Condition: Ulcerative Colitis · Sponsor: InDex Pharmaceuticals
The purpose of this study was to evaluate efficacy of cobitolimod treatment at different dose levels and frequencies compared to placebo in patients with moderate to severe left-sided ulcerative colitis.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
Inclusion Criteria: * Age ≥ 18 years old * Established diagnosis of Ulcerative Colitis (UC) * Moderately to severely active left sided UC assessed by central reading * Current oral 5-Aminosalicylic Acid (5-ASA)/ Sulphasalazine (SP) use or a history of oral 5-ASA/SP use * Current Glucocorticosteroids (GCS) use or history of GCS dependency, refractory, or intolerance * Demonstrated an inadequate response, loss of response, or intolerance to at least one of the following agents: * Immunomodulators * Tumor Necrosis Factor alpha (TNF-α) inhibitors and/or anti-integrins Exclusion Criteria: * Suspicion of differential diagnosis * Acute fulminant UC and/or signs of systemic toxicity * UC limited to the rectum (disease which extend \<15 cm above the anal verge) * History of malignancy * History or presence of any clinically significant disorder * Concomitant treatment with cyclosporine, methotrexate, tacrolimus, TNF-α inhibitors, anti-integrins or similar immunosuppressants and immunomodulators * Treatment with rectal GCS, 5-ASA/SP or tacrolimus * Long term treatment with antibiotics or non-steroidal anti-inflammatory drugs (NSAIDs) * Serious active infection * Gastrointestinal infections * Currently receiving parenteral nutrition or blood transfusions * Females who are lactating or have a positive serum pregnancy test * Women of childbearing potential not using reliable contraceptive methods * Concurrent participation in another clinical study * Previous exposure to cobitolimod
Reproduced word-for-word from the public registry record — the study team can answer questions about it.
| 1 | Prague, Czechia | — |
| 2 | Amiens, France | — |
| 3 | Caen, France | — |
| 4 | Clichy, France | — |
| 5 | Grenoble, France | — |
| 6 | Nice, France | — |
| 7 | Pierre-Bénite, France | — |
| 8 | Saint-Etienne, France | — |
| 9 | Toulouse, France | — |
| 10 | Vandœuvre-lès-Nancy, France | — |
| 11 | Augsburg, Germany | — |
| 12 | Berlin, Germany | — |
+ 52 more locations — full list on the registry record.
This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice. By subscribing you agree to our Terms of Use and Privacy Policy.