JPRN-jRCTb030230286招募中1 期
The safety and efficacy of autologous peripheral blood mononuclear cell ex vivo culture amplified cells (MNC-QQ) for alopecia: Phase 1 / 2 clinical study - Phase 1/2 clinical trial using MNC-QQ for alopecia
Ikeda Yoshio0 个研究点目标入组 5 人开始时间: 2023年8月10日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 发起方
- 入组人数
- 5
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
- 年龄范围
- >= 18age old 至 < 75age old（—）
- 性别
- All
入选标准
- •1. Patients with written informed consent.
- •2. Patiens are at the age of 18 to 75 at the time of informed consent.
- •3. Patients affected alopecia and want to receive regenerative therapy.
排除标准
- •1. Patients with HbA1c(NGSP) more than 10.0 with the medication for diabetes.
- •2. Patients with systemic infection.
- •3. Patients with severe anemia.
- •4. Patients with malignancy, or within 5 years after recover from malignant tumor (10 years after breast cancer), except for cutaneous basal cell carcinoma.
- •5. Patients with hematopoietic disorders such as leukemia, myeloproliferative disease, marrow dysplasia syndrome.
- •6. Pregnant women.
- •7. Patients infected with HIV, active HBV, HCV, HTLV, or syphilis in screening test.
- •8. Patients not expect to live for a year or more.
- •9. Patients enrolled in any other clinical trial within 90 days before informed consent.
- •10. Patients who can't consent not to change medication.
- •11. Any other reason that the Clinical Researchers may have for considering a case unsuitable for the study.
研究者
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