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Safety and Efficacy of Imatinib in Combination With Artemether-Lumefantrine for Uncomplicated Malaria

2026年6月24日 更新者:Quentin Awori、Victoria Biomedical Research Institute

Evaluating the Safety and Efficacy of Imatinib in Combination With Artemether and Lumefantrine for Treatment of Uncomplicated Malaria

This study is investigating an innovative approach to treating uncomplicated malaria by adding a drug called Imatinib to the current standard of care, Artemether + Lumefantrine (AL). The researchers hope this combination, known as ALIM, will clear infections faster and stop the spread of drug-resistant parasites that are becoming a major threat in Africa

研究概览

详细说明

Most antimalarial drugs work by directly attacking the Plasmodium falciparum parasite, but this approach carries a fundamental weakness: the parasite can slowly rewrite its own biology to shrug off these chemical assaults. Imatinib, a drug already proven safe in cancer treatment for over two decades, takes a radically different tack. Instead of targeting the invader, it targets the human red blood cell that the parasite infects. Specifically, Imatinib inhibits a human enzyme called Syk kinase a key that the parasite turns to pry open the cell and burst forth into the bloodstream. By jamming this lock, the drug traps the parasite inside the cell, where toxic byproducts accumulate and ultimately kill it. Because the parasite cannot alter human biology the way it alters its own, researchers believe resistance to Imatinib will be extraordinarily difficult if not impossible for malaria to evolve.

To test this promising strategy, a clinical trial is now underway at the Alupe sub county hospital in Busia County, Kenya, a region bearing some of the nation's highest malaria burdens. The study unfolds in three cautious phases. First, between ninety and two hundred ten adults will receive varying doses of Imatinib starting at 400 milligrams twice daily to determine the safest regimen. If side effects prove too severe, the dose will be lowered to 600 or 400 milligrams once per day. Once the optimal dose is identified, the second phase will enroll 516 adults to confirm that adding Imatinib to the standard artemether lumefantrine (AL) regimen is as safe as AL alone, and to test whether a two day course works as well as the conventional three days. Finally, because children under five account for nearly eighty percent of malaria deaths, the third phase will extend the trial to younger participants from twelve months to seventeen years using weight based dosing.

Participants who enroll must remain in the hospital for forty eight to seventy two hours of close observation. Medical staff will draw frequent blood samples, often via finger prick, to count parasites and monitor liver and kidney health. After discharge, patients return for follow up visits on days seven, twenty one, and thirty five to ensure the infection has not recurred. To compensate for time and lost wages, each participant receives 1,500 Kenyan shillings per day, and the study covers all travel and medical expenses.

Safety is reinforced by clear boundaries. Although Imatinib is already FDA approved and widely used for cancer, its combination with AL is novel. To avoid dangerous drug interactions, anyone taking medications for high cholesterol, high blood pressure, or HIV cannot enroll. Pregnant or breastfeeding women are also excluded, as Imatinib can harm a developing fetus, and female participants must use birth control throughout the trial.

The study operates under rigorous ethical oversight. It has been reviewed by the Jaramogi Oginga Odinga Teaching and Referral Hospital and the Pharmacy and Poisons Board, while an independent Data Safety Monitoring Board composed of doctors and scientists will continuously review the data to determine whether the trial remains safe to proceed. All participant information is protected under the Kenyan Data Protection Act, ensuring personal privacy is never compromised. Overall, the trial expects to enroll between 906 and 1,116 participants by the end of 2027, with the ultimate goal of delivering a more powerful, resistance proof tool for malaria elimination.

研究类型

介入性

注册 (估计的)

1116

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

学习地点

      • Kisumu、肯尼亚、40100
        • 招聘中
        • Victoria Biomedical Research Institute
        • 接触:
        • 接触:
        • 首席研究员:
          • Dr. Quentin Awori MBChB
        • 副研究员:
          • Dr. Lucas Otieno Tina, MBChB
        • 副研究员:
          • Dr. Diana Irene Odhiambo, MBChB
        • 首席研究员:
          • Dr. Karson Putt Phd
        • 副研究员:
          • Dr. Simon Kariuki Phd
        • 副研究员:
          • Dr Antony Oindo MBChB

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子
  • 成人

接受健康志愿者

不

描述

Inclusion Criteria:

For Part 1 and 2 of the study design, all individuals must meet all the inclusion criteria below:

  • Patients diagnosed with symptomatic mild to moderate P. falciparum malaria with a parasite density of >= 5000 parasites/μl
  • Adult male, age 18-55 years old or adult female, age 18-55 years that are post-menopausal, or test negative on a pregnancy test and will be on active birth control through to the end of the follow up period.
  • Provision of informed consent and agrees to hospital admission for 48-72hrs
  • Good health condition other than malaria
  • The patient has not taken anti-malarial drugs in the past 4 weeks

For Part 3 of the trial, all individuals must meet all the inclusion criteria below:

  • Patients diagnosed with symptomatic mild to moderate P. falciparum malaria and a parasite density of >= 5000 parasites/μl
  • Age 12 months to below 18 years
  • Presented by parent or legally accepted representative (LAR) who has consented to the participation of the child in the trial and agrees to hospital admission for 48-72hrs.
  • Hb levels > 5mg/dL
  • Child has not taken anti-malarial drugs in the past 6 weeks.

Exclusion Criteria:

  • Prospective study participant, LAR and/or impartial witness (where applicable) declines to provide informed consent.
  • Symptoms and signs of severe or complicated malaria including:

    • significant confusion or impaired consciousness (including unarousable coma)
    • multiple convulsions (more than two episodes within 24 hours),
    • respiratory distress
    • circulatory collapse (systolic blood pressure <80mm Hg with evidence of impaired perfusion)
    • clinical jaundice plus evidence of other vital organ dysfunction
    • simultaneous infection of unrelated origin
  • Parasite density > 200,000 parasites /μl
  • In the case of female participants: currently pregnant or lactating
  • Other neurological or psychiatric symptoms or disorders
  • Abnormal bleeding
  • Resting heart rate lower than 55 or higher than 100 bpm
  • History of cardiac disease
  • Signs, symptoms and laboratory results of impairment of vital organs such as liver, lungs, kidney and cardiovascular system
  • Abnormal blood chemistry:

    • hemoglobin < 9.0 g/dL in adults or < 5.0 g/dL in children 12 months-18 years
    • WBC not in the range of 4800-10,000/mm3
    • RBC if < 4.0x106/ mm3
    • Platelet < 1.3x105/ mm3
    • ALAT not in the normal range (4 to 36 U / l)
    • ASAT not in the normal range (8 to 33 U / l)
    • Total bilirubin 0.1 to 1.2 mg / 100 ml
    • Serum protein if < 5.5 g/dL
  • 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 attend/meet study staff on follow up visits
  • Concomitant use of medicines, including:

    • medicines used to treat high cholesterol (such as atorvastatin, lovastatin, simvastatin);
    • medicines used to treat hypertension and heart problems (such as diltiazem, nifedipine, nitrendipine, verapamil, felodipine, amlodipine);
    • medicine used to treat HIV (antiretroviral medicines) including 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 including barbiturates (such as phenobarbital), carbamazepine or phenytoin;
    • medicines used after organ transplantation and in autoimmune diseases (such as cyclosporin, tacrolimus);
    • nefazodone (used to treat depression);
    • aprepitant (used to treat nausea);

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
有源比较器:Artemether Lumefantrine Alone
Standard 3-day course. Used as control in all parts.
There is no difference
实验性的:Artemether Lumefantrine and Imatinib 400mg Twice Daily (3 days)
3-day course with imatinib 400mg twice daily.
There is no difference
实验性的:Artemether Lumefantrine and Imatinib (Optimal Dose, 3 days)
3-day course with optimal dose determined from Part 1.
There is no difference
实验性的:Artemether Lumefantrine and Imatinib (Optimal Dose, 2 days)
2-day imatinib course (optimal dose) with 3-day AL.
There is no difference
实验性的:Pediatric: Artemether Lumefantrine and Imatinib (Weight-based)
Weight-based imatinib (340 or 260 mg/m²/day, max 600mg) plus weight-based AL for 3 days.
There is no difference

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Dose of Imatinib (in mg) Required to Eliminate Viable Parasites
大体时间:48 hours post-first dose
Identification of imatinib dose that eliminates all viable parasites after 2 days of dosing, determined by absence of viable parasites on blood culture from samples taken immediately after 48 hours of study drug administration.
48 hours post-first dose
Number of Participants with Treatment-Emergent Adverse Events (TEAEs) by Severity Grade
大体时间:Up to Day 35
Safety and tolerability of imatinib mesylate combined with artemether-lumefantrine (AL+IM) compared to artemether-lumefantrine alone (AL). Non-inferior safety defined as insignificant increase (p > 0.05) in number and severity of adverse events in AL+IM cohorts versus AL alone.
Up to Day 35
Number of Participants with PCR-Corrected Recrudescence
大体时间:Day 35
Non-inferiority of 2-day AL+IM dosing compared to 3-day AL dosing as determined by PCR-corrected recrudescence using strain genotyping. Non-inferiority defined as insignificant increase (p > 0.05) in recrudescence in 2-day AL+IM cohorts versus 3-day AL alone.
Day 35

次要结果测量

结果测量
措施说明
大体时间
Change from Baseline in Parasite Density (parasites/μL)
大体时间:Days 1, 2, and 3
Accelerated parasite clearance of AL+IM compared to AL alone. Superior efficacy defined as significant decrease (p < 0.05) in average parasite density in AL+IM cohorts versus AL cohort.
Days 1, 2, and 3
Change from Baseline in Body Temperature (°C)
大体时间:Days 1, 2, and 3
Accelerated decrease in body temperature in AL+IM compared to AL alone. Superior efficacy defined as significant decrease (p < 0.05) in elevated average body temperature in AL+IM cohorts versus AL cohort.
Days 1, 2, and 3
Percentage Reduction in Parasite Density from Baseline
大体时间:Days 1, 2, and 3
Faster parasite clearance in participants with starting parasite density >10,000 parasites/μL compared to those with <10,001 parasites/μL in AL+IM cohorts. Defined as significant decrease (p < 0.05) in percentage of parasites after first drug administration between high and low baseline density groups.
Days 1, 2, and 3

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

合作者

调查人员

  • 首席研究员:Dr. Quentin Awori MBChB、Victoria Biomedical Research Institute

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年1月20日

初级完成 (估计的)

2027年6月30日

研究完成 (估计的)

2027年6月30日

研究注册日期

首次提交

2026年4月23日

首先提交符合 QC 标准的

2026年4月23日

首次发布 (实际的)

2026年4月30日

研究记录更新

最后更新发布 (实际的)

2026年6月29日

上次提交的符合 QC 标准的更新

2026年6月24日

最后验证

2026年6月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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