SBIR/STTR Research Award

Novel anti-oxidant catalyst to treat IL-2 toxicity

Award identifier 6332e614db0d2bd6349a8c80f30a35fd8c052914a8cc38520e25f2c34de8e5c8Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$340,727

Program and phase

SBIR · Phase I

Award year

2003

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Inotek Pharmaceuticals Corporation
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): IL-2 biotherapy of refractory malignancies may produce cardiovascular toxicities and hemodynamic alterations that are indistinguishable from those seen in septic shock. These host responses include a massive capillary leak syndrome, manifested as non-cardiogenic pulmonary edema and consequent respiratory failure. There is now substantial evidence that the inflammatory process to IL-2 biotherapy is mediated by profound alterations in the biosynthesis of the free radicals nitric oxide and superoxide anion, and their reaction product peroxynitrite. An effective anti-inflammatory treatment would reduce the toxicity of IL-2 treatment and encourage increased use of this highly promising antineoplastic therapy. To address this unmet need, Inotek is developing a novel class of ultrapotent peroxynitrite decomposition catalysts. The lead compound, the metalloporphyrin INO-1080, is dramatically protective in experimental models of systemic inflammatory shock. The investigators propose to establish "proof-of-principle" that INO-1080 reduces the hemodynamic biochemical, and histopathologic alterations in an experimental model of IL-2 biotherapy. First, the investigators will ensure that INO-1080 does not adversely impact the anti-tumor activity of IL-2. They will carry out these investigations in a murine model of pulmonary metastasis by syngeneic melanoma cells. Second, they will document in a large animal model that INO-1080 ameliorates shock and tissue injury induced by IL-2. The investigators will utilize a well-established ovine model of IL-2 induced shock. The investigators expect INO-1080 will reduce tissue injury, capillary leak, pulmonary hypertension, lipid peroxidation, and nitrotyrosine formation, and attenuate the loss of systemic vascular resistance. Confirmation of efficacy, coupled with evidence that INO-1080 does not adversely impact on the anti-tumor activity of IL-2, would justify clinical testing in population with refractory malignant melanoma.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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