Table 1.
Emerging topical treatments for HS
| Drug name (MOA) | Author or clinical trial # | Study type | Study goal and primary endpoint(s) | Patients enrolled | (Anticipated) completion date | Results or recruitment status |
|---|---|---|---|---|---|---|
| Ruxolitinib 1.5% cream (JAK 1/2 inhibitor) | NCT05635838 | Phase 2 randomized, double-blind vehicle-controlled |
Evaluate efficacy in patients with mild to moderate HS Endpoint: change from baseline in AN count at week 16 |
60 | March 2024 | Recruiting |
| Ruxolitinib 1.5% cream (JAK 1/2 inhibitor) | NCT04414514 | Phase 2 open label |
Evaluate efficacy and effects on skin inflammation in patients with HS Endpoint: percentage of patients who achieve HiSCR at week 16 |
24 | January 2025 | Recruiting |
| AT193 (aryl hydrocarbon agonist) | NCT04989517 | Phase 1 randomized, double-blind placebo-controlled |
Evaluate safety and tolerability in patients with HS Endpoint: incidence of TEAEs up to week 10 |
44 | February 2023 | Active, not recruiting |
| LTX-109 3% gel (lytic peptidomimetic) | NCT04756336 | Phase 2 proof of concept |
Evaluate safety and efficacy in patients with HS Endpoints: investigator and patient assessed signs and symptoms, respectively, of local reactions to the product until week 6 |
11 | July 2021 | Completed |
| Gentian violet (antiseptic) | NCT04388163 | Phase 2 open-label |
Evaluate efficacy in patients with HS Endpoint: skin redness, drainage, and pain at baseline and 1 month post-treatment |
16 | December 2023 | Not yet recruiting |
| Povidone-iodine cream (antimicrobial) | NCT01818167 | Prospective multi-center blinded, randomized, controlled clinical trial |
Compare efficacy of povidone-iodine topical cream to 10% benzoyl peroxide topical body wash for the treatment of early stage HS Endpoint: HS European Research Group scale up to 4 months |
25 | January 2015 | Results submitted |
AN abscesses and inflammatory nodules, HiSCR hidradenitis suppurativa clinical response, HS hidradenitis suppurativa, JAK Janus kinase, MOA mechanism of action, TEAEs treatment emergent adverse events