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Allopregnanolone-induced rise in intracellular calcium in embryonic hippocampal neurons parallels their proliferative potential

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About the Alzheimer’s Drug Discovery Foundation (ADDF)

The Alzheimer’s Drug Discovery Foundation’s (ADDF) sole mission is to rapidly

accelerate the discovery and development of drugs to prevent, treat and cure

AD, related dementias and cognitive aging.

ADDF was established in 2004 to expand upon the programs initiated by the

Institute for the Study of Aging (ISOA) Inc., a private foundation founded by the

Estée Lauder family in 1998. We use a venture philanthropy investment model to

bridge the global funding gap between basic research and later-stage

development, recycling any return on investment to support new research.

ADDF has an impressive track record of selecting and supporting excellent

Alzheimer’s disease (AD) drug discovery research. Our scientists have created

entirely new classes of drugs in development for AD, screened millions of

compounds, identified hundreds of leads, executed tens of patents and

licenses, and have advanced compounds into clinical trials. To date, we have

awarded over $33M for more than 240 research programs and conferences in

12 countries.

8

th

International Conference on Alzheimer’s Disease Drug Discovery

The Alzheimer’s Drug Discovery Foundation’s (ADDF) organizes an annual

two-day global conference for research scientists to engage in discussion and cross

fertilization of ideas focusing on Alzheimer’s drug discovery research. Designed

specifically for academic and industry scientists, the conference gives

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8

TH

INTERNATIONAL CONFERENCE ON

ALZHEIMER’S DISEASE DRUG DISCOVERY

FINAL PROGRAM

MONDAY, OCTOBER 15, 2007

7:45 – 8:30 am Registration & Continental Breakfast

8:30 – 8:40 Welcome & Opening Remarks Howard Fillit, MD, Executive Director, ADDF

8:40 – 9:10 Plenary Talk

Jeffrey S. Nye, MD, PhD, Johnson and Johnson

Pharmaceutical R&D, LLC

I. NEUROPROTECTION

Session Chair Frank Longo, MD, PhD, Stanford University

9:10 – 9:30

The Nrf2 Mediated Pathway as a Therapeutic Target in

Alzheimer's Disease Jari Koistinaho, MD, University of Kuopio

9:30 – 9:50

Novel C-terminal Proteolysis of APP as a Therapeutic Target

for Alzheimer’s Disease Varghese John, PhD,Buck Institute

9:50 – 10:10

Small Molecule p75 NTR and TrkB Ligands for Alzheimer's

Disease Therapeutics Frank Longo, MD, PhD, Stanford University

10:10 – 10:30 Panel Discussion

10:30 – 10:50 Break

10:50 – 11:10

Combinatorial Approaches to Small Molecule NGF Receptor Agonists

Nicholas Webster, PhD, Veterans Medical

Research Foundation

11:10 – 11:30

Why Do We Need Novel Multimodal Neuroprotective and Neurorestorative Drugs for Alzheimer's Disease?

Moussa B.H. Youdim, PhD, Technion -Israel

Institute of Technology

11:30 – 11:50 Bone Marrow-Mobilizing Agents for Alzheimer's Disease

Juan Sanchez-Ramos, MD, PhD,University of

South Florida 11:50 am –

12:10 pm The CKI Pathway in Age-Related Diseases Igor Roninson, PhD, Senex Biotechnology, Inc.

12:10 – 12:30 Panel Discussion

12:30 – 2:00 Lunch

II. ANTI-AMYLOID AND MISFOLDING

Session Chair

Michael Wolfe, PhD,Brigham and Women’s

Hospital and Harvard Medical School

2:00 – 2:20

Hsp90, Degradation and Tau: Clinical implications of Basic

Research Leonard Petrucelli, PhD, Mayo Clinic

2:20 – 2:40 ApoE Amyloid Connection Thomas Wisniewski, MD, New York University

2:40 – 3:00

Anti-amyloidogenic Properties of Resveratrol and its Analogues

Philippe Marambaud, PhD, NSLI Jewish

Research Inst.

3:00 – 3:20

Commercialization of BRI-based Peptides for the Treatment of Alzheimer's Disease

Luciano D'Adamio, MD, PhD,Albert Einstein

College of Medicine

3:20 – 3:40 Panel Discussion

3:40 – 4:00 Break

4:00 – 4:20 Efficacy of Small Molecule Assembly Blockers

William F. Goure, PhD, Acumen

Pharmaceuticals

4:20 – 4:40 Selective Amyloid-lowering Agents

Michael Wolfe, PhD,Brigham and Women’s

Hospital and Harvard Medical School 4:40 – 5:00 Panel Discussion

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Final Program (cont.)

TUESDAY, OCTOBER 16, 2007

7:45 – 8:30 am Continental Breakfast

III. MISFOLDING II

8:30 – 8:50

Plant-based Primary Screen and Animal-based Secondary Screens for Chaperone Inducing Drugs Against Protein

Misfolding in Alzheimer's Disease Pierre Goloubinoff, PhD, University of Lausanne

8:50 – 9:10

Development of Hsp90 Inhibitors as Novel Therapeutics for AD

Gabriela Chiosis, PhD, Memorial

Sloan-Kettering Cancer Center

9:10 – 9:30

NADPH Oxidase as a Therapeutic Target in Alzheimer's Disease

Michelle Block, PhD, Virginia Commonwealth

University 9:30 – 9:50 Panel Discussion

9:50 – 10:10 Break

IV. ANTI-TANGLES

Session Chair

Eva-Maria Mandelkow, MD, PhD,

Max-Planck-Unit for Structural Mol. Biology

10:10 – 10:30 Molecular Targets for Tau Pathology

Eva-Maria Mandelkow, PhD, Max Planck Unit

for Structural Biology

10:30 – 10:50

Distal Cis-Elements and Compounds that Regulate Tau Splicing

Jianhua Zhou, PhD, University of Massachusetts

Medical School

10:50 – 11:10

p25/Cdk5, the Missing Link to a Reactivation of the Cell Cycle in Neurofibrillary Degeneration

Luc Buee, PhD, French National Institute for Health and Medical Research

11:10 – 11:30

Tau-focused Drug Discovery for

Alzheimer's Disease and Related Tauopathies

John Trojanowski, MD, PhD, University of

Pennsylvania

11:30 – 11:50

Allopregnanolone as a Neurogenic and Cognition Enabling Therapeutic for Alzheimer's Disease: Preclinical Evidence

Roberta Brinton, PhD, University of Southern

California 11:50 am – 12:1 0

pm Panel Discussion

12:10 – 1:10 Lunch

V. IMMUNOLOGY AND ANTI-INFLAMMATION STRATEGIES

Session Chair

D. Martin Watterson, PhD,Northeastern

University

1:10 – 1:30

Immune Defects in Alzheimer’s Disease: New Medications Development

John Cashman, PhD, Human Biomolecular

Research Institute

1:30 – 1:50

Small Molecule Modulators of CNS Proinflammatory Cytokine Production

D. Martin Watterson, PhD, Northwestern

University

1:50 – 2:10 Agonists of TGFβSignaling to Treat Alzheimer's Disease Tony Wyss-Coray, PhD, Stanford University

2:10– 2:30 Panel Discussion

2:30 – 2:50 Break

VI. COGNITIVE ENHANCERS

Session Chair Antony Horton, PhD,ADDF

2:50 – 3:10

IRAP-a Novel Target for the Development of

Memory-Enhancing Agents Siew Yeen Chai, PhD, Howard Florey Institute

3:10 – 3:30

Cognitive-enhancing Effects ff Angiotensin IV: An

Investigation of Molecular Mechanisms Paul Gard, PhD, University of Brighton

3:30 – 3:50

Clinical Efficacy of AC-1202 (Ketasyn™) in Mild to Moderate Alzheimer’s Disease

Lauren C. Costantini, PhD, Accera, Inc.

(confirmed) 3:50 – 4:10 Panel Discussion

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