SBIR-STTR Award

Novel Reagents For The Detection Of Low Abundance Cancer Specific Glycoforms
Award last edited on: 5/18/11

Sponsored Program
SBIR
Awarding Agency
NIH : NCI
Total Award Amount
$194,005
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Michael J Ciocci

Company Information

Toph Biologicals Inc

3805 Old Easton Road
Doylestown, PA 18902
   (215) 489-4944
   N/A
   N/A
Location: Single
Congr. District: 01
County: Bucks

Phase I

Contract Number: 1R43CA153822-01
Start Date: 9/1/10    Completed: 8/31/11
Phase I year
2010
Phase I Amount
$194,005
Hepatocellular carcinoma (HCC) is one of the most common solid malignancies worldwide and the incidence in the United States is increasing. It has been estimated that the number of cases of HCC will continue to increase by 81% (from a baseline of about 13,000 a year) by the year 2020, primarily due to the hepatitis C (HCV) epidemic. Despite advances in medical technology, the 5-year survival between 1981 and 1998 improved only 3%, likely due to the fact that the majority of patients with HCC are diagnosed at advanced stages leading to an overall 1-year survival of 25% in the United States. Early diagnosis of HCC in patients at risk for liver disease will help improve outcome. N-linked glycosylation changes of specific serum biomarker proteins occur with the development of liver cancer. The specific aims of this grant are focused on developing high affinity binding lectins (carbohydrate binding proteins) that recognize the glycsoylation changes that occur on serum biomarkers of HCC (Specific Aim 1) and using these recombinant lectins in an ELISA based format on archived patient serum samples to test their sensitivity and specificity for predicting liver disease and HCC (Specific Aim 2). , ,

Public Health Relevance:
The incidence of hepatocellular carcinoma (HCC) is increasing worldwide with a poor prognosis for survival related to the lack of predictive assays for early detection. Sensitive, specific, non-invasive assays that are predictive for diagnosing HCC in patients at risk for liver disease are urgently needed.

Thesaurus Terms:
2-Acetamido-2-Deoxy-D-Glucose;2-Acetamido-2-Deoxyglucose;A1pi;Acetylglucosamine;Affinity;Agaricales;Archives;Assay;Binding;Binding (Molecular Function);Binding Sites;Bioassay;Biologic Assays;Biological;Biological Assay;Blinded;Blood;Blood Serum;Blood Tests;Cancers;Carcinoma Of The Liver Cells;Cirrhosis;Clinical;Clinical Research;Clinical Study;Cohort Studies;Combining Site;Complex;Concurrent Studies;D-Glucose, 2-(Acetylamino)-2-Deoxy-;Data;Deoxygalactose;Detection;Development;Diagnosis;Diagnostic;Disease;Disease Progression;Disorder;Elisa;Early Diagnosis;Engineering;Engineerings;Enzyme-Linked Immunosorbent Assay;Epidemic;Fetoprotein;Forecast Of Outcome;Fucose;Glycans;Glycoproteins;Grant;Hbv;Hcc;Hcv;Hcv Liver Cancer;Hcv Infection;Hematologic Tests;Hematological Tests;Hematology Testing;Hepatic Cancer;Hepatic Cirrhosis;Hepatic Disorder;Hepatitis B Virus;Hepatitis C;Hepatitis C Virus;Hepatitis C Virus Infection;Hepatitis Virus, Homologous Serum;Hepatitis, Viral, Non-A, Non-B, Parenterally-Transmitted;Hepatitus C;Hepatocellular Carcinoma;Hepatocellular Cancer;Hepatoma;Incidence;Laboratories;Lectin;Link;Liquid Substance;Liver Cirrhosis;Liver Diseases;Malignant Neoplasms;Malignant Tumor;Malignant Neoplasm Of Liver;Medical Technology;Metabolic Glycosylation;Methods;Minor;Molecular Interaction;Monitor;Mushrooms;N Acetylglucosamine;N-Acetyl-D-Glucosamine;N-Acetyllactosamine;Nanbh;Oligosaccharides;Outcome;Pt-Nanbh;Parenterally-Transmitted Non-A, Non-B Hepatitis;Patients;Performance;Persons;Phase;Polysaccharides;Primary Carcinoma Of The Liver Cells;Prognosis;Proteins;Reactive Site;Reagent;Recombinants;Reticuloendothelial System, Blood;Risk;Risk Marker;Sampling;Screening For Hepatocellular Cancer;Selection Criteria;Sensitivity And Specificity;Serum;Serum Markers;Site;Solid;Specificity;Staging;Structure;Testing;Trypsin Inhibitor, Alpha 1-Antitrypsin;United States;Whblood;Whole Blood;Alpha 1 Antiprotease;Alpha 1-Antiproteinase;Alpha 1-Antitrypsin;Alpha 1-Protease Inhibitor;Alpha 1-Proteinase Inhibitor;Alpha-Fucose;Base;Biomarker;Carbohydrate Binding Protein;Cohort;Commercialization;Disease Risk;Disease/Disorder;Disorder Risk;Early Detection;Early Liver Cancer Detection;Fluid;Gene Product;Glycosylation;Hepatitis Non A Non B;Hepatitis Nona Nonb;Hepatopathy;Improved;Liquid;Liver Cancer;Liver Cancer Detection;Liver Disorder;Malignancy;Malignant Liver Tumor;Mutant;Neoplasm/Cancer;Non A Non B Hepatitis;Non A, Non B Hepatitis;Non-A Non-B Hepatitis;Non-A, Non-B Hepatitis;Novel;Outcome Forecast;Public Health Relevance;Screening For Liver Cancer;Sugar

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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