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CTRI Number  CTRI/2025/11/097059 [Registered on: 07/11/2025] Trial Registered Prospectively
Last Modified On: 04/11/2025
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Drug 
Study Design  Randomized, Parallel Group, Placebo Controlled Trial 
Public Title of Study   A study to assess whether tofacitinib can be safely stopped in patients with ulcerative colitis who are symptom free for at least 6 months. 
Scientific Title of Study   Discontinuation of tofacitinib in patients with ulcerative colitis in sustained clinical remission on combination therapy with 5-aminosalicylates and tofacitinib: The STOP Trial 
Trial Acronym  STOP 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Ajit Sood 
Designation  Professor and Head 
Affiliation  Dayanand Medical College and Hospital 
Address  Department of Gastroenterology, 3rd Floor Ward 312 Endosurgical Complex Dayanand Medical College and Hospital, Tagore Nagar, Civil Lines

Ludhiana
PUNJAB
141001
India 
Phone  09815400718  
Fax    
Email  ajitsood10@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Ajit Sood 
Designation  Professor and Head 
Affiliation  Dayanand Medical College and Hospital 
Address  Department of Gastroenterology, 3rd Floor Ward 312 Endosurgical Complex Dayanand Medical College and Hospital, Tagore Nagar, Civil Lines

Ludhiana
PUNJAB
141001
India 
Phone  09815400718  
Fax    
Email  ajitsood10@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Ajit Sood 
Designation  Professor and Head 
Affiliation  Dayanand Medical College and Hospital 
Address  Department of Gastroenterology, 3rd Floor Ward 312 Endosurgical Complex Dayanand Medical College and Hospital, Tagore Nagar, Civil Lines

Ludhiana
PUNJAB
141001
India 
Phone  09815400718  
Fax    
Email  ajitsood10@gmail.com  
 
Source of Monetary or Material Support  
Dayanand Medical College and Hospital, Ludhiana 
 
Primary Sponsor  
Name  Dayanand Medical College and Hospital, Ludhiana, Punjab 
Address  Department of Gastroenterology, 3rd Floor Ward 312 Endosurgical Complex Dayanand Medical College and Hospital, Tagore Nagar, Civil Lines 
Type of Sponsor  Private medical college 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Ajit Sood  Dayanand Medical College and Hospital  Department of Gastroenterology, Dayanand Medical College and Hospital, Tagore Nagar, Civil Lines, Ludhiana.
Ludhiana
PUNJAB 
09815400718

ajitsood10@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Drug Trials Ethics Committee Dayanand Medical College and Hospital  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: K519||Ulcerative colitis, unspecified,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  Drug: 5-ASA and Tofacitinib  Participants will continue oral 5-Aminosalicylates at a stable dose plus tofacitinib 5 mg twice daily, for the study duration. This represents the standard combination therapy. 
Intervention  Placebo replacing Tofacitinib 5-ASA to continue  Participants will continue oral 5-Aminosalicylates at a stable dose, with placebo replacing tofacitinib, for the study duration. This group tests discontinuation of tofacitinib in patients in sustained clinical remission. 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  75.00 Year(s)
Gender  Both 
Details  1. Adults aged 18 years or older with a confirmed diagnosis of ulcerative colitis based on standard clinical, endoscopic, and histological criteria as per ECCO guidelines.
2. Composite remission at enrolment, defined as:
a) Clinical remission, indicated by a Partial Mayo Clinic score of less than or equal to 1 with no individual sub-score greater than 1 and a rectal bleeding sub-score of 0, together with biochemical remission demonstrated by fecal calprotectin levels less than 250 micrograms per gram on two different occassions three months apart.
b) Endoscopic remission, defined as ulcerative colitis endoscopic index of severity (UCEIS) of 0 or 1 within three months of enrolment.
3. Stable maintenance therapy with both 5-aminosalicylates and tofacitinib 5 mg twice daily for at least three months prior to enrolment.
4. Willingness to provide informed consent.
5. Willingness to comply with study procedures, assessments, and follow-up. 
 
ExclusionCriteria 
Details  1. Evidence of active disease at the time of enrolment (clinical, biochemical, or endoscopic activity).
2. Use of systemic corticosteroids, biologics, or immunomodulators (e.g., azathioprine, methotrexate) within the last 3 months.
3. Change of therapy or change in dose of existing therapy for UC.
4. History of colorectal cancer, dysplasia, or colectomy.
5. Significant comorbidities, including severe hepatic, renal, cardiac, respiratory, psychological or neurological diseases.
6. Pregnancy, breastfeeding, or plans to conceive during the study period.
7. Active substance abuse, including alcohol, which may interfere with adherence to the study protocol.
8. Any condition or circumstance that, in the investigator’s opinion, would make the patient unsuitable for participation or interfere with the study objectives. 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Participant and Investigator Blinded 
Primary Outcome  
Outcome  TimePoints 
Proportion of patients experiencing disease flare within 12 months  12 months 
 
Secondary Outcome  
Outcome  TimePoints 
1. Time to disease flare within 12 months
2. Proportion of patients recapturing clinical response at 8 weeks following therapy escalation
3. Proportion of patients maintaining symptomatic and biomarker remission at 12 months
4. Incidence of adverse events (AEs) and serious adverse events (SAEs) during the study period 
All the groups will be assessed on efficacy outcomes at baseline and every 4 weeks till 48 weeks 
 
Target Sample Size   Total Sample Size="110"
Sample Size from India="110" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   Phase 4 
Date of First Enrollment (India)   01/12/2025 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="1"
Months="6"
Days="0" 
Recruitment Status of Trial (Global)   Not Applicable 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  

Ulcerative colitis (UC) is a chronic relapsing disease requiring long-term therapy. Tofacitinib, an oral Janus kinase inhibitor, is effective for moderate-to-severe UC, while 5-aminosalicylates (5-ASA) remain standard for mild-to-moderate disease. In clinical practice, many patients in sustained remission continue both drugs, though the necessity of combination therapy is uncertain. Prolonged tofacitinib use carries risks such as infections, thromboembolism, cardiovascular events, and high treatment costs. Whether patients in deep remission can safely discontinue tofacitinib while continuing 5-ASA is unknown.

The STOP Trial is a double-blind, randomized controlled study enrolling 110 adult UC patients in composite remission (clinical, biochemical, and endoscopic) on stable 5-ASA and tofacitinib 5 mg twice daily for at least three months. Participants will be randomized (1:1) into two arms: (1) continuation of 5-ASA + tofacitinib, or (2) discontinuation of tofacitinib and continuation of 5-ASA 

The primary outcome is the proportion of patients experiencing relapse within 12 months, defined by Partial Mayo score greater than or equal to 2 with rectal bleeding score greater than or equal to 1, Mayo endoscopic score greater than or equal to 1, and fecal calprotectin more than 250 micrograms per gram. Secondary outcomes include time to flare, recapture of response after escalation, maintenance of remission at 12 months, and safety outcomes. 

This trial will provide prospective evidence on tofacitinib withdrawal in sustained remission. Results may guide de-escalation strategies, reduce unnecessary drug exposure, lower risks, and improve cost-effectiveness in UC management.



 
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