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SCEMBLIX®▼(asciminib) is the first and only STAMP inhibitor1–3
Learn how the unique MOA of SCEMBLIX enhances its specificity in treating CML.1
SCEMBLIX targets a different site on BCR-ABL1 – the myristoyl pocket1-3
In people who do not have CML, the myristoyl pocket is occupied by the N-terminal portion of ABL1, maintaining the protein in an inactive conformation.4,5
In BCR-ABL1, the myristoyl pocket is vacant, activating the kinase.4,5
SCEMBLIX is a first-in-class STAMP inhibitor. Binding specifically to the myristoyl pocket, it potently inactivates BCR-ABL1 via allosteric inhibition.1
With its unique MOA, SCEMBLIX offers a different approach for treating CML.4–6
Learn about the efficacy of SCEMBLIX
ATP, adenosine triphosphate; CML, chronic myeloid leukaemia; MOA, mechanism of action; STAMP, specifically targeting the ABL1 myristoyl pocket; TKI, tyrosine kinase inhibitor.
SCEMBLIX is indicated for the treatment of adult patients with Philadelphia chromosome-positive chronic myeloid leukaemia (Ph + CML) in chronic phase (CP), previously treated with two or more tyrosine kinase inhibitors, and without a known T315I mutation.7
For further information please refer to the Summary of Product Characteristics.
References
- Réa D, et al. Blood 2021;138(21):2031–2041.
- Redaelli S, et al. J Clin Oncol 2009;27(3):469–471.
- Schoepfer J, et al. J Med Chem 2018;61(18):8120–8135.
- Hughes TP, et al. N Engl J Med 2019;381(24):2315–2326.
- Manley PW, et al. Leuk Res 2020;98:106458.
- Iacob RE, et al. PLoS One 2011;6(1):e15929.
- SCEMBLIX (asciminib) Summary of Product Characteristics.