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Serum Pharmacokinetic Disposition and Urinary Excretion of Albendazole

Serum Pharmacokinetic Disposition and Urinary Excretion of Albendazole and Its Metabolites in Non-infected Human Volunteers.

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03192449
Enrollment
8
Registered
2017-06-20
Start date
2016-11-21
Completion date
2017-01-20
Last updated
2017-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neglected Tropical Diseases, Soil Transmitted Helminthiasis

Brief summary

Mass drug administration (MDA) of albendazole (ABZ) to school-age and pre-school-age children is the currently recommended strategy for controlling soil-transmitted helminthiasis (STH) in endemic areas. Recent mathematical modelling suggests that community-wide MDA will be required in order to interrupt transmission of STH. DEWORM3 aims to determine the feasibility of eliminating STH through expanded and intensified MDA strategies. In order to ensure rigorous trial results, it is crucial that the definition of such MDA coverage is informed by unbiased, empirical data. The Centro de Investigación Veterinaria de Tandil (CIVETAN) and Instituto de Investigaciones en Enfermedades Tropicales Universidad Nacional de Salta collaborate on scientific research related to pharmacokinetic studies of ABZ. This proposal describes the request for funding from DEWORM3 to conduct a study of the serum pharmacokinetic characteristics and urinary excretion of ABZ and its metabolites in non-infected human volunteers to better understand the use of urinary analysis of ABZ as a measure of MDA adherence in the context of DEWORM3.

Detailed description

Objective 1.To characterize the plasma disposition kinetics of ABZ and its main metabolites (ABZ sulphoxide and ABZ sulphone) in non-infected human volunteers. Objective 2. To characterize the pattern of albendazole (ABZ) and its main metabolites (ABZ sulphoxide and ABZ sulphone) urinary excretion in non-infected human volunteers. Objective 3. To determine the optimal and the longest period time after treatment where either ABZ and/or its metabolites can be measured in urine as an indirect assessment of an individual's adherence to treatment.

Interventions

Single dose 400mg orally

Sponsors

CIVETAN CONICET, Facultad de Ciencias Veterinarias, UNCPBA. Tandil
CollaboratorUNKNOWN
Universidad Nacional de Salta
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

Pharmacokinetics

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

1. Weight between 45 and 75 Kg. 2. Physical exam without significant abnormal findings.

Exclusion criteria

1. Intake of ABZ or other benzimidazole drugs within the last 30 days. 2. Malabsorption or other GI syndromes that could compromise the tolerability or absorption of ABZ. 3. History of hypersensitivity or intolerance to ABZ or its inactive ingredients. 4. Acute clinical conditions. 5. Pregnancy or breast feeding.

Design outcomes

Primary

MeasureTime frameDescription
Albendazole in urineUp to 72 hoursUrinary excretion of albendazole (ABZ) and its main metabolites (ABZ sulphoxide and ABZ sulphone) in non-infected human volunteers. PK parameters (Cmax, AUC, Tmax) from levels measured through HPLC

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026