Study on the Long-Term Safety and Effectiveness of Upadacitinib for Patients with Moderate to Severe Crohn’s Disease

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What is this study about?

This clinical trial is focused on studying Crohn’s Disease, a condition that causes inflammation in the digestive tract, leading to symptoms like abdominal pain, severe diarrhea, fatigue, weight loss, and malnutrition. The trial is testing a medication called Upadacitinib, also known by its code name ABT-494. This medication is taken as a modified-release tablet, which means it is designed to release the drug slowly over time. The study also includes a comparison with a placebo, which looks like the medication but does not contain the active ingredient.

The purpose of the study is to evaluate the effectiveness and safety of Upadacitinib as a maintenance therapy for people with moderately to severely active Crohn’s Disease who have already responded to initial treatment with this medication in previous studies. The study is divided into two parts: the first part is a randomized, double-blind phase where participants will receive either Upadacitinib or a placebo to see how well the medication works in maintaining their health. The second part is a long-term extension to assess the ongoing safety and benefits of using Upadacitinib over a longer period.

Participants in the study will take the medication orally and will be monitored over time to see how their condition responds. The study aims to determine if Upadacitinib can help maintain clinical remission, which means keeping the symptoms of Crohn’s Disease under control, and to observe any potential side effects. The trial will also look at the impact of the medication on the need for hospitalizations and surgeries related to Crohn’s Disease. The study is expected to continue until 2027, providing valuable information on the long-term use of Upadacitinib for managing this chronic condition.

1 joining the study

Participation begins after completing previous studies M14-431 or M14-433 with a clinical response.

Eligibility is confirmed based on completion of specific study procedures and achieving a clinical response.

2 sub-study 1: maintenance phase

This phase involves a randomized, double-blind, placebo-controlled study.

Participants receive either upadacitinib or a placebo. Upadacitinib is administered as a modified-release tablet taken orally.

The goal is to evaluate the effectiveness and safety of upadacitinib as a maintenance therapy for Crohn’s disease.

The primary focus is on achieving clinical remission and endoscopic response by Week 52.

3 sub-study 2: long-term extension

Participants who complete Sub-study 1 enter the long-term extension phase.

This phase assesses the long-term safety and effectiveness of upadacitinib.

The focus is on maintaining clinical remission and monitoring for any hospitalizations or surgeries related to Crohn’s disease over time.

4 medication details

Upadacitinib is taken orally as a modified-release tablet.

The dosage and frequency are determined by the study protocol and are consistent throughout the trial phases.

5 study duration

The estimated end date for the trial is September 3, 2027.

The study includes multiple assessments to monitor progress and response to treatment.

Who Can Join the Study?

  • Participants must have Crohn’s Disease, which is a condition that causes inflammation in the digestive tract.
  • Participants must have taken part in Study M14-431 or Study M14-433 and shown improvement after receiving the study treatment.
  • Participants must have completed the required procedures at Week 12 or Week 24 in Study M14-431 or Study M14-433. If an endoscopy, which is a procedure to look inside the digestive tract, could not be done due to the COVID-19 pandemic, it may be missing.
  • For the long-term extension study, participants must have completed the first part of Study M14-430. The endoscopy at Week 52 may be missing if it could not be done due to the COVID-19 pandemic.
  • Participants must have shown improvement at Week 24 and completed the required procedures in Part 3/Cohort 3 of Study M14-431.
  • Participants can be of any gender.
  • The study includes individuals who may be considered vulnerable, meaning they might need extra care or protection.

Who Cannot Join the Study?

  • Patients who have not responded to the initial treatment with the study medication cannot participate.
  • Individuals with other serious health conditions that might interfere with the study results are excluded.
  • Pregnant or breastfeeding women are not allowed to join the study.
  • Participants who are currently involved in another clinical trial are not eligible.
  • People with a history of severe allergic reactions to similar medications are excluded.
  • Individuals with a history of substance abuse or addiction may not participate.
  • Patients with certain infections, like tuberculosis, are not allowed to join.
  • Anyone who has had a recent surgery or plans to have surgery during the study period is excluded.
  • Individuals with a compromised immune system, meaning their body’s defense against infections is weakened, cannot participate.
  • Patients who have received certain treatments that might affect the study results are not eligible.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Other Sites

Site Name City Country Status
Centre Hospitalier Universitaire De Nice Nice France
Hospital Universitari De Girona Doctor Josep Trueta Girona Spain
Centre Hospitalier De Valenciennes Valenciennes France
Nouvelles Cliniques Nimoises Nimes France
Cabinet Particular Policlinic Algomed S.R.L. Timisoara Romania
Sjukhusen I Vaester-Vaestra Goetalandsregionen Alingsas Sweden
CHU UCL Namur Yvoir Belgium
Crwkvpgeo Ufgurufpjixrtl Sxkrhqtei Woluwe-Saint-Lambert Belgium
Ujvyosxizr Ot Dfxxmmpv Debrecen Hungary
Hnamfs Hxexeroc Herlev Denmark
Upaywfphebkjvctwrrfwr Etulrecc Ave Erlangen Germany
Aleb Gsoobc Ozyztaug Mxylferscafxd Nstscmby Milan Italy
Cljwzt Hixhqgbjlai Unbzmiczyysej Ds Tmtmvcul Toulouse France
Vpmoaouc usqqogpmefar leyvcjoc Sxrsadpm kxmiodjn Vfo Vilnius Lithuania
Csyr Dh Nuulz Vandoeuvre Les Nancy France
Cijxsv Hatilcxtgfq Uelkbhwcqrmjj Amvzog Plxeezvr Amiens France
Pawxyykcjfd Szpfdr dpepzp Zagreb Croatia
Kdy Ssjgm Split Croatia
Cbijtr hmoxljenveg uxkzcfxlclpui dl Ldooy Liege Belgium
Cpdysk Hvlpwsytqui Lrqn Stj Pierre Benite France
Hqnozlai Uekpgwybpjjbk Matunur Di Vlcipqpqkl Santander Spain
Feemckptb Puil Lv Ihzaszjbdggrh Beppeiiwi Dbz Hdwqalsq Ussyyerhgvtbi Lq Pkl Madrid Spain
Umdplihcht Gtyqcuh Hrnkswyq Oz Htjoxwyrm Heraklion Greece
Eo Gsutr Shq z otiy Warsaw Poland
Phlku Sgmrbxgd Clbbkeqy Uxefwrdrff Hnampswx Riga Latvia
Rvxfwacb srpjet Prague Czechia
Cbch dw Tcckgz Hjeqwuq Tlmswihcr Chambray Les Tours France
Imqyefaj dp Cvmzzhynbste Hlmbttxotkh Uyjitpodigtqe dv Stzux Eionkaz (qvasawo Saint Priest En Jarez France
Orqrsb Eajtaxrnkxyqv Cbquqtn Ktrm Dunaújváros Hungary
Nwdjwdgcm Cjmsx Bvrryicgxo aoem Ceske Budejovice Czechia
Aojarmg Ogfeyebadrl Psb Lcgbegfvmojrpaolz Crnmxyyhxg Catania Italy
Snzxlzaun Rmieapi Ubhphiaaqs Mhxvqav Cjzgfr Nijmegen The Netherlands
Awbafmmzm Uis Amsterdam The Netherlands
Hetcvqzwouznehjpvnvanopf Hq sgwhcu Hradec Kralove Czechia
Kn Mmkapcxgqv shbzm s rkwn Nitra Slovakia
Veyeewlrf cbwigr axmvqbuzr An Riga Latvia
Upvnawasln Oi Prcf Pecs Hungary
Apai Fptfcqkbauptujga Smero Milan Italy
Fwdqbdff Dl Rrywbto Ckjppl Blcyfyogtuvyyuikvl Dtqecbvgfjxikugl Blcbccnakuw Amapvf Pe I Sarqtl Barcelona Spain
Hiellrcq Hnkrzvbe Hvidovre Denmark
Modmokxuzqhcxuqyyrxnjeosiw Hzcitcufglyuvhgh Halle (Saale) Germany
Lvzixval svcjlaxnz mwvdrk urwwdrchvonw lgsvupcl Klyld kmmanrtd Kaunas Lithuania
Khbomkxaanivyleca Vrsnuysiq Sziqr Blddtvm Ktekdh Tatabanya Hungary
Mzulvftoemh Cxcugsq Kbmebpgzu Cracow Poland
En Hivxdzho Uywurrlokzowb Dr Gxet Cuxabbt Drr Nfqwid Las Palmas De Gran Canaria Spain
Nzaaplazvxpqnr Hoyorcfi Hillerød Denmark
Asiqxqq Oxnssghyroy Uncwyyjpgkiqa Msmiy Dcnadw Catanzaro Italy
Wca Whlsdv Ita Pibfd Ppclknec Khjdftl Warsaw Poland

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Austria Austria
Not recruiting
21.03.2018
Belgium Belgium
Not recruiting
21.03.2018
Croatia Croatia
Not recruiting
21.03.2018
Czechia Czechia
Not recruiting
21.03.2018
Denmark Denmark
Not recruiting
21.03.2018
France France
Not recruiting
21.03.2018
Germany Germany
Not recruiting
21.03.2018
Greece Greece
Not recruiting
21.03.2018
Hungary Hungary
Not recruiting
21.03.2018
Italy Italy
Not recruiting
21.03.2018
Latvia Latvia
Not recruiting
21.03.2018
Lithuania Lithuania
Not recruiting
21.03.2018
Poland Poland
Not recruiting
21.03.2018
Portugal Portugal
Not recruiting
21.03.2018
Romania Romania
Not recruiting
21.03.2018
Slovakia Slovakia
Not recruiting
21.03.2018
Spain Spain
Not recruiting
21.03.2018
Sweden Sweden
Not recruiting
21.03.2018
The Netherlands The Netherlands
Not recruiting
21.03.2018

Trial locations

Investigated Drugs:

Upadacitinib is a medication being studied for its effectiveness and safety in treating Crohn’s disease, a condition that causes inflammation in the digestive tract. In this clinical trial, upadacitinib is being tested as a maintenance therapy for patients who have already shown improvement with this medication in previous studies. The trial aims to see if upadacitinib can help maintain the health of patients with moderate to severe Crohn’s disease over a longer period.

Crohn’s Disease – Crohn’s disease is a chronic inflammatory condition of the gastrointestinal tract, primarily affecting the small intestine and colon. It is characterized by periods of flare-ups and remission, where symptoms can vary in intensity. During flare-ups, individuals may experience abdominal pain, diarrhea, fatigue, and weight loss. The inflammation can penetrate deep into the layers of the bowel tissue, leading to complications such as strictures or fistulas. The exact cause of Crohn’s disease is unknown, but it is believed to involve a combination of genetic, environmental, and immune system factors. The progression of the disease is unpredictable, with some individuals experiencing mild symptoms and others facing more severe challenges.

Trial ID:
2023-504951-29-00
Protocol code:
M14-430
NCT ID:
NCT03345823
Trial Phase:
Therapeutic confirmatory (Phase III)

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