Ivermectin and Human Immunity

Ivermectin Clinical Trial

Official title:

The Effects of Ivermectin on Human Innate Immunity Against Filarial Parasites

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03459794
• Other study ID #: STUDY00005069
• Status: Completed
• Phase: Early Phase 1
• Start date: February 12, 2018
• Est. completion date: November 30, 2018

Study information

• Verified date: April 2019
• Source: University of Georgia
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

We hypothesize that ivermectin, a drug used to treat parasitic worm infections, interacts with the human innate immune system and that this contributes to its anti-parasitic effects. Participants will donate blood before and after being administered the normal human dose of the drug. We will compare the cell types present in the blood and the chemicals known to influence the human immune system before and after the drug is given, as well as measuring any changes in gene expression in white blood cells 4 and 24hrs after the drug is taken.

Description:

Subjects will visit the University of Georgia (UGA) Clinical & Translation Research Unit (CTRU) twice on consecutive days and blood will be drawn from them. On the first occasion they will be weighed and will complete the consent process. They will have been randomly assigned to the test (Stromectol) or control (placebo) group, with 8 participants in the test group and 4 participants in the control group. Stromectol will be obtained from a medical supply distributor and a placebo will be obtained through the UGA School of Pharmacy. Drugs will be prescribed by Jonathan Murrow MD. They will be stored in their original packaging at room temperature in a drug locker in the lab at CTRU. Participants will be identified by number and allocated to groups using a block randomization protocol. Randomization and drug dispensation will be done by CTRU. Eighteen ml of blood will drawn in a fasting state and they will be administered 150 mcg/kg Stromectol or the equivalent number of placebo tablets immediately after blood is drawn. Participants will remain at CTRU for four hours after they take the drug, then another 15ml of blood will be drawn. On the second day they will attend CTRU at the same time and the third blood sample will be drawn 24 hrs after administration of the drug. On each occasion the drawn blood will be coded by CTRU staff prior to being collected by a member of the Department of Infectious Diseases and taken to the laboratory (Wildlife Health G0007) for the isolation of leukocyte populations (peripheral monocytes, lymphocytes and polymorphonuclear cells (PMNs)) and for the preparation of serum. Complete blood counts will also be carried out. Sera will be analyzed on the Luminex for cytokine/chemokine content. RNA will be isolated from the cell populations for RNASeq analysis.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 12
• Est. completion date: November 30, 2018
• Est. primary completion date: April 9, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Weight over 110 pounds and under 185 pounds

Exclusion Criteria:

• Pregnancy or nursing mothers.

• Immunosuppressed individuals.

• Hypersensitivity to ivermectin, cellulose, starch, magnesium stearate, butylated hydroxyanisole, or citric acid powder (inert ingredients of Stromectol).

• Recent (last 3 years) travel to West or Central Africa, or any other country where onchocerciasis is present

• Hepatitis/HIV

• Currently taking warfarin

• Lactose intolerance (Lactose present in placebo)

• Currently taking Steroid medications (inhaled, oral or injection)

• Currently taking Barbiturates, Benzodiazepines such as Xanax or Klonopin, Valproic acid (Lithium), Calcium channel blockers, Statins (cholesterol medication)

• Liver or renal dysfunction

Related Conditions & MeSH terms

• Ivermectin

Intervention

Drug:
• Ivermectin
150 mcg/kg ivermectin, by mouth.

Other:
• Placebo
An oral placebo will be administered, once

Locations

Country	Name	City	State
United States	University of Georgia	Athens	Georgia

Sponsors (1)

Lead Sponsor	Collaborator
University of Georgia

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The Number of Cytokines Showing Statistically Significant Changes From Pre-treatment Levels Will be Recorded.	Changes in serum levels of a panel of 41 cytokines will be compared to baseline levels using Luminex methods (HCYTOMAG-60K-PX41 kit from EMD Millipore). No pre-specified threshold was set for biological significance, and the number of cytokines showing a statistically significant (p=<0.05) change from time 0 for each group will be reported. The number of cytokines with significant changes is taken from a comparison of the mean levels in each of the groups, not at the level of individual participants.	Pre-treatment, 4 hours and 24 hours post-treatment
Primary	Number of Transcripts in PBMC With Statistically Significant Changes From Pre-treatment Levels.	Changes in expression levels of approximately 770 genes involved in innate immunity will be measured in peripheral blood mononuclear cells (PBMC) before and after treatment. The number of transcripts with significant changes is taken from a comparison of the mean levels in each of the groups, not at the individual participant level. No pre-determined threshold was set for the biological significance of these changes.	Pre-treatment, 4 hours and 24 hours post-treatment
Secondary	Complete Blood Counts (CBC)	CBCs will be performed before treatment and 24 hrs later	Pre-treatment (0hrs), 24 hours