Study on the Effectiveness and Safety of Guselkumab and Golimumab 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 and diarrhea. The study is testing a combination of treatments to see if they can help people with moderate to severe Crohn’s disease. The treatments being studied include Guselkumab, Golimumab, and a new combination therapy known as JNJ-78934804. These treatments are given as injections under the skin using a pre-filled syringe.

The purpose of the study is to evaluate how effective the combination therapy is compared to using Guselkumab or Golimumab alone. Participants in the study will receive either the combination therapy, one of the individual treatments, or a placebo. The study will last for about 48 weeks, during which the participants’ health and response to the treatment will be monitored closely.

Throughout the study, participants will have regular check-ups to assess their condition and any changes in their symptoms. The goal is to see if the combination therapy can lead to clinical remission, which means a significant reduction in symptoms, and an endoscopic response, which is an improvement seen during an examination of the digestive tract. This study aims to provide new insights into the treatment of Crohn’s disease and potentially offer a more effective therapy option for those affected by this condition.

1 joining the study

Upon joining the study, the diagnosis of Crohn’s disease must be confirmed. This includes a review of medical history and assessment of disease activity using specific scores.

Eligibility is determined based on previous treatment responses and specific criteria related to the condition.

2 initial treatment phase

The initial phase involves receiving a combination of medications: guselkumab and golimumab. These are administered as injections under the skin.

The dosage and frequency of these medications are determined by the study protocol and are monitored by the study team.

3 maintenance treatment phase

After the initial treatment phase, the focus shifts to maintaining the treatment effects. This involves continued administration of the medications as per the study schedule.

The goal is to evaluate the long-term effectiveness and safety of the combination therapy.

4 evaluation at week 48

At week 48, the study assesses the effectiveness of the treatment. This includes checking for clinical remission and endoscopic response.

The results are compared with those from participants receiving only one of the medications to determine the benefits of the combination therapy.

Who Can Join the Study?

  • Must have been diagnosed with Crohn’s disease for at least 3 months before starting the study. Crohn’s disease is a condition that causes inflammation in the digestive tract.
  • Must have a confirmed diagnosis of moderate to severe Crohn’s disease. This is determined by specific scores that measure disease activity, stool frequency, abdominal pain, and results from an endoscopic exam.
  • Must have shown an inadequate response, lost response, or been intolerant to at least one advanced therapy for inflammatory bowel disease (IBD). This includes treatments like biologics or oral medications that work similarly to biologics.
  • If female and able to have children, must follow specific requirements for contraception and reproduction during the study.

Who Cannot Join the Study?

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
IRCCS Humanitas Research Hospital Rozzano Italy
Unidade Local De Saúde De Santa Maria, E.P.E. Lisbon Portugal
Medical University Of Vienna Vienna Austria
Oncopole Claudius Regaud Toulouse France
Technische Universitaet Dresden Dresden Germany
Fondazione Policlinico Universitario Agostino Gemelli IRCCS Rome Italy
Oslo Universitetssykehus HF Oslo Norway
Medizinische Hochschule Hannover Hanover Germany
Hospital Universitario De Navarra Pamplona Spain
CHU Grenoble Alpes La Tronche France
CENTRUM MEDYCZNE REUMA PARK Warsaw Poland
Rostock University Medical Center Rostock Germany

Other Sites

Site Name City Country Status
Ospedale San Raffaele S.r.l. Milan Italy
Karolinska University Hospital Solna Sweden
Semmelweis University Budapest Hungary
Centre Hospitalier Universitaire De Nantes Nantes France
Centre Hospitalier Universitaire De Nice Nice France
Hopital Beaujon Clichy France
Klinikum Wels-Grieskirchen GmbH Wels Austria
Uniteversity Muliprofile Hospital For Active Treatment Tsaritsa Yoanna-Isul EAD Sofia Bulgaria
Vojenska Nemocnice Brno Brno-Zidenice Czechia
University Medical Center Ljubljana Ljubljana Slovenia
Centrum Diagnostyczno Lecznicze Barska Sp. z o.o. Wloclawek Poland
A.O.U. Policlinico G. Martino Di Messina Messina Italy
Gyongyosi Bugat Pal Korhaz Gyongyos Hungary
University Hospital Consorziale Policlinico Bari Italy
CED-Studienzentrum Karlshorst Berlin Germany
Hpkiipfmqcuf Hqnxciln Athens Greece
Uobbzmuwenxtlwlpbnlgp Nwyxkxmmbg Ht Tromsø Norway
Lrazp Geogidc Hpthpkkx Oa Atixmm Athens Greece
Dvguynrzmedxsigfmxfggjj coniqw “xkpiwvhriaumewe Esdk Sofia Bulgaria
Hoduub Hwdolwbz Herlev Denmark
Uukhiokjwaqktywuhzdbf Eelkguoh Awt Erlangen Germany
Anepbwgcr Uwj Amsterdam The Netherlands
Awfcabcgjq Piqwfacq Hxzmtola Dt Mrfwhvjpd Marseille France
Upmxvwcxkxni Mxgvxex Cvzzphf Uhrjgwf Utrecht The Netherlands
Awrbgjpi Uejnbnbbwl Hwgxmjuf Lorenskog Norway
Fepxiuwq Nweayuevc Bhlv Brno Czechia
Enmrgfh Uymgkkhrhuyg Mzfhabm Crcyshs Rnunadofi (xnthfnr Mzo Rotterdam The Netherlands
Aemzeqa Ovvmgijulre Uxvxjmwbhqiay Cfbqsfswyhsz Drfkq Swaytl E Dbqcg Sohqiqu Dk Thzign Turin Italy
Cvtu Dh Nahoh Vandoeuvre Les Nancy France
Unofcebgjaiwbxucbxygz Hxukghpymc Apx Heidelberg Germany
Rxaedi Mcswlftnfet Aarhus Denmark
Uppjlmylyv Oc Skinkp Szeged Hungary
Cbshno Hqcsnokapbq Uappuzuqsbraz Azzwrp Pahuerdp Amiens France
Umonybjvlr Hqzusfup Mmalydeyeg Maastricht The Netherlands
Cjfxwu Hcafmzrtexv Ubtmjqzqdtfsg Dl Rynobk Rennes France
Ktw Sfkfw Split Croatia
Rilrtu Ojqbeec Lnqi Orebro Sweden
Cmqqhw Hjwcqwlvdbd Lfft Ssz Pierre Benite France
Hqlbsbbl Uvgkygawwefoz Mjeekkr Do Vsrxxzpfmm Santander Spain
Fzatyhzam Pwpt Lm Ibkashyvophhe Bphiglicb Doo Hyzceqjf Umdbqdozroejm Lb Pvz Madrid Spain
Vwnql Sint-Niklaas Belgium
Bwadke Smjrtmy Gjettum Norway
Cndngnrx Hlorefezkhzc Uwtmpaxjnsbhc Do Pevajxjasm Pontevedra Spain
Fxojkicfjr Idxmf Siu Gtijquo Dyh Tyqnayn Monza Italy
Iabrjhsnsl Gxbvuck Hwbqbamv Oi Tvsieswvckxo Thessaloniki Greece
Cqjyfq Hjcttusjqtz Di Sbkdzgxyroez Saint-Brieuc France
Uqachoiaagr Seekifxs Salzburg Austria
Pzzw Tcvvd Huxehzlq Upvoemswetrw Sabadell Spain
Tpibj Psrfbdbakvx Pckfjrrepy Cujidld Mtzvhkqz Std z oenv Poznan Poland
Ejliz Sphnhpodqibqw Hcdmsaip Stockholm Sweden
Uvrxyefdfk Taaamcty Hbkswkka Mlgzihndficv Szombathely Hungary
Bdlpcuhpgu Slk z oacg suqsp Warsaw Poland
Aephqwb Ozarplxokdk Obwyedzq Regrnzn Vgoud Scegn Cmqhcpst Palermo Italy
Gisqqxayiwjtxifem Osyskxvtlhj Kassel Germany
Mti Pfxiul 1k Munster Germany
Iyhndoex dq Clnipewzkpyd Hdyfipqufzn Utainufrarfet do Sxlta Eeubyod (yqqgtzr Saint Priest En Jarez France
Mhntzvaq Si z obpz Bydgoszcz Poland
Imrpv Omwglmtu Slirr Cbnjw Dja Cbjgagrv Negrar di Valpolicella Italy
Mxecba Mdxhsxm smk z ogcq Wroclaw Poland
Atspqnnujm Padxpxvr Hphiayqf Dr Plbdj Paris France
Aypalzq Ovpxafofgls Pkx Lywgjycfmydlujmqh Cczvjjcbub Catania Italy
Tdfah Uqimesrfvr Hskygxxm Tartu Estonia
Bxjkwneq Udnswssnkt Hkwqrvbb Crfpmy Besançon France
Pgsdhwdaz Ikllrkzq Mudxzpzq Mxgrnzxkpgvz Sdcmx Wgxejqykmjar I Aooloybplugxj Warsaw Poland
Lfdqgohppjpzkq Kveypghhfx Aa Pohja-Tallinna Linnaosa Estonia
Ghidmoeca Sbg z oobg Torun Poland
Eyue Trgisst Czqbvsl Hatsfuhp Tallin Estonia
Candfh Mhpleq Ctdvakqjqes Ayrmdqhq Ptvy Hrqqkyup Neuilly-Sur-Seine France
Hdyyn Mbeog Ob Rfomsou Hb Aalesund Norway
Cgzzvjx Mzudtxgl Mfozq Sid z oenf Rzeszow Poland
Aspz Facgxdjzjrnvqmab Srjpr Milan Italy
Rzuakw Obkfopfymgypna Linkoping Sweden
Inkkbu aigr Prague Czechia
Mislepjiijlcqjwlkavzzxepjy Hffkuthjkjxzodmx Halle (Saale) Germany
Udlefjo Lxfgo Dm Sckht Do Gqhlwzdmrqos Eflixk Vila Nova De Gaia Portugal
Kcyufepkxvo Wdrefblxsh epoi Berlin Germany
Csywtyi Mutcdyey Kjugydus 2 Szw z oyxv Zamosc Poland
Kldxpwt zpngsdmwh apnw Teplice Czechia
Pgaqgb Psfqfd Rwxcsxrldf Sgm jk Cracow Poland
Cetqpwr Mlxkvyvk Ptqoeno Mmztyyizh Ccpqckqx Lbffivfydw Mnoeru Zbbtvuwxh swdhz Cracow Poland
Nzhgixwl Icibknvsp Od Gmjjvuniwgftpqsq Swuhglz Dj Bywzad Rgltxmmn Hmwmgmaq Castellana Grotte Italy
Rrgoul See z opyx Lublin Poland
Sanmlcr Sxv z ojci Szczecin Poland
Csrzlau Mjhynpcb Orqypv Wroclaw Poland
Umalhyv Lacgg Da Swtcr De Egnnf O Djvee E Vkcdy Evgmal Santa Maria Da Feira Portugal
Ewclqxhk Grki Leipzig Germany
Etawjgyaau Sxo z oxus Sopot Poland
Wcxrsdpjco Smzqywt Shefrldyvxntfti W Opjzowlki Olsztyn Poland
Kjiejpmeolc Dvm Bobsvsrcxohy Bopzjwq Wvao Vienna Austria
Rerhkiqh Scs z otwp Poznan Poland
Agxzuzt Oipymzgskgx Ubqdrdwzifamo Dd Cmiphrbf Monserrato Italy
Sanppeduvwpekvthwku Btg Uy (xyoonigxggjbkglhbnai Halle (Saale) Germany
Mvy Gpvpmy Btxbbo Berlin Germany
Bdakpzjzro Hkblrvsg Copenhagen Denmark
Nagz Vxoyakt Jfthujm Mngql Warsaw Poland
Olfnoa Uftcbsscpt Htclwjac Odense Denmark
Wfb Wqqctt Iqm Prucn Plkymtim Kjooixs 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
21.02.2023
Belgium Belgium
Not recruiting
21.02.2023
Bulgaria Bulgaria
Not recruiting
21.02.2023
Croatia Croatia
Not recruiting
21.02.2023
Czechia Czechia
Not recruiting
21.02.2023
Denmark Denmark
Not recruiting
21.02.2023
Estonia Estonia
Not recruiting
21.02.2023
France France
Not recruiting
21.02.2023
Germany Germany
Not recruiting
21.02.2023
Greece Greece
Not recruiting
21.02.2023
Hungary Hungary
Not recruiting
21.02.2023
Italy Italy
Not recruiting
21.02.2023
Norway Norway
Not recruiting
21.02.2023
Poland Poland
Not recruiting
21.02.2023
Portugal Portugal
Not recruiting
21.02.2023
Slovenia Slovenia
Not recruiting
21.02.2023
Spain Spain
Not recruiting
21.02.2023
Sweden Sweden
Not recruiting
21.02.2023
The Netherlands The Netherlands
Not recruiting
21.02.2023

Trial locations

Investigated Drugs:

Guselkumab is a medication used in this trial to treat Crohn’s Disease. It works by targeting specific proteins in the immune system that are involved in inflammation. By blocking these proteins, guselkumab helps reduce inflammation in the gut, which can alleviate symptoms of Crohn’s Disease.

Golimumab is another medication used in the trial for Crohn’s Disease. It is an anti-inflammatory drug that targets a protein called tumor necrosis factor (TNF). By inhibiting TNF, golimumab helps decrease inflammation and can improve symptoms in patients with Crohn’s Disease.

JNJ-78934804 is an investigational therapy being studied in this trial. It is being tested to see how effective it is when used in combination with guselkumab and golimumab for treating Crohn’s Disease. The goal is to determine if this combination therapy can provide better results than using each medication alone.

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 active phases, 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 involves an abnormal immune response. The disease can affect any part of the digestive tract, from the mouth to the anus, but most commonly impacts the end of the small intestine.

Trial ID:
2023-504741-32-00
Protocol code:
78934804CRD2001
NCT ID:
NCT05242471
Trial Phase:
Therapeutic exploratory (Phase II)

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