Anagrelide
| Clinical data | |
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| Trade names | Agrylin |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a601020 |
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| Routes of administration | By mouth |
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| Pharmacokinetic data | |
| Metabolism | Liver, partially through CYP1A2 |
| Elimination half-life | 1.3 hours |
| Excretion | Urine (<1%) |
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| ECHA InfoCard | 100.317.113 |
| Chemical and physical data | |
| Formula | C10H7Cl2N3O |
| Molar mass | 256.09 g·mol−1 |
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Anagrelide (Agrylin/Xagrid, Shire and Thromboreductin, AOP Orphan Pharmaceuticals AG) is a drug used for the treatment of essential thrombocytosis (also known as essential thrombocythemia), or overproduction of blood platelets. It also has been used in the treatment of chronic myeloid leukemia.[2]
Anagrelide controlled release (GALE-401) is in phase III clinical trials by Galena Biopharma for the treatment of essential thrombocytosis.[3]
- ^ "Prescription medicines: registration of new generic medicines and biosimilar medicines, 2017". Therapeutic Goods Administration (TGA). 21 June 2022. Retrieved 30 March 2024.
- ^ Voglová J, Maisnar V, Beránek M, Chrobák L (2006). "[Combination of imatinib and anagrelide in treatment of chronic myeloid leukemia in blastic phase]". Vnitr̆ní Lékar̆ství (in Czech). 52 (9): 819–22. PMID 17091608.
- ^ "Galena Biopharma Confirms Regulatory Pathway for GALE-401 (Anagrelide Controlled Release)". Galena Biopharma, Inc. (Press release). 2016-12-28 – via globenewswire.com.