EUCTR2021-004732-29-PT进行中(未招募)1 期
A Phase 3 Study of the Hepcidin Mimetic Rusfertide (PTG-300) in Patients with Polycythemia Vera
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 250
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Male and female subjects aged 18 (or the minimum country specific age of consent if >18) years or older.
- •3. Meet revised 2016 World Health Organization (WHO) criteria for the diagnosis of polycythemia vera and have either JAK2 V617F mutation or JAK2 exon 12 mutation
- •4. Phlebotomy requiring defined as:
- •a. At least 3 phlebotomies due to inadequate hematocrit control in 6 months before randomization or at least 5 phlebotomies due to inadequate hematocrit control in 1 year before randomization, and
- •5. CBC values immediately prior to randomization:
- •a. Hematocrit <45%,
- •b. WBC 4000/µL to 20,000/µL (inclusive), and
- •c. Platelets 100,000/µL to 1,000,000/µL (inclusive).
- •11. Subjects receiving cytoreductive therapy at randomization must be on a stable PV therapy regimen
- •12. Subjects treated with phlebotomy alone at randomization must have stopped cytoreductive therapy 2 to 6 months before screening.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 200
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 50
排除标准
- •1. Clinically meaningful laboratory abnormalities at Screening
- •2. Subjects who require phlebotomy at hematocrit levels lower than 45%.
- •4. Clinically significant thrombosis (e.g., deep vein thrombosis or splenic vein thrombosis) within 2 months prior to randomization.
- •5. Active or chronic bleeding within 2 months prior to randomization.
- •10. History of invasive malignancies within the last 5 years, except localized cured prostate cancer and cervical cancer.
- •11. Subjects with non-invasive non-melanomatous (e.g., squamous cell or basal cell carcinoma) skin cancer during screening unless adequately treated before randomization.
- •15. Received busulfan, pipobroman or 32Phosphorus within 7 months prior to screening.
研究者
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