Phase 3
Completed N=60
(CB-01-02/06) Oral Budesonide-Multi-Matrix System (MMX) 9mg Extended Release Tablets
Colitis, Ulcerative
Source: ClinicalTrials.gov NCT01100112 ↗
Enrolled (actual)
60
Serious AEs
3.3%
Results posted
Jun 2014
Primary outcomePrimary: The Percentage of Patients Achieving Clinical Remission — 25 percentage of patients
Summary
Open-label, 8 week study, to assess the efficacy and safety of oral Budesonide-MMX 9 mg Extended-release Tablets in patients with mild to moderate, active ulcerative colitis who are not in remission based on the Ulcerative Colitis Disease Activity Index in study CB-01-02/01 (parent study [NCT00679432]).
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY The Percentage of Patients Achieving Clinical Remission |
25 | — |
| SECONDARY The Secondary Efficacy Endpoint is Clinical Improvement |
26.7 | — |
| SECONDARY Safety Evaluations: the Numbers of Patients Who Experience Serious Adverse Events (SAEs) or Other Nonserious Adverse Events (AEs) During the Course of the Study. |
2; 29 | — |
| SECONDARY Endoscopic Improvement |
40 | — |
Eligibility Criteria
Inclusion Criteria
- Male and female patients 18 to 74 years of age, who are able to understand and voluntarily provide written informed consent
- Completed all Final Visit assessments for study CB-01-02/01 (NCT00679432) and are not in clinical remission
- Diagnosis of ulcerative colitis of mild to moderate severity with an Ulcerative Colitis Disease Activity Index (UCDAI) 10)
- Patients with infectious colitis
- Evidence or history of toxic megacolon
- Severe anemia, leucopenia, or granulocytopenia
- Use of immunosuppressive agents in the last 8 weeks before the study
- use of anti-tumor necrosis factor alpha agents in the last three months
- Concomitant use of any rectal preparation for the treatment of ulcerative colitis
- Concomitant use of antibiotics
- Concurrent use of cytochrome P-450 3A4 (CYP3A4) inducers and CYP3A4 inhibitors.
- Patients with verified, presumed of expected pregnancy or ongoing lactation
- Patients with liver cirrhosis, or evident hepatic or renal disease or insufficiency and/or severe impairment of the bio-humoral parameters (i.e., 2x upper limit of normal for alanine aminotransferase, aspartate aminotransferase, gamma-glutamyl transpeptidase, or creatinine)
- Patients with severe disease(s) in other organs of systems
- Patients with local of systemic complications of other pathological states requiring a therapy with corticosteroids and/or immunosuppressive agents
- Patients diagnosed with Type 1 diabetes
- Patients diagnosed with or with a family history of glaucoma
- Patients with known hepatitis B, hepatitis C, or with human immunodeficiency virus (HIV), according to the local privacy policy
- Any other medical condition that in the principal investigator's opinion would make the administration of the study drug or study procedures hazardous to the subject or obscure the interpretation of adverse events
Data sourced from ClinicalTrials.gov (NCT01100112). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.