Study to Assess Efficacy and Safety of NS-018 Compared to BAT in Patients With Myelofibrosis (NCT04854096) | Clinical Trial Compass
TerminatedPhase 2
Study to Assess Efficacy and Safety of NS-018 Compared to BAT in Patients With Myelofibrosis
Stopped: The study was stopped due to a business decision.
United States, Germany7 participantsStarted 2023-01-31
Plain-language summary
This study will enroll male and female subjects who are 18 years of age or older with Primary Myelofibrosis, post-polycythemia Vera Myelofibrosis, or post-essential Thrombocythemia Myelofibrosis with severe thrombocytopenia (platelet count \<50,000/µL) including subjects with intermediate-2 or high-risk MF according to the Dynamic International Prognostic Scoring System (DIPSS).
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* Primary MF, post-PVMF or post-ETMF according to the DIPSS risk categories of intermediate-2 or high-risk MF
* Average platelet count of \<50,000/µL at Screening based on 2 measurements taken on different days; both measurements must be \<50,000/µL.
* ECOG performance status ≤2.
* Life expectancy \>6 months.
* Spleen volume of at least 450 cm3 measured by MRI (or by CT for applicable subjects).
* Total Symptom Score (TSS) ≥10 on the Myelofibrosis Symptom Assessment Form (MFSAF) version 4.0.
* Peripheral blast count \<10%.
* No MF-directed treatment for at least 2 weeks prior to initiation of NS-018, including JAK inhibitor, erythropoietic, thrombopoietic agent, or any use of corticosteroids for MF symptom or blood count management. Low dose corticosteroids \<10 mg/day prednisone or equivalent is allowed for non-MF purposes.
Exclusion Criteria:
* Active, uncontrolled systemic infection.
* Any prior treatment with more than two JAK inhibitors.
* Previous treatment with NS-018.
* Subjects actively receiving a concurrent investigational agent.
* Subjects with any unresolved AE greater than Grade 1 other than hematological AEs from previous anticancer therapy.
* Currently taking medication that is substantially metabolized by cytochrome P450 (CYP) 1A2 or CYP3A4 (see Appendix 5) or taking medication known to be strong inhibitors or inducers of CYP3A4 (see Appendix 5).
* Radiation therapy for splenomegaly within 6 months prior to study entry (screening).
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