PROTEIN DRUG DELIVERY BASED ON STABILIZED PROTEIN

Information

  • Research Project
  • 6014575
  • ApplicationId
    6014575
  • Core Project Number
    R44DK053108
  • Full Project Number
    2R44DK053108-02
  • Serial Number
    53108
  • FOA Number
  • Sub Project Id
  • Project Start Date
    8/1/1997 - 26 years ago
  • Project End Date
    7/31/2001 - 22 years ago
  • Program Officer Name
    MCKEON, CATHERINE T
  • Budget Start Date
    9/30/1999 - 24 years ago
  • Budget End Date
    7/31/2000 - 23 years ago
  • Fiscal Year
    1999
  • Support Year
    2
  • Suffix
  • Award Notice Date
    9/30/1999 - 24 years ago

PROTEIN DRUG DELIVERY BASED ON STABILIZED PROTEIN

Design of stable and efficient formulation of proteins for their use as drugs has been the major focus of several biotechnology and pharmaceutical companies. In the Phase I, we developed a stable, focus of several biotechnology and pharmaceutical companies. In the Phase I, we developed a stable, active formulation of lipase from Candida rugosa, TheraCLEC-lipase, for use in the treatment of pancreatic insufficiency in cystic fibrosis. TheraCLEC-lipase exhibited characteristics much superior to commercially available pancreatic lipase products exhibiting very high activity against triglycerides and stability under low pH and towards various proteases present in the intestine. Moreover, in preliminary investigations, the TheraCLEC-lipase did not show any toxicity when animals were fed at a concentration of 5,000mg/kg-body weight. Based on these results, in Phase II, we will prepare a drug product prototype for the use in the treatment of pancreatic insufficiency, and steatorrhea in cystic fibrosis patients. As a first step, we will crystallize and crosslink the amylase for use in a final formulation. This final formulation of TheraCLEC lipase will be tested for efficacy in digestion of fat in dogs with ligated pancreatic ducts. Using radiolabeled TheraCLEC-lipase, we will follow the lack of absorption or absorption into systemic circulation. In addition, we will test the subacute, subchronic and long-term effects of feeding TheraCLEC-lipase in two species. If successful, TheraCLEC-lipase prototype will be ready to enter clinical trials, and will provide a novel potent, efficient drug for the treatment of pancreatic insufficiency in cystic fibrosis. PROPOSED COMMERCIAL APPLICATIONS: Currently, there are 25,000 CF patients in the US and additional 20,000 in the ret of the world. In addition, the number of alcohol-induced pancreatic insufficiency ranges from 10,000-13,000 in the US to 20,000 worldwide. The prototype TheraCLEC-lipase has enormous commercial potential over the currently available pancreatic lipase products. The worldwide market is currently $400 million with a $200 million portion being derived from US sales.

IC Name
NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
  • Activity
    R44
  • Administering IC
    DK
  • Application Type
    2
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    847
  • Ed Inst. Type
  • Funding ICs
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
  • Organization Name
    ALTUS PHARMACEUTICALS, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    CAMBRIDGE
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    021394807
  • Organization District
    UNITED STATES