Informazioni generali
  • Categoria della malattia Altro (BASEC)
  • Stato di reclutamento reclutamento in corso (BASEC/ICTRP)
  • Luogo dello studio
    Basilea, Berna, San Gallo
    (BASEC)
  • Responsabile dello studio Jens Lachmann Jens.Lachmann@iconplc.com (BASEC)
  • Fonte dati BASEC: Importato da 15.05.2025 ICTRP: N/A
  • Ultimo aggiornamento 15.05.2025 21:45
HumRes65690 | SNCTP000006035 | BASEC2024-00570

A study to investigate the efficacy and safety of TAK-279, administered orally, in patients with moderate to severe active Crohn's disease

  • Categoria della malattia Altro (BASEC)
  • Stato di reclutamento reclutamento in corso (BASEC/ICTRP)
  • Luogo dello studio
    Basilea, Berna, San Gallo
    (BASEC)
  • Responsabile dello studio Jens Lachmann Jens.Lachmann@iconplc.com (BASEC)
  • Fonte dati BASEC: Importato da 15.05.2025 ICTRP: N/A
  • Ultimo aggiornamento 15.05.2025 21:45

Descrizione riassuntiva dello studio

Crohn's disease (CD) is a serious, long-term condition that can lead to inflammation and painful ulcers in the intestine. Common symptoms include diarrhea, intestinal bleeding, and abdominal pain. There is no known cure, but some treatments can reduce inflammation and lower the likelihood of the disease returning. TAK-279 is a potential treatment for Crohn's disease and is taken as capsules orally. The study involves participants with Crohn's disease who are experiencing flare-ups (moderate to severe active Crohn's disease). They take either one of three doses of TAK-279 or a placebo once daily for up to 52 weeks (1 year). The placebo looks like the TAK-279 capsule but contains no active ingredient. The main objective is to determine whether TAK-279 reduces intestinal inflammation and symptoms compared to placebo.

(BASEC)

Intervento studiato

- The 4 study treatments consist of TAK-279 in 3 different doses (low, medium, and high) and placebo. Participants take 3 capsules once daily for up to 52 weeks (1 year). If the disease progresses in participants taking the placebo after 12 weeks of treatment, they will be switched to the medium dose of TAK-279. Participants taking TAK-279 will continue to take their assigned dose for the remainder of the treatment in the study. 28 days after the last treatment day, a safety follow-up appointment will take place.

- Willingness to undergo a colonoscopy to examine the intestine and obtain small tissue samples (biopsy) during screening. This procedure involves using a small flexible tube with a camera on the end to examine the intestine and obtain samples.

(BASEC)

Malattie studiate

Moderate to severe active Crohn's disease

(BASEC)

Criteri di partecipazione
Adults aged 18 to 75 years may participate in this study if they meet the following key study rules: - Participants must have a documented diagnosis of Crohn's disease (endoscopic with histology) for at least 30 days prior to screening. (BASEC)

Criteri di esclusione
Participants with indeterminate or unclassified chronic inflammatory bowel disease (IBD), microscopic colitis, ischemic colitis, infectious colitis, or radiation colitis, as well as diverticular disease associated with colitis and/or clinical/histological findings suggestive of ulcerative colitis. (BASEC)

Luogo dello studio

Basilea, Berna, San Gallo

(BASEC)

non disponibile

Sponsor

Jens Lachmann ICON Clinical Research (Switzerland) GmbH c/o Experfina AG Picassoplatz 8, 4052 Basel, Switzerland

(BASEC)

Contatto per ulteriori informazioni sullo studio

Persona di contatto in Svizzera

Jens Lachmann

+41 79 593 4489

Jens.Lachmann@iconplc.com

ICON Clinical Research (Switzerland) GmbH c/o Experfina AG Picassoplatz 8, 4052 Basel, Switzerland

(BASEC)

Informazioni scientifiche

non disponibile

Nome del comitato etico approvante (per studi multicentrici solo il comitato principale)

Commissione d'etica Berna

(BASEC)

Data di approvazione del comitato etico

22.08.2024

(BASEC)


ID di studio ICTRP
non disponibile

Titolo ufficiale (approvato dal comitato etico)
A Phase 2b, Multicenter, Randomized, Double-blind Induction, Placebo-Controlled, Dose-Ranging Study to Evaluate the Efficacy and Safety of Oral TAK-279 in Subjects with Moderately to Severely Active Crohn’s Disease (BASEC)

Titolo accademico
non disponibile

Titolo pubblico
non disponibile

Malattie studiate
non disponibile

Intervento studiato
non disponibile

Tipo di studio
non disponibile

Disegno dello studio
non disponibile

Criteri di inclusione/esclusione
non disponibile

non disponibile

Endpoint primari e secondari
non disponibile

non disponibile

Data di registrazione
non disponibile

Inclusione del primo partecipante
non disponibile

Sponsor secondari
non disponibile

Contatti aggiuntivi
non disponibile

ID secondari
non disponibile

Risultati-Dati individuali dei partecipanti
non disponibile

Ulteriori informazioni sullo studio
non disponibile


Risultati dello studio

Riepilogo dei risultati

non disponibile

Link ai risultati nel registro primario

non disponibile