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  Targeted Drug Delivery and Prodrug Focus Group

Targeted drug delivery, which also refers to drug targeting or site specific drug delivery, is to site-specifically deliver or activate the therapeutic compounds in the site of action. Thus, the targeted drug delivery is expected to enhance drug efficacy by increasing local active drug concentration in disease tissues, and to decrease side effect by minimizing drug exposure in normal tissues. Several targeted drug delivery technologies have been studied for enhancing drug efficacy and reducing drug toxicity, which have achieved certain degree of success. These technologies include: Intratumoral drug administration, Liposomal drug delivery, Tumor-activated prodrug therapy (TAP), Antibody-directed enzyme prodrug therapy (ADEPT), Gene-directed enzyme prodrug therapy (GDEPT), Folate-targeted drug delivery, Transferrin targeted drug delivery, Albumin-drug conjugate for targeted delivery, and prodrug targeted delivery.

Prodrug strategies have traditionally been used to address ADMET liabilities of marketed compounds or as tools in late-stage problem solving for drug development candidates. However, prodrugs are now increasingly being integrated into early drug discovery as a means of expanding the chemical space of drugable molecules.

The Targeted Drug Delivery and Prodrug Focus Group was evolved from prodrug focus group, which was formed in 2004. The Targeted Drug Delivery and Prodrug Focus Group affiliated with the following section: Physical Pharmacy and Biopharmaceutics (PPB), Drug Design and Discovery (DDD), and Pharmacokinetics, Pharmacodynamics and Drug Metabolism (PPDM).

The goals of the Targeted Drug Delivery and Prodrug Focus Group are to expand drug targeting technologies and prodrug knowledge through education, impact the direction of targeted drug delivery and prodrug research through long-range programming, encourage interdisciplinary collaborations, encourage innovative use of new technologies to solve drug targeting problems, and provide a common forum for universities, industry, and government.

To achieve these goals, we will continue to build interdisciplinary programming between PPB, DDD, and PPDM sections, develop a young and sustainable leadership pool for the Targeted Drug Delivery and Prodrug Focus Group, plan an intermediate-range program so researchers can anticipate future forums for innovative research, provide an inclusive environment for programming ideas into workshops, symposia, roundtables, and short courses; and foster interdisciplinary collaborations and research that, in turn, would advance the discipline, health care, consumer interests, and AAPS programming quality. To achieve this, the Targeted Drug Delivery and Prodrug Focus Group will serve as a forum for targeted drug delivery and prodrug scientists/enthusiasts in many areas including drug delivery and targeting; metabolism; chemical synthesis; molecular biology; biotechnology; drug safety; clinical trial testing; as well as drug approval and regulation.


Goals

The goals of the Targeted Drug Delivery and Prodrug Focus Group are to:

  • expand targeted drug delivery and prodrug knowledge through education
  • impact the direction of drug targeting and prodrug research through long-range programming
  • encourage interdisciplinary collaborations in drug targeting technologies and prodrug research
  • encourage innovative use of new technologies to solve drug targeting and prodrug problems
  • provide a common forum for universities, industry, and government

To achieve these goals we will:

  • develop interdisciplinary programming between PPB, PPDM & DDD
  • develop a young and sustainable leadership pool for the Targeted Drug Delivery and Prodrug Focus Group
  • plan an intermediate-range program so researchers can anticipate future forums for innovative research
  • provide an inclusive environment for programming ideas into workshops, symposia, roundtables, and short courses
  • foster interdisciplinary collaborations and research that, in turn, would advance the discipline, health care, consumer interests, and AAPS programming quality. Our working assumption is that by providing such a forum for targeted drug delivery and prodrug designers in the areas of:
    • Targeted Drug Delivery
    • Site specific drug activation
    • Metabolism
    • Chemical Synthesis
    • Molecular Biology
    • Biotechnology
    • Drug Safety
    • Clinical Trial Testing
    • Drug Approval and Regulation

Drug targeting and Prodrugs will be used more often and sooner as a means of enhancing drug efficacy, reducing drug toxicity, overcoming the physical/chemical liabilities of active therapeutic agents so that more innovative therapies will reach the market place.


Past Programming

  • Prodrug approaches for organ specific targeted therapy
    November 20, 2008

  • Effective Interactions from Pre-IND to IND and Beyond: “getting your Ducks in the Row” with the FDA
    November 20, 2008

  • The World Within and Beyond P-gp: Do we Underestimate or Overestimate P-gp?
    November 19, 2008

  • Transporters as Prodrug Carriers for Oral Drug Delivery
    November 19, 2008

  • Accurate Prediction of Metabolic DDI - from Preclinical Discovery to Clinical Development
    November 19, 2008

  • Tumor Imaging and Targeted Drug Delivery
    November 19, 2008

  • Rational Drug and Prodrug Design Via Computational Modeling
    November 18, 2008

  • PK/PD of Biologics: from Discovery to Successful Development
    November 18, 2008

  • Prodrug Approaches for Site-Specific Cellular Targets Roundtable
    November 15, 2007

  • Tumor-activated Prodrug and Tumor-targeting Technologies: ADEPT, GDEPT and PDEPT to Increase Drug Efficacy and Reduce Drug Toxicity Roundtable
    November 14, 2007

  • Solving ADMET Problems with Prodrug, Soft-Drug & Co-Drugs Roundtable, November 2, 2006
    Panel members: Howard Ando, Paul Erhardt, Peter Crooks
    Moderators: Howard Ando and Tycho Heimbach

  • Strategies & Technologies for Transdermal and Ocular Drug Delivery Roundtable, November 1, 2006
    Panel members: Bo Michniak-Kohn, Diane Tang-Liu, Ken Sloan
    Moderators: Jarkko Rautio and Ken Sloan

  • Facilitating Parent-Prodrug R&D and Regulatory Approval Roundtable, October 30, 2006
    Panel members: Yuanchao Zhang, Mary Beth Wire, Reza Oliyai
    Moderators: Tycho Heimbach and Paul Erhardt


JOIN THE PRODRUG FOCUS GROUP

To join the Prodrug Focus Group, click here.

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  Leadership

Chair
Victor R Guarino
Bristol-Myers Squibb
Princeton, NJ UNITED STATES



Chair-Elect
Jeffrey Wang
Western University of Health Sciences
Pomona, CA United States



Steering Committee Member
Howard Y. Ando, Ph.D.

, UNITED STATES



Steering Committee Member
Dr. Dakshina M. Chilukuri, Ph.D.
US Food and Drug Administration
Silver Spring, MD United States



Steering Committee Member
Paul W. Erhardt
University of Toledo College of Pharmacy
Toledo, OH UNITED STATES



Steering Committee Member
Tycho H. Heimbach, Ph.D.
Novartis Pharmaceuticals Corporation
East Hanover, NJ UNITED STATES



Steering Committee Member
Anthony Marfat
Pfizer
,



Steering Committee Member
Dooman Alex Oh, Ph.D.
Halozyme Therapeutics, Inc.
San Diego, CA United States



Steering Committee Member
Prof. Jarkko Rautio, Ph.D.
University of Kuopio
Kuopio, Finland



Steering Committee Member
Balvinder S. Vig, Ph.D
Bristol Myers Squibb
New Brunswick, NJ UNITED STATES




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