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临床试验/NCT04654689
NCT04654689已完成2 期

Impact of the Combined Treatment of Curcumin and Resveratrol Liposomed Polyphenols With G04CB02 on the Clinical Improvement of ALS Patients

Fundación Universidad Católica de Valencia San Vicente Mártir1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2021年11月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
90
试验地点
1
主要终点
Electromyography

研究概览

简要总结

Amyotrophic lateral sclerosis (ALS) is a disease of an inflammatory nature, which causes progressive muscle weakness associated with cognitive and behavioural disorders. Pathogenically, it is characterised by loss of oxidative control, excitotoxicity due to excess glutamate and intestinal dysbiosis. In the absence of curative treatment, the aim of the study is to assess the impact at a clinical level of the combination of liposomed polyphenols to improve their effectiveness, with the drug G04CB02 which shows great anti-ALS properties by Molecular Topology methodology. A prospective, longitudinal, mixed, analytical, experimental and double-blind study is proposed, with a population sample of 60 patients distributed randomly in 30 patients in the intervention group who will receive treatment for 2 months, and 30 patients in the control group who will receive a placebo for the same period. The assessment will be at time 0, and at 2 months and 4 months after treatment, with functional, cognitive and behavioural tests, and of the state of inflammation and oxidation; and at time 0 and 2 months, of the intestinal microbiota.

详细描述

Amyotrophic lateral sclerosis (ALS) is the most common neurodegenerative disease of an inflammatory nature among those affecting motor neurons, with a life expectancy of 3 to 5 years. It is characterised by the loss of motor neurons, and can be of the bulbar type when the pathology begins to affect the motor neurons located in the spinal bulb, or of the medullary type when it begins with a loss of strength and weakness in the extremities. Both types eventually lead to an affectation of both motor neurons that results in progressive paralysis of the voluntary muscles until the patient dies. In addition, the pathology presents cognitive and behavioural alterations. Specifically, deficits have been described in verbal fluency, memory, emotional processing or social cognition, which appear to be mainly associated with hypoperfusion of the prefrontal area or hypometabolism.

Pathogenically, ALS is characterised by an alteration in mitochondrial energy use at a neuronal level, mainly linked to a lower activity of the enzymes of the electron transport chain in the spinal cord. This alteration is a consequence of loss of oxidative control, excessive generation of oxidative free radicals, accumulation of neurofilaments, and excitotoxicity linked to an increase in the neurotransmitter glutamate.

In this respect, it has been suggested that bacterial dysbiosis, related to cognitive and behavioural worsening, could also contribute to this adverse neuroinflammatory state, having been associated with a greater risk of suffering from neurodegenerative diseases. Specifically in ALS, a variation in intestinal microbial composition has recently been observed, with an increased abundance of E. coli and enterobacteria, and a low abundance of total yeast, in patients suffering from ALS; and lower levels of non-butyrate producing bacteria needed to maintain the integrity of the intestinal barrier, immune competition and energy metabolism. In contrast, increased Akkermansia muciniphila has been associated with higher levels of nicotinamide and improved disease symptoms in the animal model of the disease.

This evidence, associated with the lack of medical treatment to cure the disease, makes it necessary to look for new therapeutic alternatives of a non-pharmacological nature. These include the administration of effective antioxidants, which reverse the high oxidative stress and inflammation characteristic of the disease. This type of treatment (specifically the association of the antioxidants Pterostilbene and Nicotinamide riboside) has already been applied by our research group to patients with ALS, achieving significant clinical improvements such as: greater functional capacity, greater respiratory capacity, increased muscle strength and electrical activity in the upper and lower limbs, as well as an increase in the percentage of skeletal muscle associated with fat loss. In this sense, several polyphenols have also been tested in animal models, among which the activity shown by Resveratrol stands out, with a high antioxidant power and great neuroprotective capacity, which is associated with an increase in the expression and activation of SIRT1 and AMPK in the ventral part of the spinal cord after its administration. Both mediators promoted the normalization of autophage flow and, more importantly, increased mitochondrial biogenesis in SOD1-G93A mice. However, their beneficial effects are strongly limited by their low availability. This limitation can be overcome by administering Resveratrol and its natural analogues, incorporated in liposomes or nanoparticles, as this is the best option for guaranteeing stability and bioavailability, after administration and absorption of the antioxidant.

Moreover, the effects of the polyphenol Curcumin have already been studied in ALS. In a paper by Chico et al, its effects were studied in ALS patients at doses of 600mg/day for 6 months. In this study they found that Curcumin generated a slight slowdown in the progression of the disease, improving aerobic metabolism and oxidative damage. Furthermore, the use of nanobiotechnology with Curcumin (80mg/day) in the treatment of ALS patients obtained positive results showing that nanocurcumin is safe and could improve the probability of survival as an additional treatment in these patients, especially those with existing bulbar symptoms. In short, the use of both antioxidants in liposome form improves the bioavailability and effects of both, and their liposome combination has already been successfully tested in vivo in prostate cancer patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All ALS patients, over 18 years of age and with a clear diagnosis and symptomatology of ALS since at least 6 months.

排除标准

  • Women under 50 years of age and childbearing age.
  • Tracheotomy patients.
  • Patients with invasive or non-invasive ventilation with positive ventilatory pressure
  • Patients with evidence of dementia.
  • Patients with alcohol or drug abuse dependency.
  • Patients infected with B or C hepatitis, or HIV positive
  • Renal patients with creatinine levels twice as high as normal markers.
  • Liver patients with liver markers (ALT, AST) elevated 3 times above normal levels.
  • Patients included in other research with drugs or therapies in the experimental phase.
  • Patients treated with anticoagulants or with haemostatic problems

研究组 & 干预措施

Intervention group

Experimental

30 patients will be given the combination of resveratrol and curcumin liposomed with G04CB02, in a single daily dose for 2 months.

干预措施: Liposomed polyphenols resveratrol and curcumin (Dietary Supplement)

Intervention group

Experimental

30 patients will be given the combination of resveratrol and curcumin liposomed with G04CB02, in a single daily dose for 2 months.

干预措施: Isocaloric Diet (Dietary Supplement)

Intervention group

Experimental

30 patients will be given the combination of resveratrol and curcumin liposomed with G04CB02, in a single daily dose for 2 months.

干预措施: G04CB02 (Drug)

Control group

Placebo Comparator

30 patients, who will receive a placebo with the same dosage pattern and for the same period of time. The placebo will consist of water with sucrose replacing the liposomal polyphenols, and a soft capsule of microcrystalline methylcellulose instead of G04CB02. Both the packaging and the capsule format will be identical to those of the treatment administered in the intervention group

干预措施: Placebo for liposomed resveratrol and curcumin (Other)

Control group

Placebo Comparator

30 patients, who will receive a placebo with the same dosage pattern and for the same period of time. The placebo will consist of water with sucrose replacing the liposomal polyphenols, and a soft capsule of microcrystalline methylcellulose instead of G04CB02. Both the packaging and the capsule format will be identical to those of the treatment administered in the intervention group

干预措施: Isocaloric Diet (Dietary Supplement)

Control group

Placebo Comparator

30 patients, who will receive a placebo with the same dosage pattern and for the same period of time. The placebo will consist of water with sucrose replacing the liposomal polyphenols, and a soft capsule of microcrystalline methylcellulose instead of G04CB02. Both the packaging and the capsule format will be identical to those of the treatment administered in the intervention group

干预措施: Placebo microcrystalline methylcellulose (Other)

结局指标

主要结局

Electromyography

时间窗: 4 months

Motor Variables

Measurement of forced vital capacity

时间窗: 4 months

Motor Variables

Revised Amyotrophic Lateral Sclerosis Functional Rating Scale associated with ALS

时间窗: 4 months

Maximum value: 48 points; Means better outcome motor variables Minimum value: 0 points

次要结局

  • Quantitative measurement of plasma PCR.(4 months)
  • Quantitative measurement of TEAC (oxidation).(4 months)
  • Edinburgh Cognitive and Behavioral ALS Screen(4 months)
  • Quantitative measurement of plasma IL-6 and TNF-alpha.(4 months)
  • Quantitative measurement of plasma 8-oxoG.(4 months)
  • Quantitative measurement of plasma haptoglobin.(4 months)
  • Frontal Assessment Battery(4 months)
  • Quantitative measurement of plasma MDA.(4 months)

研究者

发起方
Fundación Universidad Católica de Valencia San Vicente Mártir
申办方类型
Other
责任方
Principal Investigator
主要研究者

José Enrique de la Rubia Ortí, Ph

Director

Fundación Universidad Católica de Valencia San Vicente Mártir

研究点 (1)

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