Phase 2
Completed N=69
Study to Evaluate of the Efficacy and Safety of Ruxolitinib Cream in Participants With Hidradenitis Suppurativa
Source: ClinicalTrials.gov NCT05635838 ↗Enrolled (actual)
69
Serious AEs
3.0%
Results posted
Nov 2024
Primary outcomePrimary: Change From Baseline in Abscess and Inflammatory Nodule (AN) Count at Week 16 — -3.61; -2.42 ANs — p=0.0215
Summary
The purpose of this study is to evaluate the efficacy and safety of Ruxolitinib cream in participants with Hidradenitis Suppurativa. This is a randomized 16-week double-blind, vehicle-controlled (DBVC) study followed by a 16 week open label extension period (OLE) with an active treatment for participants who complete the DBVC period.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change From Baseline in Abscess and Inflammatory Nodule (AN) Count at Week 16 |
-3.61; -2.42 | 0.0215 sig |
| SECONDARY Percentage of Participants Achieving AN50, AN75, AN90, and AN100 at Week 16 |
79.2; 56.3; 54.2; 25.0; 20.8; 12.5 | — |
| SECONDARY Change From Baseline to Week 16 in Total AN Count in Anatomical Areas With Pre-existing ANs at Baseline |
-3.85; -3.17 | 0.1671 |
| SECONDARY Change From Baseline in Skin Pain Numeric Rating Scale (NRS) Score at Week 16 |
-1.90; -2.09 | 0.7982 |
| SECONDARY Change From Baseline in Itch NRS Score at Week 16 |
-1.45; -2.39 | 0.2031 |
| SECONDARY Percentage of Participants Who Achieve Hidradenitis Suppurativa Clinical Response (HiSCR) at Week 16 |
79.2; 50.0 | — |
| SECONDARY Change From Baseline in the International Hidradenitis Suppurativa Severity Score System (IHS4) Score at Week 16 |
-3.58; -2.76 | 0.2387 |
| SECONDARY Number of Participants With Any Treatment-emergent Adverse Event (TEAE ) in the Double-blind, Vehicle-controlled (DBVC) Period |
13; 15 | — |
| SECONDARY Number of Participants With Any Grade 3 or Higher TEAE in the DBVC Period |
0; 2 | — |
| SECONDARY Number of Participants With Any TEAE in the Open-label Extension (OLE) Period |
8; 15 | — |
| SECONDARY Number of Participants With Any Grade 3 or Higher TEAE in the OLE Period |
0; 3 | — |
Eligibility Criteria
Inclusion Criteria
- Diagnosis of HS based on clinical history and physical examination for at least 3 months.
- Diagnosis of HS (Hurley I or II) with the following:
- A total AN count of 3 to ≤ 10, with no draining tunnels at screening and baseline visits. AND
- The AN count at the screening AND baseline visits:
- AN of 3 should affect at least 1 distinct anatomical area
- AN of > 3 to ≤ 10 should affect at least 2 distinct anatomical areas.
- Baseline Skin Pain or Itch NRS score ≥ 1.
- Agreement to NOT use topical and systemic antibiotics for treatment of HS during the study.
- Agreement to NOT use a diluted beach bath or topical antiseptic washes containing chlorhexidine gluconate or benzoyl peroxide on the areas affected by HS lesions during the study.
- Willingness to avoid pregnancy or fathering children
Exclusion Criteria
- Presence of draining tunnels at screening or at baseline visits.
- Concurrent conditions and history of other diseases:
- Active ongoing inflammatory diseases of the skin other than HS that might confound the evaluation of HS.
- Any other concomitant skin disorder (eg, generalized erythroderma such as Netherton's syndrome), pigmentation, or extensive scarring that in the opinion of the investigator may interfere with the evaluation of HS AN or compromise participant safety.
- Immunocompromised (eg, lymphoma, acquired immunodeficiency syndrome, or Wiskott-Aldrich syndrome).
- Chronic or acute infection requiring treatment with systemic antibiotics, antivirals, antiparasitics, antiprotozoals, or antifungals within 2 weeks before baseline.
- Active acute bacterial, fungal, or viral skin infection (eg, herpes simplex, herpes zoster, chicken pox, clinically infected AD, or impetigo) within 2 weeks before baseline.
- Laboratory values outside of the protocol-defined criteria.
- Use of any prohibited medications per protocol-defined criteria.
- Pregnant or lactating participants, or those considering pregnancy during the period of their study participation.
- Other exclusion criteria may apply.
Data sourced from ClinicalTrials.gov (NCT05635838). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.