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SNDX

Syndax Pharmaceuticals (SNDX)

Syndax Pharmaceuticals Inc
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15/01/202519:34PR Newswire (US)Incyte and Syndax Announce U.S. Food and Drug Administration (FDA) Approval of Niktimvo™ (axatilimab-csfr) 9 mg and 22 mg Vial SizesNASDAQ:SNDXSyndax Pharmaceuticals Inc
13/01/202509:00PR Newswire (US)Syndax Highlights Recent Accomplishments and Anticipated 2025 Milestones at the 43rd Annual J.P. Morgan Healthcare ConferenceNASDAQ:SNDXSyndax Pharmaceuticals Inc
07/01/202523:20PR Newswire (US)Kuehn Law Encourages Investors of Syndax Pharmaceuticals, Inc. to Contact Law FirmNASDAQ:SNDXSyndax Pharmaceuticals Inc
07/01/202509:00PR Newswire (US)Syndax Announces Presentation at 43rd Annual J.P. Morgan Healthcare ConferenceNASDAQ:SNDXSyndax Pharmaceuticals Inc
03/01/202518:05PR Newswire (US)Syndax Pharmaceuticals Reports Inducement Grants Under NASDAQ Listing Rule 5635(c)(4)NASDAQ:SNDXSyndax Pharmaceuticals Inc
20/12/202419:00Edgar (US Regulatory)Form 8-K - Current reportNASDAQ:SNDXSyndax Pharmaceuticals Inc
09/12/202409:30PR Newswire (US)Syndax Announces Additional Positive Data for Revuforj® (revumenib) from AUGMENT-101 Trial in Relapsed or Refractory mNPM1 AML and BEAT AML Frontline Combination TrialNASDAQ:SNDXSyndax Pharmaceuticals Inc
07/12/202420:15PR Newswire (US)Syndax Presents Positive Revuforj® (revumenib) Data in Acute Leukemias from Multiple Trials, Including the SAVE Combination and AUGMENT-101 Trials, at 66th ASH Annual MeetingNASDAQ:SNDXSyndax Pharmaceuticals Inc
06/12/202418:28Edgar (US Regulatory)Form SC 13G/A - Statement of Beneficial Ownership by Certain Investors: [Amend]NASDAQ:SNDXSyndax Pharmaceuticals Inc
27/11/202409:00PR Newswire (US)Syndax Announces Participation at the Citi 2024 Global Healthcare ConferenceNASDAQ:SNDXSyndax Pharmaceuticals Inc
15/11/202419:29PR Newswire (US)Syndax Announces FDA Approval of Revuforj® (revumenib), the First and Only Menin Inhibitor to Treat Adult and Pediatric Patients with Relapsed or Refractory Acute Leukemia with a KMT2A TranslocationNASDAQ:SNDXSyndax Pharmaceuticals Inc
12/11/202409:00PR Newswire (US)Syndax Announces Positive Pivotal Topline Results from Relapsed or Refractory mNPM1 AML Cohort in AUGMENT-101 Trial of RevumenibNASDAQ:SNDXSyndax Pharmaceuticals Inc
05/11/202418:03Edgar (US Regulatory)Form 10-Q - Quarterly report [Sections 13 or 15(d)]NASDAQ:SNDXSyndax Pharmaceuticals Inc
05/11/202418:01PR Newswire (US)Syndax Reports Third Quarter 2024 Financial Results and Provides Business UpdateNASDAQ:SNDXSyndax Pharmaceuticals Inc
05/11/202411:01PR Newswire (US)Syndax to Host ASH Investor Event in Person and via Webcast on December 9, 2024NASDAQ:SNDXSyndax Pharmaceuticals Inc
05/11/202411:00PR Newswire (US)Syndax Announces Revumenib Abstracts to Be Presented at the 66th ASH Annual MeetingNASDAQ:SNDXSyndax Pharmaceuticals Inc
05/11/202411:00PR Newswire (US)Syndax Announces New Data from Secondary Analysis of the Pivotal AGAVE-201 Trial of Niktimvo™ (axatilimab-csfr) in Chronic Graft-Versus-Host Disease to Be Presented at 66th ASH Annual MeetingNASDAQ:SNDXSyndax Pharmaceuticals Inc
04/11/202418:01PR Newswire (US)Syndax Pharmaceuticals and Royalty Pharma Enter into $350 Million Royalty Funding Agreement for Niktimvo™NASDAQ:SNDXSyndax Pharmaceuticals Inc
01/11/202408:00PR Newswire (US)Syndax Announces Participation in November Investor ConferencesNASDAQ:SNDXSyndax Pharmaceuticals Inc
29/10/202408:00PR Newswire (US)Syndax to Announce Third Quarter 2024 Financial Results and Host Conference Call and Webcast on November 5, 2024NASDAQ:SNDXSyndax Pharmaceuticals Inc
18/09/202418:15PR Newswire (US)Incyte and Syndax Announce New England Journal of Medicine Publication of Data from Pivotal AGAVE-201 Trial of Niktimvo™ (axatilimab-csfr) in Chronic Graft-Versus-Host DiseaseNASDAQ:SNDXSyndax Pharmaceuticals Inc
15/08/202417:15Business WireIncyte und Syndax melden FDA-Zulassung von Niktimvo™ (Axatilimab-csfr) zur Behandlung der chronischen Graft-versus-Host-Krankheit (GvHD)NASDAQ:SNDXSyndax Pharmaceuticals Inc
15/08/202407:26Business WireIncyte et Syndax annoncent l’approbation par la FDA américaine de Niktimvo™ (axatilimab-csfr) pour le traitement de la maladie chronique du greffon contre l’hôte (GVHD)NASDAQ:SNDXSyndax Pharmaceuticals Inc
14/08/202418:34Business WireIncyte and Syndax Announce U.S. FDA Approval of Niktimvo™ (axatilimab-csfr) for the Treatment of Chronic Graft-Versus-Host Disease (GVHD)NASDAQ:SNDXSyndax Pharmaceuticals Inc
12/08/202408:00PR Newswire (US)Syndax Announces Publication in the Journal of Clinical Oncology of Data from the Pivotal AUGMENT-101 Trial of Revumenib in Relapsed/Refractory KMT2Ar Acute LeukemiaNASDAQ:SNDXSyndax Pharmaceuticals Inc
01/08/202417:05PR Newswire (US)Syndax Reports Second Quarter 2024 Financial Results and Provides Clinical and Business UpdateNASDAQ:SNDXSyndax Pharmaceuticals Inc
29/07/202408:01PR Newswire (US)Syndax Announces PDUFA Action Date Extension for Revumenib NDA for Relapsed or Refractory KMT2Ar Acute LeukemiaNASDAQ:SNDXSyndax Pharmaceuticals Inc
25/07/202408:00PR Newswire (US)Syndax to Announce Second Quarter 2024 Financial Results and Host Conference Call and Webcast on August 1, 2024NASDAQ:SNDXSyndax Pharmaceuticals Inc
17/06/202410:26Edgar (US Regulatory)Form 4 - Statement of changes in beneficial ownership of securitiesNASDAQ:SNDXSyndax Pharmaceuticals Inc
14/06/202408:00PR Newswire (US)Syndax Presents Updated Positive Data from BEAT AML and AUGMENT-102 Phase 1/2 Combination Trials of Revumenib in Patients with Acute Leukemias at EHA 2024 CongressNASDAQ:SNDXSyndax Pharmaceuticals Inc
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