A Study to Assess the Efficacy, Safety and Tolerability of IRL201104 in Adults With Active Eosinophilic Esophagitis

NCT ID: NCT05084963

Last Updated: 2025-05-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 36 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-10-29
• Study Completion Date: 2022-10-24

Brief Summary

The purpose of this study is to asses the efficacy, safety and tolerability of repeat doses of IRL201104 in Adult Participants with Active Eosinophilic Esophagitis (EoE)

Conditions

Eosinophilic Esophagitis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Arm 1: IRL201104 Dose A

IRL201104 IV on Days 0, 7, and 14

Group Type: EXPERIMENTAL

IRL201104

Intervention Type: DRUG

lyophilised powder for reconstitution for IV dosing

Arm 2: IRL201104 Dose B

IRL201104 IV on Days 0, 7, and 14

Group Type: EXPERIMENTAL

IRL201104

Intervention Type: DRUG

lyophilised powder for reconstitution for IV dosing

Arm 3: Placebo

Placebo IV on Days 0, 7, and 14

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Matching placebo for IRL201104

Interventions

IRL201104

lyophilised powder for reconstitution for IV dosing

Intervention Type: DRUG

Placebo

Matching placebo for IRL201104

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Age 18 to 75 years old, inclusive, at the time of signing the informed consent form.

2. Documented diagnosis of EoE by endoscopy prior to screening. Note: Must include a demonstration of intraepithelial eosinophilic infiltration (peak cell count ≥ 15 eos/hpf [400×]) from esophageal biopsy specimens from endoscopy.

3. History (by participant report) of on average at least 2 episodes of dysphagia (with intake of solids off anti-inflammatory therapy) per week in the 4 weeks prior to screening, and on average at least 2 episodes of documented dysphagia per week during any 2 consecutive weeks (qualifying period) between screening and baseline; dysphagia is defined as trouble swallowing solid food, or having solid food stick, by participant report; and completed the DSQ on ≥ 70% of days during the qualifying period prior to baseline (Visit 1).

4. Must remain on a stabilized diet for at least 6 weeks prior to screening and during the course of the study; stable diet is defined as no initiation of single or multiple elimination diets or reintroduction of previously eliminated food groups.

5. Must be willing and able to continue any dietary therapy and/or medical regimens (including gastric acid suppression) in effect at the screening visit. There should be no change to these regimens during the study participation.

6. Willing and able to comply with all clinic visits and study-related procedures.

7. Able to understand and complete study-related questionnaires.

8. Provide signed informed consent.

9. Esophagogastroduodenoscopy (EGD) with photographs performed at screening (qualifying EGD), with a demonstration of intraepithelial eosinophilic infiltration (peak cell count ≥15 eos/hpf) in at least 2 of the 3 biopsied esophageal regions (proximal, mid, or distal).

Exclusion Criteria

1. Prior participation in an IRL201104 clinical study.

2. Has any current disease of the gastrointestinal tract (aside from EoE) that may impact, in the investigator's opinion, the patient's EoE disease status. This includes, but not limited to: eosinophilic gastritis, eosinophilic enteritis, eosinophilic duodenitis, eosinophilic colitis, or proctitis; inflammatory bowel disease; or celiac disease.

3. Has other causes of esophageal eosinophilia or the following diseases: hypereosinophilic syndromes, Churg-Strauss vasculitis (eosinophilic granulomatosis with polyangiitis), or peripheral blood absolute eosinophil count of > 1500 eosinophils/μL.

4. Has presence of oral or esophageal mucosal infection of any type.

5. Has any condition affecting the esophageal mucosa or altering esophageal motility other than EoE.

6. History of achalasia, active Helicobacter pylori infection, Crohn's disease, ulcerative colitis, celiac disease, and prior esophageal surgery (with the exception of a surgical repair of an EoE complication).

7. Any esophageal stricture unable to be passed with a standard, diagnostic, adult (9 to 10 mm) upper endoscope or any critical esophageal stricture that requires dilation at screening; or dilation within 2 months prior to screening.

8. On a pure liquid diet or any mouth or dental condition that prevents normal eating.

9. Has initiated, discontinued, or changed dosage regimen of PPIs within the 4 weeks prior to the qualifying EGD, between the qualifying EGD and baseline visit (Visit 1), or anticipates changes in the use of PPI during the study. PPI must remain constant throughout the study.

10. History of bleeding disorders or esophageal varices.

11. Use of anticoagulants within 2 weeks prior to screening. Participants should not stop these agents solely to become eligible for entry into this study.

12. Treatment with an investigational drug within 2 months or within 5 half-lives (if known), whichever is longer, prior to screening.

13. Use of systemic corticosteroids within 3 months or swallowed topical corticosteroids within 6 weeks prior to screening.

14. Treatment with oral immunotherapy (OIT) within 6 months prior to screening.

15. Allergen immunotherapy (sublingual immunotherapy [SLIT] and/or subcutaneous immunotherapy [SCIT]), unless on a stable dose for at least 1 year prior to screening.

16. The following treatments within 3 months before the screening visit, or any condition that, in the opinion of the investigator, is likely to require such treatment(s) during the study:

Systemic immunosuppressive/immunomodulating drugs (eg, omalizumab, cyclosporine, mycophenolate-mofetil, interferon [IFN]γ, Janus kinase inhibitors, azathioprine, methotrexate, and other biologics that are ongoing [eg, dupilumab, benralizumab, mepolizumab, or vedolizumab]).

17. Diagnosed with active parasitic infection; or suspected parasitic infection, unless clinical and (if necessary) laboratory assessments have ruled out active infection before randomization.

18. Chronic or acute infection requiring treatment with systemic antibiotics, antivirals, or antifungals within 1 month prior to screening.

19. Use of oral antibiotics/anti-infectives within 2 weeks prior to screening.

20. Known or suspected immunosuppression, including history of invasive opportunistic infections (eg, tuberculosis, non-tuberculous mycobacterial infections, histoplasmosis, listeriosis, coccidioidomycosis, pneumocystosis, aspergillosis) despite infection resolution, or otherwise recurrent infections of abnormal frequency, or prolonged infections suggesting an immunocompromised status, as judged by the investigator.

21. Known history of human immunodeficiency virus (HIV) infection.

22. Positive or indeterminate hepatitis B surface antigen (HBsAg) or hepatitis C antibody at screening.

23. Moderate or severe renal impairment (eGFR <60 mL/min/1.73 m2) or end stage renal disease.

24. Elevated transaminases (alanine aminotransferase [ALT] and/or aspartate aminotransferase [AST]) > 3 times the upper limit of normal (ULN) at screening.

25. History of malignancy within 5 years prior to screening, except completely treated in situ carcinoma of the cervix and completely treated and resolved nonmetastatic squamous or basal cell carcinoma of the skin.

26. Any other medical or psychological condition including relevant laboratory abnormalities at screening that, in the opinion of the investigator, suggest a new and/or insufficiently understood disease, may present an unreasonable risk to the participant as a result of his/her participation in this clinical study, may make the participant's participation unreliable, or may interfere with study assessments. The specific justification for participants excluded under this criterion will be noted in study documents (eg, chart notes, electronic case report form). These may include participant-reported alcohol or drug abuse and severe concomitant illness(es).

28. Treatment with a live (attenuated) vaccine within 3 months prior to screening and/or treatment of a killed vaccine within 30 days prior to screening, until the end of the study with the exception of a coronavirus disease of 2019 (COVID-19) vaccine, as described in Section 9.2.1.

29. Pregnant or breastfeeding women, or women planning to become pregnant or breastfeed during the study.

30. Women unwilling to use adequate birth control, if of reproductive potential* and sexually active. Adequate birth control is defined as agreement to consistently practice an effective and accepted method of contraception throughout the duration of the study and for 30 days after the last dose of study treatment. These include: hormonal contraceptives, intrauterine device, or double barrier contraception (ie, condom and diaphragm), or male partner with documented vasectomy.

• For females, menopause is defined as at least 12 consecutive months without menses; to include laboratory confirmation of post-menopausal status (ie, a follicle stimulating hormone (FSH) of 2.25 U/mL must be documented). Hysterectomy, bilateral oophorectomy, or bilateral tubal ligation must be documented, as applicable; if documented, women with these conditions are not required to use additional contraception.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Revolo Biotherapeutics

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Michael Weinreich, MD, PhD

Role: STUDY_DIRECTOR

Senior Director, Revolo Biotherapeutics

Locations

Revolo Investigational Site

Little Rock, Arkansas, United States

Revolo Investigational Site

Murrieta, California, United States

Revolo Investigational Site

Centennial, Colorado, United States

Revolo Investigational Site

New Port Richey, Florida, United States

Revolo Investigational Site

Orlando, Florida, United States

Revolo Investigational Site

Sandy Springs, Georgia, United States

Revolo Investigational Site

Iowa City, Iowa, United States

Revolo Investigational Site

Crowley, Louisiana, United States

Revolo Investigational Site

Marrero, Louisiana, United States

Revolo Investigational Site

Boston, Massachusetts, United States

Revolo Investigational Site

Boston, Massachusetts, United States

Revolo Investigational Site

Farmington Hills, Michigan, United States

Revolo Investigational Site

Great Neck, New York, United States

Revolo Investigational Site

Chapel Hill, North Carolina, United States

Revolo Investigational Site

Durham, North Carolina, United States

Revolo Investigational Site

Raleigh, North Carolina, United States

Revolo Investigational Site

Mentor, Ohio, United States

Revolo Investigational Site

Chattanooga, Tennessee, United States

Revolo Investigational Site

Kingsport, Tennessee, United States

Revolo Investigational Site

Baytown, Texas, United States

Revolo Investigational Site

Harlingen, Texas, United States

Revolo Investigational Site

Riverton, Utah, United States

Revolo Investigational Site

Salt Lake City, Utah, United States

Countries

United States

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

RVLO 121-04

Identifier Type: -

Identifier Source: org_study_id