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OpenTrials
Completed

NCT Number: NCT00827996

To Assess the Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Hidradenitis Suppurativa

The trial is a 12-week phase 2 study. Subjects will be given subcutaneous injections at weeks 0 (160mg), 2 (80mg), and then every other week (40mg) until week 12 in subjects with moderate to severe hidradenitis suppurativa.

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Key information

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Subjects with moderate to severe HS as defined by a HSSI > 8 AND at least ONE of the following:

  • HS >1 year duration with multiple ER or doctors visits related to HS
  • Intralesional kenalog injection >5/year, however none within 2 weeks of entry
  • Failed systemic retinoids, but not within 3 months of entry
  • Failed at least one prior course of antibiotic therapy, which must not have been administered within 2 weeks of entry to the study (excluding the recommended antibiotic regimen given for evidence of active infection immediately before enrollment)
  • History of surgery (reconstructive), but not within 3 months of entry

Exclusion criteria

  • Women who are pregnant, nursing, or planning pregnancy within 6 months after the last injection (this includes father's who plan on fathering a child within 6 months after their last injection).
  • Use of other systemic anti-inflammatory medication except NSAIDs and low dose systemic steroids (equal or less than 10 mg daily prednisolone or equivalent).
  • If found to have an active infection, patients must have completed topical or oral antibiotic therapy at least 7 days before first injection.
  • Have a known history of serious infections (e.g., hepatitis, pneumonia or pyelonephritis) in the previous 3 months.
  • Have or have had an opportunistic infection (e.g., herpes zoster [shingles], cytomegalovirus, Pneumocystis carinii, aspergillosis, histoplasmosis, or mycobacteria other than TB) within 6 months prior to screening.
  • Have a history of lymphoproliferative disease, including lymphoma or signs suggestive of possible lymphoproliferative disease such as lymphadenopathy of unusual size or location (e.g., nodes in the posterior triangle of the neck, infraclavicular, epitrochlear, or periaortic area), or splenomegaly.
  • Have a concomitant diagnosis or history of congestive heart failure.
  • Have a history of latent or active granulomatous infection, including TB, histoplasmosis, or coccidioidomycosis, prior to screening.

Treatment and study plan

Adalimumab

Drug

Subjects will be given subcutaneous injections at weeks 0 (160mg), 2 (80mg), and then every other week (40mg) until week 12

Primary outcomes

  1. To assess the efficacy and safety of adalimumab in subjects with moderate to severe hidradenitis suppurativa. Efficacy will be evaluated using the included Hidradenitis Suppurativa Severity Index (HSSI).

    Time frame: 13 weeks

Secondary outcomes

  1. To evaluate the role of TNF alpha in the pathogenesis of hidradenitis suppurativa.

    Time frame: 13 weeks

  2. To evaluate the ability of adalimumab to maintain suppression of the disease.

    Time frame: 13 weeks

Sponsors and collaborators

Lead sponsor

Florida Academic Dermatology Centers

Other

Collaborators

  • Abbott

Registry information

Official study title

Open Label,Phase Two Study to Assess the Efficacy and Safety of Adalimumab in Subjects With Moderate to Severe Hidradenitis Suppurativa

Acronym: HIDRI2007

Important dates

Study start
2007
Primary completion
2007
Study completion
2008
First posted
Jan 23, 2009
Registry last updated
Jan 23, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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