SBIR/STTR Research Award

Development of PT523 for the treatment of lung cancer

Award identifier 401cd3318ad7126a635fb8f0a8a0960677bdd7b2408ae0a129e73f64fa92229eAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$159,000

Program and phase

SBIR · Phase I

Award year

2005

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Hana Biosciences, Inc.
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
PHS2005-2
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): The long-term goal of this proposal is to develop PT523 [Nalpha-(4-amino-4-deoxypteroly)-Ndelta-hemiphthaloyl-L-ornithine], a water soluble, non-polyglutamtable analog of methotrexate (MTX), for the treatment of advanced lung cancer. Lung cancer is among the most commonly occurring malignancies in the world and is one of the few that continues to show an increasing incidence. In the US, lung cancer is the leading cause of cancer death. Most patients with lung cancer present with locally advanced or metastatic disease at the initial diagnosis, and the current standard care for these patients is systemic chemotherapy with a two-drug combination regimen that included a platinum agent. Although the current combination chemotherapy reduces the rate of death attributed to lung cancer, disease progress is inevitable and the dose-limiting toxicities restrict their use. Therefore, development of new combination therapies that aims to inhibit tumor growth and progression while sparing normal cells will improve the quality of life of lung cancer patients. The Specific Aims are: (1) To determine the effect of PT523 in combination with various cytotoxic and targeted therapeutic agents on tumor cell proliferation in vitro. Lung cancer cell lines will be treated with PT523 and various anti-cancer agents alone and in combination for 48 to 96 hours. The cytotoxic agents will include currently approved chemotherapy drugs for lung cancer and targeted therapeutic agents will include small molecule inhibitors for EGFR. The EGFR expression profile in various lung cancer cell lines will be determined by quantitative PCR and immunocytochemistry. The effect of various treatments on lung cancer cell proliferation will be quantified by MTT assay. The agents that work synergistically with PT523 in inhibition of cell growth will be determined. (2) To determine the efficacy of PT523 in combination with various cytotoxic and targeted therapeutic agents on tumor growth in xenograft models. Before evaluating the antitumor activity of PT523 with different agents, the maximum tolerated dose (MTD) of various agents alone or in combination will be determined in athymic mice. The growth inhibition activity of PT523 in combination with various agents will be evaluated in athymic mice bearing human lung carcinomas as s.c. transplants. The agent(s) that are most efficacious in inhibition of tumor growth and best tolerated in combination with PT523 will be selected.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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