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Suspected adverse reactions reported for Treosulfan
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
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Suspected adverse reactions reported for Treosulfan
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3 branded products available
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.
NHS prescribing volume and spending trends
Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(3)
Treosulfan with fludarabine for malignant disease before allogeneic stem cell transplant (TA640)
Treosulfan with fludarabine before allogeneic stem cell transplant for people aged 1 month to 17 years with non-malignant diseases (terminated appraisal) (TA945)
Non-Hodgkin lymphoma: diagnosis and management (NG52)
Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
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Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
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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 the 50 most relevant studies.
Reviews & meta-analyses: 10 · Randomised trials: 9 · 1998–2026
Showing the 50 most relevant studies, sorted by most relevant.
Wanliang Wu, Ning Xue, Hanfang Yang, et al.
Journal of Pediatric Hematology/Oncology, 2023
D. Beelen, R. Trenschel, M. Stelljes, et al.
The Lancet. Haematology, 2020
M. Rehman, M. K. Khan suheb, Haddaya Umar, et al.
Journal of Clinical Oncology, 2023
Abdulrahman Nasiri, Eman M. Nagiub, Mahmoud Aljurf, et al.
Journal of Clinical Medicine, 2026
Background: Allogeneic hematopoietic stem cell transplantation (allo-HCT) is the only curative therapy for myelofibrosis (MF), but its use is limited by substantial transplant related morbidity and mortality, particularly in older or comorbid patients. Treosulfan has emerged as a less toxic alternative to busulfan, with potential advantages in myeloablative and reduced intensity conditioning. Methods: We conducted a comprehensive, multi-database literature search (PubMed, Scopus/EMBASE, Cochrane Library, Web of Science, and grey literature) for studies published between 2000 and 2025 evaluating treosulfan-based conditioning in MF patients undergoing allo-HCT. Data on patient characteristics, conditioning regimens, engraftment, graft-versus-host disease (GVHD), and survival outcomes were synthesized. Results: Eight studies including more than 800 patients were analyzed. Treosulfan was most commonly combined with fludarabine, with or without additional agents. Engraftment rates were consistently high at 94 to 100%, with low non-relapse mortality (NRM) and favorable progression-free survival (PFS). An EBMT registry study demonstrated superior survival and significantly lower NRM compared with busulfan based regimens. Benefits were observed across older patients, alternative donors, and second transplants. Higher treosulfan doses were associated with increased toxicity in some cohorts. Conclusions: Treosulfan based conditioning offers an effective and better tolerated option for MF transplantation. Prospective trials are needed to refine dosing and patient selection.
Abstract licence: CC BY 4.0
Hafsa Shahid, Mudassar Nisar, Fatima Hussain, et al.
Blood, 2025
Ahmad Zulaid, Mahnoor Baloch, Faiqa Amin, et al.
Blood, 2025
M. Faheem, F. Sawaira, Sai Sushrutha Mudupula Vemula, et al.
Blood, 2025
Sheng Zhu, Gang Liu, Jing Liu, et al.
Frontiers in Oncology, 2020
K. Sykora, R. Beier, A. Schulz, et al.
Bone Marrow Transplantation, 2023
- Graft vs Host Disease
- Hematopoietic Stem Cell Transplantation
- Busulfan
D. Beelen, M. Stelljes, P. Remenyi, et al.
American Journal of Hematology, 2022
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
0.4 hours
Mechanism
Treosulfan - specifically its active epoxide metabolites - function as a DNA alk…
Food interactions
None known
Human targets
1 target
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
211 hr
[L52550]
Half-life
0.4 hours
[L52550]
Volume of distribution
[L52550]
Metabolism
Elimination
42%
[L52550]…
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
It was approved by the EMA in June 2019[L16965] and by the FDA in January 2025 for use in combination with [fludarabine].[L52575]
[L52245]
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 298 interactions
[L52245]
The principal toxic effect of treosulfan in cases of overdose are myeloablation and prolonged pancytopenia, mucositis, skin toxicity, nausea, vomiting and gastritis.
[L52245]
Avoid exceeding the recommended treosulfan dosage.
[L52245]
In case of overdosage, monitor blood counts frequently and provide vigorous supportive measures as medically indicated.
In mice, the oral LD50 is 3360 mg/kg body weight and the intravenous LD50 is >2500 mg/kg body weight.
[L52545]
In rats the oral LD50 is 2575 mg/kg body weight and the intraperitoneal LD50 is >2860 mg/kg body weight.
[L52545]
How the body processes this drug — absorption, distribution, metabolism, and elimination
[L52550]
[L52550]
[L52550]
[L52550][A265130]
Treosulfan itself is a CYP2D6 substrate, and its monoepoxide intermediate SS-EBDM is a CYP2C8 substrate.
[L52550]
[L52550]
Enzymes involved in drug metabolism — important for understanding drug interactions
ATC L01AB02
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)
Treosulfan
Additional database identifiers
Drugs Product Database (DPD)
2109
ChemSpider
8057780
ZINC
ZINC000001671094
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2625
GenAtlas
CYP2D6
GeneCards
CYP2D6
GenBank Gene Database
M20403
GenBank Protein Database
181350
Guide to Pharmacology
1329
UniProt Accession
CP2D6_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2622
GenAtlas
CYP2C8
GeneCards
CYP2C8
GenBank Gene Database
M17397
Guide to Pharmacology
1325
UniProt Accession
CP2C8_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2621
GeneCards
CYP2C19
GenBank Gene Database
M61854
GenBank Protein Database
181344
Guide to Pharmacology
1328
UniProt Accession
CP2CJ_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2637
GenAtlas
CYP3A4
GeneCards
CYP3A4
GenBank Gene Database
M18907
Guide to Pharmacology
1337
UniProt Accession
CP3A4_HUMAN
DrugBank citations
If you use DrugBank data in your research, please cite the following publications:
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Structured knowledge from the free knowledge base
ATC classifications (Wikidata)
Linked open data from Wikidata (Q7838652), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication.