A Study of SPY072 in Adults With Moderate to Severe Hidradenitis Suppurativa (The SKYLIGHT Trial)
Spyre Therapeutics, Inc. · NCT07766005
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–75 · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 2
- Target enrollment
- 150
- US sites recruiting
- 7
- Study start
- September 2026
- Record last updated
- October 19, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This Phase 2 study will test whether the investigational medicine, SPY072, improves hidradenitis suppurativa (HS) in adults with moderate to severe disease receiving advanced standard of care treatment. About 150 participants will be assigned by chance to receive either SPY072 or placebo for 16 weeks. Participants will be followed after the treatment period to evaluate safety and how long treatment effects may last.
Being studied: SPY072; Placebo; bimekizumab
Conditions: Hidradenitis Suppurativa (HS)
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Clinical diagnosis of Hidradenitis Suppurativa with symptoms for at least 6 months before screening.
- Hidradenitis suppurativa lesions in at least 2 distinct anatomical areas, with at least 1 area meeting Hurley Stage II or III criteria at screening and Day 1.
- Total abscess and/or inflammatory nodule count of at least 5 at screening and Day 1.
- Documented inadequate response, intolerance, or contraindication to at least 1 systemic therapy for hidradenitis suppurativa.
Exclusion Criteria
- More than 20 draining tunnels at screening or Day 1.
- Hidradenitis suppurativa lesion expected to require incision and drainage within 4 weeks before Day 1, or major hidradenitis suppurativa surgery within 12 weeks before Day 1.
- Another inflammatory or skin condition that could interfere with assessment of hidradenitis suppurativa.
Recruiting US locations
Site 101
Indianapolis, IN 46250
Site contact: SKYLIGHT Trial Center
Site 100
Bowling Green, KY 42104
Site contact: SKYLIGHT Trial Center
Site 116
Owensboro, KY 42303
Site contact: SKYLIGHT Trial Center
Site 102
New York, NY 10023
Site contact: SKYLIGHT Trial Center
Site 104
The Bronx, NY 10455
Site contact: SKYLIGHT Trial Center
Site 125
Nashville, TN 37211
Site contact: SKYLIGHT Trial Center
Site 107
Tyler, TX 75703
Site contact: SKYLIGHT Trial Center
Study contacts (from the official record)
- SKYLIGHT Trial Center · 1-702-602-7976 · info@SKYLIGHT-trial.com
Similar studies in Indiana
All dermatology studies in Indiana →- RecruitingHealthy volunteersPhase 1
Ph 1a/1b Single Ascending Dose and Multiple Ascending Dose Study of ARQ-234
Arcutis Biotherapeutics, Inc.
- Location
- Plainfield, IN + 6 other US sites
- Eligibility basics
- Ages 18–65
- RecruitingHealthy volunteersPhase 1
A 3-part Study of SYX-5219 in Healthy Volunteers and Participants With Atopic Dermatitis
Sitryx Therapeutics Ltd
- Location
- Plainfield, IN + 5 other US sites
- Eligibility basics
- Ages 18–65
- RecruitingPhase 2
An Open-Label Extension Study of ORKA-001 in Participants With Plaque Psoriasis
Oruka Therapeutics, Inc.
- Location
- Plainfield, IN + 22 other US sites
- Eligibility basics
- Ages 18+
- RecruitingPhase 3
A Study to Evaluate the Safety and Effectiveness of Upadacitinib in Pediatric Participants With Alopecia Areata
AbbVie
- Location
- Indianapolis, IN + 8 other US sites
- Eligibility basics
- Ages 6–17