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临床试验/RPCEC00000115
RPCEC00000115已完成3 期

se of alpha interferon in the treatment of the maintenance phase of multiple myeloma.

Center for Genetic Engineering and Biotechnology (CIGB), in Havana.0 个研究点目标入组 65 人开始时间: 2011年5月19日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
65

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
N/a: Single Arm Study. Masking: Open. Control Group: Uncontrolled. Assignment: Single Group. Purpose: Treatment

入排标准

年龄范围
18 years 至 /A (No limit)(—)
性别
All

入选标准

  • 1) Patients over 18 years. 2) Willingness of the individual by signing written consent. 3) Patients with multiple myeloma stage II / III according to Salmon and Durie classification. 4) Patients who have received favorable response to chemotherapy with a minimum of 6 months of treatment.

排除标准

  • 1) Pregnancy or lactation. 2) Women of childbearing age who are hormonal contraceptive therapy or have no control over fertility. 3) Hypersensitivity to interferon or other preparations used in the study. 4) Acute or chronic liver (twice the normal value of TGP and TGO and / or total bilirubin > 1.5). 5) Decompensated heart failure. 6) Organic brain disease with symptoms that interfere with patient assessment so as to consent (eg Parkinson disease). 7) Major psychiatric disorder or other constraints that prevent the patient's consent. 8) Autoimmune diseases not related to multiple myeloma.

研究者

发起方
Center for Genetic Engineering and Biotechnology (CIGB), in Havana.

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