SBIR-STTR Award

Topical Anti-TNF Antibody for Oral Mucositis
Award last edited on: 8/16/10

Sponsored Program
SBIR
Awarding Agency
NIH : NIDCR
Total Award Amount
$125,242
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Barbara S Fox

Company Information

Avaxia Biologics Inc (AKA: Cirrcle33 LLC)

128 Spring Street Suite 620
Lexington, MA 02421
   (781) 861-0062
   info@avaxiabiologics.com
   www.avaxiabiologics.com
Location: Single
Congr. District: 05
County: Middlesex

Phase I

Contract Number: 1R43DE019735-01
Start Date: 9/15/09    Completed: 3/31/10
Phase I year
2009
Phase I Amount
$125,242
To develop an effective drug for oral mucositis Background: Oral mucositis is a painful dose-limiting side effect of many forms of cancer radiation and chemotherapy. According to a recent report by the National Comprehensive Cancer Network, mucositis is the most significant adverse symptom of cancer therapy reported by patients. There is only a single medication approved for mucositis, and it is only used in a limited set of patients. There is a compelling need for new, more effective therapeutics to reduce the severe pain and morbidity associated with this serious condition. Avaxia is developing a topical polyclonal anti-TNF antibody therapeutic for oral mucositis. TNF is an inflammatory cytokine that is believed to play a central role in the development of mucositis. We hypothesize that anti-TNF antibody will shut down the inflammatory response; preliminary data demonstrate that topical application of a rabbit polyclonal anti-TNF antibody significantly reduced both the severity and duration of radiation-induced mucositis in hamsters. In this proposal, Avaxia is isolating anti- TNF antibody from the early milk (colostrum) of immunized cows. Bovine colostral antibodies have a long history of safe human exposure, making them ideal for delivery to the oral cavity. The goal of the work described in this SBIR phase I application is to evaluate the technical feasibility of treating radiation- induced oral mucositis with topical anti-TNF bovine colostral antibody. The specific aims are as follows: To test the activity of the anti-TNF antibody in vitro (SA#1). To test the activity of topically applied anti-TNF antibody in hamsters with radiation-induced oral mucosits (SA#2). To define the distribution of topically applied anti-TNF antibody in hamsters with oral mucositis (SA#3). If these studies are successful, the SBIR Phase II application will evaluate the antibody in fractionated radiation regimens that more closely mimic clinical radiation therapy. Together, these studies will define the commercial opportunity offered by the bovine antibody and will form the basis of the pre-clinical pharmacology package to be used in support of an IND filing.

Public Health Relevance:
Oral mucositis is a serious and painful dose-limiting side effect of many forms of cancer radiation and chemotherapy. The goal of the work described in this application is to evaluate the technical feasibility of treating radiation-induced oral mucositis with a topical antibody. The long term goal is the development of a safe and effective medication.

Public Health Relevance Statement:
Oral mucositis is a serious and painful dose-limiting side effect of many forms of cancer radiation and chemotherapy. The goal of the work described in this application is to evaluate the technical feasibility of treating radiation-induced oral mucositis with a topical antibody. The long term goal is the development of a safe and effective medication.

Project Terms:
Acute; Adverse effects; Animal Model; Animal Models and Related Studies; Antibodies; Blood Circulation; Bloodstream; Bovine Species; Bucca; Buccal Cavity; Buccas; Cancer Radiotherapy; Cancer Treatment; Cancers; Cattle; Cavitas Oris; Cell/Tissue, Immunohistochemistry; Cheek; Cheek structure; Circulation; Clinical; Clinical Pharmacology; Colostrum; Colostrums; Cricetinae; DIF; Data; Development; Disease; Disorder; Dose; Dose-Limiting; Drug Administration, Topical; Drugs; Funding; Goals; Hamsters; Hand; Head and Neck, Buccal Cavity; History; IHC; Immunohistochemistry; Immunohistochemistry Staining Method; In Vitro; Inflammatory; Inflammatory Response; Lead; Malignant Neoplasm Therapy; Malignant Neoplasm Treatment; Malignant Neoplasms; Malignant Tumor; Mammals, Hamsters; Mammals, Rabbits; Measures; Medication; Membrane; Milk; Modeling; Morbidity; Morbidity - disease rate; Mouth; Mucosal Inflammation; Mucositis; NCCN; National Comprehensive Cancer Network; Oral; Oral cavity; Oryctolagus cuniculus; Pain; Painful; Patients; Pb element; Pharmaceutic Preparations; Pharmaceutical Preparations; Phase; Pilot Projects; Play; Protocols, Treatment; RGM; Rabbit, Domestic; Rabbits; Radiation; Radiation therapy; Radiotherapeutics; Radiotherapy; Recording of previous events; Regimen; Reporting; Role; SBIR; SBIRS (R43/44); Severities; Small Business Innovation Research; Small Business Innovation Research Grant; Spinal Column; Spine; Symptoms; TNF; TNF A; TNF gene; TNFSF2; Testing; Therapeutic; Therapeutic antibodies; Time; Topical application; Treatment Protocols; Treatment Regimen; Treatment Schedule; Treatment Side Effects; Tumor Necrosis Factor Gene; Vertebral column; Work; anticancer therapy; backbone; base; bovid; bovine; cancer therapy; chemotherapy; cow; cytokine; design; designing; disease/disorder; drug/agent; exposed human population; heavy metal Pb; heavy metal lead; human exposure; irradiation; malignancy; membrane structure; model organism; neoplasm/cancer; oral mucositis; oromucositis; pilot study; pre-clinical; preclinical; ray (radiation); side effect; social role; therapy adverse effect; topical administration; topical drug application; topically applied; treatment adverse effect

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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