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Completed

NCT Number: NCT02998190

First-in-Human Single and Multiple Dose of EB8018

The purpose of this study is to determine the safety profile of single and multiple doses of EB8018 in healthy male subjects, to determine the pharmacokinetic profile of single and multiple doses of EB8018 in healthy male subjects and to assess preliminary effects of EB8018 on the healthy male gut microbiome.

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Key information

Conditions

Age range

18 year–55 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Quotient Clinical

Ruddington, Nottingham, NG11 6JS, United Kingdom

About this study

Crohn's Disease is a chronic inflammatory disease of the gastrointestinal tract. Emerging evidence suggests that the microbiome plays an important role in triggering an abnormal mucosal immune response in patients with Crohn's Disease. Independent studies have demonstrated an imbalance of the microbiome with a significant increase of E coli with invasive properties, termed adherent-invasive E coli (AIEC). These AIEC bacteria attach to the gut wall of susceptible patients via the fimbrial adhesion protein FimH, and subsequently trigger inflammation by invading and proliferating within the gut wall. EB8018 is an oral small molecule that is designed to block FimH thereby preventing the entry of AIEC into the gut wall thereby disarming the bacteria without disrupting the gut microbiome.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy males
  • Age ≥ 18 to ≤ 55 years of age
  • Body mass index of 19.0 to 30.0 kg/m2
  • Normal ECG, showing no clinically relevant deviations, as judged by the investigator (QTcF ≤450 ms)

Exclusion criteria

  • Subjects who have received any Investigational Medicinal Product in a clinical research study within the previous 3 months.
  • History of any drug or alcohol abuse in the past 2 years
  • Regular alcohol consumption in males >21 units per week
  • Current smokers and those who have smoked within the last 12 months
  • Positive drugs of abuse test result
  • Presence or history of clinically significant allergy requiring treatment, as judged by the investigator. Hayfever, even inactive, is not allowed.
  • Chronic infection or acute significant infection or fever within the previous 5 weeks prior to the start of IMP administration
  • Malignancy or prior malignancy, with a disease-free interval of less than 5 years after diagnosis and intervention

Treatment and study plan

Single Ascending Doses of EB8018

Drug

Single Ascending Doses of placebo

Drug

Multiple Ascending Doses of EB8018

Drug

Multiple ascending doses of Placebo

Drug

Primary outcomes

  1. Number of Treatment Related Adverse Event, including Abnormal Laboratory Events to evaluate the safety and tolerability profile of single ascending and multiple ascending doses of EB8018 compared with placebo in healthy subjects

    Time frame: Between screening and 7-10 days after the last dose

    The variables for analysis will be the difference of EB8018 compared with placebo for incidence, severity and type of adverse events, including changes in vital signs, physical examinations, laboratory safety tests and ECGs

Secondary outcomes

  1. The amount of EB8018 in plasma

    Time frame: Between Day 1 predose and 48 hours after the (last) dose

    To characterize the amount of EB8018 in plasma over time - pharmacokinetics (PK) - after a single oral dose and multiple oral doses in healthy subjects

  2. The amount of EB8018 in urine

    Time frame: Between Day 1 predose and 48 hours after the (last) dose

    To characterize the amount of EB8018 in urine over time - pharmacokinetics (PK) - after a single oral dose and multiple oral doses in healthy subjects

  3. The amount of EB8018 in stool

    Time frame: Between predose and 48 hours after the (last) dose

    To characterize the amount of EB8018 in urine over time - pharmacokinetics (PK) - after a single oral dose and multiple oral doses in healthy subjects

  4. Analysis of microbiome richness

    Time frame: Between predose and 48 hours after the (last) dose

    To compare the abundance of gene richness, all phyla and certain species such as E. Coli

Sponsors and collaborators

Lead sponsor

Enterome

Industry

Collaborators

  • Quotient Clinical

Registry information

Official study title

A Randomised, Double-Blind, Placebo-Controlled Study of a Single Ascending Dose (SAD) and Multiple Ascending Dose (MAD) of a FimH Antagonist, EB8018, in Healthy Volunteers.

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Dec 20, 2016
Registry last updated
Feb 13, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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