DRKS00033264招募中不适用
A non-interventional study of melphalan flufenamide (melflufen, Pepaxti) in combination with dexamethasone in patients with relapsed and/or refractory multiple myeloma (RRMM) according to the approved label. - OP-113 / HARBOUR
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 one（—）
- 性别
- All
入选标准
- •1. The patient fulfils basic eligibility criteria as described in the observational plan
- •2. Be at least 18 years of age.
- •3. Ability to provide signed and dated informed consent.
- •4. Decision for treatment with the combination therapy melflufen and dexamethasone is made before inclusion in the study.
排除标准
- •1. Patients who are currently participating in any interventional clinical study (unless the patient only remains in survival follow-up).
- •2. Any assessment of effectiveness of ongoing melflufen treatment has been performed.
- •3. Previous treatment with melflufen, or ongoing treatment with melflufen has been longer than 28 days.
研究者
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