Triple Antimalarial Combination (Imatinib-DHA-PPQ) to Accelerate the Parasite Clearance and to Prevent the Selection of Resistant Parasites
试验速览
- 阶段
- 2 期
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Occurrence of Severe Adverse Events
研究概览
简要总结
The purpose of this study is to provide a new drug combination for a better treatment of P. falciparum for a faster parasite clearance and to counteract artemisinin resistance.
详细描述
According to WHO, resistance to artemisinin derivatives (ART) is emerging in many areas of the Greater Mekong Region as a delayed parasite clearance following a standard treatment by artemisinin combined therapy (ACT). Artemisinin resistance is often accompanied by the resistance to the partner drugs such as piperaquine (PPQ), mefloquine (MEF), amodiaquine (AQ) and lumefantrine (LF).
The slow and incomplete clearance of parasites following ACT treatment is considered to permit the selection of resistant parasites.
The availability of new, more efficient treatments accelerating the clearance of parasites is therefore needed to counteract the selection of ART resistant strains.
Imatinib (IMA) has been demonstrated to increase the efficacy of ART in a synergic fashion. This positive effect is further potentiated by low concentrations of PPQ.
IMA is active both on the intra-erythrocyte asexual forms and on gametocytes. It is therefore expected that the combination DHA-PPQ-IMA should lead to faster and radical clearance of the parasites, therefore reducing the frequency of healthy carriers and transmission.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Sequential
- 主要目的
- Treatment
- 盲法
- None
盲法说明
The research method will be a Phase 2 trial, 2 arms, randomized, open label (only the microscopist will be blinded), adaptive, dose de-escalation, trial conducted in adult male subjects with uncomplicated P.falciparum malaria.
In all phases, patients will be treated by a triple combination IMA-DHA-PPQ (ARM 1) or by the standard DHA-PPQ treatment (ARM 2).
入排标准
- 年龄范围
- 18 Years 至 55 Years（Adult）
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •Patients diagnosed with mild to moderate P. falciparum malaria
- •Adult male, age 18-55 years
- •Good health conditions other than malaria
- •The patient did not take anti-malarial drugs in the past 4 weeks
排除标准
- •unable to provide Informed Consent or Patient History Form
- •symptoms and signs of severe or complicated malaria including: continuous high fever over 39 °C, confusion, convulsions
- •parasitemia<150.000 parasites /microliter
- •other neurological or psychiatric symptoms or disorders
- •abnormal bleeding
- •resting hearth rate lower than 60 and higher than 100 bpm
- •abnormal ECG, history of cardiac diseases
- •male adults with corrected QT intervals > 450ms
- •signs, symptoms and laboratory results of impairment of vital organs such as liver, lungs, kidney and cardiovascular system
- •hemoglobin < 9.0 gm/100ml
- •symptoms and signs of infection such as pneumonia, dengue fever, and other viral or bacterial infection.
- •patients with symptoms of gastrointestinal infections or any sign of malabsorption that may interfere with drug absorption
- •concomitant infection by plasmodium species other than P. falciparum
- •inability to meet daily with local doctor during period of clinical trial
- •concomitant medicines like:
- •medicines used to treat high cholesterol in the blood (such as atorvastatin, lovastatin, simvastatin);
- •medicines used to treat hypertension and heart problems (such as diltiazem, nifedipine, nitrendipine, verapamil, felodipine, amlodipine);
- •medicined used to treat HIV (antiretroviral medicines): protease inhibitors (such as amprenavir, atazanavir, indinavir, nelfinavir, ritonavir), non-nucleoside reverse transcriptase inhibitors (such as efavirenz, nevirapine);
- •medicines used to treat microbial infections (such as telithromycin, rifampicin, dapsone);
- •medicines used to help you fall asleep: benzodiazepines (such as midazolam, triazolam, diazepam, alprazolam), zaleplon, zolpidem;
- •medicines used to prevent/treat epileptic seizures: barbiturates (such as phenobarbital), carbamazepine or phenytoin;
- •medicines used after organ transplantation and in autoimmune diseases (such as cyclosporin, tacrolimus);
- •sex hormones, including those contained in hormonal contraceptives (such as gestodene, progesterone, estradiol), testosterone; - glucocorticoids (hydrocortisone, dexamethasone); - omeprazole (used to treat diseases related to gastric acid production);
- •paracetamol (used to treat pain and fever);
- •theophylline (used to improve bronchial air flow);
- •nefazodone (used to treat depression);
- •aprepitant (used to treat nausea);
研究组 & 干预措施
imatinib-Dihydroartemisinin-piperaquine
triple combination
干预措施: Imatinib (Drug)
Dihydroartemisinin-piperaquine
standard of care
干预措施: Dihydroartemisinin-piperaquine (Drug)
结局指标
主要结局
Occurrence of Severe Adverse Events
时间窗: From baseline to day 42
Occurrence of Severe Adverse Events over 42 days observation period
Occurrence of Adverse Events
时间窗: From baseline to day 42
Occurrence of Adverse Events over 42 days observation period
Occurrence of Abnormal Physical Symptoms
时间窗: From baseline to day 42
Occurrence of Abnormal Physical Symptoms (Clinical Abnormalities) over 42 days observation period
Occurrence of Abnormal Laboratory Values
时间窗: From baseline to day 42
Occurrence of Abnormal Laboratory Values over 42 days observation period
次要结局
- Frequency of residual parasitemia: % of patients with >1000 parasites/ ul at day 3 and 28(day 3 and day 28)
- Frequency of fever and malaria symptoms(day 3 and day 28)
- Mean parasitemia in the control and investigational arms(day 2 and day 5)
- Parasite half-life measured at 12 and 24 hours(from baseline to 24 hours post-treatment)