USTekinumab in Fistulising Perianal Crohn's Disease (USTAP)

Crohn's Disease Clinical Trial

— USTAP  

Official title:

USTekinumab in Fistulising Perianal Crohn's Disease (CD): The USTAP CD Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04496063
• Other study ID #: GT-2019-01
• Status: Recruiting
• Phase: Phase 4
• Start date: November 16, 2020
• Est. completion date: June 30, 2025

Study information

• Verified date: January 2024
• Source: Groupe d'Etude Therapeutique des Affections Inflammatoires Digestives
• Contact: Benjamin PARIENTE, MD PhD
• Phone: + 33 20 44 47 97
• Email: Benjamin.PARIENTE[@]CHRU-LILLE.FR
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Phase IV Trial design : Multicentre, randomized, double-blind, placebo-controlled study Population : Moderate to severe Crohn's disease with at least one active perianal fistula track Investigational treatment : Group 1: Ustekinumab (UST) IntraVenous (IV) induction (6mg/kg) followed by UST SubCutaneous (SC) 90mg every 8 weeks. Group 2: Placebo IV followed by Placebo SC The trial duration for each patient will be 48 weeks. Trial objective : To evaluate the efficacy and safety of ustekinumab in fistulizing perianal Crohn's disease. Number of patients : A total of 146 patients will be included in 20 sites in France Trial duration : First patient in: Q3 2020 - Last patient first visit: Q3 2022 Last patient last visit: Q3 2023

Description:

Main endpoint: The primary endpoint will be combined remission at week 12 defined as: - 100% of the fistula tracts without any drainage by the external openings (occurring spontaneously or after gentle finger compression) And - absence of collections >2 cm of the treated perianal fistulas confirmed by masked central MRI Patient requiring UST optimization will be considered in failure but will be followed until week 48 Secondary endpoints: Definition - Clinical remission: 100% of the fistula tracts without any drainage by the external openings (i.e, absence of any drainage by all fistula openings occurring spontaneously or after gentle finger compression) - Clinical response (closure of at least 50% of all treated external openings that were draining at baseline) - Radiological remission: absence of collections >2 cm of the treated perianal fistulas confirmed by masked central MRI - Combined clinical and radiological remission at week 24 and 48. - Clinical remission (i.e, absence of any drainage by all fistula openings occurring spontaneously or after gentle finger compression) at week 12, 24 and 48 - Absence of collections >2 cm of the treated perianal fistulas confirmed by masked central MRI at week 12, 24 and 48 - Evaluation of the magnetic resonance novel index for fistula imaging in CD at week 12, 24 and 48 - Clinical response (closure of at least 50% of all treated external openings that were draining at baseline) at week 12, 24 and 48 - Combined clinical response and radiological remission at week 48 - Perineal Disease Activity Index (PDAI), Crohn Disease Activity Index (CDAI) at week 12, 24 and 48 - Quality of life will be assessed with the Inflammatory Bowel Disease questionnaire (IBDQ) scores at week 24 and 48 - Correlation between response and remission and UST trough levels and antidrug (UST) antibodies at week 12, 24, 48 - Clinical response of UST optimization at week 48 (closure of at least 50% of all treated external openings that were draining at week 12) - Clinical response at week 48 of UST introduction at W12 (closure of at least 50% of all treated external

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 146
• Est. completion date: June 30, 2025
• Est. primary completion date: June 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age =18 years
• Adults with moderate to severe Crohn's disease for at least six months
• Patients with at least one active perianal fistula track (between the anus or low rectum and the perineum or vulva) confirmed by MRI within the previous 12 weeks
• Patients either naïve to anti-TNF therapy (50%) or refractory to anti-TNF therapy (50%).
• If female, subject is either not of child bearing potential, defined as post-menopausal for at least1 year, surgically sterile (bilateral tubal ligation, bilateral oophorectomy or hysterectomy), or is of childbearing potential and practicing one of the following methods of birth control during the study and for 150

days after the last dose:

• Condoms, sponge and foam, jellies with diaphragm or intrauterine device (IUD). IUDs may fail during azathioprine treatment. Alternative or additional contraceptive measures are advised, if azathioprine is initiated
• Oral or parenteral contraceptives for 3 months prior to study drug administration
• A vasectomized partner
• Male subjects must agree to use an acceptable form of birth control, listed above at the start of azathioprine administration and for 90 days after last dose of azathioprine. Males should also commit to inform his partner(s) about it and to report any pregnancy to the investigator.
• If female, subject is not breast-feeding throughout the study and for 150 days after last dose.
• Subjects or his/her legal representative have voluntarily signed and dated an informed consent approved by and compliant with the requirements of this study protocol which has been approved by an Institutional Review Board (IRB)/Independent Ethics Committee (IEC)
• Adequate cardiac, renal and hepatic function as determined by the Principal Investigator and demonstrated by Screening laboratory evaluations, questionnaires and physical examination results that do not indicate an abnormal clinical condition which would place the subject at undue risk and thus preclude subject participation in the study
• Subject with a negative tuberculosis (TB) Screening Assessment [(including a Purified Protein Derivative (PPD) test < 5 mm and/or negative QuantiFERON-TB Gold test or equivalent and negative Chest X-Ray (CXR) (PA and lateral view)] at screening

Exclusion Criteria:

• Absence of written consent. People unable to give their consent (because of their physical or mental state)
• Pregnancy or breastfeeding
• Rectovaginal fistulas
• Rectal and/or anal stenosis
• Diverting stomas
• Abscess or collections >2 cm which are not properly drained ((i.e not drained at least 3 weeks before baseline and adequately treated provided that there is no anticipated need for any further surgery)
• History of colectomy.
• History of colonic mucosal dysplasia or adenomatous colonic polyps that are not removed.
• Screening stool trial positive for enteric pathogens or Clostridium difficile toxin. History of ongoing, chronic or recurrent infectious disease
• Positive HIV, Hepatitis B Virus (HBV),Hepatitis C Virus (HCV)
• Severe infection, chronic infection, history of recurrent infections, active infection including TB
• Malignancies or history of malignancies
• History of congestive heart failure (NYHA: Grade III and IV), demyelinating disease, current signs or history of severe/ progressive/uncontrolled renal, hepatic, endocrine, pulmonary, cardiac, neurologic, cerebral, or psychiatric disease, or systemic lupus erythematosus (SLE).
• History of transplanted organ, lymphoproliferative disease, any known malignancy
• Previous allergy immunotherapy for anaphylaxis, hypersensitivity to ustekinumab or to any excipients, or metronidazole or ciprofloxacin
• Previous use of a biologic agent targeting Interleukin 12 (IL12) and/or Interleukin 23 (IL 23), including but not limited to ustekinumab
• Oral corticosteroids at a dose > 40 mg prednisone or its equivalent per day at inclusion (oral steroids should be at stable dose at least 7 days before inclusion)
• Any current or previous use of the following within 8 weeks before the first trial agent injection : cyclosporine, tacrolimus, anti-TNF biologic agents or other agents intended to suppress or eliminate Tumor Necrosing Factor (TNF), and other biologics, including anti-integrin antibodies (approved or investigational), Janus Kinase (JAK) inhibitors (approved or investigational), or any current or previous use of an investigational agent
• Non-autologous stem cell therapy or biologic agents that deplete B or T cells <12 months prior to baseline
• Current or recent (less than 4 weeks) vaccination with attenuated live vaccines
• Patients using a prohibited medication
• Patients participating in another trial or being in a follow-up period for another trial

Related Conditions & MeSH terms

• Crohn Disease
• Crohn's Disease

Intervention

Drug:
• Ustekinumab
Intravenous induction (6mg/kg) followed by Ustekinumab subcutaneous 90mg every 8 weeks
• Placebo
Placebo intravenous followed by Placebo subcutaneous every 8 weeks

Locations

Country	Name	City	State
France	Chu Amiens	Amiens
France	Chu Besancon	Besançon
France	CHU Clermont Ferrand	Clermont-Ferrand
France	APHP- Hopital Beaujon	Clichy
France	Hôpital Louis Mourier	Colombes
France	Hôpital Kremlin Bicêtre	Le Kremlin Bicêtre
France	CHRU Lille	Lille
France	CHU Montpellier - St Eloi	Montpellier
France	Hôpital Hôtel Dieu	Nantes
France	CHU Nice- Hopital l'Archet	Nice
France	CHU Nîmes - Hôpital Universitaire Caremeau	Nîmes
France	Hôpital Bichat	Paris
France	Hôpital Saint-Antoine	Paris
France	Hôpital St Louis	Paris
France	CHU LYON- Hopital Lyon Sud	Pierre-Bénite
France	CHU Rennes	Rennes	Bretagne
France	CHU Roubaix	Roubaix
France	CHU Saint-Etienne	Saint-Priest-en-Jarez
France	CHU de Tours - Hopital Trousseau	Tours
France	CHU Nancy - Hôpital de Brabois	Vandœuvre-lès-Nancy

Sponsors (2)

Lead Sponsor	Collaborator
Groupe d'Etude Therapeutique des Affections Inflammatoires Digestives	Janssen, LP

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Combined clinical and radiological remission	Number of participants with 100% of the fistula tracts without any drainage by the external openings (occurring spontaneously or after gentle finger compression); - Number of participants with absence of collections >2 cm of the treated perianal fistulas confirmed by masked central MRI.	Week 12
Secondary	Combined clinical and radiological remission	Number of participants with 100% of the fistula tracts without any drainage by the external openings (occurring spontaneously or after gentle finger compression); - Number of participants with absence of collections >2 cm of the treated perianal fistulas confirmed by masked central MRI.	week 24 and week 48
Secondary	Clinical response	Number of participants with closure of at least 50% of all treated external openings that were draining at baseline	week 12, week 24 and week 48
Secondary	MAGNIFI-CD26	Evaluation of the magnetic resonance novel index for fistula imaging in CD (MAGNIFI-CD26)	week 12, week 24 and week 48
Secondary	PDAI	Perineal Disease Activity Index	week 12, week 24 and week 48
Secondary	IBDQ scores	Quality of life will be assessed with the Inflammatory Bowel Disease questionnaire scores	week 24 and week 48
Secondary	UST trough levels and antidrug	Correlation between response and remission and UST trough levels and antidrug (UST) antibodies	week 12 and week 24
Secondary	Clinical response of UST optimization	Number of participants with closure of at least 50% of all treated external openings that were draining at week 12	week 24 and week 48
Secondary	Clinical response of UST introduction at week 12	Number of participants with closure of at least 50% of all treated external openings that were draining at week 12	week 24 and week 48
Secondary	CDAI	Crohn Disease Activity Index	week 12, week 24 and week 48