Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06095596

Efficacy and Safety of Vedolizumab Combined With Upadacitinib in Patients With Ulcerative Colitis

Led by Sixth Affiliated Hospital, Sun Yat-sen University · Updated on 2026-04-28

334

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

It's of great importance to effectively induce and maintain disease remission in patients with moderate to severe ulcerative colitis (UC). Vedolizumab (VDZ) is known for its high safety profile and confirmed therapeutic efficacy in UC treatment. However, according to the experience in clinical practice, the effect onset speed of vedolizumab is relatively slow. Upadacitinib (UPA), however, works quickly, which complements the defect of slow onset of VDZ induction. However, the safety of UPA used in situations such as infection and tumors is inferior to that of VDZ, and long-term use requires testing for the risk of adverse events such as deep vein thrombosis. Therefore, if the advantages of long-term maintenance therapy safety of VDZ and rapid induced remission of UPA are fully utilized, the combination of VDZ and UPA induction for 8 weeks, followed by the use of single drug VDZ in maintenance therapy, can maximize the clinical benefits of UC patients. Due to the lack of high-level clinical research data at home and abroad, we plan to conduct a multicenter prospective randomized controlled clinical study to provide the evidence-based basis for the efficacy analysis of the sequential treatment of moderate to severe UC patients with VDZ and UPA.

CONDITIONS

Official Title

Efficacy and Safety of Vedolizumab Combined With Upadacitinib in Patients With Ulcerative Colitis

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed ulcerative colitis for at least 3 months with endoscopic and histopathological evidence
  • Moderate to severe ulcerative colitis with modified Mayo score 2 4 and endoscopic subscale 2 2
  • Indications for vedolizumab or upadacitinib treatment
Not Eligible

You will not qualify if you...

  • Unable to take oral upadacitinib or receive regular intravenous vedolizumab infusions
  • Presence of toxic megacolon at screening
  • Previous extensive colectomy, subtotal resection, total colectomy, ileostomy, or colostomy due to ulcerative colitis
  • Require or plan elective surgery for ulcerative colitis during the study
  • Severe, progressive, or uncontrolled kidney, liver, blood, endocrine, respiratory, mental, or neurological diseases
  • Active hepatitis B or C infection at screening

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

the Sixth Affiliated Hospital of Sun Yat-Sen University

Guangzhou, Guangdong, China, 501655

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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