Clinical trial · Interventional
Study of COLAL-PRED to Treat Moderate to Severe Ulcerative Colitis
A Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study of COLAL-PRED in the Treatment of Patients With Moderate to Severe Ulcerative Colitis
NCT00676832CI-TRIAL-00003975completedPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this study is to determine whether COLAL-PRED is a safe and effective treatment for patients with moderate to severe ulcerative colitis.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Colitis, Ulcerative | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| COLAL-PRED | Drug | — | UNRESOLVED |
| Placebo | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (5)
- type
- PLACEBO_COMPARATOR
- label
- Group 1
- interventionNames
- Drug: Placebo
- type
- EXPERIMENTAL
- label
- Group 2
- interventionNames
- Drug: COLAL-PRED
- type
- EXPERIMENTAL
- label
- Group 3
- interventionNames
- Drug: COLAL-PRED
- type
- EXPERIMENTAL
- label
- Group 4
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria:
* Females must be of non-childbearing potential evidenced by being surgically sterile, postmenopausal for at least 12 months or be using acceptable contraception methods such as contraceptive pill, or two forms of barrier contraception.
* Disease Activity Index (DAI) Score of 6-10 (inclusive) at the Baseline Visit.
* Previous colonoscopic and biopsy diagnosis of ulcerative colitis with negative evaluation of the ileum within 3 years of the screening visit.
* Endoscopic evidence of moderate or severe mucosal disease as assessed by flexible sigmoidoscopy, with a minimum confirmed diagnosis of moderate ulcerative colitis.
* The following concomitant prescription medications for ulcerative colitis are permitted if the following conditions are met:
1. Oral 5-aminosalicylic acid (5-ASA )therapy if the following 2 criteria are met:
1. Must be on a stable dose 2 weeks prior to baseline
2. Must maintain the stable dose until treatment end.
2. Azathioprine or 6-mercaptopurine or methotrexate if the 4 following criteria are met:
1. On therapy continually for at least 3 months prior to baseline.
2. And on a stable dose for at least 2 weeks prior to baseline.
3. And must maintain the stable dose until the end of study drug treatment.
Exclusion Criteria:
* History of colonic or rectal surgery, excluding hemorrhoidal surgery or an appendectomy.
* Pregnant or breast-feeding females.
* Diagnosis of diabetes, heart failure, unstable angina, hepatic cirrhosis, kidney failure, adrenocortical insufficiency, or any other unstable medical condition.
* Known hypersensitivity to corticosteroids
* Use of oral 5-aminosalicylic acid (5-ASA) or oral corticosteroids during the immediate screening period.
* Use of immunosuppressive drugs or antibiotics at any time within four weeks prior to screening.
* Diagnosis of Crohn's disease; indeterminate colitis; microscopic colitis; ischemic, infectious (e.g., salmonella, shigella, etc.), or amebic colitis; or gonococcal proctitis; Clostridium difficile colitis.
* History of tuberculosis or HIV
* Clinically significant abnormal laboratory test results, unless regarded by the Investigator as related to ulcerative colitis
* History of alcohol or drug abuse
* Known malignancy or history of malignancy that would reduce life expectancy
* Recent immunization with live viral vaccines
* History of or active peptic ulcer disease or gastritis
* Generalized infections such as systemic fungal or hepatitis B or C
* History of steroid induced severe hypertension, steroid-induced psychosis, or any other severe steroid-related adverse reactionReferences
Publications (0)
Data not yet available
No reference posted for this study.