Safety and Efficacy of EcoActive on Intestinal Adherent Invasive E. Coli in Patients With Inactive Crohn's Disease

Crohn Disease Clinical Trial

Official title:

A Phase 1/2a Double-Blind, Randomized, Placebo-Controlled Trial to Assess the Safety and Efficacy of Oral Administration of EcoActive on Intestinal Adherent Invasive Escherichia Coli (AIEC) in Patients With Inactive Crohn's Disease (CD)

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03808103
• Other study ID #: ITX/EA-002
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: May 1, 2019
• Est. completion date: September 30, 2024

Study information

• Verified date: November 2023
• Source: Intralytix, Inc.
• Contact: Jennifer Schwartz, PhD
• Phone: 667-215-2597
• Email: jschwartz[@]intralytix.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will evaluate the safety of oral administration of EcoActive to patients with inactive Crohn's disease and how it affects the levels of AIEC in stool.

Description:

The purpose of this study is to determine if EcoActive is safe and effective in people with Crohn's disease. EcoActive is a collection of bacteriophages. Bacteriophages (or phages) are viruses that infect only bacteria. The phages in EcoActive infect a specific type of bacteria called Adherent Invasive Escherichia coli (AIEC).

The cause of Crohn's disease is poorly understood. However, the presence of AIEC in the intestines is associated with worsening inflammation in this disease. Inflammation is the presence of redness, irritation, and ulcers in the intestines. By using phages that only infect and kill this specific type of bacteria (AIEC), it is the hope this can be used to improve the course of Crohn's disease. The phages would only target the AIEC, without affecting the natural, often helpful, bacteria of the intestines. EcoActive may also lessen the use of antibiotics to control symptoms. When antibiotics are used, they can have major effects on the rest of the bacteria in the intestines. Also, repeated use can cause intestinal bacteria to become resistant to antibiotics. Reduced use of antibiotics would limit both of these risks.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 30
• Est. completion date: September 30, 2024
• Est. primary completion date: September 30, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Male or female = 18 years of age

2. Inactive Crohn's disease in clinical and objective remission with a Harvey-Bradshaw Index (HBI) < 4

3. Permitted CD medications expected to remain stable during the period of the study (see Section 7 "Concomitant Crohn's Disease Medications" for allowed and prohibited drugs).

4. Crohn's disease history = 6-month duration

5. CRP (C-reactive protein) within normal range at the Screening visit (based on normal range of the local laboratory)

6. Fecal calprotectin level = 150 µg/g at the Screening visit

7. AIEC detected in the stool

8. Females of childbearing age must be using an effective method of contraception to prevent pregnancy and agree to continue to practice an acceptable method of contraception for the duration of participation in the study (contraceptive measures considered adequate are: intrauterine devices, hormonal contraceptives, such as contraceptive pills, implants, transdermal patches, hormonal vaginal devices or injections with prolonged release).

9. Negative pregnancy test for women of childbearing age (menarche to menopause)

10. Patient understands the study procedures, and can sign the informed consent, and the authorization to release relevant protected health information to the Study Investigator.

Exclusion Criteria:

1. Active Crohn's disease with a Harvey-Bradshaw Index (HBI) = 4

2. Ongoing gastrointestinal pathology: colorectal tumor, gastrointestinal bleeding

3. Active malignancies or any malignant disease within the past 5 years

4. Indeterminate colitis, ulcerative colitis

5. Colectomy or partial colectomy (less than ileo-transverse colonic anastomosis).

6. Colonic or small bowel stoma

7. Active perianal lesions

8. Women who are pregnant or nursing, or plan to become pregnant during the study period

9. Severe uncontrolled diseases that could increase the risk for subjects participating in the study, including but not limited to: heart diseases, congestive heart failure, hypertension, lung diseases; endocrine diseases; clinically significant renal disease characterized by a glomerular filtration rate < 60mL/min, hepatic diseases, haematological disorders, or other conditions that in the opinion of the Investigator could interfere with the interpretation of the study results.

10. Taking supplemental probiotics in the form of pills or tablets.

11. History or planned procedures specifically aimed at modifying the gastrointestinal microbiota within the past year.

12. Topical gastrointestinal treatment (e.g., enemas) in the 2 weeks prior to the Screening visit or planned during the study period

13. Use of bowel cleansing or preparation for endoscopy, TDM or MRI in the 4 weeks prior to the Screening visit or planned during the study period.

14. Receipt of antibiotics 4 weeks before the Screening visit or planned during the study period.

15. Known allergy or hypersensitivity to an excipient in the study drug or placebo

16. Psychological or linguistic incapability to sign the informed consent.

17. Lack or expected lack of cooperation or compliance with the study.

18. Receipt of mesalamine based therapies within 4 weeks of the screening visit.

19. Severe psychiatric, psychological, or neurological disorders.

20. Alcohol, drug or medication abuse within the past year.

21. Subject who cannot be contacted in case of emergency.

Related Conditions & MeSH terms

• Crohn Disease

Intervention

Biological:
• Placebo
Orally, twice a day, for a period of fifteen days
• Bacteriophage preparation
Orally, twice a day, for a period of fifteen days

Locations

Country	Name	City	State
United States	Johns Hopkins Green Spring Station	Lutherville	Maryland
United States	Icahn School of Medicine at Mount Sinai Hospital	New York	New York

Sponsors (3)

Lead Sponsor	Collaborator
Intralytix, Inc.	Icahn School of Medicine at Mount Sinai, Johns Hopkins University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence of adverse events	The number of solicited and unsolicited adverse events will be recorded.	Up to 6 months
Primary	Severity of adverse events	The severity will be graded according to the definitions and values stated in CTCAE V04 v4.	Up to 6 months
Primary	Effect on Harvey Bradshaw Index (HBI)	The effect on Crohn's disease activity will be evaluated using the HBI.	Up to 6 months
Primary	Effect on inflammation, as indicated by C-reactive protein (CRP)	The changes in CRP from baseline will be evaluated.	Up to 6 months
Primary	Effect on inflammation, as indicated by fecal calprotectin	The changes in fecal calprotectin levels from baseline will be evaluated.	Up to 6 months
Secondary	Effect on the incidence and levels of AIEC	The secondary objective is to assess the effect of oral phage administration on the AIEC (CFU/g) in stools of patients receiving phages vs. patients receiving placebo.	Up to 6 months