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Clinical Trials in the UK / NCT06843239
Active, not recruiting Phase 2

Tibulizumab Systemic Sclerosis Understanding and Response Evaluation (TibuSURE)

NCT06843239 · tracked via the Priya Life Science UK tracker
Sponsor
Zura Bio Inc
Phase
Phase 2
Started
2025-02-06
Last updated
2026-07-20

Condition(s) studied

Systemic Sclerosis (SSc)Scleroderma

Investigational drug(s) / intervention(s)

TibulizumabPlacebo

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

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Male or female, 18 to 75 years of age * Body mass index between 18.0 and 38.0 kg/m² * Fulfills classification criteria for SSc according to ACR/EULAR 2013 criteria * Has diffuse cutaneous SSc, defined as mRSS \>0 over at least one skin area proximal to the elbows and/or knees, in addition to acral fibrosis * Has had SSc (defined as the first non-Raynaud's phenomenon (RP) symptom or sign attributed to SSc) for ≤7 years * mRSS ≥15 and ≤45 at screening. Additional requirements for participants ≥2 years to ≤7 years from SSc onset and RNA Polymerase III antibody positive * FVC \>50% predicted * Diffusing capacity of the lungs for carbon monoxide (DLCO) ≥40% predicted (corrected for hemoglobin) Exclusion Criteria: * Has any of the following complications: * Left ventricular failure * Pulmonary arterial hypertension * Renal crisis within previous 6 months * Gastrointestinal dysmotility within previous 3 months * Digital ischemia with gangrene, amputation, or unscheduled hospitalization within previous 3 months * Current rheumatic disease other than SSc that could interfere with assessment of SSc * Lung disease requiring continuous oxygen therapy * Evidence or suspicion of active or latent tuberculosis * Active Crohn's Disease or ulcerative colitis

Primary outcome measure(s)

Trial sites (60)

FacilityCityRegionStatus
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.

Official registry record

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