Difference between revisions of "Asciminib (Scemblix)"

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*2022-03-28:  Newly indicated for the treatment of [[Chronic myeloid leukemia|chronic myelogenous leukemia]] with resistance or intolerance to prior drug therapies.
 
*2022-03-28:  Newly indicated for the treatment of [[Chronic myeloid leukemia|chronic myelogenous leukemia]] with resistance or intolerance to prior drug therapies.
 
==Also known as==
 
==Also known as==
*'''Code name:''' ABL001
+
*'''Code name:''' ABL-001
 
*'''Brand name:''' Scemblix
 
*'''Brand name:''' Scemblix
  

Revision as of 02:09, 11 August 2023

Mechanism of action

From the NCI Drug Dictionary: An orally bioavailable, allosteric Bcr-Abl tyrosine kinase inhibitor with potential antineoplastic activity. Designed to overcome resistance, asciminib binds to the Abl portion of the Bcr-Abl fusion protein at a location that is distinct from the ATP-binding domain, and is a so-called STAMP (Specifically Targeting the ABL Myristoyl Pocket) inhibitor. This binding results in the inhibition of Bcr-Abl-mediated proliferation and enhanced apoptosis of Philadelphia chromosome-positive (Ph+) hematological malignancies.

Diseases for which it is used

History of changes in FDA indication

  • 2021-10-29: Granted accelerated approval for patients with Philadelphia chromosome-positive chronic myeloid leukemia (Ph+ CML) in chronic phase (CP), previously treated with two or more tyrosine kinase inhibitors (TKIs). (Based on ASCEMBL)
    • 2022-10-12: Converted to regular approval.
  • 2021-10-29: Approved for adult patients with Ph+ CML in CP with the T315I mutation. (Based on CABL001X2101)

History of changes in EMA indication

  • 2022-08-25: Initial authorization

History of changes in Health Canada indication

  • 2022-06-22: Initial notice of compliance

History of changes in PMDA indication

Also known as

  • Code name: ABL-001
  • Brand name: Scemblix