Business address

KATHLEEN TOUPS, MD, DFAPA
Functional Medicine Neuropsychiatry
Adult and Geriatric
BUSINESS ADDRESS
PLACE OF BIRTH
New Orleans, Louisiana
CURRENT POSITIONS
Executive and Medical Director- 2012 - present
Bay Area Wellness – Functional Medicine Clinic
Lafayette, California
EDUCATION
University of California, Davis
Davis, California
Bachelor of Science, with Honors, Anthropology
1980-82
POSTGRADUATE EDUCATION
University of California, Davis
Davis, California
Department of Genetics - Graduate Division
Graduate Fellowship Recipient
1982-1983
MEDICAL EDUCATION
Louisiana State University Medical School
New Orleans, Louisiana
Doctor of Medicine
May, 1987
POSTDOCTORAL TRAINING
Mercy Hospital and Medical Center
San Diego, California
Transitional Internship
1987-1988
University of California, San Diego La Jolla, California Psychiatry Residency 1989-1992 Functional Medicine Certification Program CERTIFICATION
Federal Licensure Examination (FLEX), 1987
American Board of Psychiatry and Neurology - Diplomate, 1994
Added Qualifications in Geriatric Psychiatry (ABPN) - Diplomate, 1995
Certified Clinical Research Investigator (ACRP) - 2003
LICENSURE
California A45048, l988
HOSPITAL AFFILIATIONS
Mt. Diablo Medical Pavilion – Courtesy Staff Privileges
Concord, California
ACADEMIC POSITIONS
Assistant Professor of Clinical Psychiatry,
University of California, Davis, CA, 1994 – 1996
VA Chief of Inpatient Psychiatry, 1994-1996 Residency Training Site Director for UC Davis Medical School David Grant Medical Center Travis Air Force Base, CA OTHER APPOINTMENTS
AstraZeneca Advisory Board – 1998 - 2001 Expert Consultant - Forest Laboratories and Parke-Davis Pharmaceuticals Lilly Atomoxetine Advisory Board - 2001 - 2003 National Alliance for the Advancement of ADHD Care (NAAAC) - Board of Directors-2002 - 2004 Expert Consultant MDS Pharma Services - 2006 Phi Kappa Phi National Honor Society, 1982 Departmental Citation in Anthropology, University of California, Davis, 1982 American Association for Geriatric Psychiatry Mead-Johnson Fellowship, 1991-1993 Fellow, American Psychiatric Association – 2007 Distinguished Fellow, American Psychiatric Association - 2009 CLINICAL, ADMINISTRATIVE AND ACADEMIC POSITIONS
Research Assistant in Human Genetics, 1981-1982 University of California, Davis Davis, California Archaeologist in the California Great Basin, summer 1982 University of California, Davis Davis, California Teaching Assistant in Physical Anthropology, 1982-1983 University of California, Davis Davis, California General Practitioner in Family Medicine, 1988-1989 San Ysidro Community Health Center San Ysidro, California Urgent Care Physician, 1988-1991 Readicare Medical Group San Diego, California Private Practice, Psychiatry, 1991-1993 Affiliated Mental Health Professionals San Diego, California Psychiatry ER Physician, Consult-Liaison Psychiatry, and O/P Psychiatry, 1993 Merrithew Memorial Hospital and Pittsburgh Community Clinic Contra Costa County Mental Health Martinez and Pittsburgh, California Staff Psychiatrist, 1993-1994 Kaiser Permanente Medical Center Department of Mental Health Walnut Creek, California VA Chief of Inpatient Psychiatry, 1994-1996 Residency Training Site Director David Grant Medical Center Travis Air Force Base, California Assistant Professor of Clinical Psychiatry, 1994-1996 University of California, Davis Davis, California Private Practice - Adult and Geriatric Psychiatry, 1996-1997 Antioch, California Intensive Outpatient Psychiatry Program and Consultant to Home Health Nursing, 1997-1998 Kaiser Permanente Medical Center Walnut Creek and Martinez, California Executive and Medical Director- 1997 to 2010 Bay Area Research Institute, Clinical Trials Research Center Lafayette, California ACADEMIC ACTIVITIES
UC Davis Residency Training Site Director David Grant Medical Center, 1994-1996 Chair: Junior Faculty Group, Department of Psychiatry UC Davis Medical School, 1995-1996 Faculty Advisor: Third Year Medical Students UC Davis Medical School, 1995-1996 Lecturer and Discussion Group Leader: Introduction to Psychopathology UC Davis Medical School, Spring, 1995 and 1996 Discussion Group Leader: Human Sexuality UC Davis Medical School, 1996 Organizer and Instructor: Weekly Special Topics Seminar for Psychiatry Residents David Grant Medical Center, 1994-1996 Organizer and Coordinator: Psychiatry Grand Rounds David Grant Medical Center, 1994-1996 Member: Training Advisory Group UC Davis Department of Psychiatry, 1994-1996 PROFESSIONAL APPOINTMENTS/OFFICES
Organizer/Administrator, Bay Area Functional Medicine Group, 2011 – present Administrator, Bay Area Functional Medicine ListServe, 2013 - present President, East Bay Psychiatric Association, 2009 – 2012 Board of Trustees, Northern CA Psychiatric Society, 2008 - 2012 Councilor-At-Large, Northern CA Psychiatric Society, 2008 – 2011 Vice President, East Bay Psychiatric Association, 2007 – 2009 Secretary, East Bay Psychiatric Association, 2006 – 2007 Liaison to Northern CA Psych Society for East Bay Psych Assoc, 2009 - 2010 Delegate to the Medical Student Section of the AMA, 1985-1987 Developed Impaired Medical Student Program at LSU (Phoenix Society), 1985 Councilor, Phoenix Society (Impaired Medical Student Program), 1985-1987 American Medical Student Association (AMSA) Trustee, Region VII, AMSA National Board, 1986-1987 AMSA Representative to the American Psychiatric Association Internal Steering Committee on Alcohol and Other Drug Abuse Project, 1986-1987 Chairperson, Reference Committee on Corporatization of Health Care - AMSA National Convention, 1986 Louisiana State Delegation Leader - AMSA National Convention (Coordinated Congressional lobbying efforts), 1986 Panelist on Impaired Medical Student Programs - AMSA National Convention, 1986 Co-Chairperson, AMSA Chemical Dependency Project - Advisory Board, 1985-1986 President, LSU Medical Center Chapter AMSA, 1984-1985 Secretary, LSU Medical Center Chapter AMSA, 1983-1984 Member, AMSA Legislative Affairs Task Force, 1983-1987 COMMITTEES
Louisiana State Medical Society Mental Health Task Force, 1986-1987 Mercy Hospital and Medical Center: House Staff Committee Liaison Coordinator, 1987-1988 San Ysidro Health Center: Quality Assurance Committee, 1988-1989: Medical Forms Committee, 1988-1989 San Diego Society of Psychiatric Physicians: Mental Health Services Committee (Access to Health Care), 1988-1989 UCSD Department of Psychiatry: Graduate Education Committee, 1989-1990 American Association for Geropsychiatry: Private Practice and Medicare Committee, 1991-1993 American Association for Geropsychiatry: Board of Directors (Resident Representative), 1991-1993 Pittsburgh Community Clinic: Quality Assurance Committee, 1993 Kaiser Permanente: Biological Psychiatry Committee, 1994 Chair, Kaiser Permanente: Department of Psychiatry Medical Education, 1994 VA: Clozaril Committee, 1994-1996 VA: Quality Assurance Committee, 1994-1996 VA: David Grant Medical Center Operations Committee, 1995-1996 VA/Air Force: Mental Health Flight Committee, 1995-1996 VA/Air Force: Executive Committee, 1995-1996 VA: Pharmacy and Therapeutics Committee, 1996 Walnut Creek Hospital: Pharmacy and Therapeutics Committee, 1998 -1999 Chair, Nominations Committee, East Bay Psychiatric Assoc, 2007 – 2009 East Bay Psych Assoc: Arrangements Committee, 2008 – 2009 Integrative Psychiatry Steering Committee, Northern CA Psychiatric Society, 2010 – present Co-Chair, Integrative Psychiatry Conference, Northern CA. Psychiatric Society, 2010-2011 Nominations Committee, Northern CA Psychiatric Society, 2010 - 2012 PROFESSIONAL SOCIETIES
Contra Costa County Organization of Women Psychiatrists GOOD CLINICAL PRACTICE TRAINING
2005 - Investigator Training for Medical Research Western Institutional Review Board (WIRB) February 3, 2005 2004 - Good Clinical Practices (GCP) and DNA Sampling ePharmaLearning November 11, 2004 2004 - NIH Clinical Research Training Course February 19, 2004 2003 - Informed Consent Training Coast IRB January 31, 2003 2001 - Investigator Support Initiative Training in Good Clinical Practices Pharmacia March 19-21, 2001 Scottsdale, AZ RESEARCH
2009 - Primary Investigator Johnson & Johnson -31001074ATT2001 A Randomized, Double-Blind, Placebo-and Active-Controlled, Parallel-Group, Multicenter Study of 3 Dosages of JNJ-31001074 in the Treatment of Adult Subjects with Attention-Deficit/Hyperactivity Disorder 2009 - Primary Investigator Sonexa ST101-A001-202 A Double-Blin Placebo-Controlled Preliminary Study of the Efficacy, Safety and Tolerability of ST101 in the Treatment of Alzheimer’s Disease in Subjects Concurrently Receiving Donezepil (Aricept) 2008- Primary Investigator Sepracor 360-029 A Double-Blind, Randomized, Placebo-Controlled Study Examining the Safety, Efficacy, and Tolerability of SEP-225289 in Subjects with Major Depressive Disorder (including Atypical and Melancholic Features) 2008 - Primary Investigator Takeda LuAA21004_310 A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Fixed-Dose Study Comparing the Efficacy and Safety of 2 Doses of Lu AA21004 in Acute Treatment of Adults With Generalized Anxiety Disorder. 2008 - Primary Investigator Abbott M10-425 (ADHD) The Long Term Safety and Tolerability of ABT-089 in Adults with Attention Deficit/Hyperactivity Disorder (ADHD): An Open-Label Extension Study for Subjects Completing Study M10-346. 2008 - Primary Investigator Abbott M10-346 (ADHD) A Pilot, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2 Study of the Safety, Tolerability and Efficacy of 40mg QD and 80 mg QD ABT-89 in Adults with Attention Deficit/Hyperactivity Disorder (ADHD). 2008 - Primary Investigator Elan ELN115727-301 and 302 (Alzheimer's Disease) A Phase III, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Groups, Efficacy and Safety Trial of Bapineuzumab (AAB 001, ELN115727) in patients with Mild to Moderate Alzheimer's Disease who are Apolipoprotein E-4 Non-Carriers and Carriers. 2008 - Primary Investigator J&J Alza C-2007-008 (ADHD) A Multi-Center, Double-blind, Placebo-Controlled, Randomized, Parallel-Group Study to investigate the safety and Efficacy of J&J-31001074 in Adults with Attention Deficit/Hyperactivity Disorder. 2008 - Primary Investigator Pfizer A8801004 (ADHD) A Phase IIA, Randomized, Double Blind Placebo-Controlled, Three-Treatment, Two-Period Crossover Study of the Efficacy and Safety of Two Doses of PF-03654746 in Adults with Attention Deficit Hyperactivity Disorder. 2008 – Primary Investigator Pfizer A6061053 (Fibromyalgia) A Multi-center, Long-Term, Open-Label Extension Study of [S,S]-Reboxetine (PNU-165442G) Administered Once Daily in Patients With Fibromyalgia. 2008 - Primary Investigator Pfizer A6061043 (Fibromyalgia) A 14 Week, Randomized, Double Blind, Placebo-Controlled, Multicenter Study of [S,S]-Reboxetine (PN165442G), Administered Twice Daily in Patients with Fibromyalgia. 2007 - Primary Investigator Sanofi-EFC6607 (Depression) A multi-center, double-blind, parallel groups, fixed dose, 4-arm, placebo and paroxetine controlled 8-week efficacy study of 2 oral doses of SR58611A (175mg or 350mg, b.i.d.) in adult outpatients with Major Depressive Disorder. 2007 - Primary Investigator Sanofi-EFC5582 (GAD) An Eight-Week, Multicenter, Randomized, Double-blind, Placebo-controlled Study, Evaluating the Efficacy, Safety and Tolerability of Two Fixed Doses (100 mg and 30 mg Once Daily) of Saredutant in Patients with Generalized Anxiety Disorder. 2007 - Primary Investigator Abbott - M06-889 The Long-Term Safety and Tolerability of ABT-089 in Adults with Attention Deficit-Hyperactivity Disorder (ADHD): An Open-Label Extension Study for M06-855 2007 - Primary Investigator Abbott - M06-855 A Randomized, Double-Blind, Placebo-Controlled, Phase 2 Dose-Ranging Study of the Safety and Efficacy of ABT-089 in Adults with Attention Deficit-Hyperactivity Disorder (ADHD). 2007 - Primary Investigator Novartis - A2301E (MDD) Treatment of Major Depressive Disorder (MDD), a 52-week, open-label extension for A2301. 2007 - Primary Investigator Novartis - A2301(MDD) An 8-week, randomized, double-blind, fixed-dosage, placebo-controlled, parallel-group, multi-center study of the efficacy, safety and tolerability of Agomelatine 25 mg and 50 mg in the treatment of Major Depressive Disorder (MDD). 2007 - Primary Investigator New River - NRP104.304 A Long-Term, Open-Label, and Single-Arm Study of NRP104 30 mg, 50 mg, or 70 mg in Adults with Attention Deficit Hyperactivity Disorder (ADHD). 2007 - Primary Investigator Myriad MPC-7869-04-005 Open-Label Protocol MPC-7869-05-009.001: Open Label STudy of the Effect of Daily Treatment with MPC-7869 in Subjects with Dementia of the Alzheimer's Type. 2006 - Primary Investigator New River - NRP104.303 A Phase III, Randomized, Double-blind, Multi-center, Placebo-controlled, Parallel-group, Forced Dose Titration, Safety and Efficacy Study of NRP104 in Adults with Attention-Deficit Hyperactivity Disorder (ADHD). 2006 - Primary Investigator Cephalon - 2027 A 9-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Dose-Finding Study to Evaluate the Efficacy and Safety of Modafinil (255, 340, 425, and 510 mg/day) as Treatment for Adults With Attention-Deficit/Hyperactivity Disorder. 2005 - Primary Investigator New River - NRP104.303 A Phase III, Randomized, Double-blind, Multi-center, Placebo-controlled, Parallel-group, Forced Dose Titration, Safety and Efficacy Study of NRP104 in Adults with Attention-Deficit Hyperactivity Disorder (ADHD). 2005 – Primary Investigator Voyager-VP-AD-301 A Double-Blind Placebo-Controlled Study of VP4896 for the Treatment of Mild-to-Moderate Alzheimer's Disease. 2005 - Primary Investigator Voyager-VP-AD-104E Open Label Extension of a Double-Blind Placebo-Controlled Study of Leuprolide Acetate Depot in the Treatment of Alzheimer's Disease in Men. 2005 - Primary Investigator Eisai, Inc. - E2020-A001-412 A One Year Multi-Center, Randomized, Double-Blind, Placebo-Controlled Evaluation of the Efficacy and Safety of Donepezil Hydrochloride (E2020) in Subjects with Mild Cognitive Impairment. 2005 - Primary Investigator Cortex - CX717-051 A Randomized, Double-Blind, Two-Period Crossover Study to Assess the Efficacy and Safety of the Ampakine Compound, CX717, Versus Placebo in Adults with Attention-Deficit Hyperactivity Disorder 2005 - Primary Investigator Shire SPD465.304 A Phase III, Multi-Center, Open-Label Safety Study to Evaluate the Safety and Efficacy of SPD465 in Adults with ADHD for a 12-Month Period. 2005 - Primary Investigator Shire SPD465.303 A Phase III, Randomized, Double-blind, Multi-Center, Placebo-controlled, Parallel- group, Forced Dose Titration, Safety and Efficacy Study of SPD 465 in Adults with Attention-Deficit Hyperactivity Disorder (ADHD). 2005 - Primary Investigator Medicinova-MN-305-CL-001 A Phase II, Randomized, Double-blind, Placebo-controlled, Multi-center Study to Evaluate the Efficacy and Safety of Two Flexible Dosing Regimens of MN-305 in Patients with DSM-IV Defined Generalized Anxiety Disorder (GAD). 2005 - Primary Investigator Shire SPD485.303 A Phase III, Multi-center, Open-label Study of Methylphenidate Transdermal System (MTS) in Pediatric Patients aged 6-12 with Attention-Deficit/Hyperactivity Disorder (ADHD). 2005 - Primary Investigator Merck-0928(014-00) A Double-Blind, Randomized, Multicenter, Placebo-Controlled, Parallel-Group Efficacy and Safety Extension Study of MK-0928 15 mg and 10 mg in the Treatment of Adult Outpatients With Primary Insomnia. 2005 - Primary Investigator Myriad - MPC-7869-04-005 Phase III Multicenter, Randomized, Double Blind, Placebo Controlled Study of the Effect of Daily Treatment with MPC-7869 on Measures of Cognitive and Global Function in Subjects with Mild to Moderate Dementia of the Alzheimer's Type. 2005 - Primary Investigator Saegis - SGS742-CL03 A Double-Blind, Double Dummy, Placebo Controlled, Two-Period Crossover Study in Adults with Attention Deficit Hyperactivity Disorder (ADHD). 2004 - Primary Investigator Shire - SPD465.301 A Phase III, Randomized, Double-Blind, Multi-Center, Placebo-Controlled, Parallel-Group, Safety and Efficacy Study of SPD465 in Adults With Attention Deficit Hyperactivity Disorder (ADHD). 2004-05 - Primary Investigator Johnson & Johnson - R096769-PRE-3002 A Placebo-Controlled, Double-Blind, Randomized, Parallel Study of the Withdrawal Effects of Chronic Daily and as needed Dosing With Dapoxetine in the Treatment of Premature Ejaculation. 2004-05 - Primary Investigator Sention - C105 22020 A randomized, double-blind, placebo-controlled, parallel-group study to assess the safety, tolerability, and efficacy with mild cognitive impairment (MCI). 2004-05 - Primary Investigator GSK - 100368 A Twelve-week, Multi-center, Randomized, Double-blind, Double-dummy, Parallel-group, Active controlled, Escalating Dose Study to Compare the Effects on Sexual Functioning of Bupropion Hydrochloride Extended-release and Extended-release Venlafaxine in Subjects with Major Depressive Disorder. 2004 - Primary Investigator Shire SPD485.302 A Phase III, Randomized, Double-Blind, Multi-Center, Parallel-group, Placebo-controlled, Dose Optimization Study, Designed to Evaluate the Safety and Efficacy of Methylphenidate Transdermal System (MTS) vs. Concerta in Pediatric Patients aged 6-12 with Attention-Deficit/Hyperactivity Disorder (ADHD). 2004 - Primary Investigator Lilly B4Z-US-LYCU Efficacy and Safety of Once-Daily Atomoxetine Hydrochloride in Adults with ADHD Over an Extended period of Time: With a Brief Evaluation of Executive Cognition. 2004 - Primary Investigator Voyager-VP-AD-104 A Double-Blind Placebo-Controlled Study of Leuprolide Acetate Depot in the Treatment of Alzheimer's Disease in Men. 2004 - Primary Investigator Shire - SLI381-312 Open-Label, Multi-Center Study to Assess Safety, Tolerability, and Effectiveness Associated with the use of ADDERALL XR in Adults with Attention Deficit Hyperactivity Disorder and Evaluate an ADHD-specific Novel Quality of Life Measure. 2004-05 - Primary Investigator Cephalon, Inc. - CEP10953 A 12-Month, Open-Label, Flexible-Dosage (100 to 250 mg/day) Study of the Safety of the Safety and Efficacy of CEP-10953 in the Treatment of Patients With Excessive Sleepiness Associated With Narcolepsy, Obstructive Sleep Apnea/Hypopnea Syndrome, or Chronic Shift Work Sleep Disorder. 2003 - Primary Investigator Abbott Laboratories - M03-594 A Randomized, Double-Blind, Placebo-Controlled, 4-Period Crossover Pilot Study of the Safety of the Safety and Efficacy of Multiple Doses of ABT-089 in Adults with Attention Deficit-Hyperactivity Disorder (ADHD). 2003 - Primary Investigator Shire Pharmaceutical Development Inc. - SLI381.315 A Phase III, Randomized, Multi-Center, 18-month, Open-label Safety, Tolerability and Efficacy Study of ADDERALL XR in the Treatment of Adolescents aged 13-18 with Attention Deficit Hyperactivity Disorder (ADHD). 2003-04 - Primary Investigator Shire Pharmaceutical Development Inc. - SPD473.203 A Phase II, Randomized, Multi-Center, Double-Blind, Parallel-Group, Placebo-Controlled Safety and Efficacy Study of SPD473 in Adults Aged 18-55 with Attention Deficit Hyperactivity Disorder (ADHD). 2003-04 - Primary Investigator Alza Corporation - C2002-014 An Open Label Study of the Long-term Safety of Dapoxetine HCI in the Treatment of Rapid Ejaculation. 2003-04 - Primary Investigator Alza Corporation - C2002-013 A Placebo-Controlled, Double-Blind, Randomized, Parallel Study of the Efficacy and Safety of Dapoxetine HCI in the Treatment of Rapid Ejaculation. 2003-04 - Primary Investigator Shire Pharmaceutical Development Inc. - SLI381.314 A Phase III, Randomized, Multi-Center, Double-Blind, Parallel-Group, Placebo-Controlled Safety and Efficacy Study of ADDERALL XR with an Open-label Extension, in the Treatment of Adolescents aged 13-17 with Attention Deficit Hyperactivity Disorder (ADHD). 2003-04 - Primary Investigator Takeda Pharmaceuticals - 01-02-TL-375-022 A Phase III, Open-Label, Fixed-Dose Study to Determine the Safety of Long-Term Administration of TAK-375 in Subjects with Chronic Insomnia. 2003-04 - Primary Investigator Novartis Pharmaceuticals Corporation - E2302 A 5-week, multicenter, double-blind, randomized, placebo-controlled, parallel-group, fixed-dosed study of the efficacy and safety of Focalin LA (dexmethylphenidate hydrochloride) administered once daily in adults with Attention-Deficit/Hyperactivity Disorder. 2003-04 - Primary Investigator Ortho McNeil-CAPSS-169 The Effect of Ortho Tri-Cyclen on Bone Mineral Density in Pediatric Subjects with Anorexia Nervosa: A Double-Blind, Placebo-Controlled Study. 2002-03 - Primary Investigator GlaxoSmithKline AK130934 An 8-Week, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Flexible-Dose Comparison of Extended-Release Bupropion Hydrochloride to Assess the Efficacy, Safety and Effects on Health Outcomes in the Treatment of Adults with Attention-Deficit Hyperactivity Disorder. 2002-03 - Primary Investigator Lilly B4Z-MC-LYBM A Double-Blind Study of Treatment Optimization with Atomoxetine Hydrochloride in Adults with DSM-IV Attention Deficit/Hyperactivity Disorder. Somerset S9303-P0204 A Phase III, Open Label Study of the Safety, Tolerability, and Efficacy of the Selegiline Transdermal System in Elderly Subjects with Major Depression. 2002 - Primary Investigator Shire 381.303 A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study of ADDERALL XR in Adults with Attention Deficit Hyperactivity Disorder. 2002-04 - Primary Investigator Shire 381.304 A 12-Month, Open-Label Study of ADDERALL XR in Adults with Attention Deficit Hyperactivity Disorder. 2001-02 - Primary Investigator GlaxoSmithKline SB-659746-A002 A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating Efficacy and Safety of Three Doses of SB-659746-A (5mg, 10 mg and 20 mg) Versus Placebo in Patients with Major Depressive Disorder. 2001-03 - Primary Investigator Merck - MK-0869 A Double-Blind, Multicenter, Placebo- and Active-Controlled Acute and Extension Study of MK-0869 in the Treatment of Patients With Major Depressive Disorder. 2001-02 - Primary Investigator Lilly F1D-US-HGJU A Controlled Trial of Olanzapine Versus Ziprasidone in the Treatment of Schizophrenic and Schizoaffective Subjects with Comorbid Depression. A Long-Term, Open-Label, Safety Study of Tomoxetine Hydrochloride in Patients, 6 years and older. 2001-02 - Primary Investigator B4Z-MC-LYAQ Safety and Efficacy of Atomoxetine or Atomoxetine Plus Fluoxetine in the Treatment of Mixed Attentional and Affective Disorders. 2001-02 - Primary Investigator Pfizer A1481074 A parallel Group, Multicenter flexible dose study with a double blind, randomized, placebo-controlled phase and an open-label phase to evaluate the efficacy and safety of Viagra (Sildenafil Citrate) in males with Serotonergic Antidepressant associated Erectile Dysfunction. 2000-01 - Primary Investigator AstraZeneca 5077IL/0041 A Multicenter, Double-blind, Randomized Comparison of the Efficacy and Safety of Sustained-release Formulation Quetiapine Fumarate (SEROQUEL) and Placebo in the treatment of Patients with Schizophrenia. 2000-01 - Primary Investigator AstraZeneca 5077IL/0099 A Placebo-Controlled Trial of the Safety and Efficacy of SEROQUEL as Add-on Therapy with Lithium or Divalproex in the Treatment of Acute Mania. 2000-04 - Primary Investigator B4Z-MC-LYAR A Long-Term Open-Label Safety Study of Tomoxetine Hydrochloride In Adult Outpatients with DSM-IV Attention Deficit/Hyperactivity Disorder. 2000 - Primary Investigator Parke-Davis 1088-090-025 A Placebo-Controlled Study of Pregabalin in Elderly Patients With Generalized Anxiety Disorder. Primary Investigator Pharmacia & Upjohn M/2020/0047 Reboxetine, Placebo, and Paroxetine Comparison in Patients with Major Depressive Disorder 2000-01 - Primary Investigator Lilly B47-MC-LYAO A phase III randomized, double-blind comparison of placebo and tomoxetine in adult outpatients with DSM-IV Attention-Deficit/Hyperactivity Disorder. 2000-02 - Primary Investigator Lilly B47-MC-LYAB A phase III open label, long-term, safety and efficacy study of tomoxetine hydrochloride in outpatients with ADHD, ages 6 to 18 years. 2000-01 - Primary Investigator Pfizer 0501015 A 24-week, open-label extension study of Zoloft in children & adolescent outpatients previously diagnosed with Major-Depressive Disorder. 2000 - Subinvestigator Shire-381.301 A randomized, double-blind, placebo-controlled, parallel-group study of SL1381 in children with Attention Deficit Hyperactivity Disorders. 2000 - Subinvestigator Shire-381.302 A 12-month, open-label study of SL1381 in children with Attention Deficit Hyperactivity Disorder. 2000 - Subinvestigator Alza C-99-018 Open-label study to evaluate participants use and safety of OROS (methylphenidate HCI) in participants with ADHD in a community setting. 2000-2003 - Primary Investigator Bristol-Myers Squibb CN138-005 A multicenter, randomized, double-blind, placebo controlled flexible-dose study of Aripiprazole in the treatment of institutionalized patients with psychosis associated with dementia of the Alzheimer’s type. 2000-01 - Primary Investigator Bristol-Myers Squibb CN 138-007 A randomized, double-blind, placebo-controlled , flexible -dose study of two fixed doses of Aripiprazole in the treatment of patients with Acute Mania. 2000-01 - Primary Investigator Bristol-Myers Squibb CN 138-010 A randomized, double-blind, placebo-controlled study of Aripiprazole in the maintenance treatment of patients with Bipolar Disorder. 2000 - Primary Investigator Lilly F1D-US-HGHC Prevalence of Hyperprolactinemia in Schizophrenic patients treated with anti-psychotic drugs. 2001 - Primary Investigator Lilly F1D-US-HGHH Olanzapine in the reduction of Hyperprolactinemia and associated morbidity in Schizophrenic patients. 1999-01 - Primary Investigator Lilly F1D-MC-HGIP Open-Label Combination of Olanzapine and Fluoxetine in Major Depressive Disorder. 1999-00 - Primary Investigator Lilly F1D-MC-HGHZ The combination of Olanzapine and Fluoxetine in Treatment Resistant Depression without Psychotic features 1999-00 - Primary Investigator Pfizer 0501017 A multicenter 10-week randomized double-blind placebo controlled flexible dose outpatients study of Sertraline in children and adolescents with Major Depressive Disorder. 1999-00 - Primary Investigator Forest SCT-MD-01 Fixed dose comparison of the safety and efficacy of Lu 26-054, Citalopram, and placebo in the treatment of Major Depressive Disorder. 1999-00 - Primary Investigator Forest SCT-MD-03 Open-Label study of Lu26-054 in the treatment of Major Depressive Disorder. 1999-00 - Primary Investigator Lilly F1D-MC-HGHX A double-blind placebo-controlled comparison of the efficacy and safety of short-acting IM Olanzapine, short-acting IM Lorazepam, and IM placebo in treating agitation in patients with Dementia of the Alzheimer’s Type, Vascular Dementia, and Mixed Dementia. 1999-00 - Primary Investigator Lilly F1D-US-HGHQ Olanzapine versus Divalproex in the treatment of acute mania. 1998-99 - Primary Investigator Roche WV15825 A double-blind, randomized, placebo-controlled study of Ro 64-0796 used in elderly subjects for the prevention of clinical influenza during the influenza season. 1998-99 - Primary Investigator Abbott M97-696 A multi-center, double-blind, placebo-controlled study to evaluate the safety and efficacy of Depakote CR in the treatment of acute mania in bipolar disorder patients. 1998-99 - Primary Investigator Abbott M97-738 A multi-center, double-blind, placebo-controlled study of Depakote in the treatment of signs and symptoms of mania in elderly patients with dementia. 1998-01 - Primary Investigator Abbott M98-817 A multi-center, open-label study of Depakote in the treatment of signs and symptoms of mania in elderly patients with dementia. 1997-98- Primary Investigator Zeneca 5077US/0004 A multi-center randomized comparison of Seroquel and Risperdal, to assess efficacy, safety, and tolerability in treatment of psychotic disorders. 1993-94- Primary Investigator Bristol-Myers Squibb A multi-center open label study to evaluate efficacy of Serzone in treatment of major depression. 1992-93- Co-Investigator Mental Status Changes with Steroid Prophylaxis in Cardiac Angiography Veterans Administration Hospital Department of Psychiatry and Radiology University of California, San Diego 1992-93 - Primary Investigator Withdrawal of Neuroleptics in Geriatric Patients Veterans Administration Hospital Department of Psychiatry, Geropsychiatry Division University of California, San Diego Developed research protocol for 5-year study to evaluate cognitive deficits associated with neuroleptics, course of relapse off medication, medication withdrawal symptoms, and withdrawal emergent dyskinesias in geriatric patients. PRESENTATIONS
Management of the Aggressive Patient in an Urgent Care Medical Facility Grand Rounds, Kaiser Permanente Department of Urgent Care Walnut Creek, CA May, 1994 Eating Disorders UC Davis School of Medicine March, 1995 and February, 1996 Pharmacologic Issues in Psychiatry UC Davis School of Medicine August, 1995 Pharmacologic and Case Management of a Complicated Dementia Patient Interdisciplinary Grand Rounds - Department of Mental Health David Grant Medical Center, Travis Air Force Base September, 1995 Nefazadone: Has It Fulfilled It's Promise? San Francisco, CA March, 1996 New Treatments for Depressed and Anxious Patients San Francisco, CA August, 1996 Depressed Patients with Symptoms of Anxiety Grand Rounds - Veteran's Administration Oakland Mental Health Clinic September, 1996 A Clinician’s Perspective: The Ins and Outs of Seroquel Zeneca District Emphasis Meeting Reno, Nevada May, 1998 Focus on Quetiapine Oakland, CA May, 1998 Clinical Impressions of Seroquel: The First Year Roundtable Discussion San Francisco, CA June, 1998 Update on Seroquel San Mateo County Psychiatric Association San Mateo, CA June, 1998 Use of Quetiapine in Clinical Practice Kaiser Permanente Update on Atypical Antipsychotics Psychiatry Research Unit San Francisco General Hospital San Francisco, CA September, 1998 Practical Issues in the Clinical Use of the Newest Antipsychotic Agents McCauley Psychiatric Institute St. Mary's Hospital San Francisco, CA September, 1998 New Uses for Atypical Antipsychotic Agents Program Directors' Meeting Heritage Oaks Hospital Sacramento, CA October, 1998 Updated Issues on Diagnosis and Management of Depression Parke-Davis & Forest Pharmaceuticals, Inc. Santa Rosa, CA October, 1998 Review of Atypical Antipsychotics: Focus on Quetiapine San Mateo, CA November, 1998 Atypical Antipsychotics in Clinical Practice San Jose, CA January, 1999 Clinical Uses and Case Studies with Atypical Antipsychotics Southern California Psychiatric Association San Bernadino, CA January, 1999 An Update on the Use of Atypical Antipsychotics Inland Region-California Psychiatric Association San Bernadino, CA January, 1999 Quetiapine: Dosing Strategies and Case Studies Zeneca District Emphasis Meeting Las Vegas, Nevada February, 1999 Atypical Antipsychotics in Acute Psychiatric Patients Grand Rounds, Nevada State Hospital Reno, Nevada February, 1999 Use of Atypical Antipsychotics in Adult and Geriatric Patients Grand Rounds, Summit Senior Bridges Hospital Oakland, CA February, 1999 Update on Antipsychotics: A Review of the QUEST Trial Grand Rounds, Dept. of Psychiatry UC Irvine, Medical Center March, 1999 Atypical Antipsychotics: Clinical Uses and Dosing Strategies Brea, CA March, 1999 Update on Atypical Antipsychotics: Focus on Seroquel Eureka, CA March, 1999 Clinical Perspectives on Atypical Antipsychotics Community Mental Health Department Ukiah, CA March, 1999 Use of Atypical Antipsychotics in the Geriatric Population Grand Rounds, Laguna Honda Hospital San Francisco, CA March, 1999 Valley Area Physician Talk Santa Barbara & Burbank June, 1999 Roundtable Dinner Program on Psychosis Phoenix, AZ August, 1999 Grand Rounds, Regional Office of Mental Health New Orleans, LA August, 1999 Atypical Antipsychotics with Focus on Quetiapine Burbank, CA September, 1999 Atypical Antipsychotics: Side Effect Profiles & Dosing Stratagies Tucson, AZ September, 1999 Dosing Strategies with Quetiapine Seroquel National Speakers Update Meeting, Phoenix, AZ November, 1999 Grand Rounds Yuba/Sutter Mental Health Sacramento, CA November, 1999 Comparing Atypical Antipsychotics Managed Care Meeting Yountville, CA November, 1999 Atypical Antispychotics Seattle, WA March, 2000 Parkinson’s Disease and Psychosis Kahului, HI March, 2000 Side Effect Profiles and Dosing Strategies with Atypical Antipsychotics Santa Barbara, CA April, 2000 New Applications and Dosing Strategies with Atypical Antipsychotics Vista Del Mar, CA April, 2000 Review & Update of Atypical Antipsychotics Family & Child Therapy Center Racine, WI August, 2000 Atypical Antipsychotics Milwaukee, WI August, 2000 A New Atypical Antipsychotic Allina Behavioral Health Teleconference Minneapolis, MN September, 2000 Pharmacologic Profiles of Newer Antipsychotics Grand Rounds, Veteran’s Administrative Hospital Tucson, AZ November, 2000 Update on Side Effects of Antipsychotic Therapy Tucson, AZ November, 2000 Seroquel Faculty Update Meeting Chairperson, Moderator, Speaker Sonoma, CA December, 2000 Issues in the Management of Schizophrenia Sonoma, CA December, 2000 Side Effect Profiles with of Antipsychotic Therapy Whitehall, WI February, 2001 Update on Side Effects of Antipsychotic Therapy Chinatown/North Beach Mental Health Clinic San Francisco, CA March, 2001 Update on Side Effects of Antipsychotic Therapy Citywide Community Focus Center San Francisco, CA April, 2001 Pharmacologic Profiles of Newer Antipsychotics San Mateo, CA April, 2001 Issues in the Management of Schizophrenia Santa Rosa, CA October, 2001 Case Studies of Psychosis San Francisco, CA November, 2001 Antipsychotic Use in Special Populations Grand Rounds, San Joaquin County Mental Health Stockton, CA April, 2002 Issues in the Management of Schizophrenia Chinatown Mental Health Clinic San Francisco, CA May, 2002 Psychiatric Case Study Program San Francisco, CA May, 2002 Antipsychotic Use in Special Populations Grand Rounds, Dominican Hospital Santa Cruz, CA July, 2002 The Ups and Downs of the Newer Atypical Antipsychotic Medications Redwood City, CA July, 2002 Using Medical Consequences of Atypical Antipsychotics to Guide Choices in Special Populations Grand Rounds, Alameda County Mental Health Oakland, CA October, 2002 Are Therapeutic Targets in ADHD Keeping Pace With Advancements in Treatment? Moderator Seattle, WA December, 2002 Recognition, Diagnosis, and Treatment of Adult ADHD: Clinical Perspectives Strattera Speaker Bureau Summit Santa Ana Pueblo, NM March 2003 Clinical Perspectives on a New Treatment Option for ADHD Walnut Creek, CA March 2003 ADHD in Women: Evidence, Diagnosis, and Treatment Kaiser-Permanente Northern California Region Annual Conference for Psychiatry and Chemical Dependency Clinicians. San Francisco, CA April 2003 Case Study in the Management of Schizophrenia Lafayette, CA May 2003 ADHD in Adults: The Often Missed Diagnosis "Introducing a New Diagnostic Tool for Primary Care Physicians." NAAAC (National Alliance for the Advancement of ADHD Care) Houston, TX June 2003 Antipsychotic Use in Special Populations Eden Community Support San Leandro, CA January 2004 Adult ADHD Danville, Berkeley, Lafayette, CA March 2004 Clinical Insights: Antipsychotic Therapy for Bipolar Mania Lafayette, CA April 2004 A Conversation About Medications NAMI Contra Costa General Meeting Concord, CA February 2004 Update on New Psychotropic Medications NAMI Contra Costa General Meeting Concord, CA 2008 Clinical Trials 101: Development of New Medications from Ethics and Oversight to Rating Scales and Beyond Northern CA Psychiatric Society Annual Meeting Monterey, CA March, 2009 PUBLICATIONS/POSTERS
Efficacy and Safety of Lisdexamphetamine Dimesylate in the Treatment of Non-Caucasian Children and Adults with Attention-Deficit/Hyperactivity Disorder – Valerie Arnold, M.D., Michael McManus, M.D., Kathleen Toups, M.D., Joseph Biederman, M.D. – APA New Research Poster Session – May 7, 2008

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