Astellas Pharma Gelecekteki Büyüme

Future kriter kontrolleri 3/6

Astellas Pharma kazanç ve gelirin sırasıyla yıllık 25.6% ve 0.6% oranında artacağı tahmin edilmektedir. EPS'nin yıllık 26% oranında büyümesi beklenmektedir. Özkaynak kârlılığının 3 yıl içinde 11.9% olacağı tahmin edilmektedir.

Anahtar bilgiler

25.6%

Kazanç büyüme oranı

26.0%

EPS büyüme oranı

Pharmaceuticals kazanç büyümesi	21.5%
Gelir büyüme oranı	0.6%
Gelecekteki özkaynak getirisi	11.9%
Analist kapsamı	Good
Son güncelleme	25 Nov 2024

Gelecekteki son büyüme güncellemeleri

Recent updates

Kazanç ve Gelir Büyüme Tahminleri

DB:YPHA - Analistlerin gelecek tahminleri ve geçmiş finansal verileri (JPY Millions )
Tarih	Gelir	Kazançlar	Serbest Nakit Akışı	Faaliyetlerden Nakit	Avg. Analist Sayısı
3/31/2027	1,972,110	217,037	305,069	385,624	15
3/31/2026	1,853,429	143,323	309,061	339,335	16
3/31/2025	1,781,945	85,590	246,600	340,341	16
9/30/2024	1,772,155	54,746	125,654	200,804	N/A
6/30/2024	1,701,806	21,519	92,795	172,877	N/A
3/31/2024	1,603,672	17,045	100,981	172,475	N/A
12/31/2023	1,543,324	4,198	136,404	216,089	N/A
9/30/2023	1,523,572	38,090	151,562	236,992	N/A
6/30/2023	1,511,818	107,031	205,852	291,133	N/A
3/31/2023	1,518,619	98,714	239,438	327,767	N/A
12/31/2022	1,468,235	136,430	183,399	260,759	N/A
9/30/2022	1,406,682	148,911	214,107	257,916	N/A
6/30/2022	1,351,811	118,211	215,849	266,193	N/A
3/31/2022	1,296,163	124,086	205,277	257,444	N/A
12/31/2021	1,300,914	120,167	236,959	290,559	N/A
9/30/2021	1,285,714	119,360	248,993	331,268	N/A
6/30/2021	1,268,702	100,863	261,235	325,326	N/A
3/31/2021	1,249,528	120,589	229,402	306,843	N/A
12/31/2020	1,253,215	138,307	196,679	276,851	N/A
9/30/2020	1,265,853	139,722	146,751	235,299	N/A
6/30/2020	1,273,678	187,306	135,534	236,186	N/A
3/31/2020	1,300,843	195,411	144,110	221,998	N/A
12/31/2019	1,289,855	220,751	151,021	225,239	N/A
9/30/2019	1,309,722	246,925	182,693	248,203	N/A
6/30/2019	1,311,397	226,224	176,251	228,863	N/A
3/31/2019	1,306,348	222,265	206,502	258,630	N/A
12/31/2018	1,305,901	213,600	254,876	300,955	N/A
9/30/2018	1,307,658	186,429	265,976	309,442	N/A
6/30/2018	1,306,830	176,770	N/A	290,301	N/A
3/31/2018	1,300,316	164,679	N/A	312,614	N/A
12/31/2017	1,305,521	182,515	N/A	264,549	N/A
9/30/2017	1,299,746	185,754	N/A	260,795	N/A
6/30/2017	1,296,484	194,556	N/A	276,954	N/A
3/31/2017	1,311,665	218,701	N/A	235,612	N/A
12/31/2016	1,312,627	207,940	N/A	325,459	N/A
9/30/2016	1,336,878	205,818	N/A	308,800	N/A
6/30/2016	1,366,799	215,678	N/A	302,245	N/A
3/31/2016	1,372,706	193,687	N/A	313,737	N/A
12/31/2015	1,360,153	185,659	N/A	207,806	N/A
9/30/2015	1,340,307	168,805	N/A	182,815	N/A
6/30/2015	1,295,761	144,617	N/A	156,675	N/A
3/31/2015	1,247,259	135,856	N/A	187,686	N/A
12/31/2014	1,205,276	124,154	N/A	N/A	N/A
9/30/2014	1,177,660	112,663	N/A	224,809	N/A
6/30/2014	1,159,218	104,614	N/A	N/A	N/A
3/31/2014	1,139,909	90,874	N/A	214,257	N/A
12/31/2013	1,137,824	79,679	N/A	N/A	N/A

Analist Gelecek Büyüme Tahminleri

Kazançlar ve Tasarruf Oranları: YPHA 'nin tahmini kazanç büyümesi (yıllık 25.6% ) tasarruf oranının ( 1% ) üzerindedir.

Kazançlar ve Piyasa: YPHA şirketinin kazançlarının (yıllık 25.6% ) German pazarından (yıllık 20.9% ) daha hızlı büyümesi öngörülüyor.

Yüksek Büyüme Kazançları: YPHA şirketinin kazançlarının önümüzdeki 3 yıl içerisinde önemli ölçüde artması bekleniyor.

Gelir ve Pazar: YPHA şirketinin gelirinin (yıllık 0.6% ) German pazarından (yıllık 5.6% ) daha yavaş büyümesi öngörülüyor.

Yüksek Büyüme Geliri: YPHA şirketinin gelirinin (yıllık 0.6% ) yıllık 20% oranından daha yavaş büyümesi öngörülüyor.

Hisse Başına Kazanç Büyüme Tahminleri

Gelecekteki Özkaynak Getirisi

Gelecekteki ROE: YPHA 'nin Özsermaye Getirisi'nin 3 yıl içinde düşük olması tahmin ediliyor ( 11.9 %).

Astellas Pharma Gelecekteki Büyüme

Future kriter kontrolleri 3/6

Anahtar bilgiler

Gelecekteki son büyüme güncellemeleri

Astellas Pharma Inc. Revises Consolidated Earnings Guidance for the Year Ending March 31, 2024

Astellas Pharma Inc. Revises Consolidated Earnings Guidance on Full Basis for the Full-Year 2023

Astellas Pharma Inc. Reaffirms Consolidated Earnings Guidance for the Fiscal Year Ending March 31, 2023

Recent updates

Astellas Pharma Inc. Vyloy™ (Zolbetuximab-Clzb) Approved by U.S. Fda for Treatment of Advanced Gastric and Gej Cancer

Astellas Pharma Inc. to Report Q2, 2025 Results on Oct 30, 2024

Astellas Pharma Inc. to Report Q2, 2025 Results on Oct 30, 2024

Astellas Pharma Inc. Receives Approval from the European Commission for VYLOY in Combination with Chemotherapy for Advanced Gastric and Gastroesophageal Junction Cancer

Astellas Pharma Inc. to Present VEOZAH (fezolinetant) Data at 2024 Annual Meeting of The Menopause Society

European Commission Approves Astellas Pharma Inc.'s PADCEV in Combination with KEYTRUDA (Pembrolizumab) for First-Line Treatment of Advanced Urothelial Cancer

Astellas Pharma Inc. Initiates Phase 3 Clinical Study of Fezolinetant for VMS in Women with Breast Cancer Receiving Adjuvant Endocrine Therapy

Astellas Pharma Inc. Announces Center for Drug Evaluation of China's National Medical Products Administration Approves Padcev (Enfortumab Vedotin) for Treatment of Locally Advanced or Metastatic Urothelial Cancer

Astellas Pharma Inc. Receives Positive Chmp Opinion for Zolbetuximab in Combination with Chemotherapy for Treatment of Advanced Gastric and Gastroesophageal Junction Cancer

Astellas Pharma Inc. to Report Q1, 2025 Results on Aug 01, 2024

U.S. Food and Drug Administration Acknowledges Astellas Pharma Inc.’ Resubmission of Biologics License Application for Zolbetuximab and Sets New Action Date

Astellas Pharma Inc., Annual General Meeting, Jun 20, 2024

Astellas Pharma Inc. Announces European Commission Approval for Use in Additional Recurrent Early Prostate Cancer Treatment Setting

Astellas Pharma Inc. Revises Consolidated Earnings Guidance for the Year Ending March 31, 2024

Astellas Pharma Inc. to Report Fiscal Year 2024 Results on Apr 25, 2024

U.S. FDA Accepts Astellas’ Supplemental New Drug Application for Izervay (Avacincaptad Pegol Intravitreal Solution) for Geographic Atrophy

China's National Medical Products Administration Accepts Astellas and Pfizer's Supplemental Biologics License Application for Enfortumab Vedotin with Keytruda (Pembrolizumab) for First-Line Treatment of Advanced Bladder Cancer

Astellas Pharma Inc.'s Vyloy™? (zolbetuximab) Approves in Japan for Treatment of Gastric Cancer

Astellas Pharma Inc. Receives Positive CHMP Opinion for XTANDI™ in Additional Recurrent Early Prostate Cancer Treatment Setting

Astellas Pharma Initiates Phase 3 Clinical Studies of Fezolinetant for VMS Associated with Menopause in Japan

Astellas Pharma Inc. Announces Japan's Ministry of Health, Labour and Welfare Grants Priority Review for the Company's Supplemental New Drug Application (sNDA) for PADCEV with KEYTRUDA

Astellas Pharma Inc. Submits Supplemental New Drug Application in Japan for PADCEV with KEYTRUDA for First-Line Treatment of Advanced Bladder Cancer

European Medicines Agency Validates Type II Variation Application for PADCEV®? (enfortumab Vedotin) with KEYTRUDA®? (Pembrolizumab) for First-Line Treatment of Advanced Bladder Cancer

Astellas Pharma Inc. Provides Update on Zolbetuximab Biologics License Application in U.S

Astellas Pharma Inc. to Report Q3, 2024 Results on Feb 05, 2024

Astellas Pharma Inc. Announces EMA Recommends Arpraziquantel for Treatment of Schistosomiasis in Preschool-Aged Children

Astellas Pharma Inc. Announces That Its VEOZA™ (fezolinetant) Approved by European Commission for Treatment of Vasomotor Symptoms Associated with Menopause

Astellas Pharma US, Inc. Announces FDA Approves Expanded Use of CRESEMBA® (isavuconazonium sulfate) in Children with Invasive Aspergillosis and Invasive Mucormycosis

Astellas Pharma Inc. and Seagen Inc. Announces FDA Grants Priority Review for Supplemental Biologics License Application of Padcev with Keytruda for First-Line Treatment of Advanced Bladder Cancer

Astellas' Fezolinetant Reduces Frequency and Severity of VMS Associated with Menopause in Women Considered Unsuitable for Hormone Therapy

Pfizer and Astellas' Xtandi Approve by U.S. FDA in Earlier Prostate Cancer Treatment Setting

Seagen Inc. and Astellas Pharma Inc. Announces Results from the Phase 3 EV-302 Clinical Trial for PADCEV (Enfortumab Vedotin-Ejfv) in Combination with Keytruda (Pembrolizumab) Versus Chemotherapy

Astellas to Share New Data Across Hard-to-Treat Cancers During ESMO Congress 2023

Astellas Receives Positive Chmp Opinion for Veoza (Fezolinetant)

Astellas Pharma Inc. to Report Q2, 2024 Results on Nov 01, 2023

Astellas Pharma Inc. and Seagen Inc. Announces Positive Topline Results from the Phase 3 Ev-302 Clinical Trial

Astellas Pharma Inc. Announces China's National Medical Products Administration Accepts New Drug Application for Xtandi®? (Enzalutamide) in Metastatic Hormone-S Sensitive Prostate Cancer

Astellas Pharma Inc. Announces Positive 24-Month Topline Results from the Phase 3 GATHER2 Clinical Trial Evaluating the Efficacy and Safety of IZERVAY

European Medicines Agency Validates Type II Variation for Astellas' XTANDI (enzalutamide) for Treatment of Non-Metastatic Hormone-Sensitive Prostate Cancer with High-Risk Biochemical Recurrence

Sandoz AG completed the acquisition of Product Rights of MYCAMINE from Astellas Pharma Inc. (TSE:4503).

Sandoz AG completed the acquisition of Product Rights of MYCAMINE from Astellas Pharma Inc. (TSE:4503).

FDA Grants Priority Review for XTANDI in Non-Metastatic Castration-Sensitive Prostate Cancer with High-Risk Biochemical Recurrence

Astellas Pharma Inc. Announces European Medicines Agency Accepts for Regulatory Review the Marketing Authorization Application for Avacincaptad Pegol

U.S. FDA Accepts Astellas Pharma US, Inc.'s sNDA for CRESEMBA® (isavuconazonium sulfate) in Children

Astellas Pharma Inc. Announces the U.S. Food and Drug Administration Approves Izervay (Avacincaptad Pegol Intravitreal Solution) for the Treatment of Geographic At the 12-Month Primary Endpoint Across Two Phase 3 Clinical Trials

Astellas Pharma Inc. Revises Consolidated Earnings Guidance on Full Basis for the Full-Year 2023

China's National Medical Products Administration Accepts Astellas' Biologics License Application for Zolbetuximab

European Medicines Agency Accepts Astellas' Marketing Authorization Application for Zolbetuximab

Astellas Pharma Inc. to Report Q1, 2024 Results on Aug 01, 2023

Astellas Announces U.S. FDA Grants Priority Review for Zolbetuximab Biologics License Application

Astellas Pharma Inc. Announces Positive Topline Results from the Phase 3b DayLIGHT Clinical Trial for Fezolinetant

Astellas Pharma Inc. Confirms Unfavorable District Court Decision in Myrbetriq U.S. Patent Trial

Astellas Pharma Inc. Announces Submission of New Drug Application to Japan's Ministry of Health, Labour and Welfare for Zolbetuximab

Astellas' Veozah Tm (Fezolinetant) Approved by U.S. Fda for Treatment of Vasomotor Symptoms Due to Menopause

Astellas Pharma Inc. Provides Update on Fezolinetant New Drug Application in U.S

Astellas Pharma Inc. Reaffirms Consolidated Earnings Guidance for the Fiscal Year Ending March 31, 2023

Astellas Pharma Inc. Announces CEO Changes, Effective April 1, 2023

Sandoz AG agreed to acquire Product Rights of MYCAMINE from Astellas Pharma Inc. (TSE:4503).

Sandoz AG agreed to acquire Product Rights of MYCAMINE from Astellas Pharma Inc. (TSE:4503).

Astellas Announces Hold Lifted by FDA on FORTIS Clinical Trial of AT845 Investigational Treatment for Adult Patients with Late-Onset Pompe Disease

Astellas Pharma Inc. Presents Positive Findings from Phase 3 SPOTLIGHT Trial of Zolbetuximab during 2023 ASCO GI Cancers Symposium

Astellas Pharma Inc. Receives SBTi Approval for Revised Science-Based Climate Goals to Reduce Greenhouse Gas Emissions

Astellas Pharma Inc. to Report Q3, 2023 Results on Feb 06, 2023

Seagen, Astellas and Merck Announce FDA Acceptance of sBLAs for PADCEV® (enfortumab vedotin-ejfv) with KEYTRUDA® (pembrolizumab) for the First-Line Treatment of Certain Patients With Locally Advanced or Metastatic Urothelial Cancer

Astellas Pharma Inc. Announces Positive Topline Results from the Phase 3 GLOW Clinical Trial

Astellas Pharma Inc. Appoints Steve Sabus as Chief Commercial Officer

Astellas Announces Zolbetuximab Meets Primary Endpoint in Phase 3 SPOTLIGHT Trial as First-Line Treatment

Kazanç ve Gelir Büyüme Tahminleri

Analist Gelecek Büyüme Tahminleri

Hisse Başına Kazanç Büyüme Tahminleri

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