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NCT06734637Recruiting

Efficacy and Safety of Peginterferon in ET and PV.

A Single-arm, Single-center Study to Explore the Safety and Efficacy of Pegylated Interferon Alpha in Chinese Patients With ET (Essential Thrombocythemia) and PV (Polycythemia Vera).

Source: ClinicalTrials.gov · Last updated 16 Dec 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is a single-arm, single-center study aims to recruit 40 participants with Essential Thrombocythemia (ET) and Polycythemia Vera (PV). Eligible participants will receive a subcutaneous injection of Peginterferon α-2b 180 mcg once a week and follow-up,and efficacy and safety will be evaluated.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
40 (estimated)
First submitted
11 Dec 2024
Start date
20 Nov 2024
Primary completion date
20 Nov 2026
Lead sponsor
Zhenya Hong
NCT number
NCT06734637

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From 20 Nov 2024 to the primary completion date, 20 Nov 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous treatment with Peginterferon α-2b.
  • ET patients who do not meet the criteria for cytoreductive therapy as per the 2016 Chinese Expert Consensus on Primary Thrombocythemia.

Other illness

  • Allergy to the active ingredient, α-interferon, or any excipients of this product.
  • History of psychiatric illness, or allergy to interferon.
  • Severe cardiac disease, liver insufficiency, chronic kidney disease, and neurological disorders (such as depression or mania).
  • History of other malignant tumors within the past three years.
  • Autoimmune chronic hepatitis.
  • Any condition deemed unsuitable for inclusion by the investigator.

Lab values

  • Plasma total bilirubin greater than twice the normal value.

Who the study is looking for

  • Meet the 2016 WHO diagnostic criteria for ET (Essential Thrombocythemia) and PV (Polycythemia Vera)
    • ET (Essential Thrombocythemia) major criteria:
    • Platelet count \> 450 \* 10\^9/L; (2) Bone marrow biopsy shows marked megakaryocytic proliferation with increased mature megakaryocyte volume and increased nuclear lobulation. There is no significant granulocytic proliferation, left shift, or erythroid proliferation, with grade 1 fibrosis observed in a few cases; (3) Does not meet the WHO diagnostic criteria for BCR-ABL1+ CML, PV, PMF, MDS, or other myeloproliferative neoplasms; (4) JAK2, CALR, or MPL mutation positive.
    • Secondary criteria: (1) Presence of a clonal marker or absence of evidence for reactive thrombocytosis.
    • The diagnosis of ET requires the fulfillment of all four main criteria, or the first three main criteria plus one secondary criterion.
    • PV (Polycythemia Vera) main criteria: (1) Hemoglobin \> 16.5 g/dL in males, \> 16 g/dL in females, or Hematocrit \> 49% in males, \> 48% in females, or an increase in red cell volume of 25% or more above the normal value; (2) Bone marrow biopsy shows increased cellularity inappropriate for age, with marked erythroid, granulocytic, and megakaryocytic proliferation, and the presence of mature megakaryocytes of varying sizes and morphologies; (3) JAK2 V617F mutation positive or JAK2 exon 12 mutation positive.
    • Secondary criteria: Serum Epo (Erythropoietin) level below the lower limit of the normal range.
    • The diagnosis of PV requires the fulfillment of three major criteria, or the first two main criteria plus one secondary criterion.
  • For ET patients, the criteria for cytoreductive therapy must be met, as follows:
    • (1) For patients without a history of thrombosis: Age ≥ 60 years, regardless of the presence of cardiovascular risk (CVR) or JAK2V617 mutation; Any age with a platelet count \> 1500 × 109/L. (2) For patients with a history of arterial thrombosis: Any age, regardless of the presence of CVR and JAK2V617 mutation; (3) For patients with a history of venous thrombosis: Any age, regardless of the presence of CVR and JAK2V617 mutation; 3.ECOG score ≤ 2. 4.Cardiac ejection fraction (EF) ≥ 60%. 5.The participant voluntarily signs the informed consent form.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Tongji Medical College, Huazhong University of Science and Technology
Coordinator of this site? Confirm its status
WuhanChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.