Medications Discovery & Toxicology Branch (MDTB)

What We Do:

The MDTB plans and implements a preclinical Addiction Treatment Discovery Program (ATDP), with the goal of identifying potential medications to treat drug dependence disorders. The Program is implemented by coordinating the extramural activities of the MDTB and the Chemistry & Pharmaceutics Branch (CPB) and through close interactions with chemists and pharmaceutical company contacts. Within the ATDP, contract-supported activities range from in vitro receptor activity profiling to compound evaluations in advanced animal models. The MDTB also supports grants aimed at evaluating potential new pharmacotherapies to treat drug dependence.

Beyond medications discovery, the MDTB plans and implements a comprehensive preclinical Toxicology Program. Through contracts, the Toxicology Program supports all of the standard Good Laboratory Practices (GLP) preclinical safety studies required for IND and NDA filings with the FDA. In addition, contracts have been established to support specialized preclinical drug interaction studies in which the safety of potential medications is established in the presence of drugs of abuse.

Staff Biographies and Research Interests:

  • Jane B. Acri, Ph.D., - Chief
    Supervises staff responsible for coordinating the Division's contract- and grant-based medications discovery and preclinical safety assessment efforts. Oversees grant-related issues in medications discovery and activities of the Addiction Treatment Discovery Program, Toxicology Program, and branch participation in the Safety Assessment Candidate team. Project officer on related contracts and grants. Has served as a project leader on a number of drug development projects. Eight years of direct experience in drug abuse research at Uniformed Services University of the Health Sciences and the NIDA Intramural Research Program prior to joining DTMC in 1996.
  • Nathan M. Appel, Ph.D., - Health Scientist Administrator
    Director of the Division's Toxicology Program. Project Officer on related contracts and member of most drug development project teams. Program Official or Science Officer on grants and cooperative agreements involving preclinical safety assessment. Joined the NIDA Extramural Program in 1999. Eight years previous experience at the Food and Drug Administration (FDA).
  • Carol Hubner, Ph.D., - Health Scientist Administrator & Associate Director, Addiction Treatment Discovery Program
    Associate Director of the Addiction Treatment Discovery Program. Project Officer on rodent behavioral pharmacology contracts supporting this program. Seven years of preclinical research experience studying drugs of abuse (primarily cocaine) at the Scripps Clinic and Research Foundation, University of Maryland, and the National Institute of Mental Health. Joined DTMC in 1992.
  • Matthew A. Seager, Ph.D., - Health Scientist Administrator
    Serves as Project Officer on in vitro receptor profiling and safety/discovery pharmacology contracts and supports the Addiction Treatment Discovery Program (ATDP) and the Toxicology Program.  Twelve years of previous experience in preclinical neuroscience drug discovery at Eli Lilly, Merck, and Bristol Myers Squibb. Joined DTMC in 2020.
  • David A. White, Ph.D., - Health Scientist Administrator & Director, Addiction Treatment Discovery Program
    Serves as Director of the Addiction Treatment Discovery Program Team and is a Project Officer on related contracts. Serves as a NIDA representative to the Interagency Committee on Drug Control (ICDC). More than six years of previous research experience in the area of drug abuse at Emory University's School of Medicine in the Department of Pharmacology. Joined DTMC in 2006.