ASPARLAS® calaspargase pegol for injection1 | |
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Indication in ALL | ASPARLAS® is indicated as a component of a multi-agent chemotherapeutic regimen for the treatment of ALL in pediatric and young adult patients age 1 to 21 years. |
Half-life | 16.1 days IV infusion1 Half-life based on PK data after a single dose of ASPARLAS® 2500 IU/m2 |
Recommended dose | 2500 U/m2 IV no more than every 21 days1 |
Shelf life | Proposed shelf life of 36 months. Store ASPARLAS® refrigerated at 2°C to 8°C in the original carton to protect from light. Do not shake or freeze product. Unopened vials may be stored at room temperature (15°C to 25°C) for no more than 48 hours. Diluted solution may be stored for up to 4 hours at room temperature (15°C to 25°C) or refrigerated at 2°C to 8°C for up to 24 hours. Discard any unused portion left in a vial. |
Data from separate Product Monographs and regulatory documents; comparative clinical significance has not been proven.
Consult the individual Product Monographs for complete dosing and administration information.
*The recommended dose of ASPARLAS® is 2500 U/m2 IV no more than every 21 days.
†The recommended dose of ONCASPAR® for patients with BSA >0.6 m2 and aged ≤21 years is 2500 U (equivalent to 3.3 mL ONCASPAR®)/m² body surface area IV or IM every 14 days.
‡The recommended dosage of RYLAZE™ is 25 mg/m2 on Monday and Wednesday and 50 mg/m2 IM on Friday, for a total of six doses to replace each planned dose of pegaspargase.
= intravenous infusion
= intramuscular
Data from separate Product Monographs; comparative clinical significance has not been proven.
See individual Product Monographs for complete dosing and administration information.
Learn more about Servier Canada’s treatment options in ALL
Consult the ASPARLAS® Product Monograph
aBFM: augmented Berlin-Frankfurt-Münster; AE: adverse event; ALL: acute lymphoblastic leukemia; ALP: alkaline phosphatase; ALT: alanine aminotransferase; aPTT: activated partial thromboplastin time; AST: aspartate aminotransferase; BFM: Berlin-Frankfurt-Munster; BSA: body surface area; CSF: cerebrospinal fluid; CTCAE: Common Terminology Criteria for Adverse Events; DFCI: Dana-Farber Cancer Institute; IM: intramuscular; IV: intravenous; NCCN: National Comprehensive Cancer Network®; NPAA: nadir plasma arparaginase activity; NSAA: nadir serum asparaginase activity; NSAID: non-steroidal anti-inflammatory drug; PD: pharmacodynamics; PK: pharmacokinetics; TDM: therapeutic drug monitoring.
* Comparative clinical significance has not been established.
† Fictitious cases. May not be representative of all patients.
‡ Clinical significance has not been established.
References:
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