Development of Puerarin to Reduce Alcohol Drinking

Information

  • Research Project
  • 6993082
  • ApplicationId
    6993082
  • Core Project Number
    R44AA015220
  • Full Project Number
    2R44AA015220-03A2
  • Serial Number
    15220
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/30/2006 - 18 years ago
  • Project End Date
    8/31/2009 - 15 years ago
  • Program Officer Name
    EGLI, MARK
  • Budget Start Date
    9/30/2006 - 18 years ago
  • Budget End Date
    8/31/2007 - 17 years ago
  • Fiscal Year
    2006
  • Support Year
    3
  • Suffix
    A2
  • Award Notice Date
    9/30/2006 - 18 years ago

Development of Puerarin to Reduce Alcohol Drinking

[unreadable] DESCRIPTION (provided by applicant): This application is a resubmission in response to AA-04-002 from the National Institute on Alcohol Abuse and Alcoholism to continue our STTR (Phase I and II) study on the development of NPI-031G (Puerarin), an Isoflavone-C-glycoside isolated from Puerira lobota (Kudzu), as a botanical anti-craving agent for the treatment of alcohol drinking problems. [unreadable] In STTR Phase II, we showed that chronic oral administration of NPI-031G (150 mg/kg/day) suppressed daily alcohol drinking by almost 50 percent in animals throughout a 4-week study (see Preliminary Data Section C). [unreadable] Recently, we demonstrated that the extract of kudzu, which contains 20 percent NPI-031G, reduces alcohol intake significantly in heavy alcohol drinkers. In this continuing application, we propose to complete the preclinical work, including a toxicity study in year 01 and 02, a prerequisite for an IND application. In year 03, we will focus on clinical evaluation in human alcoholics. Specifically, we will conduct the following studies. [unreadable] Year 01: 1) Synthesis of radio-labeled NPI-031G; 2) Purification of NPI-031G (>99.0 percent) for clinical study; 3) Bioavailability and pharmacokinetic study; and 4) Toxicity studies (mutagenic, acute toxicity). [unreadable] Year 02: 1) Chronic toxicity study; 2) In vitro and in vivo drug metabolism studies; 3) Preparation of Drug Master File (DMF); 4) Request for IRB approval, 5) Submission of IND application; and 6) Phase I safety and alcohol challenge study in humans. [unreadable] Year 03: 1) Preparation of NPI-031G and placebo capsules under GMP conditions; 2) Effects on brain alcohol levels (humans); 3) Effects on cerebral blood flow in human; and 4) Human alcohol self-administration in natural setting. [unreadable] The proposed pre-clinical and clinical studies are necessary steps toward the commercial development of NPI-031G. NPI, Inc. has also prepared a comprehensive business plan for further development of NPI-031G as an anti-craving agent in collaboration with a pharmaceutical company in the US (Business Plan in Appendix). [unreadable] [unreadable]

IC Name
NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM
  • Activity
    R44
  • Administering IC
    AA
  • Application Type
    2
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    895187
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    273
  • Ed Inst. Type
  • Funding ICs
    NIAAA:895187\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    NATURAL PHARMACIA INTERNATIONAL, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    Burlington
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    01803
  • Organization District
    UNITED STATES