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NCT07766005 · Spyre Therapeutics, Inc.

A Study of SPY072 in Adults With Moderate to Severe Hidradenitis Suppurativa (The SKYLIGHT Trial)

What this study is about

This Phase 2 study will test whether the experimental medicine, SPY072, improves hidradenitis suppurativa (HS) in adults with moderate to severe disease receiving advanced the usual treatment treatment. About 150 participants will be assigned by chance to receive either SPY072 or placebo for 16 weeks.

View original scientific description

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.

Interventions

DRUG

SPY072

Solution for SC injection

DRUG

Placebo

Matching placebo for SC injection

DRUG

bimekizumab

Advanced standard of care

Primary outcome measures

Percentage of Participants Achieving Hidradenitis Suppurativa Clinical Response 75 (HiSCR75)

Time frame: Week 16

HiSCR75 is defined as at least a 75% reduction from baseline in total abscess and inflammatory nodule count, with no increase in abscess count and no increase in draining tunnel count

Who can participate

This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.

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.

Where

  • Birmingham, Alabama
  • Rogers, Arkansas
  • Irvine, California
  • Coral Gables, Florida
  • Atlanta, Georgia
  • Indianapolis, Indiana
  • Bowling Green, Kentucky
  • Owensboro, Kentucky
  • Baton Rouge, Louisiana
  • Boston, Massachusetts
  • Detroit, Michigan
  • Las Vegas, Nevada

And 11 more locations — see the full list below.

Related conditions & keywords

Hidradenitis Suppurativa (HS)Hidradenitis suppurativaHidradenitisSkin diseasesSweat gland diseasesSkin and connective tissue diseases

Frequently asked questions

What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Data: ClinicalTrials.gov · synced Oct 19, 2026 · Source of record for eligibility and locations

📊
1 of 150 participants interested
1% interest

See if this study fits

A short prescreen based on this study's listed criteria. A coordinator confirms eligibility — this is not a medical assessment.

Preparing your pre-screening questions…

Study locations

Choose your preferred location, or select flexible during enrollment.

NOT_YET_RECRUITING

Birmingham

Alabama

Location available
NOT_YET_RECRUITING

Rogers

Arkansas

Location available
NOT_YET_RECRUITING

Irvine

California

Location available
NOT_YET_RECRUITING

Coral Gables

Florida

Location available
NOT_YET_RECRUITING

Atlanta

Georgia

Location available
RECRUITING

Indianapolis

Indiana

Location available
RECRUITING

Bowling Green

Kentucky

Location available
RECRUITING

Owensboro

Kentucky

Location available
NOT_YET_RECRUITING

Baton Rouge

Louisiana

Location available

And 17 more locations available.

Express your interest

Share your contact details and a study coordinator can follow up about screening.

Secure & Confidential

Your information is protected and will only be shared with the research team.

What participation can include

  • Study-related care provided by the research team
  • Close monitoring by medical professionals
  • Possible compensation for time and travel*
  • The option to withdraw at any time
  • Contributing to medical research that may help future patients

*Compensation varies by study. Confirm details with coordinator.

Typical next steps

  1. 1.Submit this form
  2. 2.Phone screening
  3. 3.In-person assessment if eligible
  4. 4.Begin participation

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Looking for Hidradenitis Suppurativa (HS) Treatment in Birmingham?

Join others in Alabama exploring innovative treatment options through clinical research

Hidradenitis Suppurativa (HS) Treatment Options in Birmingham, Alabama

If you're searching for Hidradenitis Suppurativa (HS) treatment in Birmingham, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Birmingham, Rogers, Irvine and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with Hidradenitis Suppurativa (HS). All study-related care is provided at no cost to participants.

Local Sites
3 locations in Alabama
Now Enrolling
Up to 150 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for Hidradenitis Suppurativa (HS)?

Potential Benefits

  • ✓Access to new treatment approaches before public availability
  • ✓Close monitoring by experienced medical professionals
  • ✓Study-related care provided at no cost
  • ✓Contribute to medical research for Hidradenitis Suppurativa (HS)

What to Expect

  • →Initial screening to determine eligibility
  • →Regular check-ups and monitoring visits
  • →Possible compensation for time and travel
  • →You can withdraw at any time

Frequently Asked Questions About This Hidradenitis Suppurativa (HS) Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT07766005. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.