DelveInsight’s, “Chronic Myelomonocytic Leukemia Pipeline Insight 2024” report provides comprehensive insights about 20+ companies and 22+ pipeline drugs in Chronic Myelomonocytic Leukemia pipeline landscape. It covers the pipeline drug profiles, including clinical and nonclinical stage products. It also covers the therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.
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Key Takeaways from the Chronic Myelomonocytic Leukaemia Pipeline Report
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Chronic Myelomonocytic Leukaemia Emerging Drugs Profile
Ruxolitinib is a selective Janus kinase (JAK) inhibitor primarily used for treating myelofibrosis and polycythemia vera, and it has shown promise in chronic myelomonocytic leukemia (CMML). In CMML, ruxolitinib targets the JAK1 and JAK2 pathways, which are crucial for cytokine signaling and hematopoiesis. The mechanism of action involves inhibiting the dysregulated JAK-STAT signaling pathway, which is often activated in myeloproliferative neoplasms, leading to abnormal cell proliferation and inflammation. Clinical trials have demonstrated that ruxolitinib can reduce splenomegaly and improve disease-related symptoms in CMML patients, particularly those with high symptom burdens or splenomegaly, by decreasing inflammatory cytokines and promoting hematologic improvement. Currently, the drug is in Phase II stage of its development for the treatment of CMML.
NMS-03592088 is a novel, potent inhibitor of FLT3, KIT and CSF1R, all relevant targets in AML. NMS-03592088 showed superior preclinical activity compared with approved FLT3 inhibitors in different FLT3-driven models. In addition, NMS-03592088 is active on FLT3 gatekeeper mutation F691L causing resistance to f irst generation FLT3 inhibitors. Currently, the drug is in Phase I/II stage of its clinical trial for the treatment of Chronic Myelomonocytic Leukemia (CMML).
IO-202 is a first-in-class IgG1 antibody with specific, high-affinity binding to LILRB4 and depletes LILRB4 positive cells via antibody-dependent cellular cytotoxicity and antibody-dependent cellular phagocytosis. As such, IO-202 is a targeted therapy with broad potential in blood cancers and autoimmune and inflammatory diseases.The U.S. Food and Drug Administration granted IO-202 Fast Track Designations for the treatment of patients with relapsed or refractory acute myeloid leukemia (AML) and relapsed or refractory CMML, respectively. The FDA has also granted IO-202 Orphan Drug Designations for the treatment of AML and CMML, respectively. Currently, the drug is in Phase I stage of its clinical trial for the treatment of CMML.
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Chronic Myelomonocytic Leukemia pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration
Chronic Myelomonocytic Leukaemia Products have been categorized under various Molecule types such as
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Scope of the Chronic Myelomonocytic Leukaemia Pipeline Report
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