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A Study of SPY072 in Rheumatic Disease

RECRUITINGPhase 2Sponsored by Spyre Therapeutics, Inc.
Actively Recruiting
PhasePhase 2
SponsorSpyre Therapeutics, Inc.
Started2025-08-21
Est. completion2026-10-31
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations13 sites

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

Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria:

For rheumatoid arthritis:

* Moderate-to-severely active RA as defined by the presence of ≥4 swollen joints (based on 28 joint count) and ≥4 tender joints (based on 28 joint count) at Screening and Day 1.
* Documentation of ≥1 of the following:

  1. Positive test results for rheumatoid factor or anti-citrullinated peptide antibodies at Screening, OR
  2. Radiology report documenting bony erosions in hands or feet consistent with RA on previous radiographs
* Inadequate response (defined as signs and symptoms of persistently active disease, loss of response, or intolerance) to:

  1. ≥1 csDMARD treatment; AND/OR
  2. ≤2 classes of bDMARD/tsDMARD treatment (\>2 classes of bDMARDs and/or tsDMARDs is exclusionary)

For axial spondyloarthritis:

* Moderate-to-severely active axSpA defined by BOTH of the following at Screening AND Day 1:

  1. BASDAI ≥4, AND
  2. Back pain ≥4 (from BASDAI Item 2)
* hsCRP greater than the ULN per the central laboratory at Screening
* Inadequate response (defined as signs and symptoms of persistently active disease, loss of response, or intolerance) to:

  1. 2 different NSAIDs given at the maximum tolerated dose for ≥4 weeks or intolerant to or has a contraindication to NSAID therapy; AND/OR
  2. ≤2 classes of bDMARD (anti-TNF or anti-IL-17)/tsDMARD at an approved dose for ≥12 weeks (\>2 classes of bDMARDs/tsDMARDs is exclusionary)

For psoriatic arthritis:

* Screening and Day 1 TJC ≥3 out of 68 and SJC ≥3 out of 66 (dactylitis counts as 1 joint each)
* ≥1 active plaque psoriasis lesion and/or a documented history of psoriasis
* Inadequate response (defined as signs and symptoms of persistently active disease, loss of response, or intolerance) to:

  1. ≥1 NSAID treatment; AND
  2. ≥1 csDMARD treatment; AND/OR ≤2 classes of bDMARD/tsDMARD treatment (\>2 classes of bDMARDs and/or tsDMARDs is exclusionary)

Exclusion Criteria:

* Inadequate response to \>2 classes of bDMARDs/tsDMARDs
* Other autoimmune, rheumatologic, inflammatory diseases or pain-amplification syndromes that might confound the evaluations of efficacy of SPY072

Conditions9

ArthritisAxSpAAxial SpondyloarthritisPsA (Psoriatic Arthritis)Psoriatic ArthritisRheumatic DiseasesRheumatic Joint DiseaseRheumatoid ArthritisRheumatologic Disease

Locations13 sites

Site 113
Avondale, Arizona, 85392
SKYWAY-RD Trial Center
Site 114
Chula Vista, California, 91910
SKYWAY-RD Trial Center
Site 111
Covina, California, 91722
SKYWAY-RD Trial Center
Site 108
Tujunga, California, 91042
SKYWAY-RD Trial Center
Site 112
Upland, California, 91786
SKYWAY-RD Trial Center

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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

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