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Clinical Trial Summary

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 fruquintinib maleate tablet group, high-dose fruquintinib maleate tablet group, or the ruxolitinib tablet group. Stratification factors include the Dynamic International Prognostic Scoring System (DIPSS) risk classification (intermediate-2 and high risk)


Clinical Trial Description

n/a


Study Design


NCT number NCT06457425
Study type Interventional
Source Chengdu Zenitar Biomedical Technology Co., Ltd
Contact Liangkun Sun
Phone 15885742617
Email liangkunsun@zenitar.cn
Status Recruiting
Phase Phase 2
Start date May 6, 2024
Completion date July 6, 2026