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Study identifier: NCT03178669 Synced from ClinicalTrials.gov · August 11, 2026
● Study status: CompletedCONDUCT

The Efficacy of Cobitolimod in Patients With Moderate to Severe Active Ulcerative Colitis

Condition: Ulcerative Colitis  ·  Sponsor: InDex Pharmaceuticals

PhasePhase 2
Planned participants213
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where64 locations · 10 countries
For sponsors, CROs & site teams
Professional view of this study — listed sites, countries and recruiting context from the public registry. Everything below is written for patients and caregivers.See where this study is running →

About this study

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.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

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.

Locations (64)

1Prague, Czechia
2Amiens, France
3Caen, France
4Clichy, France
5Grenoble, France
6Nice, France
7Pierre-Bénite, France
8Saint-Etienne, France
9Toulouse, France
10Vandœuvre-lès-Nancy, France
11Augsburg, Germany
12Berlin, Germany

+ 52 more locations — full list on the registry record.

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

PragueAmiensCaenClichy

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