SBIR-STTR Award

Novel Therapeutic Approach To Psoriasis
Award last edited on: 3/5/07

Sponsored Program
STTR
Awarding Agency
NIH : NIAMS
Total Award Amount
$682,784
Award Phase
2
Solicitation Topic Code
-----

Principal Investigator
Harrihar A Pershadsingh

Company Information

Bethesda Pharmaceuticals Inc

1016 Lakeview Way
Redwood City, CA 94062
   (661) 664-9640
   N/A
   N/A

Research Institution

University of Michigan

Phase I

Contract Number: 1R41AR44767-01
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
1997
Phase I Amount
$99,510
There is no text on file for this abstract.

Thesaurus Terms:
drug screening /evaluation, hormone receptor, psoriasis, skin disorder chemotherapy, thiazole astrocytoma, cell proliferation, keratinocyte, oral administration, smooth muscle SCID mouse, histology, human tissue, organ culture, tissue /cell culture

Phase II

Contract Number: 2R42AR044767-02A2
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
2001
(last award dollars: 2002)
Phase II Amount
$583,274

Psoriasis is a common, inflammatory disease of the skin characterized by hyper-proliferation of keratinocytes. A variety of antipsoriatic therapies are available, however, due to problems with side effects and variability in clinical response, intense clinical and commercial interest remains in the development of new treatments. Thiazolidinediones, a novel class of compounds that activate the nuclear hormone receptor PPAR gamma, have recently been found to reversibly inhibit the proliferation of both normal and psoriatic human keratinocytes in vitro, and ameliorate the histologic abnormalities of psoriatic skin in organ culture and in the scid mouse/human skin transplant model of psoriasis. In the current proposal, we will: 1) perform pilot studies of the antipsoriatic effects of orally administered thiazolidinediones in humans; 2) investigate the cellular mechanisms that mediate the antipsoriatic effects of thiazolidinediones, and 3) investigate the antipsoriatic potential of a recently developed series of novel thiazolidinediones that are expected to be more effective than existing compounds with respect to ameliorating the epidermal inflammation and hyperproliferation that characterizes psoriasis. By investigating clinical efficacy, by addressing therapeutic mechanisms, and by testing novel thiazolidinediones, the current Phase II studies will significantly advance the potential for Phase III commercial development of thiazolidinediones in the treatment of psoriasis.