R&D Pipeline (As of Apr 2018) Underlined items indicate changes from the previous announcement on Jan 31, 2018.
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1 R&D Pipeline (As of Apr 2018) Underlined items indicate changes from the previous announcement on Jan 31, Oncology (1/2) MDV3100 enzalutamide Androgen receptor inhibitor Castration-resistant prostate cancer (Tablet) Approved (Feb. 2018) / Japan Pfizer New formulation Non-metastatic castration-resistant prostate cancer Filed (Jan. 2018) / US, Europe New indication Prostate cancer in patients with non-metastatic biochemical P-III / US, Europe, Asia New indication recurrence Metastatic hormone-sensitive prostate cancer New indication 55 ASP3550 degarelix AMG 103 blinatumomab ASP2215 gilteritinib GnRH antagonist Prostate cancer (3-month formulation) Filed (Nov. 2017) / Japan Injection Ferring New formulation Anti-CD19 BiTE antibody Acute lymphoblastic leukemia Filed (Jan. 2018) / Japan Injection Amgen with Amgen Astellas) FLT3/AXL inhibitor Relapsed or refractory acute myeloid leukemia Post-chemo maintenance acute myeloid leukemia Filed (Mar. 2018) / US, Japan Post-HSCT maintenance acute myeloid leukemia Newly diagnosed acute myeloid leukemia with low intensity induction of chemotherapy P-II/III / US, Europe, Japan, Asia IMAB362 zolbetuximab Anti-Claudin 18.2 Newly diagnosed acute myeloid leukemia with high intensity induction of chemotherapy P-I / US, Japan Gastric and gastroesophageal junction adenocarcinoma Injection (Ganymed) AGS-16C3F ADC targeting ENPP3 Renal cell carcinoma, Europe Injection (ADC technology in-licensed from Seattle Genetics) ASG-22ME enfortumab vedotin ADC targeting nectin-4 Urothelial cancer, Europe, Japan, Asia P-I / Japan Injection with Seattle Genetics) AGS67E Lymphoid malignancies P-I Injection (ADC technology in-licensed from Seattle Genetics)
2 Oncology (2/2) AGS62P1 Acute myeloid leukemia P-I Injection (ADC technology, EuCODE license from Ambrx) ASP8374/PTZ-201 Cancer P-I Injection Option agreement with Potenza Updates from the previous announcement (Jan. 2018): MDV3100 (enzalutamide): Approval of the tablet formulation for CRPC obtained in Japan in Feb ASP2215 (gilteritinib): Applications of market approval for FLT 3 mutation-positive relapsed or refractory acute myeloid leukemia were submitted in Japan and US in Mar
3 Urology and Nephrology YM905 solifenacin Muscarine M 3 receptor antagonist Neurogenic detrusor overactivity in pediatric patients Approved (Feb. 2018) / Europe Filed (Feb. 2017) / US Licensor* Remarks New indication EB178 solifenacin/ mirabegron ASP1517 (FG-4592) roxadustat Combination therapy of solifenacin and mirabegron HIF stabilizer Overactive bladder with symptoms of urge urinary incontinence, urgency, and urinary frequency Anemia associated with chronic kidney disease in patients not on dialysis and on dialysis Filed (Jun. 2017) / US P-III / Europe P-III / Japan FibroGen YM178 mirabegron Beta 3 receptor agonist Neurogenic detrusor overactivity in pediatric patients P-III / Europe New indication YM311 (FG-2216) HIF stabilizer Renal anemia P-II / Europe P-I / Japan FibroGen ASP8232 VAP-1 inhibitor Diabetic kidney disease P-II / Europe 57 ASP6294 ASP8302 Nerve Growth Factor (NGF) neutralization antibody Muscarine M 3 receptor positive allosteric modulator Bladder pain syndrome / Interstitial cystitis P-II / Europe Injection Underactive bladder P-II / Europe, Japan ASP7713 Underactive bladder P-I MA-0217 Acute kidney injury P-I Injection (Mitobridge) Update from the previous announcement (Jan. 2018): YM905 (solifenacin): Approval for neurogenic detrusor overactivity in pediatric patients obtained in EU in Feb 2018.
4 58 Immunology and Neuroscience FK506 tacrolimus ASP015K peficitinib ASKP1240 bleselumab ASP8062 ASP0819 ASP4070 (JRC2-LAMP-vax) ASP5094 ASP4345 Immunosuppressant Prevention of rejection after organ transplantation Filed (Jul. 2017) / US New formulation (Granule formulation in pediatric use) JAK inhibitor Rheumatoid arthritis P-III / Japan, Asia, Europe Anti-CD40 GABA B receptor positive allosteric modulator Calcium 2+ -activated K + channel opener DNA vaccine for Japanese red cedar Anti-alpha-9 integrin Dopamine D 1 receptor positive allosteric modulator Recurrence of focal segmental glomerulosclerosis in de novo kidney transplant recipients Injection Kyowa Hakko Kirin Fibromyalgia Fibromyalgia Pollinosis caused by Japanese red cedar P-II / Japan Injection Immunomic Rheumatoid arthritis P-II / Japan Injection Cognitive impairment associated with schizophrenia ASP0892 Peanut allergy P-I Injection Immunomic ASP1807 (CC8464) Neuropathic pain P-I Chromocell ASP6981 Cognitive impairment associated with schizophrenia P-I Update from the previous announcement (Jan. 2018): ASP1707: Discontinued phase 2 program for rheumatoid arthritis because phase 2 study did not meet its primary endpoint.
5 Others Licensor* Remarks AMG 785 romosozumab ipragliflozin/ sitagliptin ASP1941 ipragliflozin ASP0456 linaclotide Anti-Sclerostin Fixed dose combination of ipragliflozin and sitagliptin Osteoporosis for those at high risk of fracture Filed (Dec. 2016) / Japan Injection Amgen with Amgen Astellas) Type 2 diabetes Approved (Mar 2018) / Japan with MSD and Kotobuki) SGLT2 inhibitor Type 1 diabetes Filed (Jan. 2018) / Japan with Kotobuki) New indication Guanylate cyclase-c receptor Chronic constipation Filed (Sep. 2017) / Japan Ironwood New indication agonist fidaxomicin Macrocyclic antibiotic Infectious enteritis (bacterial target: Clostridium difficile ) Filed (Jul. 2017) / Japan Merck 59 ESN364 fezolinetant CK reldesemtiv Clostridium difficile infection in pediatric patients P-III / Europe New indication NK3 receptor antagonist Menopause-related vasomotor symptoms (Ogeda) Fast skeletal troponin activator Spinal muscular atrophy Chronic obstructive pulmonary disease Cytokinetics Amyotrophic lateral sclerosis ASP7317 Cell therapy (Retinal pigment epithelium cell) Dry age-related macular degeneration, Stargardt s macular degeneration Injection (Astellas Institute for Regenerative Medicine) MA-0211 Duchenne muscular dystrophy P-I (Mitobridge) Updates from the previous announcement (Jan. 2018): ipragliflozin/sitagliptin: Approval for the fixed dose combination of ipragliflozin and sitagliptin for Type 2 diabetes obtained in Japan in Mar ASP0113: Discontinued the phase 3 program for cytomegalovirus reactivation in hematopoietic cell transplant recipients because phase 3 study did not meet its primary endpoint. ASP1707: Discontinued the phase 2 program for endometriosis due to the comprehensive consideration including strategic prioritization.
*Compounds with "In-house" in this column include ones discovered by collaborative research.
AGS67E Lymphoid malignancies P-I Injection In-house (ADC technology in-licensed from Seattle Genetics) AGS62P1 Acute myeloid leukemia P-I Injection In-house (ADC technology, EuCODE license from Ambrx)
R&D Pipeline (As of Jul 2018) Underlined items indicate changes from the previous announcement on Apr 26, 2018.
R&D Pipeline (As of Jul 2018) Underlined items indicate changes from the previous announcement on Apr 26, 2018. Oncology (1/2) MDV3100 enzalutamide (XTANDI ) Androgen receptor inhibitor Non-metastatic
R&D Pipeline (As of April 2017)
R&D Pipeline (As of April 2017) Underlined items indicate changes from the previous announcement on January 31, 2017. Oncology (1/2) MDV3100 enzalutamide Androgen receptor inhibitor Metastatic castration-resistant
R&D Pipeline (As of Oct 2018) Underlined items indicate changes from the previous announcement on July 27, 2018.
R&D Pipeline (As of Oct 2018) Underlined items indicate changes from the previous announcement on July 27, 2018. Oncology (1/2) enzalutamide MDV3100 (XTANDI ) Androgen receptor inhibitor Non-metastatic
R&D Pipeline (As of July 2016) 1. Global Development Underlined items indicate for changes from the previous announcement on May 11, (1) Regulat
R&D Pipeline (As of July 2016) 1. Global Development Underlined items indicate for changes from the previous announcement on May 11, 2016. (1) Regulatory decision *Compounds with "" in this column include
R&D Pipeline (May 2014) 1. Global Development (1) Approved Product Name (Approval Date) Classification Target Disease Area * MDV3100 enzalutamide XTAN
R&D Pipeline (May 2014) 1. Global Development (1) Approved Product Name (Approval Date) Classification Target Disease Area * MDV3100 enzalutamide XTANDI (Mar. 2014) Androgen receptor inhibitor
(2) Phase-lll / Phase-ll (2/3) ASP7487 (OSI-906) linsitinib IGF-1R/IR tyrosine kinase inhibitor Adrenocortical carcinoma Ovarian cancer, Non-small cel
R&D Pipeline (February 2012) 1. Global Development (1) Filed YM178 mirabegron Beta 3 receptor agonist Overactive bladder associated with symptoms of urgency, urinary frequency, and urge urinary incontinece
(3) Phase-lll / Phase-ll (1/3) Stage in the most advanced territory EC905 solifenacin/ tamsulosin Concomitant use of solifenacin and tamsulosin Lower
R&D Pipeline (November 2011) 1. Global Development (1) Approved telavancin Product Name (Approval Date) VIBATIV (Sep. 2011) Classification Lipoglycopeptide antibiotic Therapeutic Target Treatment of adults
R&D Pipeline (May 2010)
R&D Pipeline (May 2010) 1 Global development (1) Filed Stage in the Most Advanced Territory YM617 tamsulosin Alpha-1 receptor antagonist Lower urinary tract syndrome in male patients (June 2007) New indication
R&D Pipeline (May 2006)
R&D Pipeline (May 2006) 1Japan (1)Approved Product Name (Code No) Vesicare (YM905) Funguard (FK463) (Approval Date ) solifenacin (April 2006) micafungin (April 2006) Urinary frequency, urinary incontinence
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