Oncologic Drugs Advisory Committee

Slides

 

September 13, 2005 AM Session

 

The committee will discuss New Drug Application (NDA) 21-491, proposed trade name Xinlay™(astrasentan hydrochloride) capsules, Abbott Laboratories, proposed indication for the treatment of men with metastatic hormone-refractory prostate cancer.

 

 

      .         Sponsor Presentation                                                    Abbott Laboratories

 

                Introduction                                                                          Gary Gordon, M.D.

                                                                                                                Oncology Vice President

 

                Unmet Need & Mechanistic Rationale                           Joel B. Nelson, M.D., Chairman of Urology

                                                                                                                University of Pittsburgh

 

                Efficacy                                                                                  Darryl J. Sleep, M.D., FCS

                                                                                                                Oncology Global Project Head

               

                Safety                                                                                     Gary Gordon, M.D.

     

                Places in Therapy                                                               Howard Scher, M.D.

                                                                                                                Chief of Genitourinary Oncology

                                                                                                                Memorial Sloan-Kettering Cancer Center

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            Supporting Slides

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      FDA Presentation      

 

Xinlay (atrasentan) FDA Review                                       Amna Ibrahim, M.D.

                                                Medical Officer, Division of Drug Oncology Products, FDA

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                                                                                        Shenghui Tang Ph.D.

                                                                                                                Statistical Reviewer, Division of Drug Oncology Products, FDA

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                                                                                                                Ralph B. D’Agostino, Ph.D.                                                               

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      Open Public Hearing Speakers

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      Questions to the Committee

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September 13, 2005 PM Sexxion

 

The committee will discuss NDA 21-743, S003, Tarceva ™(erlotinib) Tablets, OSI Pharmaceuticals, Inc, proposed indication for the first line treatment, in combination with gemcitabine, of patients with locally advanced, unresectable or metastatic pancreatic cancer.

 

      Sponsor Presentation                                             

               

Tarceva (erlotinib) Tablets                                               Pablo J. Cagnoni, MD
Pancreatic Cancer                                                            
Vice President Medical Affairs & Translational Research

                                                                                                                OSI Pharmaceuticals, Inc.

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Background of Pancreatic Cancer &                              Malcolm Moore, MD

NCIC PA.3 Study Design                                                    Professor of Medicine and Pharmacology

                                                                        Princess Margaret Hospital

University of Toronto

Chair, NCIC Clinical Trials Group—GI Committee

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Clinical Efficacy Data                                                         Gary M. Clark, PhD

Review of Study NCIC PA.3                                               Vice President Biostatistics and Data Management

OSI Pharmaceuticals, Inc.

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Clinical Safety Data                                                            Karsten Witt, MD

Review of Study NCIC PA.3                                               Vice President Drug Safety and Medical Writing

                                                                                                                OSI Pharmaceuticals, Inc.

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Tarceva® (erlotinib) Tablets                                            Mace Rothenberg, MD

Concluding Remarks and Risk/Benefit Summary        Associate Professor of Medical Oncology

                                                                                                Vanderbilt University

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      FDA  Presentation                                                     

 

Tarceva (erlotinib) FDA review                                         Adrian Senderowicz, M.D.

                                                                                        Medical Officer, Division of Drug Oncology Products, FDA

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      Open Public Hearing Speakers

 

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      Questions to the Committee

 

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