Decitabine Press Release

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Tue, 07/07/2020 - 14:32 FDA Approves New Therapy for Myelodysplastic Syndromes (MDS) That Can Be Taken at Home
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FDA
Thu, 05/14/2020 - 08:19 Tolero Pharmaceuticals Announces Expansion of the Zella 102 Study in Patients with Intermediate and High-Risk Myelodysplastic Syndromes (MDS)
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SDP Oncology
Wed, 03/25/2020 - 21:35 Tolero Pharmaceuticals Joins The Leukemia & Lymphoma Societys Groundbreaking Beat AML Master Clinical Trial for Patients with Acute Myeloid Leukemia
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SDP Oncology
Thu, 02/06/2020 - 16:12 Otsuka announces that subsidiary Astex Pharmaceuticals' NDA for ASTX727 (oral C-DEC), for the treatment of MDS and CMML, has been accepted for priority review by the U.S. FDA
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Otsuka
Mon, 12/09/2019 - 11:32 A decades-long journey in blood cancer research
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Novartis
Tue, 09/17/2019 - 17:01 Dana-Farber Cancer Institute receives $5 million gift to create the Edward P. Evans Center for Myelodysplastic Syndromes
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Dana Farber
Tue, 09/03/2019 - 18:22 Astex Pharmaceuticals announces that its novel, oral hypomethylating agent ASTX727 has been granted orphan drug designation for the treatment of myelodysplastic syndromes (including chronic myelomonocytic leukemia) by the US FDA
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Astex
Fri, 06/07/2019 - 12:28 Otsuka and Taiho Announce that Taiho Will Commercialize Two of Astex Pharmaceuticals' Drug Candidates in North America
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Otsuka
Fri, 06/07/2019 - 12:22 Otsuka and its Subsidiary Astex Pharmaceuticals, Inc. Announce Positive Results from a Phase III Clinical Trial of Anticancer Candidate ASTX727
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Otsuka
Fri, 06/07/2019 - 05:38 Taiho Oncology Announces Agreement with Otsuka to Commercialize Astex Pharmaceuticals Drug Candidates
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Astex
Thu, 12/20/2018 - 13:22 Daiichi Sankyo Initiates First Novel-Novel Combination Study of Two Investigational Agents within its AML Franchise in Patients with AML
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Daiichi Sankyo
Thu, 11/29/2018 - 18:10 Venetoclax combination approved for elderly AML
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Dana Farber
Wed, 11/21/2018 - 10:15 Roche announces FDA grants Venclexta accelerated approval for people with newly-diagnosed acute myeloid leukaemia or those who are ineligible for intensive induction chemotherapy
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Rocheusa
Tue, 10/16/2018 - 08:28 Tolero Pharmaceuticals announces first patient dosed with investigational agent Alvocidib in phase 1b/2 Zella 102 study in patients with myelodysplastic syndromes (MDS)
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SDP Oncology
Sun, 09/30/2018 - 18:31 Lupin receives FDA approval for Decitabine for Injection, 50 mg/vial, Single-Dose Vial
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Lupin
Mon, 07/30/2018 - 03:07 Astex Pharmaceuticals and Otsuka announce results of the phase 3 ASTRAL-1 study of guadecitabine (SGI-110) in treatment-naive AML patients ineligible to receive intense induction chemotherapy
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Astex
Thu, 05/18/2017 - 08:37 Helsinn Group and MEI Pharma Announce Upcoming Presentations of Gene Mutation and Clinical Response Data from Phase II Study of Pracinostat and Azacitidine in Acute Myeloid Leukemia
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MEI Pharma
Sat, 12/03/2016 - 07:28 Helsinn Group and MEI Pharma Report Prolongation of Survival Results from Phase 2 Clinical Study of Pracinostat and Azacitidine in Acute Myeloid Leukemia
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MEI Pharma
Tue, 11/29/2016 - 10:40 Astex to Showcase Its Next-Generation Hypomethylating Agents Being Developed for Treatment of AML/MDS at the 2016 Annual Meeting of the American Society of Hematology
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Astex
Mon, 08/29/2016 - 11:26 Vitamin C may boost effectiveness of acute myeloid leukemia treatment
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Van Andel
Mon, 08/08/2016 - 08:16 Helsinn Group and MEI Pharma Enter Strategic Agreement for the Development and Commercialization of Pracinostat for the Treatment of Acute Myeloid Leukemia and Other Hematologic Diseases
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MEI Pharma
Mon, 08/01/2016 - 07:11 MEI Pharma's Pracinostat Receives Breakthrough Therapy Designation from FDA for Treatment in Combination with Azacitidine of Patients with Newly Diagnosed Acute Myeloid Leukemia Unfit for Intensive Chemotherapy
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MEI Pharma
Mon, 12/07/2015 - 16:23 Combination Treatment with Decitabine Yields Higher Response for Patients with AML or MDS
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Fox Chase
Wed, 04/22/2015 - 17:54 Study illuminates role of cancer drug decitabine in repairing damaged cells
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Purdue