Difference between revisions of "Dasatinib (Sprycel)"
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==History of changes in FDA indication== | ==History of changes in FDA indication== | ||
===[[Chronic myeloid leukemia]]=== | ===[[Chronic myeloid leukemia]]=== | ||
− | * | + | *2006-06-28: Initial accelerated approval for the treatment of adults with chronic, accelerated, or myeloid or lymphoid blast phase [[Chronic myeloid leukemia | chronic myeloid leukemia]] with resistance or intolerance to prior therapy including [[Imatinib (Gleevec) | imatinib]]. ''(Based on CA180-013)'' |
− | ** | + | **2009-05-21: Converted to regular approval for the treatment of adults with chronic, accelerated, or myeloid or lymphoid blast phase [[Chronic myeloid leukemia | chronic myeloid leukemia]] with resistance or intolerance to prior therapy including [[Imatinib (Gleevec) | imatinib]]. ''(Based on CA180-035)'' |
− | *11 | + | *2007-11-08: New accelerated approval for the treatment of adults with chronic phase (CP) [[Chronic myeloid leukemia |chronic myeloid leukemia (CML)]] with resistance or intolerance to prior therapy, including imatinib mesylate. The new dosing regimen is 100 mg taken orally once daily. ''(New dosing instruction; based on CA180-034)'' |
− | *10 | + | *2010-10-28: Accelerated approval for newly diagnosed adults with [[Biomarkers#BCR-ABL1|Philadelphia chromosome-positive (Ph+)]] [[Chronic myeloid leukemia | chronic myeloid leukemia (CML)]] in chronic phase. ''(Approval expanded to the first-line setting; based on DASISION)'' |
− | ** | + | **2015-08-12: Converted to regular approval for newly diagnosed adults with [[Biomarkers#BCR-ABL1|Philadelphia chromosome-positive (Ph+)]] [[Chronic myeloid leukemia | chronic myeloid leukemia (CML)]] in chronic phase. ''(Based on DASISION)'' |
− | *11 | + | *2017-11-10: New indication for the treatment of pediatric patients with [[Biomarkers#BCR-ABL1|Philadelphia chromosome-positive]] [[Chronic myeloid leukemia |chronic myeloid leukemia]] in chronic phase. ''(Approval expanded to include the pediatric population; based on CA180-018 & CA180-226)'' |
===[[B-cell acute lymphoblastic leukemia, Ph-positive|Ph+ ALL]]=== | ===[[B-cell acute lymphoblastic leukemia, Ph-positive|Ph+ ALL]]=== | ||
− | * | + | *2006-06-28: Initial approval for the treatment of adults with [[Biomarkers#BCR-ABL1| Philadelphia chromosome-positive]] [[:Category:Acute lymphoblastic leukemias|acute lymphoblastic leukemia]] with resistance or intolerance to prior therapy. ''(Based on START-L)'' |
− | *12 | + | *2018-12-21: Approved for pediatric patients 1 year of age and older with newly diagnosed [[Biomarkers#BCR-ABL1|Ph+]] [[:Category:Acute lymphoblastic leukemias|ALL]] in combination with chemotherapy. ''(Based on COG AALL1122)'' |
==History of changes in EMA indication== | ==History of changes in EMA indication== | ||
− | *11 | + | *2006-11-20: Initial authorization |
+ | ==History of changes in Health Canada indication== | ||
+ | *2007-03-26: Initial notice of compliance with conditions | ||
+ | *2009-11-19: Conditions were met | ||
==Also known as== | ==Also known as== | ||
*'''Code name:''' BMS-354825 | *'''Code name:''' BMS-354825 | ||
Line 55: | Line 58: | ||
[[Category:EMA approved in 2006]] | [[Category:EMA approved in 2006]] | ||
[[Category:FDA approved in 2006]] | [[Category:FDA approved in 2006]] | ||
+ | [[Category:Health Canada approved in 2007]] | ||
[[Category:WHO Essential Cancer Medicine]] | [[Category:WHO Essential Cancer Medicine]] |
Revision as of 11:34, 31 March 2023
General information
Class/mechanism: Tyrosine kinase inhibitor of BCR-ABL, the SRC family (SRC, LCK, YES, FYN), c-KIT, EPHA2, and PDGFRβ. Binds to multiple conformations of the ABL kinase.[1][2][3]
Route: PO
Extravasation: n/a
For conciseness and simplicity, HemOnc.org currently will focus on treatment regimens and not list information such as: renal/hepatic dose adjustments, metabolism (including CYP450), excretion, monitoring parameters (although this will be considered for checklists), or manufacturer. Instead, for the most current information, please refer to your preferred pharmacopeias such as Micromedex, Lexicomp, UpToDate (courtesy of Lexicomp), or the prescribing information.[1]
Diseases for which it is used
Patient drug information
- Dasatinib (Sprycel) package insert[1]
- Dasatinib (Sprycel) patient drug information (Chemocare)[4]
- Dasatinib (Sprycel) patient drug information (UpToDate)[5]
History of changes in FDA indication
Chronic myeloid leukemia
- 2006-06-28: Initial accelerated approval for the treatment of adults with chronic, accelerated, or myeloid or lymphoid blast phase chronic myeloid leukemia with resistance or intolerance to prior therapy including imatinib. (Based on CA180-013)
- 2009-05-21: Converted to regular approval for the treatment of adults with chronic, accelerated, or myeloid or lymphoid blast phase chronic myeloid leukemia with resistance or intolerance to prior therapy including imatinib. (Based on CA180-035)
- 2007-11-08: New accelerated approval for the treatment of adults with chronic phase (CP) chronic myeloid leukemia (CML) with resistance or intolerance to prior therapy, including imatinib mesylate. The new dosing regimen is 100 mg taken orally once daily. (New dosing instruction; based on CA180-034)
- 2010-10-28: Accelerated approval for newly diagnosed adults with Philadelphia chromosome-positive (Ph+) chronic myeloid leukemia (CML) in chronic phase. (Approval expanded to the first-line setting; based on DASISION)
- 2015-08-12: Converted to regular approval for newly diagnosed adults with Philadelphia chromosome-positive (Ph+) chronic myeloid leukemia (CML) in chronic phase. (Based on DASISION)
- 2017-11-10: New indication for the treatment of pediatric patients with Philadelphia chromosome-positive chronic myeloid leukemia in chronic phase. (Approval expanded to include the pediatric population; based on CA180-018 & CA180-226)
Ph+ ALL
- 2006-06-28: Initial approval for the treatment of adults with Philadelphia chromosome-positive acute lymphoblastic leukemia with resistance or intolerance to prior therapy. (Based on START-L)
- 2018-12-21: Approved for pediatric patients 1 year of age and older with newly diagnosed Ph+ ALL in combination with chemotherapy. (Based on COG AALL1122)
History of changes in EMA indication
- 2006-11-20: Initial authorization
History of changes in Health Canada indication
- 2007-03-26: Initial notice of compliance with conditions
- 2009-11-19: Conditions were met
Also known as
- Code name: BMS-354825
- Brand name: Sprycel
References
Categories:
- Drugs
- Oral medications
- Mutation-specific medications
- Bcr-Abl inhibitors
- BTK inhibitors
- KIT inhibitors
- PDGFR inhibitors
- SRC inhibitors
- SYK inhibitors
- B-cell acute lymphoblastic leukemia medications
- Chronic myeloid leukemia medications
- Systemic mastocytosis medications
- EMA approved in 2006
- FDA approved in 2006
- Health Canada approved in 2007
- WHO Essential Cancer Medicine