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Latest Major R&D Pipeline

Major R&D Pipeline

As of November 8, 2024
(Updated based on quarterly financial disclosure)

  • ¡ñ£ºDevelopment progress from July 2024 onwards¡¡¡¡¡ð£ºDevelopment progress from April 2024 onwards

Neurology

Dementia

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¡¡
DiseaseStudyRegionDevelopment Stage
¡¸Leqembi¡¹(lecanemab/BAN2401)¡¡Treatment for Alzheimer’s disease (AD)/ anti-Aβ protofibril antibody¡¡In-license (BioArctic AB)¡¡Injection (intravenous infusion, subcutaneous injection)¡¡Joint development with Biogen Inc.
Early AD 301 (Clarity AD) Asia (South Korea) ¡ð Approval (April 2024)
Great Britain ¡ñ Approval (August 2024)
Europe Submission
(accepted: January 2023)
IV maintenance dosing for early AD (Additional Dosage and Administration) 201£¯301 US ¡ð Submission (June 2024)
Maintenance dosing of a subcutaneous injection formulation for early AD (Additional Formulation) 301 US ¡ñ Completion of Rolling Submission (October 2024)
Preclinical AD 303 (AHEAD 3-45) Japan/US/Europe ±Ê¢ó
E2814¡¡anti-MTBR tau antibody¡¡Collaboration (University College London)¡¡Injection
Dominantly inherited AD (in combination with lecanemab) Tau Nexgen JP/US/EU ±Ê¢ò/¢ó
Dominantly inherited AD 103 US/EU ±Ê¢ñ²ú/¢ò
Sporadic early AD (in combination with lecanemab) 202 JP/US ¡ñ ±Ê¢ò
E2511¡¡TrkA integrated synapse regenerant ±õ²Ô-³ó´Ç³Ü²õ±ð¡¡°¿°ù²¹±ô
AD - US ±Ê¢ñ
E2025¡¡Anti-EphA4 antibody¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡±õ²ÔÂá±ð³¦³Ù¾±´Ç²Ô
AD - US ±Ê¢ñ

Neurological diseases other than dementia

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DiseaseStudyRegionDevelopment Stage
¡¸Fycompa¡¹(perampanel/E2007)¡¡Antiepileptic agent / AMPA receptor antagonist¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡°¿°ù²¹±ô / Injection
Adjunctive therapy for primary generalized tonic-clonic seizures (Additional Indication) 332 China ¡ð Approval (April 2024)
¡¸Dayvigo¡¹(lemborexant/E2006)¡¡Insomnia treatment / Orexin receptor antagonist¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡°¿°ù²¹±ô
Insomnia disorder 311 China Submission (accepted: January 2024)
¡¸Rozebalamin¡¹(mecobalamin/E0302)¡¡Treatment for Amyotrophic lateral sclerosis (ALS)¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡±õ²ÔÂá±ð³¦³Ù¾±´Ç²Ô
ALS JETALS (IIS) Japan ¡ñ Approval (September 2024)
lorcaserin/E2023¡¡Treatment for Dravet syndrome / serotonin 2C receptor agonist¡¡In-license (Arena Pharmaceuticals)¡¡Oral
Dravet syndrome 304 US ±Ê¢ó
E2086¡¡Orexin receptor agonist¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡°¿°ù²¹±ô
Narcolepsy - US ±Ê¢ñb
EA4017¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡°¿°ù²¹±ô
Chemotherapy-induced peripheral neuropathy (Development conducted by EA Pharma) - Japan ±Ê¢ñ

Oncology

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DiseaseStudyRegionDevelopment Stage
¡¸Lenvima/Kisplyx¡¹(lenvatinib/E7080)¡¡Anticancer agent / kinase inhibitor¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡°¿°ù²¹±ô
In combination with anti-PD-1 therapy pembrolizumab, joint development with Merck & Co., Inc., Rahway, NJ, USA, through an affiliate (Additional Indication)
Hepatocellular carcinoma (in combination with transcatheter arterial chemoembolization) / First-line LEAP-012 JP/US/EU/CH ±Ê¢ó
Esophageal carcinoma (in combination with chemotherapy) / First-line LEAP-014 JP/US/EU/CH ±Ê¢ó
Gastric cancer (in combination with chemotherapy) / First-line LEAP-015 JP/US/EU/CH ±Ê¢ó
In combination with anti-PD-1 antibody nivolumab, joint development with Ono Pharmaceutical (Additional Indication)
Hepatocellular carcinoma - Japan ±Ê¢ñb
¡¸Halaven¡¹(eribulin/E7389)¡¡Anticancer agent / microtubule dynamics inhibitor¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡±õ²ÔÂá±ð³¦³Ù¾±´Ç²Ô
Monotherapy (Additional Formulation)
Liposomal formulation - JP/EU ±Ê¢ñ
In combination with anti-PD-1 antibody nivolumab, joint development with Ono Pharmaceutical (Additional Formulation)
Liposomal formulation 120 Japan ±Ê¢ñ²ú/¢ò
¡¸Tasfygo¡¹(tasurgratinib/E7090)¡¡Anticancer agent / FGFR1, FGFR2, FGFR3 inhibitor¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡°¿°ù²¹±ô
Biliary tract cancer with FGFR2 gene fusion 201 Japan ¡ñ Approval (September 2024)
Breast cancer - Japan ±Ê¢ñb
farletuzumab ecteribulin£¨FZEC£©/MORAb-202¡¡Anticancer agent / Folate receptor α targeted antibody drug conjugate¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡±õ²ÔÂá±ð³¦³Ù¾±´Ç²Ô
Non-small cell lung cancer 203 US/EU ±Ê¢ò
Ovarian cancer, peritoneal cancer, fallopian tube cancer 205 JP/US/EU ±Ê¢ò
Solid tumors 201 US/EU ±Ê¢ñ/¢ò
BB-1701¡¡Anticancer agent / HER2 targeted antibody drug conjugate¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡±õ²ÔÂá±ð³¦³Ù¾±´Ç²Ô
Breast cancer 205 JP/US ±Ê¢ò
E7386¡¡Anticancer agent / CBP/β-catenin interaction inhibitor¡¡Collaboration (PRISM BioLab)¡¡Oral
Solid tumors (in combination with pembrolizumab) 201 JP/US/EU ±Ê¢ñ²ú/¢ò
Solid tumors - JP/US/EU ±Ê¢ñ
Solid tumors (in combination with lenvatinib) - JP/US/EU ±Ê¢ñb
H3B-6545¡¡Anticancer agent / ERα inhibitor¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡°¿°ù²¹±ô
Breast cancer (in combination with CDK4/6 inhibitor palbociclib) - US/EU ±Ê¢ñb
E7130¡¡ Anticancer agent¡¡Collaboration (Harvard University)¡¡Injection
Solid tumors - Japan ±Ê¢ñ
E7766¡¡Anticancer agent¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡±õ²ÔÂá±ð³¦³Ù¾±´Ç²Ô
Solid tumors - US/EU ±Ê¢ñb

Global Health

¡ù×óÓҤ˥¹¥¯¥í©`¥ë¤Ç¤­¤Þ¤¹

DiseaseSponsor of studyRegionDevelopment Stage
fosravuconazole/E1224¡¡Antifungal agent / ergosterol synthesis inhibitor¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡°¿°ù²¹±ô
Eumycetoma
*Supported by GHIT fund
*Eisai is mainly responsible for non-clinical studies and the provision of the investigational drug.
DNDi?Mycetoma Research Center of the University of Khartoum Sudan ±Ê¢òb/¢ó
SJ733¡¡Antimalarial agent / ATP4 inhibitor¡¡Co-development (University of Kentucky)¡¡Oral
Malaria
*Supported by GHIT fund
*Eisai is responsible for the provision of drug substance and formulation manufacturing
University of Kentucky Peru ±Ê¢ò
AWZ1066S¡¡Antifilarial agent / antiwolbachia mechanism Co-development (Liverpool School of Tropical Medicine)¡¡Oral
Lymphatic filariasis and onchocerciasis (river blindness)
*Supported by the GHIT Fund and Medical Research Council in the UK
*Eisai is responsible for the provision of drug substance and formulation manufacturing
Liverpool School of Tropical Medicine UK ±Ê¢ñ

Gastrointestinal Disorders

¡ù×óÓҤ˥¹¥¯¥í©`¥ë¤Ç¤­¤Þ¤¹

DiseaseStudyRegionDevelopment Stage
MOVICOL/(AJG555)¡¡Chronic constipation treatment / polyethylene glycol preparation¡¡In-license (Norgine)¡¡Oral
Chronic constipation in children under 2 years of age (Additional Dosage and Administration)¡¡(Development conducted by EA Pharma) CT3 Japan ±Ê¢ó
AJM347¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡°¿°ù²¹±ô
Inflammatory bowel disease (Joint development conducted by EA Pharma with Ensho Therapeutics, Inc) - EU ±Ê¢ñ
EA1080¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡°¿°ù²¹±ô
Inflammatory bowel disease (Joint development conducted by EA Pharma with Ensho Therapeutics, Inc) - EU ±Ê¢ñ
EA3571¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡°¿°ù²¹±ô
Metabolic dysfunction-associated steatohepatitis (Development conducted by EA Pharma) - Japan ±Ê¢ñ

Other

¡ù×óÓҤ˥¹¥¯¥í©`¥ë¤Ç¤­¤Þ¤¹

DiseaseStudyRegionDevelopment Stage
¡¸URECE¡¹(dotinurad / FYU-981)¡¡Treatment for Hyperuricemia and Gout / selective URAT1 inhibitor¡¡In-license (FUJI YAKUHIN)¡¡Oral
Gout, hyperuricemia - Asia (Thailand)

¡ñ

Approval (September 2024)
Gout 301 China Submission (accepted: January 2024)
E6742¡¡Treatment for Systemic lupus erythematosus / TLR 7/8 inhibitor¡¡±õ²Ô-³ó´Ç³Ü²õ±ð¡¡°¿°ù²¹±ô
Systemic lupus erythematosus 101 Japan ±Ê¢ñ/¢ò
E8001¡¡In house¡¡Injection
Rejection reaction associated with organ transplantation - Japan ±Ê¢ñ