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AP

WKN: A41DXH | ISIN: US00510M2035 | Ticker-Symbol: 3ZO0
NASDAQ
02.10.26 | 21:59
1,280 US-Dollar
+0,79 % +0,010
Branche
Biotechnologie
Aktienmarkt
Sonstige
1-Jahres-Chart
ACURX PHARMACEUTICALS INC Chart 1 Jahr
5-Tage-Chart
ACURX PHARMACEUTICALS INC 5-Tage-Chart

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FrXFRA DELETION OF INSTRUMENTS FROM BOERSE FRANKFURT - 02.10.2026 -3-1.284The following instruments on Boerse Frankfurt do have their last trading day on 02.10.2026Die folgenden Instrumente in Boerse Frankfurt haben ihren letzten Handelstag am 02.10.2026ISIN NameKYG200801002 CBAK...
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DiAcurx enrolls first patient in recurrent C. difficile trial3
ACURX PHARMACEUTICALS Aktie jetzt für 0€ handeln
DiAcurx Pharmaceuticals, Inc.: Acurx Pharmaceuticals Announces First Patient Enrolled in PATHFINDER Clinical Trial of Ibezapolstat in Multiply-Recurrent C. difficile Infection191PATHFINDER is a ground-breaking Phase 2 clinical trial with ibezapolstat (IBZ) in patients with multiply-recurrent CDI (C. difficile Infection) (rCDI) that, together...
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19.09.New to The Street Broadcasts Tonight at 6:30 PM ET Across the United States, Latin America and MENA, Featuring BioVie, Acurx Pharmaceuticals, Lantern Pharma and SafeSpace Global966BioVie (Nasdaq:BIVI) CEO Cuong Do Discusses the Company's Recent Long COVID Clinical Results and the Potential of Bezisterim to Address Significant Unmet Patient Needs NEW YORK CITY, NY / ACCESS Newswire...
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18.09.Transcript: Acurx Pharmaceuticals Q2 2026 Earnings Conference Call2
08.09.Acurx Pharmaceuticals, Inc. - S-1, General form for registration of securities1
17.08.Acurx receives FDA conditional acceptance for ibezapolstat brand name5
17.08.Acurx Pharmaceuticals, Inc.: Acurx Pharmaceuticals Receives FDA Conditional Acceptance and USPTO Trademark Allowance for the Company's Brand Name for Ibezapolstat296The proposed proprietary name, or brand name, CIFBEZY has received conditional acceptance from the FDA and also federal trademark allowance from the USPTO These...
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14.08.Acurx outlines 20-patient PATHFINDER start in Q4 as FDA stays open to a single Phase III ASPIRE for ibezapolstat2
14.08.Earnings Call: Acurx übertrifft EPS-Prognose für Q2 2026, Aktie gibt vorbörslich jedoch nach2
14.08.Earnings Call: Acurx übertrifft EPS-Prognose für Q2 2026, Aktie gibt vorbörslich dennoch nach1
14.08.Acurx Pharmaceuticals GAAP EPS of -$0.53 misses by $0.192
14.08.Acurx Pharmaceuticals, Inc. Reports Second Quarter 2026 results and provides business update231STATEN ISLAND, N.Y., Aug. 14, 2026 /PRNewswire/ -- Acurx Pharmaceuticals, Inc. (NASDAQ: ACXP) ("Acurx" or the "Company"), a late-stage biopharmaceutical company...
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12.08.Acurx receives patents in Japan and Mexico for antibiotics2
10.08.Acurx partners with Leiden University on MRSA antibiotic research3
03.08.Acurx receives FDA guidance on single Phase 3 trial pathway1
03.08.Acurx Pharmaceuticals, Inc.: FDA Provides Further Regulatory Guidance to Acurx Pharmaceuticals for the Ibezapolstat Clinical Development Program, Including the Potential for a Single-Phase 3-Trial Registration Plan and a Trial Design to Support ...223Acurx has received FDA guidance in meeting minutes from a July 13, 2026 Type C Meeting to discuss ibezapolstat's (IBZ) Phase 3 clinical program, including the...
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16.06.Acurx Pharmaceuticals, Inc.: Acurx Pharmaceuticals Announces Presentation of Results from Leiden University Medical Center Public-Private Partnership for Its DNA pol IIIC Inhibitors at the Leiden Early Drug Discovery & Development (LED3) Scientific ...192Results are from Acurx's ongoing scientific collaboration with Leiden University Medical Center (LUMC) partially under a grant from Health Holland to further study...
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19.05.New to The Street: Acurx Pharmaceuticals Highlights FDA's New CDI Guidance That Could Accelerate Approval Path for Ibezapolstat491NEW YORK CITY, NY / ACCESS Newswire / May 19, 2026 / New to The Street's longtime featured biotechnology client, Acurx Pharmaceuticals, Inc. (Nasdaq:ACXP), highlighted a potentially transformative regulatory...
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12.05.Acurx outlines August first patient for 20-patient rCDI pilot as it weighs FDA one-trial path5
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