EFFICACY AND SAFETY OF S.C. INFLIXIMAB IN PATIENTS SWITCHED FROM I.V. FORMULATION OF INFLIXIMAB

San Donato Group (GSD)

Status: Enrolling

Conditions: Rheumatologic Disease; Inflammatory Bowel Diseases

Treatments: Drug: CT-P13

Study type: Observational

Funder types: Other

Identifiers

NCT05719389

BIO BETTER SWITCH

Details and patient eligibility

About

Phase-IV, national, multicentric, non-randomized, observational real-life study. The goal of this stud is to investigate the patient's benefits in terms of quality of life and work ability resulting from the switch from infliximab i.v. to s.c. in patients with gastroenterological or rheumatological indication at month 12.Patients who are eligible but were switched before the inclusion in this study will also be enrolled, and the data already collected according to clinical practice and consistent with the study outcome measures will be used retrospectively. All patients will be followed up according to the standard of care of each participating center.

The main questions it aims to answer are:

1. To investigate the effectiveness at month 2, 6 and 12 after switching to infliximab s.c.

2. To investigate the safety profile at month 2, 6 and 12 after switching to infliximab s.c.

3. To investigate the difference between patients with rheumatological diseases and patients with IBD in terms of quality of life and work, effectiveness and safety at month 2, 6 and 12 after switching.

4. To investigate the presence of baseline predictors for drug persistence at month 12 (sex, age, disease type, disease severity, body mass index, concomitant medications, smoking habit, presence of comorbidities).

5. To investigate whether there is any change between baseline and week 52 in the following aspects:

   • Job type and need for any authorization to go to the hospital to receive the study drug
   • Distance and duration of the travel home-hospital
   • Mode of travel home-hospital
   • Need for a caregiver to be present
   • Time spent at hospital
   • Patient's preference for the way of study drug administration expressed on a 10-grades VAS scale.

The study period for observation will be 12 months from the date of switch. At week 0, month 2, 6 and 12 from the date of the switch, clinical activity, safety data and biomarker levels will be collected.

For those patients who have had an endoscopic evaluation of the disease within 2 months of inclusion and repeat the endoscopic evaluation at 12 months ± 8 weeks, endoscopic data will also be collected (valid only in the presence of IBD).

In those centers where a blood sample to analyze the minimum levels and anti-drug antibodies of infliximab has been collected and/or stored within 2 months prior to the date of transition, the patient will be asked to give informed consent to the use of this sample and to provide a blood sample for the same analysis at week 0, month 2 and 12. These samples will be analyzed and compared to evaluate the immunogenicity of the drug. These analyzes will be centralized in one lab.

Full description

250 patients with confirmed diagnosis of Crohn's disease or ulcerative colitis, rheumatoid arthritis, ankylosing spondylitis or psoriatic arthritis;, aged≥ 18, with full ability to understand study procedures and sign an informed consent form, exposed to infliximab i.v. for at least the minimum time required by the current SmPC, and switched to infliximab s.c. 120 mg q2w since the launch date of s.c. infliximab into the Italian market will be prospectively enrolled.

Descriptive analyses will be used for all results. Since there is no control arm, a comparison will be made between the study outcomes and the expected rates reported in the literature for patients treated with infliximab. Survival analyses will be used to acquire and analyze safety and treatment persistence endpoints. Depending on the normality in the distribution of the variables, parametric and non-parametric tests will be used to perform the appropriate statistical analyzes. For all statistical analyzes, a p value <0.05 will be considered as the limit for significance.

Enrollment period:18 months after the approval of the relevant ethical committee Observational period for each patient:12 months from the date of switch

Statistical analysis and publication of results: 6 months after the last patient's follow-up time completion:

Total duration: 3 years

Enrollment: 250 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Male or female patient of ≥18 years age and no upper age limit
2. Patients with confirmed diagnosis of at least one of the following conditions: Crohn's disease; ulcerative colitis; rheumatoid arthritis4 (2010 ACR/EULAR criteria); ankylosing spondylitis (according to the ASAS modification of the Berlin algorithm for diagnosing ankylosing spondylitis)5; psoriatic arthritis (CASPAR criteria)6.
3. Exposed to i.v. infliximab for at least the minimum time required by the current SmPC, and switched to infliximab s.c. 120 mg q2w prior or at the time of to the inclusion in this study.
4. Treatment with infliximab is according to local approved label
5. Full ability to understand the study procedures and to sign an informed consent form

Exclusion criteria

a. Known intolerance/allergy/reaction to infliximab or any excipient included in the s.c. infliximab formulation

1. Non confirmed diagnosis of IBD (unclassified IBD) or not classifiable as having RA or AxSpA or PsA according to the respective criteria
2. Cardiac insufficiency grade IV according to the NYHA scale
3. Active infection at the time of inclusion
4. Pregnancy or lactation at the time of inclusion
5. Active malignancy at the time of inclusion