Crisantaspase 10,000unit powder for solution for injection vials
Requires a prescription from a doctor or prescriber
Asparaginase <em>Erwinia chrysanthemi</em> is an asparaginase-specific enzyme derived from <em>Erwinia</em> <em>chrysanthemi</em> used as an anticancer agent.
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Erwinase 10,000unit powder for solution for injection vials
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
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Codes for healthcare professionals and prescribing systems
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing all 28 studies.
Reviews & meta-analyses: 1 · Trials: 2 · 2012–2026
Showing all 28 studies, sorted by most relevant.
Martina Chiu, Saverio Tardito, Serena Pillozzi, et al.
British Journal of Cancer, 2014
- Glutamine
- Antineoplastic Agents
- Asparaginase
Renee Potashner, T. Taylor, Ally Sarna, et al.
JCO Clinical Cancer Informatics, 2025
- Antineoplastic Agents
- Asparaginase
- Medical Order Entry Systems
K. Torres-Obreque, E. K. Kleingesinds, João H. P. M. Santos, et al.
Preparative Biochemistry & Biotechnology, 2023
- Asparaginase
- Polyethylene Glycols
- Enzyme Stability
K. Hameed, Amol C Shetty, A. Emadi
Blood, 2023
CADTH
Canadian Journal of Health Technologies, 2023
Reactions Weekly, 2025
Reactions Weekly, 2025
Reactions Weekly, 2024
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
None known
Half-life
18.2 hours
Mechanism
Asparaginase Erwinia chrysanthemi is a tetrameric enzyme made up of four identic…
Food interactions
None known
Human targets
None mapped
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
80 years
Half-life
18.2 hours
Protein binding
Volume of distribution
5 L
[L1448]…
Metabolism
[L34719]…
Elimination
[L34719]
Clearance
0.31 L/h
[L34719]
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Asparaginase Erwinia chrysanthemi was first approved by the FDA in November 2011 to treat patients with acute lymphoblastic leukemia (ALL) who are allergic to E. coli-derived asparaginase: it has been used as part of multi-agent chemotherapy.[L149] In June 2021, the recombinant form of asparaginase Erwinia chrysanthemi was approved by the FDA as a component of a chemotherapy regimen to treat acute lymphoblastic leukemia and lymphoblastic lymphoma in adult and pediatric patients who are allergic to the E. coli-derived asparaginase.[L34714]
[L149][L34719]
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 63 interactions
[L149]
In clinical trials, the most common adverse effects were hypersensitivity reactions, pancreatic toxicity, blood clots, hemorrhage, and liver toxicity.
[L34714]
Pancreatitis occurs in 8-14% of pediatric patients, with adolescents at the highest risk for developing this adverse event. Pancreatitis typically occurs after the first few weeks of asparaginase administration, which suggests this complication occurs from an underlying predisposition rather than a cumulative drug effect.
[A7464]
How the body processes this drug — absorption, distribution, metabolism, and elimination
[L149]
For asparaginase Erwinia chrysanthemi (recombinant)-rywn, the median tmax is 10 hours and the mean absolute bioavailability is 37% in healthy subjects.
[L34719]
[L34719]
Asparaginase Erwinia chrysanthemi has a shorter half-life compared with the E. coli-derived preparations.
[A7464]
[L1448]
The geometric mean (%CV) apparent volume of distribution of asparaginase Erwinia chrysanthemi (recombinant)-rywn was 1.48 L/m2 (49%).
[L34719]
While asparaginases are not detectable in cerebrospinal fluid, asparagine in cerebrospinal fluid is depleted with systemic administration of any formulation of asparaginases.
[L1448]
[L34719]
[L34719]
[L34719]
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Asparaginase Erwinia chrysanthemi
Matched from: Crisantaspase
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ATC classifications (Wikidata)
Linked open data from Wikidata (Q105296036), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication.