A Study of SPY072 in Rheumatic Disease
Condition(s) studied
Investigational drug(s) / intervention(s)
SPY002-072: Experimental
Placebo: Matching Placebo
Study summary
This is a multi-center, double-blind, placebo-controlled, Phase 2, proof-of-concept basket study with the goal of assessing the efficacy and safety of SPY072 compared to placebo in adults (aged ≥18 years) with rheumatic disease (RD).
Eligibility
Primary outcome measure(s)
- Rheumatoid Arthritis: Change from baseline in Disease Activity Score in 28 joints (c-reactive protein) (DAS-CRP) — Week 12
The score is calculated based on the number of tender and swollen joints out of 28 assessed (TJC28 and SJC28), a measure of inflammation in the blood (c-reactive protein, CRP), and the subject's overall assessment of their health (patient global assessment). Scores range from 0-10. Higher scores indicate greater disease activity. - Axial Spondyloarthritis: Change from baseline in Ankylosing Spondylitis Disease Activity Score (ADAS) — Week 16
The score combines 5 disease activity variables (back pain, duration of morning stiffness, patient global assessment of disease activity, peripheral pain/swelling and measure of inflammation) to measure disease activity. Lowest score is 0.6 and increases as disease worsens. Higher scores indicate greater disease activity. - Psoriatic Arthritis: Proportion of participants who achieve an American College of Rheumatology 20 Response Criteria (ACR20) response — Week 16
The proportion of subjects who achieve at least 20% improvement in tender and swollen joint counts (TJC and SJC), and at least 20% improvement in 3 out of 5 other disease activity measures (patient global assessment, physician global assessment, patient pain assessment, health assessment questionnaire, and measure of inflammation) will be assessed.
Trial sites (64)
| Facility | City | Region | Status |
|---|---|---|---|
| Site 113 | Avondale | Arizona | |
| Site 118 | Tucson | Arizona | |
| Site 114 | Chula Vista | California | |
| Site 111 | Covina | California | |
| Site 108 | Tujunga | California | |
| Site 112 | Upland | California | |
| Site 107 | Whittier | California | |
| Site 115 | Aventura | Florida | |
| Site 109 | Hialeah | Florida | |
| Site 106 | Ormond Beach | Florida | |
| Site 110 | Tampa | Florida | |
| Site 116 | Willowbrook | Illinois | |
| Site 119 | Rockville | Maryland | |
| Site 104 | Duncansville | Pennsylvania | |
| Site 105 | Corpus Christi | Texas | |
| Site 120 | Irving | Texas | |
| Site 103 | Tomball | Texas | |
| Site 102 | Tomball | Texas | |
| Site 503 | Lovech | Lovech | |
| Site 502 | Pleven | Pleven | |
| Site 506 | Plovdiv | Plovdiv | |
| Site 505 | Plovdiv | Plovdiv | |
| Site 504 | Varna | Varna | |
| Site 706 | Hlučín | Hlučín | |
| Site 702 | Moravská Ostrava | Ostrava-město | |
| Site 704 | Pardubice | Pardubice Region | |
| Site 705 | Prague | Praha, Hlavní Mesto | |
| Site 703 | Prague | Praha, Hlavní Mesto | |
| Site 701 | Uherské Hradiště | Zlín | |
| Site 303 | Tbilisi | K'alak'i T'bilisi | |
| Site 304 | Tbilisi | K'alak'i T'bilisi | |
| Site 301 | Tbilisi | K'alak'i T'bilisi | |
| Site 307 | Tbilisi | K'alak'i T'bilisi | |
| Site 305 | Tbilisi | K'alak'i T'bilisi | |
| Site 308 | Batumi | Georgia | |
| Site 302 | Kutaisi | Georgia | |
| Site 306 | Tbilisi | Georgia | |
| Site 201 | Chisinau | Moldova | |
| Site 202 | Chisinau | Moldova | |
| Site 401 | Krakow | Lesser Poland Voivodeship |
+ 24 more sites — see the full list on the official registry below.
More Spyre Therapeutics, Inc. trials in Poland
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 NCT07148414 on ClinicalTrials.gov ↗ ← All trials in Poland