News Releases
The latest company news, press releases, and resources about Servier and everything our company has to offer.
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11.10.2025Servier's Clinical and Real-World Data at 2025 SNO Congress Showcase Leadership in IDH-Mutant Glioma
11.06.2025Servier's New and Updated Data at 2025 ASH Annual Meeting Highlight Commitment to Hematology Research
11.03.2025Servier Announces Positive Findings from Longer-Term Analysis of the Phase 3 INDIGO Trial Showing Continued Durable Treatment Effect of VORANIGO® (vorasidenib) Published in The Lancet Oncology
10.31.2025Servier's VORANIGO® (vorasidenib) Receives Prestigious 2025 Prix Galien USA Award
09.22.2025European Commission Approves Servier's VORANIGO® (vorasidenib) as the First Targeted Therapy for Grade 2 IDH-Mutant Glioma in the EU
09.08.2025Servier acquires potential treatment for Fragile X syndrome, the most common genetic cause of autism spectrum disorder
09.02.2025Servier and IDEAYA Biosciences Partner to Bring Darovasertib, a Promising Uveal Melanoma Treatment, to Patients Worldwide
08.11.2025Servier’s VORANIGO® (vorasidenib) Nominated for 2025 Prix Galien USA Award
07.28.2025Servier Announces Positive Data from Long-Term Follow-Up Analysis of the Phase 3 AGILE Trial of TIBSOVO® (ivosidenib) in IDH1-mutated Acute Myeloid Leukemia
07.25.2025Servier Receives Positive CHMP Opinion for VORANIGO® (vorasidenib) for the Treatment of Adults and Adolescents with Grade 2 IDH-mutant Diffuse Glioma
05.28.2025Servier Ranked Among Top Companies Across Several Categories in 2024 PatientView Corporate Reputation of Pharma Survey
05.22.2025Servier Presentations at ASCO 2025 Reinforce Company Leadership in IDH-Mutated Cancers
02.27.2025Servier announces the appointment of Nitza Thomasson as Executive Director R&D Neurology
01.13.2025Servier Appoints David K. Lee to Executive Committee
01.09.2025Servier Announces Expansion of its Tibsovo (ivosidenib) Development Program Investigating its Safety and Efficacy in Patients Living with IDH1-Mutated Cancers in Both Hematological Malignancies and Solid Tumors
11.19.2024Servier Partners With Local Cancer Center to Support Research Graduate Students in the Boston Area
11.13.2024Servier to Present Data Across its Hematology Portfolio at the 2024 American Society of Hematology (ASH) Annual Meeting
11.12.2024Servier to Present Data on IDH-mutant Glioma at the 2024 Society for Neuro-Oncology (SNO) Congress
08.06.2024Servier's VORANIGO® (vorasidenib) Tablets Receives FDA Approval as First Targeted Therapy for Grade 2 IDH-mutant Glioma
05.30.2024Servier Initiates Critical Dialogue on AYA Cancer Survivorship at ASCO 2024
05.23.2024Servier Highlights Commitment to Improving Cancer Outcomes at ASCO 2024
05.14.2024Servier Ranks 1st Across Several Categories in 2023-2024 PatientView U.S. Corporate Reputation Survey
04.08.2024Servier Data Presented at AACR Underscores Unwavering Dedication to Advancing Oncology R&D
02.21.2024Servier Receives Regulatory Filing Acceptances from FDA and EMA for Vorasidenib in the Treatment of IDH-Mutant Diffuse Glioma
02.20.2024FDA and EMA Accept Vorasidenib Regulatory Submissions for the Treatment of IDH-mutant diffuse glioma
12.21.2023CStone sells to Servier its exclusive rights to TIBSOVO®in Greater China and Singapore
12.09.2023Servier Showcases Leadership in Mutant Isocitrate Dehydrogenase (IDH) Inhibition Through New Data Spotlighting Real-World Treatment Patterns and Clinical Outcomes of Tibsovo® Use at ASH 2023
12.08.2023Servier Expands Base4 Partnership to Advance Neuroscience Drug Development
12.07.2023Nicolas Garnier joins Servier as Chief Patient Officer
12.05.2023Servier Data at ASH 2023 Furthers Leadership in Hard-to-Treat Hematologic Malignancies
12.05.2023Data at ASH 2023 Underscores Servier Leadership in Hard-to-Treat Hematologic Malignancies
11.18.2023New Analyses from Pivotal Phase 3 INDIGO Study Reinforce Vorasidenib's Potential to Change the Treatment Paradigm for IDH-Mutant Diffuse Glioma
11.10.2023New Vorasidenib Data at SNO 2023 Bolster Servier's Neuro-Oncology Clinical Development Program
10.24.2023Servier Announces FDA Approval of TIBSOVO® (ivosidenib tablets) for the Treatment of IDH1-Mutated Relapsed or Refractory (R/R) Myelodysplastic Syndromes (MDS)
08.15.2023Servier Announces FDA Filing Acceptance and Priority Review for TIBSOVO® (ivosidenib tablets) in the Treatment of IDH1-mutated Relapsed or Refractory (R/R) Myelodysplastic Syndromes (MDS)
06.09.2023Servier Presents Updated Results for TIBSOVO® (ivosidenib tablets) in IDH1-mutated Relapsed/Refractory Myelodysplastic Syndromes at the 2023 European Hematology Association (EHA) Congress
06.05.2023Servier Bolsters Position as the Leader in Mutant IDH Inhibition with Positive New IDH1-Mutated Acute Myeloid Leukemia Data at ASCO
06.04.2023Servier Presents Transformational Data from Pivotal Phase 3 INDIGO Trial of Vorasidenib in Recurrent or Residual Grade 2 IDH-Mutant Diffuse Glioma
05.25.2023Servier Targets Transformative Treatment of Cancer at ASCO 2023
05.10.2023Servier receives European Commission approval of Tibsovo® (ivosidenib tablets) in IDH1-mutated Acute Myeloid Leukemia and IDH1-mutated Cholangiocarcinoma
03.14.2023Servier's Pivotal Phase 3 INDIGO Trial Investigating vorasidenib in IDH-Mutant Low-Grade Glioma Meets Primary Endpoint of Progression-Free Survival (PFS) and Key Secondary Endpoint of Time to Next Intervention (TTNI)
03.09.2023Servier Announces Partnership with QIAGEN to Develop New mIDH1 Companion Diagnostic Test to Support Servier's Onco-hematology Portfolio
02.24.2023Servier receives a positive CHMP opinion for TIBSOVO® (ivosidenib tablets) in IDH1-mutated Acute Myeloid Leukemia (AML) and Cholangiocarcinoma (CCA) patients
02.02.2023Servier full year 2021/22 results confirm the transformation trajectory of the Group
01.17.2023Servier and Taiho Oncology Present Overall Survival Data for Trifluridine/Tipiracil (LONSURF®) In Combination With Bevacizumab in Patients With Refractory Metastatic Colorectal Cancer at 2023 ASCO Gastrointestinal Cancers Symposium
12.12.2022Real-World Analysis Suggests Pediatric-Inspired Regimens Lead to Higher Overall Survival in Adolescent and Young Adult Patients with Newly-Diagnosed Acute Lymphoblastic Leukemia
12.10.2022Servier Presents Patient Follow Up Data from the Phase 3 AGILE Study at ASH 2022
12.07.2022Servier Wins Reuters’ 2022 Patient Champion Award
11.03.2022New Data at ASH 2022 Bolster Servier's Leadership in Hematology Research
07.20.2022Servier Affirms Commitment to Cancer by Announcing the Opening of a Global R&D Center and Expanded Offices in Boston's Seaport
06.01.2022Servier to Showcase Growing Oncology Portfolio at the ASCO and EHA 2022 Annual Meetings
05.25.2022Servier Announces FDA Approval of TIBSOVO® (ivosidenib tablets) in Combination with Azacitidine for Patients with Newly Diagnosed IDH1-mutated Acute Myeloid Leukemia
04.21.2022Phase 3 AGILE Data of TIBSOVO® (ivosidenib tablets) in Combination with Azacitidine for Patients with Previously Untreated IDH1-mutated Acute Myeloid Leukemia Published in the New England Journal of Medicine
03.17.2022Servier Joins Everest Climb to Fight Cancer Benefitting Fred Hutchinson Cancer Research Center
03.10.2022Servier Submits a Marketing Authorization Application to the European Medicines Agency (EMA) for TIBSOVO® (ivosidenib tablets) for Patients with IDH1-mutated Acute Myeloid Leukemia (AML) and Cholangiocarcinoma
03.07.2022Servier Announces FDA Filing Acceptance and Priority Review for TIBSOVO® (ivosidenib tablets) in Combination with Azacitidine for Patients with Previously Untreated IDH1-mutated Acute Myeloid Leukemia
01.18.2022Servier Group Reports Financial Year 2020/2021 Annual Results, R&D Strategy and Pipeline
12.11.2021Phase 3 Data Demonstrate TIBSOVO® (ivosidenib tablets) in Combination with Azacitidine Significantly Improves Event-Free Survival and Overall Survival in Patients with Previously Untreated IDH1-mutated Acute Myeloid Leukemia
11.04.2021New Data at ASH 2021 Reinforces the Strength of Servier's Hematology Portfolio
08.25.2021Servier Announces FDA Approval of TIBSOVO® (ivosidenib tablets) in IDH1-Mutated Cholangiocarcinoma
08.02.2021Servier Announces Positive Topline Data from the Global Phase 3 Study of TIBSOVO® (ivosidenib tablets) in Combination with Azacitidine in Patients with Previously Untreated IDH1-mutated Acute Myeloid Leukemia
06.16.2021Servier Announces Promising Phase 1 Data for Vorasidenib in IDH Mutant Low-Grade Glioma Published in Clinical Cancer Research
06.07.2021Servier Presents Updated Translational Data from Perioperative Study of Vorasidenib and TIBSOVO® (ivosidenib tablets) in Patients with IDH Mutant Low-Grade Glioma at ASCO 2021
06.01.2021Servier Highlights Novel Approaches to Treating Cancer at the ASCO and EHA 2021 Annual Meetings
05.05.2021Servier Announces FDA Filing Acceptance and Priority Review for TIBSOVO® (ivosidenib tablets) in IDH1-mutated Cholangiocarcinoma
04.01.2021Servier Completes Acquisition of Agios Pharmaceuticals' Oncology Business
03.01.2021Agios Submits Supplemental New Drug Application to FDA for TIBSOVO® (ivosidenib tablets) for Patients with Previously Treated IDH1-Mutant Cholangiocarcinoma
01.17.2021Agios Presents Final Data from Phase 3 ClarIDHy Study of TIBSOVO® (ivosidenib tablets) in Patients with Previously Treated IDH1-Mutant Cholangiocarcinoma
01.12.2021Taiho Oncology and Servier To Present Data on LONSURF® (trifluridine and tipiracil) at 2021 ASCO Gastrointestinal Cancers Symposium (ASCO GI)
12.22.2020Servier Announces a Collaboration to Explore Immune Checkpoint Signaling in Cancer
12.21.2020Servier and Celsius Therapeutics Announce Target Discovery Collaboration in Colorectal Cancer
12.21.2020Agios to Focus on Developing and Commercializing Innovative Treatments for Genetically Defined Diseases and Sell Its Oncology Business to Servier for Up to $2 Billion Plus Royalties
12.21.2020Servier to Acquire Agios Pharmaceuticals' Oncology Business
12.04.2020Precision BioSciences Reports Positive Interim Results from PBCAR0191 Phase 1/2a Trial in Relapsed/Refractory (R/R) Non-Hodgkin Lymphoma (NHL) and R/R B-cell Acute Lymphoblastic Leukemia (B-ALL)
11.04.2020Agios to Present Broad Set of Clinical and Translational Data for Oncology and Rare Genetic Disease Programs at the Virtual 2020 ASH Annual Meeting
10.16.2020Agios Announces Withdrawal of European Marketing Authorization Application for TIBSOVO® as a Treatment for Relapsed or Refractory IDH1-mutant Acute Myeloid Leukemia
10.12.2020Servier and CureMatch® Launch Their Self-Certified CE-Marked Clinical Decision Support Software, Bionov™
09.24.2020Servier and MBC BioLabs Announce Winner of the 2020 Servier Golden Ticket
09.21.2020Agios Announces Final Overall Survival Data from Phase 3 ClarIDHy Study of TIBSOVO® (ivosidenib tablets) in Previously Treated IDH1-Mutant Cholangiocarcinoma Patients
06.12.2020Agios and Royalty Pharma Announce $255 Million Purchase Agreement for IDHIFA® Royalty
05.29.2020Agios Presents Updated Data from the Phase 1 Dose-escalation Study of Vorasidenib in Patients with IDH-mutant Non-enhancing Glioma
05.19.2020Agios Announces Publication of TIBSOVO® Phase 3 Data in The Lancet Oncology Demonstrating Significant Improvement in Progression-Free Survival Compared to Placebo in Previously Treated IDH1-Mutant Cholangiocarcinoma Patients
05.13.2020Agios to Present Updated Data from the Phase 1 Study of Vorasidenib in Non-enhancing Glioma in Oral Presentation at the American Society of Clinical Oncology Annual Meeting
03.25.2020Agios Provides Update on 2016 Collaboration Agreement with Celgene, a Wholly Owned Subsidiary of Bristol Myers Squibb
03.19.2020Coronavirus: Adapting our Approach to Continue to Serve our Patients
12.16.2019Agios Receives FDA Breakthrough Therapy Designation for TIBSOVO® (ivosidenib) for the Treatment of Adult Patients with Relapsed or Refractory Myelodysplastic Syndrome with an IDH1 Mutation
12.09.2019Agios Presents Translational Data to Further Characterize the Role of TIBSOVO® (ivosidenib) Treatment in IDH1 Mutant Acute Myeloid Leukemia (AML)
12.04.2019Servier Showcases Robust Presence at ASH 2019
11.22.2019Agios Presents New Pharmacodynamic and Response Data from Both Cohorts of the Perioperative Study of Vorasidenib and TIBSOVO® (ivosidenib) in Patients with IDH1 Mutant Positive Low-Grade Glioma
10.27.2019Agios Presents Data from Single Agent Dose-Escalation Arm of Phase 1 Study of AG-270, a MAT2A Inhibitor, in Patients with MTAP-Deleted Tumors
10.09.2019Agios to Present Data from AG-270 Phase 1 Dose-Escalation Study in Patients with MTAP-Deleted Tumors in a Proffered Papers Oral Presentation and Poster Session at the AACR-NCI-EORTC International Conference
10.01.2019Servier Acquires non-Hodgkin B-cell Lymphoma Treatment PIXUVRI® (pixantrone) from CTI BioPharma, Strengthening the Servier Oncology Portfolio
09.30.2019Data from Agios’ Phase 3 ClarIDHy Trial of TIBSOVO® Demonstrates Significant Improvement in Progression Free Survival (PFS) Compared to Placebo in Previously Treated IDH1 Mutant Cholangiocarcinoma Patients
09.10.2019Agios to Present Data From the Phase 3 ClarIDHy Study of TIBSOVO® in Previously Treated IDH1 Mutant Cholangiocarcinoma in Presidential Symposium at ESMO
06.03.2019Agios Presents Updated Data from Phase 1 Studies of TIBSOVO® (ivosidenib) in Newly Diagnosed Adult Patients with IDH1 Mutant Acute Myeloid Leukemia (AML) Not Eligible for Intensive Chemotherapy
06.03.2019Servier and MBC BioLabs Announce Winner of the 2019 Servier Golden Ticket
05.29.2019Servier Showcases Robust Presence at ASCO 2019
05.15.2019Agios to Present Clinical Data from its IDH Program at ASCO
05.09.2019Servier Cuts Ribbon on New Boston Headquarters
05.02.2019Agios Announces FDA Approval of Supplemental New Drug Application (sNDA) for TIBSOVO® as Monotherapy for Newly Diagnosed Adult Patients with IDH1 Mutant Acute Myeloid Leukemia (AML) Not Eligible for Intensive Chemotherapy
Media Contacts
Sara Noonan
sara.noonan@servier.com