Entity

Time filter

Source Type

San Diego, CA, United States

Auci D.L.,HollisEden Pharmaceuticals | Mangano K.,University of Catania | Destiche D.,HollisEden Pharmaceuticals | White S.K.,HollisEden Pharmaceuticals | And 5 more authors.
International Journal of Molecular Medicine | Year: 2010

HE3286 (17α-ethynyl-5-androstene-3β, 7β, 17β-triol) is an orally bio-available synthetic derivative of naturally occurring androstene-3β, 7β, 17β-triol. Our present data show that oral treatment with HE3286, favourably influenced the course of arthritis in the rat model of adjuvant-induced arthritis (reduced cumulative disease scores and paw edema), and in the mouse model of collagen antibody-induced arthritis (reduced clinical paw scores). Importantly, HE3286 was not immune suppressive in human mixed lymphocyte reaction or in animals challenged with Coxsackie B3 virus. HE3286 is currently in phase I/II clinical trials in rheumatoid arthritis and ulcerative colitis and these findings further strengthen the possibility that HE3286 may represent an effective anti-inflammatory agent useful for treating chronic inflammation with a more attractive safety profile than glucocorticoids or cyclooxygenase inhibitors.

Discover hidden collaborations