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INFORMATION FOR

Jesse M. Cedarbaum

MD, FAAN (Neurology), FANA
Professor Adjunct

Contact Information

Jesse M. Cedarbaum, MD, FAAN (Neurology), FANA

Office Location

Research Summary

I am a neurologist whose career focus has been on the development of novel and improved therapeutic agents for neurodegenerative and neuropsychiatric disorders. I have a unique background of over 30 years of drug development and clinical trials experience in academia, biotechnology, large and small pharmaceutical companies. My therapeutic area experience and expertise spans the spectrum of neuropsychiatric conditions, from neurodegenerative diseases (Alzheimer's, Parkinson's) to neuromuscular disorders (ALS, peripheral neuropathies) to psychiatric and ophthalmological disorders, and is represented in a body of over 120 peer-reviewed scientific publications, mostly in the area of Parkinson’s disease (PD) therapeutics. I have led teams developing both small molecule, protein and antisense therapeutics in all stages of the development process, including preclinical development, Phase 1, translational and "Proof of Concept" studies, Phase 3 clinical studies and associated regulatory activities. I have played key roles in the development of several currently marketed products, both as an academic investigator and industry team leader and executive. Most recently I led a team at Biogen that advanced 3 new compounds into the clinic for potential treatment of PD, including efforts to develop novel biomarkers and digital health technologies.

Extensive Research Description

The early focus of my work was on using neuroanatomical and neurophysiological tools to understand the pharmacology of drugs acting on the noradrenergic system of the brain, and the contribution of the locus coeruleus (LC) noradrenergic system to brain function. These efforts helped lay the groundwork for a theory of locus coeruleus function that is still widely supported – that the LC is involved in novelty detection and selective attention. Subsequent understanding of pathological changes in the LC and the correlation of loss of noradrenergic function in dementia are in keeping with this hypothesis.

My interest in the pharmacology of catecholaminergic systems in the brain led to a clinical interest in Parkinson’s disease. Significant novel clinical observations from work carried out at Cornell and the Burke Rehabilitation Center included the (at that time) novel understanding that the timing emergence of MRF and dyskinesia in the treatment of PD was related to age of onset and severity of disease, not the duration of levodopa administration. In addition, our group was among the first to report on the near-universal prevalence of dementia in advanced PD. Our group also was among the early pioneers in the utilization of enteral levodopa infusions to attempt to control MRFs, and we established the basis for the use of peripheral COMT inhibitors in PD through a combination of clinical observations and studies using novel COMT inhibitors in nonhuman primates. And finally, we described the relationship between plasma and brain pharmacokinetics levodopa and dopamine by sampling CSF from PD patients who had Ommaya reservoirs left in place following neurosurgical procedures.

Prior to initiation of clinical trials for ALS at Regeneron Pharmaceuticals, it became apparent to us that there was a need for a comprehensive clinical rating scale to be used as a clinical trial outcome measure. This work resulted in the development and validation of the ALS Functional Rating Scale (ALSFRS) and its revised, expanded version, the ALSFRS-R. Unfortunately, none of our ALS clinical trials were successful, but the ALSFRS-R continues to be the most-used outcome measure for ALS trials, and is endorsed by FDA for this use.

The neurotrophic factor trail led us to studies for treatment of retinal disorders, since the eye, after all, is a part of, and a window into, the brain. Subsequent to the completion of the ALS program, I led a series of clinical trials of an anti-VEGF agent, aflibercept, for treatment of neovascular Age Related Macular Degeneration (“wet”) AMD. This program resulted in the eventual approval of the drug, known commercially as Eyelea, for wet AMD and a variety of other retinal vascular diseases.

After leaving Regeneron, I joined Elan Pharmaceuticals. There my focus shifted back to neurodegenerative disease, in particular Alzheimer’s disease. Three publications from this period helped lay the groundwork for acceptance by both FDA and EMA of the Clinical Dementia Rating Sum of Boxes (CDR-SB), developed at Washington University in St. Louis, as a sole clinical outcome measure for trials in the MCI-early AD space, and its adoption as the outcome measure for most contemporary MCI-mild AD clinical trials.

Most recently, as we prepared for the development of novel therapeutic agents for the treatment of PD at Biogen, I established a number of external collaborative projects that resulted in the identification and preliminary validation of novel or pre-existing biomarkers for PD clinical trials, and helped lead pre-competitive collaborative efforts to secure regulatory support for the use of dopamine transporter (DaT) imaging as an enrichment biomarker for PD clinical trials.




Coauthors

Research Interests

Cerebellar Ataxia; Parkinson Disease; Supranuclear Palsy, Progressive; Motor Neuron Disease; Multiple System Atrophy; Lewy Body Disease

Public Health Interests

Clinical Trials; Pharmaceuticals and Medical Devices

Selected Publications

  • IC‐P‐108: VOLUMETRIC MRI RESULTS OF BMS AVAGACESTAT IN A PRODROMAL AD POPULATIONIstace A, Bracoud L, Berman R, Luo F, Roche F, Salloway S, Dyck C, Dubois B, Andreasen N, Brody M, Curtis C, Soininen H, Thein S, Shiovitz T, Ferris S, Grill J, Gouttard S, Schaerer J, Hayes W, Kaplita S, Belaroussi B, Yu H, Cedarbaum J, Feldman H, Pachai C, Coric V. IC‐P‐108: VOLUMETRIC MRI RESULTS OF BMS AVAGACESTAT IN A PRODROMAL AD POPULATION Alzheimer's & Dementia 2014, 10: p60-p61. DOI: 10.1016/j.jalz.2014.05.114.
  • P2‐202: VOLUMETRIC MRI RESULTS OF BMS AVAGACESTAT IN A PRODROMAL AD POPULATIONIstace A, Bracoud L, Berman R, Luo F, Roche F, Salloway S, Dyck C, Dubois B, Andreasen N, Brody M, Curtis C, Soininen H, Thein S, Shiovitz T, Ferris S, Grill J, Gouttard S, Schaerer J, Hayes W, Kaplita S, Belaroussi B, Yu H, Cedarbaum J, Feldman H, Pachai C, Coric V. P2‐202: VOLUMETRIC MRI RESULTS OF BMS AVAGACESTAT IN A PRODROMAL AD POPULATION Alzheimer's & Dementia 2014, 10: p546-p547. DOI: 10.1016/j.jalz.2014.05.879.
  • P1–343: A phase II study of the gamma‐secretase inhibitor avagacestat (BMS‐708163) in predementia Alzheimer's diseaseCoric V, Salloway S, Dyck C, Kerselaers W, Kaplita S, Curtis C, Ross J, Richter R, Andreasen N, Brody M, Sharma S, Cedarbaum J, Berman R. P1–343: A phase II study of the gamma‐secretase inhibitor avagacestat (BMS‐708163) in predementia Alzheimer's disease Alzheimer's & Dementia 2013, 9: p283-p283. DOI: 10.1016/j.jalz.2013.05.569.
  • A Study To Evaluate Safety and Tolerability of CK-2017357 (CK-357) in Patients with Amyotrophic Lateral Sclerosis Using a Twice-Daily, Dose-Titration Regimen (P04.155)Shefner J, Andrews J, Bedlack R, Berry J, Goslin K, Jackson C, Kissel J, Lange D, Licht J, Mozaffar T, Pestronk A, Rosenfeld J, Wolff A, Lee J, Masonek J, Jones D, Meng L, Cedarbaum J. A Study To Evaluate Safety and Tolerability of CK-2017357 (CK-357) in Patients with Amyotrophic Lateral Sclerosis Using a Twice-Daily, Dose-Titration Regimen (P04.155) Neurology 2012, 78: p04.155-p04.155. DOI: 10.1212/wnl.78.1_meetingabstracts.p04.155.
  • The Effects of ELND005 (Scyllo-Inositol) on Emergence of Neuropsychiatric Symptoms (NPS) in Mild/Moderate Alzheimer's Disease: Results from a 78-Week Phase 2 Study (P04.215)Tariot P, Lyketsos C, Crans G, Cedarbaum J, Hernandez C, Abushakra S. The Effects of ELND005 (Scyllo-Inositol) on Emergence of Neuropsychiatric Symptoms (NPS) in Mild/Moderate Alzheimer's Disease: Results from a 78-Week Phase 2 Study (P04.215) Neurology 2012, 78: p04.215-p04.215. DOI: 10.1212/wnl.78.1_meetingabstracts.p04.215.
  • A Study To Evaluate Safety, and Tolerability of Repeated Doses of CK-2017357 (CK-357) in Patients with Amyotrophic Lateral Sclerosis (S25.005)Shefner J, Barohn R, Boylan K, Bradshaw D, Brooks B, Heiman-Patterson T, Katz J, Maragakis N, Mitsumoto H, Pestronk A, Simmons Z, Wolff A, Lee J, Masonek J, Jones D, Meng L, Cedarbaum J. A Study To Evaluate Safety, and Tolerability of Repeated Doses of CK-2017357 (CK-357) in Patients with Amyotrophic Lateral Sclerosis (S25.005) Neurology 2012, 78: s25.005-s25.005. DOI: 10.1212/wnl.78.1_meetingabstracts.s25.005.
  • BIOMARKERS OF SARCOPENIA IN CLINICAL TRIALS RECOMMENDATIONS FROM THE INTERNATIONAL WORKING GROUP ON SARCOPENIACESARI M, FIELDING R, PAHOR M, GOODPASTER B, HELLERSTEIN M, ABELLAN VAN KAN G, ANKER S, RUTKOVE S, VRIJBLOED J, ISAAC M, ROLLAND Y, M’RINI C, AUBERTIN-LEHEUDRE M, CEDARBAUM J, ZAMBONI M, SIEBER C, LAURENT D, EVANS W, ROUBENOFF R, MORLEY J, VELLAS B. BIOMARKERS OF SARCOPENIA IN CLINICAL TRIALS RECOMMENDATIONS FROM THE INTERNATIONAL WORKING GROUP ON SARCOPENIA The Journal Of Frailty & Aging 2012, 1-9. DOI: 10.14283/jfa.2012.17.
  • O4‐06‐07: Imaging and cerebrospinal fluid biomarker results of a phase II dose‐ranging study of ELND005 (Scyllo‐inositol) in mild‐to‐moderate Alzheimer's diseasePorsteinsson A, Sperling R, Salloway S, Keren R, Dyck C, Tariot P, Arnold D, Crans G, Hernandez R, Liang E, Bairu M, Cedarbaum J, Pastrak A, Abushakra S. O4‐06‐07: Imaging and cerebrospinal fluid biomarker results of a phase II dose‐ranging study of ELND005 (Scyllo‐inositol) in mild‐to‐moderate Alzheimer's disease Alzheimer's & Dementia 2011, 7: s695-s695. DOI: 10.1016/j.jalz.2011.05.2010.
  • P2‐509: Population pharmacokinetic analysis of plasma, cerebrospinal fluid and brain ELND005 in patients with mild to moderate Alzheimer's diseaseWagg J, Green M, Yan L, Liang E, Cedarbaum J, Abushakra S. P2‐509: Population pharmacokinetic analysis of plasma, cerebrospinal fluid and brain ELND005 in patients with mild to moderate Alzheimer's disease Alzheimer's & Dementia 2011, 7: s475-s475. DOI: 10.1016/j.jalz.2011.05.1380.
  • IC‐P‐093: Predicting Initial Changes in Brain Volume with Effective Anti‐Amyloid Agents: Just Ask AliceCedarbaum J. IC‐P‐093: Predicting Initial Changes in Brain Volume with Effective Anti‐Amyloid Agents: Just Ask Alice Alzheimer's & Dementia 2011, 7: s46-s46. DOI: 10.1016/j.jalz.2011.05.058.
  • P2‐499: Safety and efficacy results of a phase II randomized, placebo‐controlled, dose‐ranging study of elnd005 (scyllo‐inositol) in mild‐to‐moderate Alzheimer's diseaseSalloway S, Porsteinsson A, Sperling R, Keren R, Dyck C, Tariot P, Gilman S, Crans G, Hernandez R, Quinn G, Bairu M, Cedarbaum J, Pastrak A, Abushakra S. P2‐499: Safety and efficacy results of a phase II randomized, placebo‐controlled, dose‐ranging study of elnd005 (scyllo‐inositol) in mild‐to‐moderate Alzheimer's disease Alzheimer's & Dementia 2011, 7: s472-s472. DOI: 10.1016/j.jalz.2011.05.1371.
  • P2‐476: A Phase 1, dose escalation study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of multiple oral daily doses of ELND006 in healthy elderly subjectsLiang E, Liu W, Lohr L, Nguyen V, Lin H, Munson M, Crans G, Cedarbaum J. P2‐476: A Phase 1, dose escalation study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of multiple oral daily doses of ELND006 in healthy elderly subjects Alzheimer's & Dementia 2011, 7: s465-s465. DOI: 10.1016/j.jalz.2011.05.1347.
  • P2‐201: Predicting initial changes in brain volume with effective anti‐amyloid agents: Just ask aliceCedarbaum J. P2‐201: Predicting initial changes in brain volume with effective anti‐amyloid agents: Just ask alice Alzheimer's & Dementia 2011, 7: s377-s378. DOI: 10.1016/j.jalz.2011.05.1086.
  • P2‐213: Oral amyloid anti‐aggregating agent ELND005 is measurable in CSF and brain of healthy adult menGarzone P, Koller M, Pastrak A, Jhee S, Ereshefsky L, Moran S, Cedarbaum J, Xu V, Ross B. P2‐213: Oral amyloid anti‐aggregating agent ELND005 is measurable in CSF and brain of healthy adult men Alzheimer's & Dementia 2009, 5: p323-p323. DOI: 10.1016/j.jalz.2009.04.526.
  • P2‐082: Defining mild cognitive impairment: Disparity of incidence and prevalence estimates with variable operationalized definitionsWard A, Michels S, Cedarbaum J, Arrighi H. P2‐082: Defining mild cognitive impairment: Disparity of incidence and prevalence estimates with variable operationalized definitions Alzheimer's & Dementia 2009, 5: p286-p286. DOI: 10.1016/j.jalz.2009.04.392.
  • Safety and pharmacokinetics of intravenous VEGF Trap in a phase I clinical trial of patients with advanced solid tumorsDupont J, Rothenberg M, Spriggs D, Cedarbaum J, Furfine E, Cohen D, Dancy I, Lee H, Cooper W, Lockhart A. Safety and pharmacokinetics of intravenous VEGF Trap in a phase I clinical trial of patients with advanced solid tumors Journal Of Clinical Oncology 2005, 23: 3029-3029. DOI: 10.1200/jco.2005.23.16_suppl.3029.
  • 132 A phase I and pharmacokinetic clinical trial of subcutaneous (sc) VEGF trap in advanced solid tumor patientsDupont J, Schwartz L, Koutcher J, Spriggs D, Gordon M, Mendelson D, Murren J, Lucarelli A, Cedarbaum J. 132 A phase I and pharmacokinetic clinical trial of subcutaneous (sc) VEGF trap in advanced solid tumor patients European Journal Of Cancer Supplements 2004, 2: 43. DOI: 10.1016/s1359-6349(04)80140-x.
  • Phase I and pharmacokinetic study of VEGF Trap administered subcutaneously (sc) to patients (pts) with advanced solid malignanciesDupont J, Schwartz L, Koutcher J, Spriggs D, Gordon M, Mendelson D, Murren J, Lucarelli A, Cedarbaum J. Phase I and pharmacokinetic study of VEGF Trap administered subcutaneously (sc) to patients (pts) with advanced solid malignancies Journal Of Clinical Oncology 2004, 22: 3009-3009. DOI: 10.1200/jco.2004.22.14_suppl.3009.
  • Phase I and pharmacokinetic study of VEGF Trap administered subcutaneously (sc) to patients (pts) with advanced solid malignanciesDupont J, Schwartz L, Koutcher J, Spriggs D, Gordon M, Mendelson D, Murren J, Lucarelli A, Cedarbaum J. Phase I and pharmacokinetic study of VEGF Trap administered subcutaneously (sc) to patients (pts) with advanced solid malignancies Journal Of Clinical Oncology 2004, 22: 3009-3009. DOI: 10.1200/jco.2004.22.90140.3009.
  • Is NT-3 a colonic prokinetic—A randomized controlled trial?Rao S, Sadeghi P, Mudipalli R, Kempf J, Stambler N, Cedarbaum J. Is NT-3 a colonic prokinetic—A randomized controlled trial? Gastroenterology 2003, 124: a569. DOI: 10.1016/s0016-5085(03)82879-2.
  • Intrathecal Ciliary Neurotrophic Factor Delivery for Treatment of Amyotrophic Lateral Sclerosis (Phase I Trial)Penn R, Kroin J, York M, Cedarbaum J. Intrathecal Ciliary Neurotrophic Factor Delivery for Treatment of Amyotrophic Lateral Sclerosis (Phase I Trial) Neurosurgery 1997, 40: 94-100. DOI: 10.1227/00006123-199701000-00021.
  • Chapter 10 Neurotrophic factors Towards a restorative therapy of Parkinson's diseaseAltar C, Wiegand S, Lindsay R, Cedarbaum J. Chapter 10 Neurotrophic factors Towards a restorative therapy of Parkinson's disease 1996, 159-185. DOI: 10.1016/b978-012525445-8/50012-6.
  • PrefaceCedarbaum J, Gancher S. Preface Neurologic Clinics 1992, 10: xi. DOI: 10.1016/s0733-8619(18)30210-x.
  • ReplyOlanow C, Cedarbaum J. Reply Annals Of Neurology 1992, 31: 114-115. DOI: 10.1002/ana.410310125.
  • Review Article: Rehabilitation Programs in the Management of Patients with Parkinson's DiseaseCedarbaum J, Toy L, Silvestri M, Green-Parsons A, Harts A, McDowell F. Review Article: Rehabilitation Programs in the Management of Patients with Parkinson's Disease Neurorehabilitation And Neural Repair 1992, 6: 7-19. DOI: 10.1177/136140969200600102.
  • L-Deprenyl, Levodopa Pharmacokinetics, and Response Fluctuations in Parkinson's Disease.Cedarbaum J, Silvestri M, Clark M, Harts A, Kutt H. L-Deprenyl, Levodopa Pharmacokinetics, and Response Fluctuations in Parkinson's Disease. Clinical Neuropharmacology 1990, 13: 269. DOI: 10.1097/00002826-199006000-00014.
  • Controlled-release SinemetCedarbaum J, Kutt H, McDowell F. Controlled-release Sinemet Neurology 1987, 37: 1567-1567. DOI: 10.1212/wnl.37.9.1567-a.
  • Effect of Supplemental Carbidopa on Bioavailability of l-dopaCedarbaum J, Kutt H, Dhar A, Watkins S, Mc Dowell F. Effect of Supplemental Carbidopa on Bioavailability of l-dopa Neurology 1985, 35: 711-711. DOI: 10.1212/wnl.35.5.711.
  • Parkinson's disease: Biochemistry, clinical pathology and treatment By W. Birkmayer and P. Riederer (translated by Gavin Reynolds with the assistance of Karl Blau and Lindsay Reynolds) New York, Springer‐Verlag, 1983 160 pp, illustrated, $39.00Cedarbaum J. Parkinson's disease: Biochemistry, clinical pathology and treatment By W. Birkmayer and P. Riederer (translated by Gavin Reynolds with the assistance of Karl Blau and Lindsay Reynolds) New York, Springer‐Verlag, 1983 160 pp, illustrated, $39.00 Annals Of Neurology 1984, 16: 625-626. DOI: 10.1002/ana.410160523.
  • CENTRAL NORADRENERGIC NEURONS: INTERACTION OF AUTOREGULATORY MECHANISMS WITH EXTRINSIC INFLUENCESAghajanian G, Cedarbaum J. CENTRAL NORADRENERGIC NEURONS: INTERACTION OF AUTOREGULATORY MECHANISMS WITH EXTRINSIC INFLUENCES 1979, 619-621. DOI: 10.1016/b978-1-4832-8363-0.50188-9.