Health Canada expands approval of Scemblix®, making it an option for newly diagnosed and previously treated chronic myeloid leukemia (CML) patients
- Scemblix® is first to show superior efficacy and a favourable safety and tolerability profile in a Phase III trial vs. all standard of care (SoC) therapies1,2
- Fifty percent of CML patients do not meet efficacy milestones (MMR) with current SoC and almost 25% discontinue or switch therapies within one year of treatments2
- Scemblix®, a new first-line option for adults with CML, is now approved for newly diagnosed and previously treated CML
In Canada, Scemblix® was previously approved for the treatment of adult patients with Ph+ CML-CP previously treated with two or more TKIs. Newly diagnosed patients will now have access to a treatment that has shown superior efficacy versus all standard of care (SoC) therapies and a favourable safety and tolerability profile.
"The approval of a new treatment option for newly diagnosed and previously treated Canadians living with CML is an important milestone," said
CML that is diagnosed in the chronic phase has a more favourable prognosis than CML that is diagnosed in the accelerated or blast phase. Although the Ph chromosome is present in everyone with CML, in rare cases it can't be found during testing. In general, Ph+ CML has a more favourable prognosis than Ph- CML.3
While TKIs have transformed CML into a chronic disease, efficacy, safety and tolerability challenges continue to hinder long-term treatment success for many patients. Many patients do not meet molecular response goals, and many discontinue or change treatment due to intolerance.4,5,6
"The approval of asciminib represents a significant step forward, expanding treatment options for CML patients," said Dr.
"We are proud that
The clinical effectiveness, safety and cost-effectiveness of Scemblix® is currently under review by Canada's
About Chronic Myeloid Leukemia (CML)
Chronic myeloid leukemia (CML) is a type of cancer that develops in the blood-forming cells of the bone marrow. In 95% of patients with CML, a genetic mutation produces an abnormal chromosome in bone marrow stem cells known as the
The Ph chromosome produces the BCR-ABL1 protein, which causes bone marrow to make too many abnormal white blood cells. These cells overcrowd healthy blood cells, which can be fatal if untreated.7
CML has three stages: chronic, accelerated, and blast phases. Most patients are diagnosed in the chronic phase, and with proper treatment, can often stay in this early stage without advancing further.7
According to the most recently available data, 665 Canadians were diagnosed with CML in 2019 and 140 Canadians died from CML in 2022.8
About Scemblix® (asciminib tablets)
Scemblix® is the first CML treatment that works by Specifically Targeting the ABL Myristoyl Pocket (referred to as a STAMP inhibitor in scientific literature).9,10 The current approved CML treatments are TKIs that target the adenosine triphosphate (ATP)-binding site (ATP-competitive).10
About the ASC4FIRST Trial
The approval of Scemblix® is based on results from the ongoing Phase III ASC4FIRST trial in patients newly diagnosed with Ph+ CML-CP.1 Data has shown:
- Nearly 20% more patients treated with Scemblix® achieved MMR versus investigator-selected (IS) SoC TKIs (imatinib, nilotinib, dasatinib and bosutinib) (68% vs. 49%, p < 0.001) and nearly 30% more patients achieved MMR versus imatinib alone (69% vs. 40%, p < 0.001) at week 48.1,2
- Scemblix® is the first CML treatment to show superior efficacy along with a favourable safety and tolerability profile verus imatinib and second generation TKIs.1,2
- In newly diagnosed Ph+ CML-CP patients, the most common adverse reaction (≥ 20%) was musculoskeletal pain. Serious adverse events occurred in 11% of patients who received Scemblix®. Serious adverse reactions in ≥ 1% included pancreatitis (1%).1,2
About Novartis
In Canada,
SCEMBLIX® is a registered trademark.
References
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1 Scemblix® (asciminib) 2025 Product Monograph. https://www.novartis.com/ca-en/content/scemblix. |
2 Hochhaus A, Wang J, |
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4 Hochhaus, A., & Ernst, T. 2021. TKI discontinuation in CML: How do we make more patients eligible? How do we increase the chances of a successful treatment-free remission? Hematology Am Soc Hematol Educ Program, 2021(1), 106–112. |
5 Hehlmann R, Cortes JE, Zyczynski T, et al. Tyrosine kinase inhibitor interruptions, discontinuations and switching in patients with chronic-phase chronic myeloid leukemia in routine clinical practice: SIMPLICITY. Am J Hematol. 2019;94(1):46-54. doi:10.1002/ajh.25306 |
6 Claudiani S, Chughtai F, Khan A. et al. Long-term outcomes after upfront second-generation tyrosine kinase inhibitors for chronic myeloid leukemia: managing intolerance and resistance. Leukemia. 2024;38:796 - 802. doi:10.1038/s41375-024-02187-w |
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9 Cortes JE, Hughes TP, Mauro MJ, et al. Asciminib, a First-in-Class STAMP Inhibitor, Provides Durable Molecular Response in Patients (pts) with Chronic Myeloid Leukemia (CML) Harboring the T315I Mutation: Primary Efficacy and Safety Results from a Phase 1 Trial. Oral presentation at: ASH Annual Meeting; |
10 Schoepfer J, Jahnke W, Berellini G, et al. Discovery of Asciminib (ABL001), an Allosteric Inhibitor of the Tyrosine Kinase Activity of BCR-ABL1. J Med Chem. 2018;61(18):8120-8135. doi:10.1021/acs.jmedchem.8b01040 |
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