Status:
RECRUITING
A Study to Investigate the Efficacy and Safety of NSI-8226 in Adults With Eosinophilic Esophagitis
Lead Sponsor:
Uniquity One (UNI)
Conditions:
Eosinophilic Esophagitis (EoE)
Eligibility:
All Genders
18-75 years
Phase:
PHASE2
Brief Summary
Phase 2 study to evaluate the safety, tolerability, PK, immunogenicity, and pharmacodynamics of solrikitug in adult participants with eosinophilic esophagitis.
Detailed Description
This is a 24-week randomized, double-blind, placebo-controlled Phase 2 clinical study with a 28-week extension to evaluate the safety, tolerability, PK, immunogenicity, and pharmacodynamics of 3 dose ...
Eligibility Criteria
Inclusion
- Key inclusion criteria
- Part A
- Participant must be 18 to 75 years of age inclusive, at the time of signing the informed consent.
- Established diagnosis of EoE with a previous EGD and esophageal biopsy confirming diagnosis of EoE.
- Participants who have symptomatic EoE as defined by a history of on average at least 2 episodes of dysphagia per week in the 4 weeks prior to Screening.
- Must remain on a stabilized diet for at least 8 weeks prior to Visit 1 and during the course of the study.
- May be on any background PPI and/or STC, during the course of the study, as long as background medications have been stable for at least 8 weeks prior to the Screening and must agree to no changes to background medication or dosage unless medically indicated.
- Discontinuation of any marketed investigational drug or biologic (monoclonal or polyclonal antibody) within 30 days or 5 half-lives prior to screening, whichever is longer.
- Participants should have previously documented standard of care treatment, which could include PPI and/or STC and/or diet.
- Key exclusion criteria
- Part A
- Female participant who is pregnant or breastfeeding.
- Have a history or presence of any other gastrointestinal disorders such as active Helicobacter pylori infection, history of achalasia, hyper eosinophilic syndrome and eosinophilic granulomatosis with polyangiitis, esophageal varices, Crohn's disease, ulcerative colitis, inflammatory bowel disease, celiac disease, eosinophilic enteritis, gastritis, colitis, diverticulitis, irritable bowel syndrome, or other clinically significant gastrointestinal conditions as per Investigator discretion.
- Esophageal stricture that prevents the easy passage of a standard endoscope or any critical esophageal stricture that requires dilation at screening.
- Esophageal dilation performed within 8 weeks prior to screening.
- Participant has a known hypersensitivity to any component of the formulation of solrikitug, including any of the excipients, or a history of anaphylactic reaction to any therapeutic monoclonal antibody.
- Part B
- Participants who, during Part A, developed a serious adverse event (SAE) and/or adverse event (AE) deemed related to study drug, which in the opinion of the investigator could indicate that continued treatment with study drug may present and unreasonable risk to the participant.
- Participants who became pregnant during Part A.
- Participants who are prematurely discontinued from study drug due to AE (patients who are prematurely discontinued from study drug due to lack of efficacy are eligible to enter Part B).
- Patients who did not undergo endoscopy with biopsies prior to receiving rescue treatment.
Exclusion
Key Trial Info
Start Date :
October 16 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 31 2027
Estimated Enrollment :
157 Patients enrolled
Trial Details
Trial ID
NCT06598462
Start Date
October 16 2024
End Date
August 31 2027
Last Update
August 12 2025
Active Locations (56)
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1
Research Site 1039
Dothan, Alabama, United States, 36305
2
Research Site 1037
Paradise Valley, Arizona, United States, 85253
3
Research Site 1018
Peoria, Arizona, United States, 85306
4
Research Site 1037
Scottsdale, Arizona, United States, 85258