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2024.
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- Dec.27.2024 R & D
- Ono Receives Supplemental Approval of Opdivo® in Combination with Cisplatin and Gemcitabine for Treatment of Unresectable Urothelial Carcinoma in Japan
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- Dec.25.2024 R & D
- Bristol Myers Squibb Receives European Commission Approval for Opdivo (nivolumab) plus Yervoy (ipilimumab) for the First-Line Treatment of Adult Patients with Microsatellite Instability–High or Mismatch Repair Deficient Metastatic Colorectal Cancer
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- Dec.24.2024 Sustainability
- ONO Earned Top Score in the Pharmaceutical Sector of the Dow Jones Sustainability Index Selected for the World Index and Asia Pacific Index for Five Straight Years
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- Dec.23.2024 R & D
- U.S. FDA Approves Pfizer’s BRAFTOVI® Combination Regimen as First-Line Treatment of BRAF V600E-Mutant Metastatic Colorectal Cancer
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- Dec.10.2024 R & D
- SK Biopharmaceuticals’ Cenobamate Demonstrates Clinical Efficacy and Safety in Epilepsy Patients across Korea, China and Japan
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- Dec.03.2024 Licensing
- Ono Enters into Drug Discovery Collaboration Agreement with Congruence Therapeutics to Generate Novel Small Molecule Correctors in the Oncology Area
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- Nov.18.2024 R & D
- Bristol Myers Squibb Receives Positive CHMP Opinion for Opdivo® (nivolumab) plus Yervoy® (ipilimumab) for the First-Line Treatment of Adult Patients with Microsatellite Instability–High or Mismatch Repair Deficient Metastatic Colorectal Cancer
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- Oct.31.2024 Management / Finance
- Revisions of Consolidated Financial Forecasts and Introduction of Core Basis in Financial Results
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- Oct.31.2024 Management / Finance
- Announcement on Financial Results for FY2024 Q2
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- Oct.15.2024 Corporate
- Notice on the Recipients of the “Osamu Hayaishi Memorial Scholarship for Study Abroad” of the FY2025 Japanese Biochemical Society
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- Oct.10.2024 Licensing
- Ono Enters into License Agreement for LCB97, an Antibody-Drug Conjugate, and Research Collaboration and License Agreement to generate novel ADC candidates by leveraging ConjuAll™ ADC platform with LigaChem Biosciences
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- Oct.10.2024 R & D
- Opdivo® Intravenous Infusion Approved in Taiwan in Combination with Cisplatin and Gemcitabine for the First-Line Treatment of Adult Patients with Unresectable or Metastatic Urothelial Carcinoma
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- Oct.07.2024 R & D
- U.S. Food and Drug Administration Approves Perioperative Treatment of Neoadjuvant Opdivo® (nivolumab) and Chemotherapy Followed by Surgery and Adjuvant Single-Agent Opdivo for Resectable Non-Small Cell Lung Cancer (NSCLC)
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- Sep.18.2024 R & D
- Bristol Myers Squibb Presents Landmark 10-Year Follow-Up Data from CheckMate -067 Which Showed Continued Durable Long-Term Survival Benefit with Opdivo® plus Yervoy® in Advanced Melanoma
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- Sep.12.2024 R & D
- Ono and Bristol-Myers Squibb KK Submit Supplemental Application of Opdivo and Yervoy in Combination Treatment in Japan to Expand the Use for Unresectable Advanced or Recurrent Microsatellite Instability-High Colorectal Cancer
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- Aug.23.2024 R & D
- Bristol Myers Squibb Receives U.S. Food and Drug Administration sBLA Acceptance for First-Line Treatment of Unresectable Hepatocellular Carcinoma
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- Aug.20.2024 Sustainability
- Ono Selected for ESG Investment Indexes Adopted by GPIF
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- Aug.16.2024 R & D
- U.S. Food and Drug Administration Accepts for Priority Review Deciphera’s New Drug Application for Vimseltinib for the Treatment of Patients with Tenosynovial Giant Cell Tumor (TGCT)
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- Aug.09.2024 R & D
- Ono and Bristol-Myers Squibb KK Submit Supplemental Application of Opdivo and Yervoy in Combination Treatment in Japan to Expand the Use for Unresectable Hepatocellular Carcinoma
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- Aug.08.2024 Sustainability
- Ono Supports TNFD Recommendations and Discloses Information Aligned with TNFD Framework
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- Aug.01.2024 Licensing
- Ono Enters into a New Option and Research Collaboration Agreement with Monash University to Discover and Create New Anti-GPCR Antibodies in the Autoimmune and Inflammatory Diseases
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- Jul.31.2024 Management / Finance
- Announcement on Financial Results for FY2024 1Q
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- Jul.22.2024 R & D
- Bristol Myers Squibb Receives European Medicines Agency Validation of Application for Opdivo (nivolumab) plus Yervoy (ipilimumab) for First-Line Treatment of Unresectable or Advanced Hepatocellular Carcinoma
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- Jul.19.2024 R & D
- European Medicines Agency Accepts Deciphera’s Marketing Authorization Application for Vimseltinib for Treatment of Patients with Tenosynovial Giant Cell Tumor (TGCT)
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- Jul.18.2024 R & D
- Opdivo® Intravenous Infusion Approved in South Korea in Combination with Cisplatin and Gemcitabine for the First-Line Treatment of Patients with Unresectable or Metastatic Urothelial Carcinoma
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- Jul.12.2024 Management / Finance
- Notice concerning Completion of Disposal of Treasury Shares as Tenure-based Restricted Stock Compensation and Performance-linked Restricted Stock Compensation
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- Jun.25.2024 R & D
- European Medicines Agency Validates Bristol Myers Squibb’s Application for Subcutaneous Nivolumab
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- Jun.20.2024 Management / Finance
- Notice of Disposal of Treasury Shares as Tenure-based Restricted Stock Compensation and Performance-linked Restricted Stock Compensation
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- Jun.11.2024 Corporate
- Ono Announces Results of Tender Offer to Acquire Deciphera Pharmaceuticals and Completion of Acquisition of Deciphera (a Wholly Owned Subsidiary of Ono)
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- Jun.05.2024 R & D
- Bristol Myers Squibb Announces Opdivo (nivolumab) Plus Yervoy (ipilimumab) Significantly Improved Overall Survival Compared to Lenvatinib or Sorafenib as First-Line Treatment for Patients with Advanced Hepatocellular Carcinoma in CheckMate -9DW Trial
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- Jun.04.2024 R & D
- Bristol Myers Squibb Presents Multiple New Analyses at 2024 ASCO Annual Meeting Highlighting Opdivo and Opdivo-based Combinations in Earlier and Advanced Stages of Non-Small Cell Lung Cancer
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- Jun.04.2024 R & D
- Bristol Myers Squibb Receives European Commission Approval for Opdivo® (nivolumab) in Combination with Cisplatin and Gemcitabine for the First-Line Treatment of Adult Patients with Unresectable or Metastatic Urothelial Carcinoma
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- May.23.2024 R & D
- Bristol Myers Squibb Announces Updated Action Date by the U.S. Food and Drug Administration for Subcutaneous Nivolumab (nivolumab and hyaluronidase)
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- May.17.2024 R & D
- Ono Receives Approvals of BRAFTOVI® and MEKTOVI® for Expanded Use for Two New Indications in Japan
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- May.13.2024 R & D
- Bristol Myers Squibb Provides Update on Phase 3 CheckMate -73L Trial
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- May.09.2024 Management / Finance
- Announcement on Financial Results for FY2023
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- May.09.2024 Management / Finance
- Notice regarding Differences in the Non-consolidated Financial Results between the Fiscal Year Ended March 31, 2024 and the Previous Fiscal Year
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- May.08.2024 R & D
- European Medicines Agency Validates Bristol Myers Squibb’s Application for Opdivo (nivolumab) Plus Yervoy (ipilimumab) for the First-Line Treatment of Adult Patients with Microsatellite Instability–High or Mismatch Repair Deficient Metastatic Colorectal Cancer
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- May.07.2024 R & D
- U.S. Food and Drug Administration Accepts Bristol Myers Squibb’s Application for Subcutaneous Nivolumab (nivolumab and hyaluronidase)
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- May.07.2024 R & D
- CHMP Adopts Positive Opinion Recommending Approval of Bristol Myers Squibb’s Opdivo® (nivolumab) in Combination with Cisplatin and Gemcitabine for the First-Line Treatment of Adult Patients with Unresectable or Metastatic Urothelial Carcinoma
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- Apr.30.2024 Corporate
- ONO Enters into a Definitive Agreement to Acquire Deciphera Pharmaceuticals
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- Apr.25.2024 Licensing
- Ono Enters into a Collaboration Agreement with PRISM BioLab to Generate Novel Drug Candidates in the Oncology Area
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- Apr.10.2024 Corporate
- Support for Earthquake Relief Efforts in Eastern Taiwan
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- Apr.05.2024 Corporate
- Announcement on Changes of the Board of Directors, Audit & Supervisory Board Members and Corporate Officers
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- Mar.29.2024 Management / Finance
- Ono Announces Completion of Cancellation of Treasury Stock
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- Mar.27.2024 Corporate
- Ono Announces General Sponsorship for the “Theme Weeks” as Bronze Partner, at the Expo 2025 Osaka, Kansai, Japan
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- Mar.22.2024 Licensing
- Ono Enters into Comprehensive Drug Discovery Collaboration Agreement with University of Oxford
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- Mar.21.2024 R & D
- ONO PHARMA Announces Enrollment is Complete for the First Arm of the PROSPECT Study of Tirabrutinib in U.S. Patients with Relapsed or Refractory PCNSL
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- Mar.21.2024 R & D
- Bristol Myers Squibb Announces CheckMate -9DW Trial Evaluating Opdivo (nivolumab) Plus Yervoy (ipilimumab) Meets Primary Endpoint of Overall Survival for the First-Line Treatment of Advanced Hepatocellular Carcinoma
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- Mar.14.2024 Licensing
- Ono Enters into a Collaboration Agreement with Sibylla Biotech to Generate Novel Drug Candidates for Neurological Disorders
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- Mar.12.2024 R & D
- U.S. Food and Drug Administration Approves Opdivo® (nivolumab), in Combination with Cisplatin and Gemcitabine, for First-Line Treatment of Adult Patients with Unresectable or Metastatic Urothelial Carcinoma
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- Mar.11.2024 Sustainability
- Ono Selected as "2024 Health & Productivity Stock"
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- Mar.11.2024 Licensing
- ONO Enters into a University-Wide, Research Alliance Agreement with Harvard University
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- Mar.06.2024 Licensing
- Ono Enters into a License Agreement with NEX-I to Develop and Commercialize NXI-101
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- Mar.05.2024 Corporate
- ONO Receives Excellence Award at the Nikkei Integrated Report Award 2023
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- Mar.04.2024 Management / Finance
- Ono Announces Status and Completion of Acquisition of Own Shares
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- Mar.01.2024 Management / Finance
- Ono Announces Status of Acquisition of Own Shares
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- Feb.21.2024 Licensing
- Ono Enters into a Drug Discovery Collaboration Agreement with EME Aiming at the Generation of Novel VHH Antibody Drugs
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- Feb.19.2024 Licensing
- Ono Enters into a Research Collaboration Agreement with InveniAI to Identify Novel Therapeutic Targets
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- Feb.14.2024 Licensing
- ONO Enters into an Option and Collaboration Agreement with Numab to Develop Multi-specific Antibody NM49
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- Feb.13.2024 Licensing
- Ono Enters into a Drug Discovery Collaboration and Option Agreement with Shattuck Labs to Generate Bifunctional Fusion Proteins
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- Feb.09.2024 R & D
- ONO Receives Supplemental Approval of Opdivo® in Japan for Expanded Use for Treatment of Unresectable Advanced or Recurrent Malignant Epithelial Tumors
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- Feb.08.2024 R & D
- Bristol Myers Squibb Announces Acceptance of U.S. and EU Regulatory Filings for Neoadjuvant Opdivo (nivolumab) and Chemotherapy Followed by Surgery and Adjuvant Opdivo in Resectable Non-Small Cell Lung Cancer
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- Feb.07.2024 Sustainability
- ONO Selected as Highest Rating A-List Company by CDP in Two Categories of “Climate Change” and “Water Security” in CDP 2023
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- Feb.01.2024 Management / Finance
- Ono Announces Status of Acquisition of Own Shares
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- Jan.31.2024 Management / Finance
- Announcement on Financial Results for FY2023 3Q
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- Jan.29.2024 R & D
- Subcutaneous Nivolumab (nivolumab and hyaluronidase) Shows Noninferiority Compared to Intravenous Opdivo (nivolumab) in Advanced or Metastatic Clear Cell Renal Cell Carcinoma in CheckMate -67T Trial
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- Jan.23.2024 R & D
- Opdivo® (nivolumab) in Combination with CABOMETYX® (cabozantinib) Demonstrates Long-Term Survival Benefits After Four Years of Follow-Up in the CheckMate -9ER Trial in First-Line Advanced Renal Cell Carcinoma
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- Jan.23.2024 R & D
- Eight-Year Data for Opdivo (nivolumab) Plus Yervoy (ipilimumab) Continue to Demonstrate Longest Survival Benefit vs. Sunitinib Reported in Patients with Previously Untreated Advanced or Metastatic Renal Cell Carcinoma
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- Jan.22.2024 R & D
- Opdivo (nivolumab) Plus Yervoy (ipilimumab) Reduced the Risk of Disease Progression or Death by 79% Versus Chemotherapy in Patients with Microsatellite Instability–High or Mismatch Repair Deficient Metastatic Colorectal Cancer in CheckMate -8HW Trial
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- Jan.11.2024 Corporate
- Notice of Changes in Representative Directors
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- Jan.09.2024 Corporate
- Support for Disasters Caused by the 2024 Noto Peninsula Earthquake
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- Jan.09.2024 R & D
- Fate Therapeutics Announces Initiation of Phase 1 Clinical Trial for FT825 / ONO-8250 in Patients with HER2-expressing Advanced Solid Tumors
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- Jan.05.2024 Management / Finance
- Ono Announces Status of Acquisition of Own Shares