A 12-month Real Life Study of IBD Patients Switched From Adalimumab Originator Humira® to One of Its Biosimilar (Rhoneswitch)

Grenoble Alpes University Hospital Center (CHU) logo

Grenoble Alpes University Hospital Center (CHU)

Status

Unknown

Conditions

IBD Patients, Originator Treatment, Biosimilar, Switch Back

Study type

Observational

Funder types

Other

Identifiers

NCT04422171
38RC19.379
2020-A00494-35 (Other Identifier)

Details and patient eligibility

About

Biosimilars represent great potential in cost saving and reinvestment opportunities in healthcare. Biosimilars of adalimumab appear to be clinically equivalent to the reference product in patients with rheumatoid arthritis and psoriasis. No data are currently available in IBD patients. Real-life data are needed. Minimizing the switch back is another clinical challenge in the current area of biosimilars. The primary objective of Rhoneswitch is to describe the magnitude of patient's switch back defined as a deterioration of symptoms without objective identification of disease activity, 12 months after the switch from ada originator Humira®. The primary endpoint is to assess the percentage of patients who switch back to originator therapy Humira® 12 months after switching from ada Humira® to ada Bs: Amgevita® ,Hulio®, Hyrimoz® or Imraldi® in IBD patients without any objective markers of inflammation.

Full description

The subject will be include during usual hospital consultation after reviewing inclusion/exclusion criteria and obtain non opposition. Data will be collected during 3 usual hospital consultations: at month 3, month 6, and month 12. The end of study will be at month 12 or at premature termination. Questionnaires will be done in addition during all usual hospital consultations.

Enrollment

400 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

INCLUSION CRITERIA

  • Documented diagnosis of CD or UC established on the basis of standard clinical, endoscopic and histological criteria at least 3 months prior to inclusion.

  • Inactive CD or UC outpatients are defined per clinical assessment as an Harvey Bradshaw Index (HBI) score ≤4 for CD patients and a Partial Mayo Score (PMS) ≤2 with each sub-score of 1 or less for UC and/or according to ECCO classification (Sturm 2019) within previous 3 months, demonstrating an adequate clinical remission to ada originator

  • May be receiving the following drugs (but must remain on stable dose for 10 weeks):

    • Oral 5-aminosalicylates (ASA) compounds or rectal formulations of 5ASA provided the dose to be stable at least 4 weeks before switching
    • Azathioprine, 6-MP or methotrexate provided the dose has been stable for 4 weeks prior to inclusion (dose must remain stable for 10 weeks after switching)
  • Non opposition required

EXCLUSION CRITERIA

  • Diagnosis of indeterminate colitis, ischaemic colitis, fulminant colitis
  • Current use of another TNF inhibitor included (but not limited to) infliximab, certolizumab, golimumab
  • Current use of vedolizumab or ustekinumab
  • Current use of JAK inhibitors or S1P modulators
  • Current use of oral corticosteroids
  • Active flaring CD or UC patients defined as a HBI > 4 for CD and a PMS>1 for UC and/or concomitant CS medication
  • Pregnancy or breast feeding
  • Subject under guardianship or subject deprived of liberty

Trial contacts and locations

1

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Central trial contact

Laure Bordy; NICOLAS MATHIEU

Data sourced from clinicaltrials.gov

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