Study Evaluating Orally Administered Moxidectin In Subjects With Onchocerca Volvulus Infection

Onchocerciasis Clinical Trial

Official title:

A Randomized, Single-Ascending Dose, Ivermectin-Controlled, Double-Blind, Safety, Tolerability, Pharmacokinetic, and Efficacy Study Of Orally Administered Moxidectin In Subjects With Onchocerca Volvulus Infection

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00300768
• Other study ID #: 3110A1-200-GH
• Secondary ID: B1751004OCRC 33
• Status: Completed
• Phase: Phase 2
• Start date: September 6, 2006
• Est. completion date: November 29, 2009

Study information

• Verified date: November 2022
• Source: Medicines Development for Global Health
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The primary purpose of this study was to determine the safety and tolerability of moxidectin in subjects infected with Onchocerca volvulus (a parasitic worm).

Description:

This was a phase 2, randomized, ivermectin-controlled, double-blind, single-ascending-dose, parallel design, inpatient/outpatient study of moxidectin administered to subjects of both sexes with different degrees of severity of O. volvulus infection. The study was conducted at a single site in Ghana.

Secondary objects are to determine the pharmacokinetics of moxidectin, to obtain initial indication of the efficacy in terms of long term effect on skin microfilaria levels and an indication of the effect on the macrofilaria that may underlie the effect on skin microfilaria levels.

Subjects were enrolled in consecutive cohorts to receive a single oral dose of 2 mg, 4 mg or 8 mg or moxidectin or ivermectin 150 µg/kg by severity of infection, based on the mean of the skin microfilariae densities at each of 4 body locations, both iliac crests and calves.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 172
• Est. completion date: November 29, 2009
• Est. primary completion date: November 2009
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

1. Written, signed (or thumb-printed), and dated informed consent

2. Aged 18 to 60 years, inclusive

3. Body weight = 40 kg for women and = 45 kg for men

4. Nonpregnant, nonbreastfeeding women. Women of child bearing potential must agree to use birth control during the first 150 days after treatment.

5. Healthy, as determined by a physician on the basis of a physical examination, ECG, and a thorough review of the medical history and clinical laboratory results

6. Adequate hematologic, renal, and hepatic function

7. Skin microfilarial density within the required range for the cohort

Exclusion Criteria:

1. Participation in any studies other than purely observational ones, within 4 weeks before test article administration.

2. Any vaccination within 4 weeks before test article administration

3. Acute infection requiring therapy within the last 10 days before test article administration

4. Administration of any medication (with the exception of medication required to treat any reactions during the screening fluorescein angiography (chlorpheniramine) or paracetamol) or herbal preparation within 10 days prior to test article administration or any condition currently requiring regular medication

5. Clinically significant ECG abnormalities or history of cardiac abnormality

6. Past or current history of neurological or neuropsychiatric disease or epilepsy

7. Subjects with orthostatic hypotension at the screening evaluation

8. History of drug or alcohol abuse or regular use of = 3 cigarettes per day

9. Use of alcohol or other drugs of abuse within 72 hours before test article administration

10. Any condition, in the investigator's opinion, that places the subject at undue risk

11. Subjects who have donated blood within 8 weeks before study entry

12. Subjects with ocular onchocerciasis in cohorts intended to enroll subjects with mild infection. Ocular onchocerciasis is defined by the presence of live or dead microfilariae, onchocercal punctate opacities, onchocercal lesions of the posterior segment or lesions that mimic those seen in onchocerciasis.

13. Subjects with hyperreactive onchodermatitis

14. Antifilarial therapy within the previous 5 years

15. Coincidental infection with Loa Loa

16. Female subjects of childbearing potential with a contraindication to DMPA if not on Norplant

17. Any other condition which the investigator feels would exclude the subject from the study

Related Conditions & MeSH terms

• Intestinal Volvulus
• Onchocerciasis

Intervention

Drug:
• 2 mg moxidectin
Single-dose, tablet encapsulated for blinding
• ivermectin 150 mcg/kg
Single-dose, tablets encapsulated for blinding
• 4 mg moxidectin
Single dose, tablets encapsulated for blinding
• 8 mg moxidectin
single dose, tablets encapsulated for blinding

Locations

Country	Name	City	State
Ghana	Onchocerciasis Chemotherapy Research Center	Hohoe	Volta Region

Sponsors (2)

Lead Sponsor	Collaborator
Medicines Development for Global Health	World Health Organization

Country where clinical trial is conducted

Ghana, 

References & Publications (1)

Awadzi K, Opoku NO, Attah SK, Lazdins-Helds J, Kuesel AC. A randomized, single-ascending-dose, ivermectin-controlled, double-blind study of moxidectin in Onchocerca volvulus infection. PLoS Negl Trop Dis. 2014 Jun 26;8(6):e2953. doi: 10.1371/journal.pntd. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence of clinical adverse events and clinically significant laboratory test results		Duration of follow up (18 months)
Secondary	Skin mf counts at day 8 and months 1, 2, 3, 6, 12 and 18		day 8 and months 1, 2, 3, 6, 12, 18
Secondary	Nodulectomy at 18 months		18 months
Secondary	Pharmacokinetics (PKs) at days 1, 2, 4, 13, and 18 and months 1, 2, 3, 6 and 12		days 1, 2, 4, 13, and 18 and months 1, 2, 3, 6 and 12

External Links

•   Awadzi et al 2014