Tibulizumab Systemic Sclerosis Understanding and Response Evaluation (TibuSURE)
Condition(s) studied
Investigational drug(s) / intervention(s)
Tibulizumab: Anti BAFF/IL-17 antibody
Placebo: Placebo (inactive)
Study summary
The study is a Phase 2, multi-center, randomized, double-blind, placebo-controlled study to evaluate the effects of tibulizumab over 24 weeks (Period 1) in adult participants with systemic sclerosis, followed by an open-label extension period where all active participants will receive tibulizumab and will be evaluated for an additional 28 weeks (Period 2)
Eligibility
Primary outcome measure(s)
- [Period 1] Change from baseline in modified Rodnan Skin Score (mRSS) at 24 weeks — Week 24
The mRSS assesses skin thickness at 17 different cutaneous sites across the body using a scale from 0 (normal skin) to 3 (severe thickening), with a total score ranging from 0 (no thickening) to 51 (severe thickening in all 17 areas) - [Period 2] Safety and tolerability of tibulizumab — Week 52
Assessed by the incidence of all treatment-emergent adverse events (TEAEs), as well as changes from baseline in vital signs, electrocardiogram (ECG) parameters, and laboratory results
Trial sites (60)
| Facility | City | Region | Status |
|---|---|---|---|
| UCSD Altman Clinical and Translational Research Institute Center for Clinical Research | La Jolla | California | |
| UCLA Department of Medicine | Los Angeles | California | |
| IRIS Research and Development LLC | Plantation | Florida | |
| University of Iowa | Iowa City | Iowa | |
| Massachusetts General Hospital | Boston | Massachusetts | |
| University of Michigan Hospital | Ann Arbor | Michigan | |
| Rheumatology Associates | Arlington | Texas | |
| STAT Research S.A. | Buenos Aires | Buenos Aires | |
| Centro de Investigaciones Médicas Tucumán | San Miguel de Tucumán | Tucumán Province | |
| Organización Médica de Investigación | Buenos Aires | Argentina | |
| Centro de Investigación y Prevención Cardiovascular-Arenales | Buenos Aires | Argentina | |
| Hospital General de Agudos Dr. José María Ramos Mejia | Buenos Aires | Argentina | |
| Instituto de Investigación Clínica TyT | Buenos Aires | Argentina | |
| Centro Medico de Estudios Clinicos y Farmacovigilancia (CECYF) | Buenos Aires | Argentina | |
| Consultorios Médicos Dr. Doreski | Buenos Aires | Argentina | |
| Consultora Integral de Salud Centro Médico Privado | Córdoba | Argentina | |
| Instituto CER S.A. | Quilmes | Argentina | |
| AES - AS - Clinica Mayo de Urgencias | San Miguel de Tucumán | Argentina | |
| CTR Estudios Clinicos | Santiago | Chile | |
| Enroll SpA | Santiago | Chile | |
| Centro de especialidades médicas Vanguardia | Temuco | Chile | |
| Clinical Research Chile SpA | Valdivia | Chile | |
| Centro de Estudios Clinicos Victoria Limitada (Cevic) | Victoria | Chile | |
| Dermacross Clinica Dermatologica | Vitacura | Chile | |
| Debreceni Egyetem Klinikai Kozpont Nagyerdei Campus | Debrecen | Hungary | |
| Pécsi Tudomanyegyetem - Vasvari Pal u. | Pécs | Hungary | |
| Mediadvance Clinical | Chihuahua City | Mexico | |
| PanAmerican Clinical Research | Guadalajara | Mexico | |
| Medical Care and Research S.A. de C.V. | Mérida | Mexico | |
| Centro de Investigación y Tratamiento Reumatológico S.C | Miguel Hidalgo | Mexico | |
| Oaxaca Site Management Organization - Clinic - OSMO - PPDS | Oaxaca City | Mexico | |
| M2M Med-ul. | Chorzów | Poland | |
| Malopolskie Badania Kliniczne Sp. z o.o. | Krakow | Poland | |
| Malopolskie Centrum Kliniczne | Krakow | Poland | |
| Centrum Medyczne Plejady | Krakow | Poland | |
| Santa Familia PTG Łódź | Lodz | Poland | |
| Twoja Przychodnia NCM | Nowa Sól | Poland | |
| Twoja Przychodnia PCM - ul. | Poznan | Poland | |
| Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji | Warsaw | Poland | |
| Klinika Reuma Park sp . zoo Sp.k. | Warsaw | Poland |
+ 20 more sites — see the full list on the official registry below.
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06843239 on ClinicalTrials.gov ↗ ← All trials in the UK