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NCT02695212 · ClinicalTrials.gov registry record · Phase 2
Single Center Study of Apremilast for the Treatment of Hidradenitis Suppurativa
A Phase 2 study of Hidradenitis Suppurativa, sponsored by Florida Academic Dermatology Centers.
- Completed
- Registry status
- Phase 2
- Development phase
- 20
- Enrollment target
- 1
- Study location
NCT02695212: Completed Phase 2 study of Hidradenitis Suppurativa, sponsored by Florida Academic Dermatology Centers.
NCT02695212 is a Phase 2 study of Hidradenitis Suppurativa that has completed, run by Florida Academic Dermatology Centers. The registered enrollment target is 20 participants, below the 598-participant average among 52 other Hidradenitis Suppurativa trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02695212, a Phase 2 study of Hidradenitis Suppurativa, has completed, sponsored by Florida Academic Dermatology Centers.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
The primary objective of this study is to evaluate the safety and efficacy of Apremilast in subjects with moderate Hidradenitis Suppurativa (HS).
Primary Outcome
defined as a 30% reduction in the total number of abscess and inflammatory nodule count with a 50% reduction as an exploratory endpoint..
Conditions Studied
Interventions
- DRUG Apremilast
Study Locations (1)
Florida
- Florida Academic Dermatology Centers - Coral Gables
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2016-07 |
| Est. Completion | 2017-08 |
| Phase | Phase 2 |
What the finished NCT02695212 record still lists
NCT02695212 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 598-participant average among 52 other Hidradenitis Suppurativa trials with a reported enrollment target (97% lower).
The record links to 1 condition, with Hidradenitis Suppurativa appearing as the primary indexed condition, and to 1 intervention - of which Apremilast is the first listed.
NCT02695212 reports a single indexed study location in Florida.
Frequently Asked Questions
What is clinical trial NCT02695212 about?
NCT02695212 is a clinical study titled "Single Center Study of Apremilast for the Treatment of Hidradenitis Suppurativa". The primary objective of this study is to evaluate the safety and efficacy of Apremilast in subjects with moderate Hidradenitis Suppurativa (HS).
What is the current status of trial NCT02695212?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2016-07. Estimated completion is 2017-08.
What conditions does trial NCT02695212 study?
This clinical trial studies the following conditions: Hidradenitis Suppurativa.
What interventions are being tested in trial NCT02695212?
The interventions under investigation include: Apremilast (DRUG).
Who is sponsoring clinical trial NCT02695212?
This trial is sponsored by Florida Academic Dermatology Centers, which has 2 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02695212 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Hidradenitis Suppurativa
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT02695212's enrollment target sits among peer trials
20 41st of 52 higher than 9 of 52 other Hidradenitis Suppurativa trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Hidradenitis Suppurativa trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
-
Topical Ruxolitinib 1.5% for Hidradenitis Suppurativa Treatment
RECRUITING · Phase 2
-
A Study for Evaluating Safety & Efficacy of Topical Roflumilast 0.3% Foam in Hidradenitis Suppurativa
RECRUITING · Phase 2
-
A Study to Investigate Efficacy and Safety With SAR445399 in Adult Participants With Moderate to Severe Hidradenitis Suppurativa
RECRUITING · Phase 2
-
A 16-Week Study to Learn About the Study Medicine Called Ritlecitinib in Adults With Long Lasting Painful Red Skin Lumps, Known by the Medical Term, Hidradenitis Suppurativa, or HS.
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-
A Study to Assess Molecular Changes in Adult Participants With Moderate to Severe Hidradenitis Suppurativa or With Moderate to Severe Atopic Dermatitis Receiving Subcutaneous Injections of Lutikizumab
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-
Brivekimig for the Treatment of Moderate to Severe Hidradenitis Suppurativa
RECRUITING · Phase 2
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