The Center for Alternatives to Animal Testing is an academic center affiliated with the Division of Toxicological Sciences in the Department of Environmental Health Sciences of the Johns Hopkins University Bloomberg School of Public Health.
Melvin E. Andersen, PhD, CIH, DABT, FATS
The Hamner Institutes for Health Science
Stanley Barone, Jr., PhD
US Environmental Protection Agency
Cynthia F. Bearer, MD, PhD
Case Western Reserve University
Kim Boekelheide, MD, PhD
Brown University
Joseph P. Bressler, PhD*
Johns Hopkins University
James S. Bus, PhD
Dow Chemical Company
Lucio G. Costa, PhD, ATS
University of Washington
Kevin M, Crofton, PhD*
US Environmental Protection Agency
Ellen Fritsche, PhD*
University of Duesseldorf, Germany
Alan M. Goldberg, PhD*
Johns Hopkins University
Thomas Hartung, MD, PhD
European Centre for the Validation of
Alternative Methods (ECVAM)
Charles Hastings, PhD
BASF
Robert J. Kavlock, PhD
US Environmental Protection Agency
Holger Knaut, PhD*
European Centre for the Validation of Alternative Methods (ECVAM)
Sue A. Leary*
Alternatives Research & Development Foundation (ARDF)
Pamela J. Lein, PhD*
Oregon Health & Science University
Tina E. Levine, PhD*
US Environmental Protection Agency
Philip G. Lewis, MD, MPH*
Rohm and Haas Company
Abby A. Li, PhD*
Exponent Health Sciences
Paul A. Locke, JD, DrPH*
Johns Hopkins University
Sue Marty, PhD*
Dow Chemical Company
Elise Miller, MEd
Institute for Children’s Environmental Health (ICEH)
William R. Mundy, PhD*
US Environmental Protection Agency
David E. Owen, PhD*
Shell Chemicals Ltd.
Stephanie Padilla, PhD
US Environmental Protection Agency
Anna Price, PhD*
European Centre for the Validation of
Alternative Methods (ECVAM)
David E. Ray, PhD*
University of Nottingham, UK
Andréa Seiler, PhD*
ZEBET
Ellen K. Silbergeld, PhD*
Johns Hopkins University
Martin L. Stephens, PhD*
Humane Society of the United States
Robert L. Tanguay, PhD*
Oregon State University
Gihan I. Tennekoon, MD*
Children’s Hospital of Philadelphia
Catherine Willett, PhD
People for the Ethical Treatment of Animals (PETA)
Marc Willuhn, PhD*
European Chemical Industry Council (Cefic)
*Steering Committee
American Chemistry Council
Cefic LRI (European Chemical Industry Council)
CropLife America
Dow Chemical Company
Environmental Protection Agency (EPA)
European Centre for the Validation of Alternative Methods
ExxonMobil
Johns Hopkins Center for Alternatives to Animal Testing (CAAT)
Rohm and Haas Company

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MAIN PAGE
Tuesday, November 11
5:30–7:30 Registration with Reception
Wednesday, November 12
8:00-9:00 Registration and Continental Breakfast
9:00-9:15 Welcome
Alan M. Goldberg, PhDObjectives of Conference
David E. Owen, PhDPLENARY
Chair: Gihan I. Tennekoon, MD9:15-10:00 Toxicity Testing in the 21st Century: Promises and Conundrums
Kim Boekelheide, MD, PhD10:00-10:45 Adverse Neurodevelopmental Outcome—
The Role for In Vitro
Cynthia F. Bearer, MD, PhD10:45-11:15 Refreshment Break
11:15-12:00 Criteria
Kevin M. Crofton, PhD12:00-1:00 Lunch
ENDPOINTS
Chair: Stanley Barone, Jr., PhD1:00-2:15 Endpoint One—Proliferation,
Differentiation, Migration and Apoptosis
Ellen Fritsche, PhD2:15-3:30 Endpoint Two—Neuronal Connectivity Including Neurite Outgrowth, Synapse Formation and
Function (Neurochemical and Electrophysiological)
William R. Mundy, PhD3:30-4:00 Refreshment Break
4:00-5:15 Endpoint Three—Glial (Function) Including
Migration, Myelination, Inflammation and Signaling
Joseph P. Bressler, PhDCRITERIA
5:15-6:00 Discussion and Re-examination of Criteria
Kevin M. Crofton, PhD6:00-7:00 Reception
Thursday, November 13
8:00-8:30 Continental Breakfast
PLENARY
Chair: Holger Knaut, PhD8:30-9:15 Models: Cell Cultures
Lucio G. Costa, PhD9:15-10:00 Models: Non-Mammalian
Pamela J. Lein, PhD10:00-10:30 Refreshment Break
10:30-12:30 CONCURRENT BREAKOUT GROUPS
Group 1: Cell Culture
Chair: Marc Willuhn, PhD
Rapporteur: Abby A. Li, PhDInvited Poster Presentations
Group 2: Models
Chair: Robert L. Tanguay, PhD
Rapporteur: Stephanie Padilla, PhDInvited Poster Presentations
12:30-1:30 Lunch
1:30-2:15 SUMMARIES OF BREAKOUT GROUPS
Chair: Anna Price, PhDGroup 1: Cell Culture
Abby A. Li, PhDGroup 2: Models
Stephanie Padilla, PhDDATA INTERPRETATION, INTEGRATION/USE, AND POLICY
Chair: Martin L. Stephens, PhD2:15-3:00 Developing Predictive Bioactivity Signatures from ToxCast’s High Throughput Screening Data
Robert J. Kavlock, PhD3:00-3:30 Refreshment Break
3:30-4:00 The Use of In Vitro Data in Understanding Human Health Effects and Risk
James S. Bus, PhD4:00-5:30 OVERVIEW TO DECISION MAKING WITH DNT DATA
Chair: Tina E. Levine, PhDOpening Statement and Charge to the Panel
Paul A. Locke, JD, DrPHPanel: Melvin E. Andersen, PhD
Thomas Hartung, MD, PhD
Abby A. Li, PhD
Elise Miller, MEd
Catherine Willett, PhD• Data needs
• Levels of decision making
>> Product development
>> Hazard assessment
>> Regulatory applications5:30-8:30 Posters and Vendor Exhibits
Reception and Buffet Dinner
Friday, November 14
8:00-8:30 Continental Breakfast
MEETING THE OBJECTIVES OF THE CONFERENCE
8:30-10:30 Policy Framework
Chair: Philip G. Lewis, MD, MPH
Panel: Charles Hastings, PhD
Robert J. Kavlock, PhD
Paul A. Locke, JD, DrPH
David E. Owen, PhD
David E. Ray, PhD
Ellen K. Silbergeld, PhDApplying DNT Data
• Prioritization for further action
• Using alternative data in conjunction with other data (e.g. animals and humans)
• Using alternative data when other data are not available10:30-11:00 Refreshment Break
11:00-12:15 Biology Framework
Opening Remarks on Goals of Session
Kevin M. Crofton, PhDPanel: Lucio G. Costa, PhD, ATS
Holger Knaut. PhD
Pamela J. Lein, PhD
Sue Marty, PhD• Criteria for evaluating alternative methods (codify criteria— which are most important?)
• What assays are ready now? Or where should we invest current efforts? Review of data presented at meeting.
• Critical research needs to move forward (endpoints, models, methods, new biology)12:15-12:30 SUMMARY AND FINAL COMMENTS FROM THE AUDIENCE
Philip G. Lewis, MD, MPHClose
12:30 Lunch