Entolimod, an Adjuvant for Vaccine Augmentation

Substance Use Disorders Clinical Trial

Official title: Entolimod, an Adjuvant for Vaccine Augmentation

Status Completed

Clinical Trial Summary

The primary objective of this pilot study to evaluate the safety of low dose Entolimod in normal, healthy, non-patient normals. This clinical trial in 40 normal humans compares a single dose of 4 ug Td (2 ug of TT and 2 ug of diphtheria toxoid + 3000 ug of alum with or without entolimod. Subjects will be randomized to: Td alone (n=15) and Td+ entolimod (n=25). The investigators expect that Td + entolimod will double the anti-TT and anti-diphtheria AB levels over Td alone.

Clinical Trial Description

This is a single-blind (participants are blinded), pilot study with no therapeutic or diagnostic intent and limited drug exposure. The study will be conducted at Baylor College of Medicine in normal, healthy, and non-drug using male volunteers who have not received the Td vaccination in the past 5 years.

The purpose of this study is to evaluate the safety and surrogate efficacy of low dose entolimod in normal, healthy, non-patient subjects by comparing anti-tetanus (TT) antibody levels between patients getting entolimod vs no entolimod combined with tetanus-diphtheria (Td) vaccine. Subjects will be randomly assigned to one of two arms in a 3:5 ratio (for every 8 subjects, 3 will be randomly assigned to the control group and 5 to the treatment group) to receive a single dose of:

Arm 1: Td (4 ug) (n=15), Arm 2: Td (4 ug) + Entolimod (1 ug) (n=25)

We propose to give the normal dose of Td given routinely to humans (i.e. TT at 2μg and diphtheria toxoid at 2 ug) for a total protein dose of 4 ug. The proposed dose of entolimod at 1 ug is 30-40 times lesser than that previously given safely to humans. We expect that Td + entolimod will double the anti-tetanus toxoid antibody (anti-TT AB) and anti-diphtheria AB levels over Td alone. We predict that this low dosing of entolimod (1μg) produces no difference in adverse effects from giving Td vaccine alone and that any adverse events will be no different than what is typical as reported in the Physicians' Desk Reference for Td vaccine in humans.

For purposes of this trial, study population age cut-off will be 40 years of age. The reason for this cut-off is that the body produces higher antibody levels in response to vaccines in younger age groups compared to older groups. Further, this study is restricted to males only as a safety measure so that women of child-bearing age are not exposed to entolimod, which has not been given to women of childbearing potential.

We consider our strategy adequate for human safety for several reasons related to risks for this new combination of an existing vaccine and new adjuvant. First, our proposed Td-Entolimod starting dose is the usual approved clinical dose of Td (4 μg containing 2 ug TT + 2 ug diphtheria toxoid). Second, the proposed dose for the adjuvant entolimod (1 μg) is supported by both animal toxicology studies and human safety/PK/PD studies cross-referenced from IND 100480. The results of these safety studies, which have given humans up to 30 μg and animals up to 100μg, strongly support that entolimod at 1μg is a safe human dose. The other adjuvant is aluminum phosphate, which is contained within the standard Td vaccine in humans. Third, further support for safety comes from the recent recommendations to boost pregnant women with Td at each pregnancy regardless whether or not they have recently received a Td shot. This recommendation of acceptable enough safety for ACIP to recommend it for pregnant women, supports that this study's single dosing with Td even at less than a 5 year interval would be relatively low risk. Fourth, other FDA approved conjugate vaccines using TT have contained 8 to 10 times greater doses of TT than in our planned dose. Fifth, we will have a randomization of 25 subjects to the Td-Entolimod combination vaccine, which will provide sufficient numbers of subjects to detect common adverse events such as fever and local site reactions in more than one human subject in our vaccinated group compared to the Td alone control group. Local injection site and systemic inflammatory changes also will be monitored in planned clinical study trials with later TT conjugate anti-addiction vaccines.

The close monitoring of objective and subjective drug effects by direct observation, blood work (CBC and Comprehensive Metabolic Panel), weekly telephone check-ins over a 6 week period from point of vaccination to close-out visit to monitor for potential adverse reactions, and a close-out physical will allow objective evaluation of the effects of the vaccines in these normal subjects. We will also have post treatment follow up period with monthly telephone visits up to 1 year from vaccination to further monitor for adverse reactions.

At 6-weeks post-vaccination, we will analyze level of anti-TT AB and anti-diphtheria AB and compare both study arms compared to baseline AB levels to determine the immune potentiating capability of entolimod. In addition to not expecting any difference in adverse events (AE) from giving Td alone compared to those AE listed in the Physicians' Desk Reference for Td in normals, we also expect the AB levels at 6 weeks post vaccination and the ratio of 6-week to baseline AB levels from Td+entolimod (n=25) to be at least double the levels from Td alone (n=15). ;

Related Conditions & MeSH terms

• Substance Use Disorders
• Substance-Related Disorders

• NCT number: NCT03063736
• Study type: Interventional
• Source: Baylor College of Medicine
• Status: Completed
• Phase: Early Phase 1
• Start date: December 8, 2017
• Completion date: December 31, 2019