Drug Translation


New drug development can be divided into two phases: (1) discovery, which tends to be chemistry-centric, and (2) translation, which focuses on animal and clinical therapeutic responses. The figure to the right illustrates how few new drugs make the journey from initial drug lead discovery to final approval in humans as a “Drug Discovery Funnel.” During the first discovery phase, only 4% of initial drug leads progress to early animal work. SMDA’s Drug Discovery working group aims to increase success rates in early drug screening and optimization by leveraging large-scale drug datasets and modifying in vitro validation assays to improve clinical validity.

In the second translational phase, a mere 0.2% of drug leads are approved for use in humans. SMDA’s Translational working group aims to increase success rates in clinical translation through modeling drug response (PK-PD) and better matching drug leads to the patient populations who will benefit from them (diagnostics).

Overall, these two working groups strive to fulfill a major strategic goal of SMDA and POH: to better integrate research across the drug development process to increase success rates and reduce drug development costs. This page provides an overview of SMDA’s Translational working group’s current priority areas and shared resources.

 

Translational Drug Data: patient-measurements vs drug-response

A key aspect of translational and clinical drug research is its focus on patient- or animal-specific physiological measurements. Diseases are often diagnosed by quantifying symptoms through various metrics such as weight, heart rate, and blood pressure. These measurements guide clinical practice by identifying diseases and evaluating their severity.

In addition to patient-specific data, molecular biomarkers from patient samples (e.g., blood, urine, biopsies) are used to more precisely define disease states and identify appropriate drugs for individual patients. Blood and biopsy samples allow for monitoring drug concentrations, evaluating immune cell populations, and assessing disease populations such as bacteria and cancer. Beyond cell type frequencies, we can now analyze genomic variants, gene expression, and protein and metabolite concentrations within both immune and disease cells (see figure to the right). This comprehensive analysis enables us to take a detailed census of the disease “battlefield” during anti-cancer, anti-viral, or anti-bacterial immune responses.

The SMDA PK-PD working group focuses on utilizing these various physiological and molecular measurements to better understand drug responses in patients across both veterinary and human medicine.

 

 

 


Tactical Priorities

  • Recruit Workforce:  with interests in molecular diagnostics and PK-PD modeling
  • Train Workforce:  to use emerging tools of
    • PK-PD modeling
    • data-science
    • machine-learning
  • Build Collaborations:  between relevant disciplines
    • clinicians
    • scientists
  • Automate:   laborious and iterative processes to:
    • increase efficiency of research
    • increase access to advanced computational methods
  • Map Community Datasets:
    • cancer genomics
    • infectious disease genomics
    • immunology

Strategic Priorities

  • Molecular Diagnostics: using biomarkers to predict
    • drug-response
    • patient survivial
  • PK-PD modeling: to better understand
    • patient variability in drug-response
    • in vivo drug response
    • clincial drug drug interactions
  • Digital Teaching Assistants: ChatBots built off of literature underlying traditional coursework
  • Textbook Mobile Apps:   mobile apps based on data and equations underlying current textbooks


Current Members

  • Eugene Douglass
  • Jonathan Mochel
  • K. Mellisa Hallow
  • Karin Allenspach
  • Silvia Carnaccini
  • Janet Grimes
  • Robin Southwood

Software Tools


Cleaned Datasets


Key Performance Indicators: summary statistics

 

KPI Category KPI Current Value
Research and Publications Number of Published Papers
Impact Factor of Journals
Citations
Conference Presentations
Collaboration and Engagement Interdisciplinary Projects
External Collaborations
Collaborative Publications %
Workshops and Seminars
Funding and Grants Research Grants Received $
Grant Applications Submitted
Grant Success Rate %
Data and Tools Datasets Published
Software Tools Developed
Tool Adoption downloads
Training and Development Students Supervised
Training Programs
Skill Development certificates
Impact and Outreach Societal Impact
Media Mentions
Public Engagement events
Operational Efficiency Project Completion Rate
Data Management Practices % compliance
Resource Utilization % efficiency
Innovation and Excellence Awards and Recognitions
Innovative Solutions breakthroughs
Feedback and Improvement Stakeholder Feedback satisfaction
Continuous Improvement # iterations

 

 

 


Key Performance Indicators: specific items list

 


Protected Content

  • Research and Publications
    • Number of Published Papers
    • Impact Factor of Journals
    • Citations
    • Conference Presentations
  • Collaboration and Engagement
    • Interdisciplinary Projects
    • External Collaborations
    • Collaborative Publications
    • Workshops and Seminars
  • Funding and Grants
    • Research Grants Received
    • Grant Applications Submitted
    • Grant Success Rate
  • Data and Tools
    • Datasets Published
    • Software Tools Developed
    • Tool Adoption
  • Training and Development
    • Students Supervised
    • Training Programs
    • Skill Development
  • Impact and Outreach
    • Societal Impact
    • Media Mentions
    • Public Engagement
  • Operational Efficiency
    • Project Completion Rate
    • Data Management Practices
    • Resource Utilization
  • Innovation and Excellence
    • Awards and Recognitions
    • Innovative Solutions
  • Feedback and Improvement
    • Stakeholder Feedback
    • Continuous Improvement