Actively Recruiting
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
Eligibility Criteria
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
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
Trial Site Locations
Total: 1 location
1
the Sixth Affiliated Hospital of Sun Yat-Sen University
Guangzhou, Guangdong, China, 501655
Actively Recruiting
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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