| 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
|
|
|
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
|
|
|
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.
|