Inqovi (decitabine and cedazuridine) vs Daurismo (glasdegib)
Inqovi (decitabine and cedazuridine) vs Daurismo (glasdegib)
Inqovi (decitabine and cedazuridine) is an oral hypomethylating agent used for the treatment of adults with myelodysplastic syndromes (MDS), including certain types of chronic myelomonocytic leukemia (CMML). Daurismo (glasdegib) is an oral hedgehog pathway inhibitor indicated in combination with low-dose cytarabine for the treatment of newly diagnosed acute myeloid leukemia (AML) in adults who are 75 years or older or who have comorbidities that preclude the use of intensive induction chemotherapy. When deciding between Inqovi and Daurismo, it is crucial to consider the specific diagnosis (MDS/CMML vs. AML), patient age, comorbidities, and the potential side effects, as these factors will guide the choice of treatment in consultation with a healthcare provider.
Difference between Inqovi and Daurismo
Metric | Inqovi (decitabine and cedazuridine) | Daurismo (glasdegib) |
---|---|---|
Generic name | Decitabine and cedazuridine | Glasdegib |
Indications | Myelodysplastic syndromes (MDS), including previously treated and untreated, de novo and secondary MDS with the following French-American-British subtypes: refractory anemia, refractory anemia with ringed sideroblasts, refractory anemia with excess blasts, and chronic myelomonocytic leukemia, as well as intermediate-1, intermediate-2, and high-risk International Prognostic Scoring System groups. | Acute myeloid leukemia (AML) for newly-diagnosed patients aged 75 years or older or who have comorbidities that preclude use of intensive induction chemotherapy, in combination with low-dose cytarabine. |
Mechanism of action | Decitabine: hypomethylating agent; Cedazuridine: cytidine deaminase inhibitor. | Hedgehog pathway inhibitor. |
Brand names | Inqovi | Daurismo |
Administrative route | Oral | Oral |
Side effects | Fatigue, constipation, hemorrhage, myalgia, mucositis, arthralgia, nausea, dyspnea, diarrhea, rash, dizziness, febrile neutropenia, edema, headache, cough, decreased appetite, upper respiratory tract infection, pneumonia, and transaminase increased. | Anemia, fatigue, hemorrhage, febrile neutropenia, musculoskeletal pain, nausea, edema, thrombocytopenia, dyspnea, decreased appetite, dysgeusia, mucositis, constipation, and rash. |
Contraindications | Hypersensitivity to decitabine, cedazuridine, or any component of the formulation. | Hypersensitivity to glasdegib or any component of the formulation. |
Drug class | Hypomethylating agent, Cytidine deaminase inhibitor | Hedgehog pathway inhibitor |
Manufacturer | Astellas Pharma US, Inc. | Pfizer Inc. |
Efficacy
Efficacy of Inqovi for Leukemia
Inqovi, which is a combination of decitabine and cedazuridine, is specifically indicated for the treatment of adult patients with myelodysplastic syndromes (MDS), including previously treated and untreated, de novo and secondary MDS with the following French-American-British subtypes (refractory anemia, refractory anemia with ringed sideroblasts, refractory anemia with excess blasts, and chronic myelomonocytic leukemia) and intermediate-1, intermediate-2, and high-risk International Prognostic Scoring System groups. This oral hypomethylating agent has shown efficacy in clinical trials by improving the hematologic parameters and reducing the need for transfusions. The effectiveness of Inqovi is measured by the rate of complete remission (CR), duration of CR, and overall response rate (ORR), which includes CR and partial remission (PR).
Results from pivotal clinical trials demonstrate that Inqovi, when used in the appropriate patient population, can lead to a significant improvement in these outcomes. Patients treated with Inqovi have been observed to achieve higher rates of complete remission compared to those who received alternative treatments. The duration of these remissions also plays a critical role in the management of MDS, as longer remissions are associated with improved quality of life and potentially better long-term outcomes.
Efficacy of Daurismo for Leukemia
Daurismo (glasdegib) is approved for the treatment of newly-diagnosed acute myeloid leukemia (AML) in adult patients who are 75 years of age or older, or who have comorbidities that preclude the use of intensive induction chemotherapy. Glasdegib, when used in combination with low-dose cytarabine (LDAC), has shown a significant improvement in overall survival compared to LDAC alone. The efficacy of Daurismo is primarily evaluated based on overall survival, event-free survival, and the rate of complete remission with full or partial hematologic recovery.
In clinical studies, patients treated with Daurismo in combination with LDAC had a median overall survival that was notably longer than that of patients who received LDAC alone. The combination therapy has been associated with a higher rate of complete remission, indicating that Daurismo can be an effective treatment option for older patients with AML or those who cannot tolerate more aggressive chemotherapy regimens. While the treatment does not cure AML, it can provide a significant survival benefit and improve the quality of life for patients with this challenging and often aggressive disease.
Regulatory Agency Approvals
Inqovi
Daurismo
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