RPCEC00000015招募中2 期
Evaluation of the immune potentiating effect of the NAcGM3/VSSP/Montanide ISA 51 formulation in HIV patients, phase II.
Center of Molecular Immunology(CIM)0 个研究点目标入组 118 人开始时间: 2010年12月29日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- 入组人数
- 118
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
- Randomized controlled trial. Masking: Double Blind. Control group: Placebo. Assignment: Parallel. Purpose: Treatment
入排标准
- 年龄范围
- 18 years 至 59 years(—)
- 性别
- All
入选标准
- •1. HIV patients with CD4+ values between 350 and 500 cells, relative CD4 values between 14 and 28% of total leukocytes, and viral load values between 30,000 and 100,000 copies.
- •2. Patients who have never undergone anti-retroviral treatment.
- •3. Patients of both sexes, aged 18 to 59 years.
- •4. Reproductive-age females with confirmed negative pregnancy test, using appropriate double contraceptive method (intrauterine devices, hormonal contraceptives, surgical sterilization, barrier methods).
- •5. Patients with Grade 0 to 2 Performance Status evaluation, according to WHO criteria.
- •6. Clinical laboratory parameters: a.-) hematopoietic parameters: Hb>100g/l- leukocytes> 4 x 109 cells/l, - granulocytes > 2 x 109 cells/l- platelets > 150 x 109 cells/l; b.-) Liver (not exceeding normal upper limit by three times)- bilirubin: 17 umol/l (LSN)- ALAT: 40 U/l (LSN)- ASAT: 40 U/L (LSN)- alkaline phosphatase: 279 U/l; c.-) Kidney: - serum creatinine < 132 umol/l; d.-) LDH (not exceeding twice the normal upper limit) – 240 - 480 U/l.
- •7. Patients who agree to participate in the trial by signing the Informed Consent.
排除标准
- •1. Patients with a diagnosis of previous oncoproliferative diseases.
- •2. Patients with other acute or chronic infectious diseases (Syphilis, Hepatitis B or C, Tuberculosis, Toxoplasmosis).
- •3. Patients with acute allergic states or history of severe allergic reactions.
- •4. Patients with autoimmune diseases or decompensated chronic diseases.
- •5. Inability to understand informed consent.
- •6. Patients who are receiving or have received in the three months prior to the study treatment with some other immunomodulator or vaccine preparation.
研究者
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