Eisai Clinical Trials

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An Open-Label Study To Evaluate the Pharmacodynamic Effects, Efficacy, Safety, and Tolerability of E2027 in Subjects With Dementia With Lewy Bodies or Parkinson’s Disease Dementia With or Without Amyloid Copathology

Registry #: NCT04764669

Protocol #: E2027-A001-203

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A Placebo-Controlled, Double-Blind, Parallel-Group, Randomized, Study To Evaluate the Efficacy, Safety and Tolerability of E2027 in Subjects With Dementia With Lewy Bodies

Registry #: NCT03467152, 2017-003728-64

Protocol #: E2027-G000-201

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A Phase 1/2 single-arm study evaluating the safety and efficacy of eribulin mesilate in combination with irinotecan in children with refractory or recurrent solid tumors

Registry #: NCT03245450, 2016-003352-67

Protocol #: E7389-G000-213

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A multicenter, uncontrolled, open-label study and extension study for verification of efficacy and safety for perampanel monotherapy in untreated patients with partial onset seizures (including secondarily generalized seizures)

Registry #: NCT03201900

Protocol #: E2007-J000-342

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A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Active Comparator, Parallel-Group Study of the Efficacy and Safety of Lemborexant in Subjects 55 Years and Older With Insomnia Disorder (SUNRISE 1)

Registry #: NCT02783729, EU CTR 2015-004347-39

Protocol #: E2006-G000-304

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A Long-Term Multicenter, Randomized, Double-Blind, Controlled, Parallel Group Study of the Safety and Efficacy of Lemborexant in Subjects With Insomnia Disorder (SUNRISE 2)

Registry #: NCT02952820, EU CTR 2015-001463-39

Protocol #: E2006-G000-303

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A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study With Open-Label Extension Phase of the Efficacy and Safety of Lemborexant in Subjects With Irregular Sleep-Wake Rhythm Disorder and Mild to Moderate Alzheimer’s Disease Dementia

Registry #: NCT03001557, 2017-003306-40

Protocol #: E2006-G000-202

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A Placebo-Controlled, Double-Blind, Parallel-Group, 24 Month Study With an Open-Label Extension Phase to Evaluate the Efficacy and Safety of Elenbecestat (E2609) in Subjects With Early Alzheimer’s Disease

Registry #: NCT02956486, EU CTR 2016-003928-23

Protocol #: E2609-G000-301

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A Placebo-Controlled, Double-Blind, Parallel-Group, Randomized, Proof-of-Concept, Dose-Finding Study To Evaluate Safety, Tolerability, and Efficacy of E2609 in Subjects With Mild Cognitive Impairment Due to Alzheimer’s Disease (Prodromal Alzheimer’s Disease) and Mild to Moderate Dementia Due to Alzheimer’s Disease

Registry #: NCT02322021, EU CTR 2014-002723-94

Protocol #: E2609-G000-202

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A Placebo-Controlled, Double-Blind, Parallel-Group, 24 Month Study With an Open-Label Extension Phase to Evaluate the Efficacy and Safety of Elenbecestat (E2609) in Subjects With Early Alzheimer’s Disease

Registry #: NCT02956486, EU CTR 2016-004128-42

Protocol #: E2609-G000-302

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A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group, Bayesian Adaptive Randomization Design, Dose Response Study of the Efficacy of E2006 in Adults and Elderly Subjects With Chronic Insomnia

Registry #: NCT01995838

Protocol #: E2006-G000-201

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An Open-Label, Single-Arm Multicenter Phase 1b/2 Study to Evaluate the Efficacy and Safety of Eribulin Mesylate in Combination With Pembrolizumab in Subjects With Metastatic Triple-Negative Breast Cancer (mTNBC)

Registry #: NCT02513472

Protocol #: E7389-M001-218

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A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Explore the Safety And Tolerability of Doses of E2007 up to a Maximum of 12 mg In Patients With Refractory Partial Seizures

Registry #: NCT00416195, EU CTR 2006-003702-26

Protocol #: E2007-G000-208

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A Multicenter, Randomized, Double-blind, Parallel-group, Placebo-controlled Study of E2020 in Patients With Dementia With Lewy Bodies (DLB), Followed by a Long-term Extension Phase

Registry #: NCT01278407

Protocol #: E2020-J081-341

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Double-blind Study of E2020 in Patients With Dementia With Lewy Bodies – Phase II

Registry #: NCT00543855

Protocol #: E2020-J081-431

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An Open-label Randomized Parallel Two-arm Multicenter Study of Eribulin Versus Vinorelbine in Female Subjects With Locally Recurrent or Metastatic Breast Cancer, Previously Treated With At Least Two and a Maximum of Five Prior Chemotherapy Regimens, Including an Anthracycline and a Taxane

Registry #: NCT02225470

Protocol #: E7389-C086-304

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A Phase 2, Open-Label, Single-Arm, Multicenter Study to Evaluate the Efficacy and Safety of Eribulin Mesylate Administered Biweekly (Q2W) for Subjects With Human Epidermal Growth Factor Receptor 2 (HER2)-Negative Metastatic Breast Cancer

Registry #: NCT02481050

Protocol #: E7389-M001-216

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A Long Term Extension Study of E2080 in Lennox-Gastaut Patients

Registry #: NCT01151540, EU CTR 2016-004953-34

Protocol #: E2080-J081-305

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A Placebo-Controlled, Double-Blind Comparative Study of E2080 in Lennox-Gastaut Syndrome Patients

Registry #: NCT01146951, EU CTR 2016-004952-30

Protocol #: E2080-J081-304

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The “EMBRACE” Trial: Eisai Metastatic Breast Cancer Study Assessing Physician’s Choice Versus E7389. A Phase III Open-Label, Randomized, Parallel, Two-arm, Multi-center Study of E7389 Versus “Treatment of Physician’s Choice” in Patients With Locally Recurrent, Metastatic Breast Cancer, Previously Treated With At Least Two and a Maximum of Five Prior Chemotherapy Regimens, Including an Anthracycline and a Taxane

Registry #: NCT00388726, EU CTR 2006-001949-34

Protocol #: E7389-G000-305

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Phase II Extension Study of E7389 for Locally Advanced or Metastatic Breast Cancer

Registry #: NCT00965523

Protocol #: E7389-J081-224

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A Phase III Open Label, Randomized Two-Parallel-Arm Multicenter Study of E7389 Versus Capecitabine in Patients With Locally Advanced or Metastatic Breast Cancer Previously Treated With Anthracyclines and Taxanes

Registry #: NCT00337103, EU CTR 2005-004009-26

Protocol #: E7389-G000-301

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A 24-week, Multicentre, Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy, Tolerability and Safety of Donepezil (Aricept) in Parkinson’s Disease Patients with Dementia.

Registry #: NCT00165815

Protocol #: E2020-E044-316

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Phase II Clinical Study of E7389 for Locally Advanced or Metastatic Breast Cancer

Registry #: NCT record obsolete. Reporting done in conjuction with study E7389-J081-224 (NCT00965523)

Protocol #: E7389-J081-221

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An Open-label Extension Study to Evaluate the Safety and Tolerability of Perampanel (E2007) Administered as an Adjunctive Therapy in Epilepsy Subjects

Registry #: NCT02427607, EU CTR 2016-004945-10

Protocol #: E2007-J000-341

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Double-Blind, Parallel-Group Comparison of 23 mg Donepezil Sustained Release (SR) to 10 mg Donepezil Immediate Release (IR) in Patients With Moderate to Severe Alzheimer’s Disease

Registry #: NCT00478205, EU CTR 2006-004888-54

Protocol #: E2020-G000-326

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Clinical efficacy and safety of donepezil on cognitive and global function in patients with Alzheimer’s disease. A 24-week, multicenter, double-blind, placebo-controlled study in Japan.

Registry #: Not available

Protocol #: E2020-J081-161

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A Randomized, Double-Blind, Placebo-Controlled Evaluation of the Effects of Donepezil Hydrochloride (E2020) in the Management of Patients with Alzheimer’s Disease in a Nursing Home Facility

Registry #: Not available

Protocol #: E2020-A001-311

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A Preliminary, Multi-Center, Randomized, Double-Blind, Placebo-Controlled Evaluation of the Safety and Efficacy of E2020 in Patients with Alzheimer’s Disease.

Registry #: Not available

Protocol #: E2020-A001-201

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A Multi-Center, Randomized, Double-Blind, Parallel Group Study With 3 Groups Receiving Placebo, 5 mg of E2020 and 10 mg of E2020

Registry #: NCT00165659

Protocol #: E2020-J081-231

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A 54-week, Randomized, Double-Blind, Placebo-Controlled Evaluation of the Effects of Donepezil Hydrochloride (E2020) on Functional Outcomes in Patients with Alzheimer’s Disease.

Registry #: Not available

Protocol #: E2020-A001-312

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A 30-Week, Multi-Center, Randomized, Double-Blind, Placebo-Controlled Evaluation of the Safety and Efficacy of E2020 in Patients with Alzheimer’s Disease.

Registry #: Not available

Protocol #: E2020-A044-304

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A 30-Week, Multi-Center, Randomized, Double-Blind, Placebo-Controlled Evaluation of the Safety and Efficacy of E2020 in Patients with Alzheimer’s Disease.

Registry #: Not available

Protocol #: E2020-A001-302

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A 24-weeks, Multi-center, Randomized, Double-blind, Placebo Controlled Study to Evaluate the Efficacy and Safety of Donepezil Hydrochloride in Chinese Subjects With Severe Alzheimer’s Disease

Registry #: NCT01404169

Protocol #: E2020-C086-339

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A 24 Week, Multicenter, Randomized, Double-Blind, Placebo-Controlled Evaluation of the Safety and Efficacy of Donepezil Hydrochloride (E2020) in Patients With Severe Alzheimer’s Disease Followed by a 12 Week Open-Label Extension Period

Registry #: NCT00096473

Protocol #: E2020-A001-315

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A 15-week, Multi-Center, Randomized, Double-Blind, Placebo-Controlled Evaluation of the Safety and Efficacy of E2020 in Patients with Alzheimer’s Disease.

Registry #: Not available

Protocol #: E2020-A001-301

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A Randomized, Double-blind, Placebo-controlled, Parallel-group Study With an Open-label Extension Phase to Evaluate the Effect of Perampanel (E2007) on Cognition, Growth, Safety, Tolerability, and Pharmacokinetics When Administered as an Adjunctive Therapy in Adolescents (12 to Less Than 18 Years of Age) With Inadequately Controlled Partial-onset Seizures

Registry #: NCT01161524, EU CTR 2010-018518-56

Protocol #: E2007-G000-235

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A Double-Blind, Placebo-Controlled, Dose-Escalation, Parallel-Group Study of E2007 Given as Adjunctive Therapy in Patients With Refractory Partial Seizures

Registry #: NCT00144690, EU CTR 2005-004199-18

Protocol #: E2007-A001-206

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A Double-Blind, Placebo-Controlled, Dose-Escalation, Parallel-Group Study to Evaluate the Efficacy and Safety of E2007 (perampanel) Given as Adjunctive Therapy in Subjects With Refractory Partial Seizures

Registry #: NCT00700310, EU CTR 2007-006169-33

Protocol #: E2007-G000-306

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A Double-Blind, Placebo-Controlled, Dose-Escalation, Parallel-Group Study to Evaluate the Efficacy and Safety of E2007 (Perampanel) Given as Adjunctive Therapy in Subjects With Refractory Partial Seizures

Registry #: NCT00699582, EU CTR 2007-006168-31

Protocol #: E2007-G000-305

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A Double-Blind, Placebo-Controlled, Dose-Escalation, Parallel-Group Study to Evaluate the Efficacy and Safety of E2007 (Perampanel) Given as Adjunctive Therapy in Subjects With Refractory Partial Seizures

Registry #: NCT00699972, EU CTR 2007-006191-11

Protocol #: E2007-G000-304

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A Study With an Open-label Extension Phase to Evaluate the Efficacy and Safety of Perampanel (E2007) Administered as an Adjunctive Therapy in Subjects With Refractory Partial-onset Seizures

Registry #: NCT01618695

Protocol #: E2007-J000-335

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Study of Lenvatinib (E7080) in Participants With Advanced Hepatocellular Carcinoma (HCC)

Registry #: NCT00946153

Protocol #: E7080-J081-202

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A Multicenter, Open-Label, Phase 3 Trial to Compare the Efficacy and Safety of Lenvatinib (E7080) Versus Sorafenib in First-Line Treatment of Subjects With Unresectable Hepatocellular Carcinoma

Registry #: NCT01761266, EU CTR 2012-002992-33

Protocol #: E7080-G000-304

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An Open-label, Multicenter, Phase 2 Study to Evaluate the Efficacy and Safety of Eribulin Mesylate in Previously Treated Subjects With Advanced or Metastatic Soft Tissue Sarcoma

Registry #: NCT01458249

Protocol #: E7389-J081-217

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Phase II Study of E7389 Administered as an IV Bolus Infusion Day 1 and Day 8 Every 3 Weeks in Pre-Treated Patients With Advanced and/or Metastatic Soft Tissue Sarcoma

Registry #: NCT00413192, EU CTR 2005-004272-20

Protocol #: E7389-E044-207

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A Randomized, Open-label, Multicenter, Phase 3 Study to Compare the Efficacy and Safety of Eribulin With Dacarbazine in Subjects With Soft Tissue Sarcoma

Registry #: NCT01327885, EU CTR 2010-024483-17

Protocol #: E7389-G000-309

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A Multicenter, Randomized, Controlled, Open-label Study to Evaluate the Cognitive Development Effects and Safety, and Pharmacokinetics of Adjunctive Rufinamide Treatment in Pediatric Subjects 1 to Less Than 4 Years of Age With Inadequately Controlled Lennox-Gastaut Syndrome

Registry #: NCT01405053, EU CTR 2010-023505-36

Protocol #: E2080-G000-303

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An Open-Label, Multicenter, Phase 1b/2 Study of E7080 Alone, and in Combination With Everolimus in Subjects With Unresectable Advanced or Metastatic Renal Cell Carcinoma Following One Prior VEGF-Targeted Treatment

Registry #: NCT01136733, EU CTR 2010-019484-10

Protocol #: E7080-G000-205 Ph2

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An Open-Label, Multicenter, Phase 1b/2 Study of E7080 Alone, and in Combination With Everolimus in Subjects With Unresectable Advanced or Metastatic Renal Cell Carcinoma Following One Prior VEGF-Targeted Treatment

Registry #: NCT01136733, EU CTR 2010-019484-10

Protocol #: E7080-G000-205 Ph1b

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A Phase 1 Study of E7080 in Subjects With Solid Tumor

Registry #: NCT01268293

Protocol #: E7080-J081-105

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An Open Label Phase I Dose Escalation Study of E7080 Administered to Patients With Solid Tumors

Registry #: NCT00280397

Protocol #: E7080-J081-103

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A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase 3 Trial of Lenvatinib (E7080) in 131I-Refractory Differentiated Thyroid Cancer

Registry #: NCT01321554, EU CTR 2010-023783-41

Protocol #: E7080-G000-303

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A Double-blind, Randomized, Placebo-controlled, Multicenter Study to Evaluate the Efficacy and Safety of Adjunctive Perampanel in Primary Generalized Tonic Clonic Seizures

Registry #: NCT01393743, EU CTR 2011-000265-12

Protocol #: E2007-G000-332 EXT

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A Double-blind, Randomized, Placebo-controlled, Multicenter Study to Evaluate the Efficacy and Safety of Adjunctive Perampanel in Primary Generalized Tonic Clonic Seizures

Registry #: NCT01393743, EU CTR 2011-000265-12

Protocol #: E2007-G000-332 CORE

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A Phase 2 Study of E7080 in Subjects With Advanced Thyroid Cancer

Registry #: NCT01728623

Protocol #: E7080-J081-208

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Phase II, Multicenter, Open-label, Single Arm Trial to Evaluate the Safety and Efficacy of Oral E7080 in Medullary and Iodine-131 Refractory, Unresectable Differentiated Thyroid Cancers, Stratified by Histology

Registry #: NCT00784303, EU CTR 2007-005933-12

Protocol #: E7080-G000-201

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