About this trial
This trial adopts a multicenter, open-label, positive drug parallel control clinical trial design, planning to enroll approximately 75 MF participants. Eligible participants will be stratified and assigned in a 1:1:1 ratio to the low-dose flonoltinib maleate tablet group, high-dose flonoltinib maleate tablet group, or the ruxolitinib tablet group. Stratification factor include the Dynamic International Prognostic Scoring System (DIPSS) risk classification (intermediate-2 and high risk)
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age ≥ 18 years, no gender restrictions;
Diagnosed with primary myelofibrosis (PMF) according to WHO criteria (2016 edition) or post-polycythemia vera myelofibrosis (PPV-MF) or post-essential thrombocythemia myelofibrosis (PET-MF) according to IWG-MRT criteria;
Evaluated as intermediate-2 or high-risk myelofibrosis according to the Dynamic International Prognostic Scoring System (DIPSS) risk classification;
Expected survival ≥ 24 weeks;
Disqualifiers
Previous anticancer treatment-related toxic reactions have not recovered to grade 1 or below (excluding alopecia and conditions specified in inclusion criteria 8 and 9), or have not fully recovered from previous surgery (major surgery within 4 weeks);
Hypersensitivity, allergic to the investigational drug or its excipients;
Previous intolerance or resistance to ruxolitinib;
Use of JAK inhibitors within 4 weeks before the first dose;
Trial design
Parallel
Treatments tested in this trial
Flonoltinib 50mg
DrugFlonoltinib 50mg, QD
Flonoltinib 100mg
DrugFlonoltinib 100mg, QD
Ruxolitinib
DrugFor patients with platelet counts between 100×10\^9/L and 200×10\^9/L, the recommended starting dose is 15 mg twice daily (bid). For patients with platelet counts \>200×10\^9/L, the recommended starting dose is 20 mg bid. For patients with platelet counts between 50×10\^9/L and \<100×10\^9/L, the recommended maximum starting dose is 5 mg bid.
Treatment groups
Trial outcomes
Primary outcomes
Percentage of subjects with ≥35% reduction in spleen volume from baseline(Evaluation by IRC)
Percentage of subjects with ≥35% reduction in spleen volume from baseline(Evaluation by IRC)
Secondary outcomes
Percentage of subjects with ≥35% reduction in spleen volume from baseline (Evaluation by researcher)
Percentage of subjects with ≥35% reduction in spleen volume from baseline(Evaluation by researcher)
Percentage of subjects with ≥35% reduction in spleen volume from baseline (Evaluation by researcher)
Percentage of subjects with ≥35% reduction in spleen volume from baseline (Evaluation by researcher)
Percentage of subjects with ≥35% reduction in spleen volume from baseline (Evaluation by IRC)
Percentage of subjects with ≥35% reduction in spleen volume from baseline( Evaluation by IRC)
Percentage of subjects with ≥50% reduction in MPN-SAF TSS scale total symptom score
Percentage of subjects with ≥50% reduction in MPN-SAF TSS scale total symptom score
Sponsors and contacts
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