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Jaktinib Versus Hydroxycarbamide in Subjects With Intermediate-2 or High-risk Myelofibrosis

Phase 3
Completed
Conditions
Myelofibrosis
Interventions
Registration Number
NCT04617028
Lead Sponsor
Suzhou Zelgen Biopharmaceuticals Co.,Ltd
Brief Summary

This study is to determine the efficacy of Jaktinib versus Hydroxycarbamid in participants with Intermediate-2 or High-risk myelofibrosis

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
105
Inclusion Criteria
  • Age ≥ 18 years old,either male or female;
  • Subjects diagnosed with a PMF according to World Health Organiztion criteria (2016 Edition), or patients diagnosed with a Post-PV-MF or Post-EF-MF according to International Working Group for Myeloproliferative Neoplasms Research and Treatment criteria;
  • High risk or intermediate-2 risk as defined by the Dynamic International Prognostic Scoring System (DIPSS) for Primary Myelofibrosis;
  • Subjects have no plan for stem cell transplantation in the near future;
  • Life expectancy of > 24 weeks;
  • ECOG performance status of 0-1;
  • Palpable splenomegaly at least 5 cm below left costal margin;
  • Peripheral blood blast count ≤ 10%;
  • Subjects who have not yet received treatment with a JAK inhibitor, or Subjects who have been treated with JAK inhibitors for ≤10 days;
  • Subjects have not received growth factor, thrombopoietin mimetics or platelet transfusion(s) within 2 weeks before the randomization; ANC≥ 1.0×10^9/L, platelet count ≥ 100×10^9/L within 2 days before the randomization;
  • Normal functions in major organs within 7 days before the randomization, fulfilling the following criteria: ALT and AST ≤ 2.5×ULN; DBIL and TBIL ≤ 2.0×ULN; serum creatinine ≤ 1.5×ULN;
  • If the subject is receiving any anti-myelofibrosis treatment (except for JAK inhibitors and hydroxyurea) at screening, the dosing regimen must remain unchanged for at least 2 weeks before screening. If the investigator judges that there is no need to continue to use, stop the use of thalidomide, androgens and prednisone> 10 mg during screening. The drugs used to improve anemia should be stopped for at least 6 half-lives or 2 weeks before randomization(whichever is the longer);
  • If the subject is receiving Hydroxycarbamide treatment at screening, the drug must be discontinued ≥ 2 weeks before the randomization;
  • Meet the requirements of the ethics committee and willing to sign the informed consent form;
  • Ability to comply with trial and follow-up procedures.
Exclusion Criteria
  • Subjects with any significant clinical and laboratory abnormalities which may affect the safety evaluation, such as uncontrolled diabetes, uncontrolled hypertension after taking two or more hypotensive drugs, peripheral neuropathy;
  • Subjects with congestive heart failure, uncontrolled or unstable angina or myocardial infarction, cerebrovascular accident, or pulmonary embolism within 24 weeks prior to screening;
  • Subjects who have not fully recovered from surgical operation within 4 weeks prior to screening;
  • Subjects suffering from arrhythmia and requiring treatment at screening;
  • Subjects with clinical symptoms of active bacterial, viral, parasitic or fungal infections requiring treatment at screening;
  • Chest X-rays suggest an active lung infection at screening;
  • Subjects who had active tuberculosis infection within 48 weeks before screening;γ-Interferon release test suggests latent tuberculosis infection at screening;
  • Subjects who had undergone splenectomy, or received radiotherapy to the spleen within 48 weeks before screening;
  • Subjects with known human immunodeficiency virus (HIV), known active infectious Hepatitis B (HepB), and/or known active infectious Hepatitis C (HepC);
  • Subjects with epilepsy or patients who have received psychotropic drug or sedatives during screening;
  • Female subjects who are pregnant, currently breastfeeding, planning to become pregnant;Subjects who are unable to adopt effective contraceptive methods during the study; Male subjects who did not use condoms during the dosing period and within 2 days after the last dose
  • Subjects who had experienced malignant tumors within the past 5 years (except for adequately treated local basal cell carcinoma of the skin and cervical carcinoma in situ that have been cured);
  • Subjects who are unsuitable to the trial in combination with other serious diseases, as identified by the investigator;
  • Subjects with suspected allergies to Jaktinib or its excipient;
  • Subjects who have participated in another clinical trial of a new drug or medical instrument within 12 weeks before screening.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
JaktinibPlacebo to match HydroxycarbamideParticipants will receive Jaktinib plus placebo to match Hydroxycarbamide.
HydroxycarbamideHydroxycarbamide TabletsParticipants will receive Hydroxycarbamide plus placebo to match Jaktinib.
HydroxycarbamidePlacebo to match JaktinibParticipants will receive Hydroxycarbamide plus placebo to match Jaktinib.
JaktinibJaktinibParticipants will receive Jaktinib plus placebo to match Hydroxycarbamide.
Primary Outcome Measures
NameTimeMethod
Splenic response rate at Week 24Week 24

Splenic response rate at Week 24 is defined as the proportion of participants achieving a ≥ 35% reduction in spleen volume at Week 24 from baseline as measured by MRI or CT

Secondary Outcome Measures
NameTimeMethod
Proportion of transfusion dependent patients converted to non-transfusion dependent patients at baselineFrom start of drug administration up to 7 days after last dose of study treatment

Trial Locations

Locations (1)

The First Affiliated Hospital of Medical School of Zhejiang University

🇨🇳

Hangzhou, Zhejiang, China

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