Golimumab in Ulcerative Colitis (UC) Patients With Loss of Response (LOR) Followed by Dose Optimization (GOLILOR)

Centre Hospitalier Universitaire de Saint Etienne

Status and phase: Completed; Phase 2

Conditions: Ulcerative Colitis

Treatments: Drug: Golimumab (Optimization); Diagnostic Test: Rectosigmoidoscopy; Biological: Blood samples

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT03182166

1608162

2016-004245-85 (EudraCT Number)

Details and patient eligibility

About

It is planned to enroll 80 UC patients who will require optimization of golimumab after secondary LOR. The review of the study protocol and its approval by an Independent Ethics Committee of the University of Saint Etienne are pending. All patients enrolled will give their written informed consent before being included. This study will be conducted in accordance with the ethical principles that have their origins in the Declaration of Helsinki, in compliance with the approved protocol, good clinical practice and applicable regulatory requirements. Patients will visit the investigator from screening visit to visit 6 at W-1, W0, W2, W4, W8, and at the end of the follow-up at wk 24. During their participation, patients will record clinical parameters required to calculate the partial Mayo score reported over 3 days prior to the visit and endoscopy at W0, W2 (optional) , W4, W8 (optional) and at the end of the follow-up to calculate total Mayo score.

Enrollment: 51 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Affiliate or beneficiary of social security
• Age>18 years
• Pregnant women or man
• Presenting primary response under golimumab induction and in loss of response during maintenance therapy
• Patient with an ulcerative colitis
• Treated with golimumab
• Signature of consent

Exclusion criteria

• Trying to become pregnant
• Mental or emotional disorders
• Patients with crohn's disease or indeterminate colitis
• cancer(<5)
• Patients not in agreement with this study protocol
• Patients with crohn's disease or indeterminate colitis
• Patients non primary responder to golimumab

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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51 participants in 1 patient group

Patients treated with golimumab

Experimental group

Description:

The optimization procedure is: * For patients treated at 50 mg of golimumab every 4 weeks (less than 80 kg) will have an increase dose of golimumab: 100 mg every 4 weeks for 8 weeks. They will have rectosigmoidoscopy for measured mayo score and blood samples for measured the concentration of golimumab antibodies. * For patients treated at 100 mg of golimumab every four weeks (more than 80 kg) will have an increase dose of golimumab: treated at 100 mg every 2 weeks for 4 weeks. They will have rectosigmoidoscopy for measured mayo score and blood samples for measured the concentration of golimumab antibodies.

Treatment:

Biological: Blood samples

Drug: Golimumab (Optimization)

Diagnostic Test: Rectosigmoidoscopy