A Phase II/III, Randomized, Double-Blind, Placebo-Controlled Trial of Uridine Supplementation in HIV Lipoatrophy
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 167
- 试验地点
- 30
- 主要终点
- Change in Limb Fat (g) From Baseline
研究概览
简要总结
Lipoatrophy, the loss of body fat from particular areas of the body, is a common side effect of antiretroviral therapy (ART). The purpose of this study was to determine the effectiveness of uridine supplementation in treating HIV infected individuals on stable ART with lipoatrophy.
详细描述
Lipoatrophy is a distressing long-term complication of ART and is associated with decreased quality of life, an increased risk of cardiovascular disease, and nonadherence to ART. The cause of lipoatrophy in HIV-infected individuals receiving ART is not completely understood. However, past research suggests that mitochondrial toxicity in subcutaneous adipose tissue caused by thymidine analogue nucleoside analogues may be responsible for the development of lipoatrophy.
Uridine is a nucleoside that has been shown to be an effective supplement in treating individuals with mitochondrial toxicity. NucleomaxX is a food supplement that consists of mitocnol, a sugar cane extract that has a high content of nucleosides, including uridine. The purpose of this study was to evaluate the effects of uridine supplementation in the form of NucleomaxX on limb fat in HIV-infected individuals receiving stable ART containing stavudine (d4T) or zidovudine (ZDV). In addition, this study evaluated the safety and tolerability of NucleomaxX.
This study lasted for 48 weeks. Participants were randomly assigned to one of two treatment arms, stratified by d4T or ZDV use. Arm A participants received NucleomaxX for uridine, while Arm B participants received a placebo for NucleomaxX. Participants in both arms received their assigned intervention three times per day, every other day, for the duration of the study. There were 8 study visits over the 48-week study duration. Blood collection and a physical exam occurred at all study visits, and participants completed an adherence assessment at most visits. Participants underwent dual energy X-ray absorptiometry scans (DEXA) within 14 days prior to or following the screening visit and at other selected visits. Specific fasting tests for glucose and lipid levels occurred at selected visits. ART was not provided by this study.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Care Provider)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •HIV-1 infected
- •Stable ART containing zidovudine or stavudine for at least 12 consecutive weeks prior to study entry
- •Cumulative ART with zidovudine or stavudine for at least 24 weeks prior to study entry
- •Viral load of 5,000 copies/ml or less within 45 days prior to study entry
- •Lipoatrophy in at least two of the following areas: face, arms, legs, OR buttocks
- •Not planning to add to or change current vitamin supplementation
- •Willing to use acceptable forms of contraception
排除标准
- •Life expectancy of less than 12 months
- •Currently enrolled in or planning to enroll in an ART interruption study
- •Plans to change current ART regimen
- •Liver failure at anytime prior to study entry
- •Greater than Grade 2 diarrhea or vomiting within 7 days prior to study entry
- •Current AIDS-defining opportunistic infection or illness. Individuals with cutaneous Kaposi's sarcoma not requiring chemotherapy are not excluded.
- •Currently receiving insulin or oral hypoglycemic products for diabetes mellitus
- •Systemic cancer chemotherapy or immunomodulating agents within 30 days prior to study entry
- •Systemic steroids for a cumulative duration of longer than 4 weeks within the 6 months prior to study entry
- •Known allergy or sensitivity to study drug or any of its components
- •Severe lactose intolerance
- •Current drug or alcohol abuse or dependence
- •Clinically significant illness requiring systemic treatment or hospitalization
- •Chronic disability or serious illness that may affect body composition
- •Received an investigational drug other than NucleomaxX or uridine for lipoatrophy within 30 days prior to study entry
- •Certain abnormal laboratory values
- •Pregnancy or breastfeeding
研究组 & 干预措施
NucleomaxX
Participants received NucleomaxX for 48 weeks
干预措施: NucleomaxX (Drug)
Placebo
Participants received NucleomaxX placebo for 48 weeks
干预措施: NucleomaxX placebo (Drug)
结局指标
主要结局
Change in Limb Fat (g) From Baseline
时间窗: Baseline and Week 48
Limb fat was measured at baseline and visit week 48 using dual-energy x-ray absorptiometry (DEXA), and change from baseline to week 48 (week 48 - baseline) was estimated for the treatment groups.
次要结局
- Change in Creatine Kinase From Baseline (Week 48 - Baseline)(Baseline and Week 48)
- Time to Safety Events (Signs/Symptoms or Laboratory Abnormalities)(Through Week 48)
- Number of Subjects Discontinuing Study Medication(Through Week 48)
- Change in Limb Fat From Baseline (Week 24 - Baseline)(Baseline and Week 24)
- HIV-1 RNA Level(At Week 48)
- Change in CD4+ Count From Baseline (Week 48 - Baseline)(Baseline and Week 48)
- Change in Fasting Lactate From Baseline (Week 48 - Baseline)(Baseline and Week 48)
- Change in Fasting Glucose From Baseline (Week 48 - Baseline)(Baseline and Week 48)
- Change in Fasting Total Cholesterol From Baseline (Week 48 - Baseline)(Baseline and Week 48)
- Change in Fasting High-density Lipoprotein (HDL) Cholesterol From Baseline (Week 48 - Baseline)(Baseline and Week 48)
- Change in Fasting Non-HDL Cholesterol From Baseline (Week 48 - Baseline)(Baseline and Week 48)
- Change in Fasting Low-density Lipoprotein (LDL) Cholesterol From Baseline (Week 48 - Baseline)(Baseline and Week 48)
- Change in Fasting Triglycerides From Baseline (Week 48 - Baseline)(Baseline and Week 48)
- Change in Hemoglobin From Baseline (Week 48 - Baseline)(Baseline and Week 48)
- Change in Leukocytes From Baseline (Week 48 - Baseline)(Baseline and Week 48)