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SNDX Syndax Pharmaceuticals
- 16.510
- +0.010+0.06%
Close Nov 27 16:00 ET
- 16.520
- +0.010+0.06%
Post 20:01 ET
1.41BMarket Cap-4535P/E (TTM)
16.725High16.300Low1.47MVolume16.630Open16.500Pre Close24.23MTurnover1.86%Turnover RatioLossP/E (Static)85.36MShares25.34052wk High3.85P/B1.31BFloat Cap15.00052wk Low--Dividend TTM79.18MShs Float29.860Historical High--Div YieldTTM2.58%Amplitude3.390Historical Low16.473Avg Price1Lot Size
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Syndax Pharmaceuticals Stock Forum
1 HOUR AGO, 5:29 PM EST
VIA PR NEWSWIRE
– Approva...
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 Translocation
FDA Approves Revumenib for Relapsed or Refractory Acute Leukemia With a Kmt2a Translocation
Syndax Announces Positive Pivotal Topline Results from Relapsed or Refractory mNPM1 AML Cohort in AUGMENT-101 Trial of Revumenib
Syndax Pharmaceuticals (SNDX)announced positive topline results from the AUGMENT-101 trial of revumenib in relapsed/refractory mNPM1 AML patients. The trial met its primary endpoint with a 23% complete remission rate (p-value = 0.0014) and achieved a 47% overall response rate in a heavily pre-treated population. The safety profil...
Syndax Pharmaceuticals Inc - Primary Endpoint Met With 23% Cr/CRH Rate in Phase 2 Trial
Dow Jones· 1 min ago
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⇨ Nikt...
5 mins ago
Incyte and Syndax Announce U.S. FDA Approval of Niktimvo™ (Axatilimab-Csfr) for the Treatment of Chronic Graft-Versus-Host Disease (Gvhd)
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