The ASCENTRA-UC study is a phase 2 study testing PALI-2108 in patients with moderate to severe ulcerative colitis. Doses of drug will be compared against a placebo to see how well it works, how safe it is, and how the body responds to it.
Eligibility
Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Key Inclusion Criteria:
* Documented clinical diagnosis of UC for ≥ 3 months prior to Screening. The diagnosis of UC must be confirmed by endoscopic and histologic evidence.
* If a histopathology report is not available in the source records, a biopsy for a local histopathology evaluation (to obtain a report) can be obtained during the screening endoscopy procedure.
* Moderately to severely active UC, defined as:
* mMS of 5 to 9 (inclusive), AND
* ES ≥ 2, AND
* RB ≥ 1.
* Participants must satisfy at least one of the criteria listed under item a OR at least one of the criteria listed under item b:
a. History of inadequate response or loss of response, or intolerance to at least one prior UC therapy, defined as: i. Oral prednisone ≥ 40 mg/day (or equivalent) or budesonide ≥ 9 mg/day for ≥ 2 weeks.
ii. Corticosteroid dependence: unable to taper \< 10 mg/day prednisone equivalent within 3 months, or relapse within 3 months of discontinuation.
iii. Immunosuppressants: azathioprine ≥ 2 mg/kg/day, 6-mercaptopurine (6-MP) ≥ 1.0 mg/kg/day (or therapeutic 6-thioguanine nucleotide \[6-TGN\] level) for ≥ 12 weeks, or methotrexate ≥ 15 mg/week subcutaneous or intramuscular.
iv. Approved advanced therapies at the approved labelled dose:
1. Anti-tumor necrosis factor (TNF), anti-integrin (vedolizumab), or anti-IL-12/23 for at least 8 weeks; anti-IL 23 for at least 12 weeks.
2. Janus kinase (JAK) inhibitor for at least 8 weeks; sphingosine-1-phosphate receptor (S1PR) modulator for at least 12 weeks.
Note: Demonstration of intolerance requires no minimum dose nor duration of use.
b. Currently receiving one or more of the following treatments: i. Stable oral prednisone at ≤ 20 mg/day (or equivalent) or budesonide ≤ 9 mg for ≥ 2 weeks prior to randomization.
ii. Stable dose of thiopurine (azathioprine or 6-MP) for ≥ 4 weeks prior to randomization, and have started the treatment ≥ 12 weeks prior to randomization.
iii. Stable dose of oral aminosalicylates for ≥ 2 weeks prior to randomization.
Key Exclusion Criteria:• Diagnosis of Crohn's disease or IBD-Unclassified (IBD-U; indeterminate colitis) or a history of ischemic colitis or radiation colitis.
* UC limited to rectum (\< 15 cm from anal verge).
* Any prior history of suicidal behavior (actual, interrupted, aborted attempt, or preparatory acts).
* Columbia-Suicide Severity Rating Scale (C-SSRS) suicidal ideation type 4 or 5, or any active suicidal ideation with some intent to act.
* Severe depression at Screening based on a validated scale threshold (e.g., Patient Health Questionnaire-9 \[PHQ-9\] ≥ 20, or PHQ-9 item 9 \> 0) at Screening.
* Failure or intolerance of \> 3 classes of approved advanced therapies or \> 4 approved individual advanced therapies.
Primary outcome measure(s)
Proportion of participants with clinical remission using the 3-component modified Mayo Score (mMS) at Week 12. — Week 12 The Modified Mayo Score (MMS) is a composite score of ulcerative colitis (UC) disease activity on a scale of increasing severity from 0-9, calculated by summing three subscores: Endoscopic subscore (ES), scored on a scale of increasing severity from 0 (normal or inactive disease) to 3 (severe disease, such as spontaneous bleeding or ulceration); Stool frequency subscore (SFS), scored on a scale of increasing frequency from 0 (normal number of stools) to 3 (≥5 stools more than normal per day for the participant); and rectal bleeding subscore (RBS), scored on a scale of increasing severity from 0 (no blood seen) to 3 (blood alone passed). Clinical Remission is defined as an ES of 0 or 1, RBS of 0, and SFS of 0 or 1 and not greater than the baseline SFS.
Trial sites (115)
Facility
City
Region
Status
Site US-022
Sun City
Arizona
Recruiting
Site US-018
San Diego
California
Not Yet Recruiting
Site US-028
Bristol
Connecticut
Not Yet Recruiting
Site US-026
Orlando
Florida
Recruiting
Site US-005
Des Plaines
Illinois
Recruiting
Site US-007
Glenview
Illinois
Recruiting
Site US-020
Gurnee
Illinois
Recruiting
Site US-008
Baton Rouge
Louisiana
Not Yet Recruiting
Site US-011
Mandeville
Louisiana
Recruiting
Site US-010
Tupelo
Mississippi
Not Yet Recruiting
Site US-006
St Louis
Missouri
Recruiting
Site US-014
Clifton
New Jersey
Recruiting
Site US-002
Albany
New York
Recruiting
Site US-016
Rochester
New York
Recruiting
Site US-025
Brunswick
Ohio
Recruiting
Site US-023
Dayton
Ohio
Recruiting
Site US-027
Westlake
Ohio
Recruiting
Site US-019
Providence
Rhode Island
Recruiting
Site US-003
Cordova
Tennessee
Recruiting
Site US-024
Garland
Texas
Recruiting
Site US-009
Georgetown
Texas
Recruiting
Site US-030
Houston
Texas
Recruiting
Site US-015
Lubbock
Texas
Recruiting
Site US-017
Mansfield
Texas
Recruiting
Site US-001
Southlake
Texas
Recruiting
Site US-004
Tyler
Texas
Not Yet Recruiting
Site US-013
Richmond
Virginia
Recruiting
Site US-021
Bellevue
Washington
Recruiting
Site US-029
Tacoma
Washington
Recruiting
Site US-012
Milwaukee
Wisconsin
Not Yet Recruiting
Site CA-005
Calgary
Alberta
Not Yet Recruiting
Site CA-004
Edmonton
Alberta
Not Yet Recruiting
Site CA-006
Greater Sudbury
Ontario
Not Yet Recruiting
Site CA-003
London
Ontario
Not Yet Recruiting
Site CA-002
Scarborough Village
Ontario
Not Yet Recruiting
Site CA-007
Montreal
Quebec
Not Yet Recruiting
Site CA-001
Montreal
Quebec
Not Yet Recruiting
Site CZ-005
Brno
Czechia
Not Yet Recruiting
Site CZ-002
Brno
Czechia
Not Yet Recruiting
Site CZ-008
Havířov
Czechia
Not Yet Recruiting
+ 75 more sites — see the full list on the official registry below.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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