Repeated Controlled Human Hookworm Infection (ReCHHI1)

Meta Roestenberg

Status: Completed

Conditions: Necator Americanus Infection

Treatments: Biological: 100 Necator americanus L3 larvae; Biological: 150 Necator americanus L3 larvae; Biological: 50 Necator americanus L3 larvae

Study type: Interventional

Funder types: Other

Identifiers

NCT03257072

ReCHHI1

Details and patient eligibility

About

Twenty-four healthy hookworm-naive volunteers will be exposed to 50 L3 Necator americanus larvae for a maximum of three times.

Full description

Twenty-four volunteers will be allocated equally into three groups (i.e. group A, B, C). Group A, B, and C will have one, two, and three infections respectively. Every infection will be performed with 50 L3 Necator americanus larvae. Group A will receive infection at week 4 only. Group B will be infected at week 2 and week 4. Group C will be infected at week 0, 2 and 4. To maintain blinding, group A and B will receive mock infections with water at week 0 and week 0 and 2 respectively. The interval between each CHHI is 2 weeks. Before every infection, the safety will be assessed by a review of adverse events data with a local safety monitor.

Sixteen weeks after the last infection (week 20), all volunteers will be offered treatment with a 3-day regimen of albendazole to abrogate infection. Volunteers with average egg counts >250 eggs per gram will be asked if they would be willing to keep their infection for a maximum of two years (chronic donors). No more than four volunteers will be selected to be chronic donors. Six months after the last infection (or after the last donation for the chronic donors) volunteers will undergo their last visit.

Enrollment: 24 patients

Sex: All

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Subject is aged ≥ 18 and ≤ 45 years and in good health.
2. Subject has adequate understanding of the procedures of the study and agrees to abide strictly thereby.
3. Subject is able to communicate well with the investigator, is available to attend all study visits.
4. Subject agrees to refrain from blood donation to Sanquin or for other purposes throughout the study period.
5. For female subjects: subject agrees to use adequate contraception and not to breastfeed for the duration of study.
6. Subject has signed informed consent.

Exclusion criteria

1. Any history, or evidence at screening, of clinically significant symptoms, physical signs or abnormal laboratory values suggestive of systemic conditions, such as cardiovascular, pulmonary, renal, hepatic, neurological, dermatological, endocrine, malignant, haematological, infectious, immune-deficient, psychiatric and other disorders, which could compromise the health of the volunteer during the study or interfere with the interpretation of the study results. These include, but are not limited to, any of the following:

   • Body Mass Index (BMI) <18.0 or >30.0 kg/m2 at screening;
   • positive HIV, HBV or HCV screening tests;
   • the use of immune modifying drugs within three months prior to study onset (inhaled and topical corticosteroids and oral anti-histamines exempted) or expected use of such during the study period;
   • having one of the following laboratory abnormalities: ferritine <10 ug/L, transferrine <2.04 g/L or Hb <7.0 mmol/L for females or <8.0 mmol/L for males;
   • history of malignancy of any organ system (other than localized basal cell carcinoma of the skin), treated or untreated, within the past 5 years;
   • any history of treatment for severe psychiatric disease by a psychiatrist in the past year;
   • history of drug or alcohol abuse interfering with normal social function in the period of one year prior to study onset.

2. Known hypersensitivity to or contra-indications for use of albendazole, including co-medication known to interact with albendazole metabolism (e.g. carbamazepine, phenobarbital, phenytoin, cimetidine, theophylline, dexamethasone)

3. Known allergy to amphotericin B or gentamicin

4. For female subjects: positive urine pregnancy test at screening

5. Positive faecal qPCR or Kato-Katz for hookworm at screening, any known history of hookworm infection or treatment for hookworm infection or possible exposure to hookworm in the past

6. Being an employee or student of the department of parasitology of the LUMC

7. Current or past scars, tattoos, or other disruptions of skin integrity at the intended site of larval application

8. Subjects with planned travel to hookworm endemic areas during this trial

9. Receipt of a vaccine within 4 weeks prior to the study initiation

10. Known food allergy

Trial design

Primary purpose: Diagnostic

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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24 participants in 3 patient groups

A: 50 Necator americanus L3 larvae

Experimental group

Description:

Mock infections with water at week 0 and 2, infection with 50 Necator americanus L3 larvae at week 4

Treatment:

Biological: 50 Necator americanus L3 larvae

B: 100 Necator americanus L3 larvae

Experimental group

Description:

Mock infections with water at week 0, infection with 50 Necator americanus L3 larvae at week 2 and 4

Treatment:

Biological: 100 Necator americanus L3 larvae

C: 150 Necator americanus L3 larvae

Experimental group

Description:

Infection with 50 Necator americanus L3 larvae at week 0, 2 and 4

Treatment:

Biological: 150 Necator americanus L3 larvae