documented Grade 2 or higher hypersensitivity reaction to native or pegylated E. coli
asparaginase or Calaspargase pegol

- Must have two remaining weeks of native E. coli asparaginase treatment or 1 remaining
dose of either Pegaspargase or Calaspargase pegol

- Direct bilirubin less than or equal to Grade 2

- Amylase and lipase within normal limits (per institutional standards)

- signed informed consent byt he patient is greater than or equal to 18 years or by the
parent if the patient is younger than 18 years old.

Exclusion Criteria:

-
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Falls Church, Virginia 22042
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4650 Sunset Blvd
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4401 Penn Avenue
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501 6th Ave S
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9000 W Wisconsin Ave #270
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