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Loiasis With Positive Blood MicrofilaremiaPhase 3STOP-FiLAR-ALBNCT06613997

21-day Double-blind Trial of Albendazole in Adults With Loa Loa Microfilaremia

A Phase 3 study testing Albendazole 400mg in people with Loiasis With Positive Blood Microfilaremia and Loiasis, run by Programme National de Lutte contre l'Onchocercose, Republic of the Congo.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record

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Trial summary

Our aim is to test the hypothesis that a 3-week course of albendazole 400 mg daily is safe and can progressively reduce Loa loa microfilarial densities in subjects with microfilaremia. Read more about this study

Who is it for?
Ages 18 to 70 years
What is being tested?
Albendazole 400mg
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
100 participants
Where
No sites listed yet
Study dates
15 Jan 2025to 31 Dec 2027
Phase
Phase 3

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 70 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Consent informed, written, signed and dated
  • Women or men aged 18 to 70 years inclusive
  • Carrier of L. loa microfilaremia
  • Body weight ≥ 40 kg and less than 90 kg

Who cannot join

  • Participation in any study other than a purely observational study, within the 4 weeks preceding this study (determined by the theoretical date of the first administration of albendazole placebo)
  • Any vaccination within 4 weeks previous to this study
  • Infection requiring treatment in the 10 days previous to this study, as determined by the anamnesis during the medical interview (e.g. pulmonary infection , digestive or skin infection; with or without antibiotic treatment)
  • Known immunosuppressive pathology (by self-report)
  • Past or present history of neurological (including epilepsy) or neuropsychiatric disease
  • Current treatment with ritonavir and/or rifampicin
Show all 17Show fewer
  • Use of cocaine or other drugs of abuse in the 72 hours preceding administration of the trial treatment, as determined by history during the medical interview
  • Past or present history of liver, kidney or bone marrow failure
  • ALAT transaminase level ≥ 3 times the upper limit of normal (3N) according to laboratory standards
  • Any condition, in the opinion of the investigator, that exposes the subject to undue risk
  • Known intolerance to ALB or benzimidazole derivatives in general
  • Subjects who donated blood in the previous 8 weeks to study entry, with a standard volume (500 mL)
  • On clinical examination: symptoms, physical signs or laboratory findings suggestive of systemic disorders, including disorders, including renal, hepatic, cardiovascular, pulmonary, skin, immunodeficiency, psychiatric and other abnormalities that could interfere with the interpretation of trial results. The physician may then give a favorable or unfavorable opinion on the participants inclusion.
  • ALB and/or mebendazole in the last month
  • IVM taken in the last month
  • Any condition which, in the opinion of the investigator, exposes the subject to undue risk
  • Positive urine pregnancy test for women of childbearing age or breastfeeding

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Jéremy CAMPILLO, PharmD PhD contact

+33 4 67 41 61 52

jeremy.campillo@ird.fr

Bachiratou SAHM contact

bachiratou.sahm@ird.fr

About this study

Official title: Randomized, Double-blind Trial Evaluating the Safety and Efficacy of a 21-day Course of Albendazole 400mg/Day in Subjects With High Loa Loa Microfilaremia

Our aim is to test the hypothesis that a 3-week course of albendazole 400 mg daily is safe and can progressively reduce Loa loa microfilarial densities in subjects with microfilaremia.

Read the detailed description

Onchocerciasis, a parasitic disease caused by Onchocerca volvulus, present in sub-Saharan Africa, is subject of control programs based on the massive annual administration of ivermectin to the entire population living in endemic zones, without prior diagnosis. These programs are hampered in certain regions: areas coendemic with loasis (due to the Loa loa parasite) due to the risk of serious adverse effects caused by ivermectin in individuals heavily infected. The aim of this research is to evaluate an albendazole-based pre-treatment strategy to reduce the microfilarial density of loasis, enabling the safe use of ivermectin in all areas affected by onchocerciasis.

The efficacy of albendazole in reducing Loa loa microfilarial densities was evaluated in less than 100 individuals in 3 clinical trials. A 3-day regimen of ALB (200 mg daily) showed no effect on Loa loa microfilarial densities. A single dose of 800 mg every two months for one year induced a significant but insufficient reduction in Loa loa microfilarial densities to eliminate the risk of post-ivermectin side effects. The most interesting results came from a trial involving 21 subjects (10 in the albendazole group and 11 in the placebo group): twice-daily treatment with 200 mg ALB for 21 days progressively reduced Loa loa microfilarial densities by 80% over six months. However, the geometric mean of Loa loa microfilarial densities and the highest Loa loa microfilarial density in the albendazole group were 2,369 and 20,200 mf/mL respectively, i.e. below the risk threshold for serious adverse effects.

This project is based on a double-blind, randomized, placebo-controlled clinical trial. It aims to evaluate the safety and efficacy of 21 days of albendazole in Loa loa microfilaremia patients. The trial will be conducted in a rural area of Congo (Niari department, Mossendjo district and Lékoumou department, Komono district). A total of 100 subjects will be included in the study. Participants will receive either albendazole 400 mg daily or a similar placebo for 21 days. The aim is to recruit as many individuals as possible with at least 20,000 mfs/mL during the screening campaign, but we will be able to include all patients with microfilaremia. The individuals included will be monitored for 6 months (50 days of close follow-up for safety and 180 days of follow-up for efficacy). Initially, the majority of analyses will be descriptive. An Intention-to-Treat analysis will be performed. A Per Protocol analysis will be performed in the event of protocol deviations. The main evaluation criteria will be :

  • Tolerance of a 21-day course of albendazole 400mg/day in L. loa-infected individuals with mfs in the bloodstream (criterion: no serious adverse events occurred in the albendazole-treated group).
  • Efficacy: describe the kinetics of L. loa microfilarial densities (measured at 2, 7, 15, 22, 30, 90 and 180 days post-treatment) and the percentage of individuals who reduced their microfilarial load by at least 30% of their initial value.

The study will implement rigorous ethical procedures to ensure the safety and well-being of participants. The main objective is to minimize risks and maximize potential public health benefits. The study will comply with all applicable local laws, regulations and ethical guidelines (including the Declaration of Helsinki and Good Clinical Practice), and will be preceded by full information given to participants. Free and informed consent will be obtained, and participation will be voluntary. Risks include mild discomfort during the fingertip prick required for microfilaremia monitoring, and possible mild side effects associated with albendazole. On the other hand, benefits include the possibility of free medical screening and a contribution to medical research. Medical follow-up is planned to manage potential side effects. The research will be carried out in suitable, secure facilities, located close to the participating villages for assistance in the event of an emergency. A data anonymization system will be put in place to protect participants. Data will be secured on a server and exchanged securely. An Independent Monitoring Committee will oversee the study to guarantee the safety and interests of participants. Finally, specific insurance will cover participants in the event of study-related harm, ensuring adequate protection in the event of complications.

If successful, this project could revolutionize onchocerciasis control in areas coendemic with loasis. The proposed pre-treatment strategy could enable ivermectin to be administered safely, helping to speed up the elimination of onchocerciasis. In addition, this project could have important implications for the individual treatment of subjects with high Loa loa microfilarial density, offering an alternative to currently complicated and ineffective treatments.

Being tested
Albendazole 400mg, Placebo
Keywords
filariasis, Albendazole, Onchocerciasis
Medical subject headings
Loiasis, Filariasis, Onchocerciasis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Albendazole 400mgDrug

    Albendazole 400mg per days for 21 consecutive days

  • PlaceboDrug

    Placebo for 21 consecutive days

Study groups in NCT06613997
Study groupRoleWhat they receive
Albendazole 21 daysExperimentalParticipants randomized in this arm will receive 21 days of albendazole 400mg/days .
Receives: Drug: Albendazole 400mg
Placebo 21 daysPlacebo comparatorParticipants randomized in this arm will receive 21 days of placebo.
Receives: Drug: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Tolerance of Albendazole 400mg/day in individuals with Loa loa microfilaremia

    The proportion of AEs and/or SAEs occurring in the treatment (ALB) and placebo groups and the proportion of AEs and/or SAEs occurring by grade in the treatment (ALB) and placebo groups

    Measured: During the treatment (21 days) and 3 month after

  2. Efficacity of Albendazole 400mg/day in individuals with Loa loa microfilaremia

    Rate of reduction of L. loa DMF in blood at D2, D7, D15, D22, D30, D90 and D180 in each of the two groups and proportion of subjects without L. loa microfilariae in blood at D2, D7, D15, D22, D30, D90 and D180 in both groups

    Measured: During the treatment (21 days) and 6 months after

Secondary outcomes (1)
  1. Comparison the safety of albendazole to placebo in individuals with Loa loa microfilaremia

    Comparison of occurrence of adverse events by proportion and grade in treatment group (ALB) and placebo group and comparison of DMF reduction rates in L. loa during treatment (D1 to D21) and those observed over the long term (D21 to D180)

    Measured: From Day 2 after the first dose to 6 months after the first dose

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Sep 2024
  2. Study start15 Jan 2025 (estimated)
  3. Primary completion31 Dec 2026 (estimated)
  4. Study completion31 Dec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
A 2-group, randomized, double-blind, parallel clinical trial: * albendazole 400 mg daily for 21 consecutive days * Placebo, daily for 21 consecutive days
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06613997
Sponsor's protocol ID
Protocole 129
Acronym
STOP-FiLAR-ALB
Status last verified
Sep 2024
First submitted
23 Sep 2024
Last updated
26 Sep 2024
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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