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WKN: A3EWWP | ISIN: US34960Q3074 | Ticker-Symbol: CNB1
NASDAQ
14.01.26 | 22:00
3,280 US-Dollar
-15,90 % -0,620
Branche
Biotechnologie
Aktienmarkt
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FORTRESS BIOTECH INC Chart 1 Jahr
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MiFortress Biotech receives FDA approval for Zycubo to treat Menkes disease7
DiFortress Bio gains on FDA approval of copper replacement therapy6
DiFortress Biotech, Inc. - 8-K, Current Report2
FORTRESS BIOTECH Aktie jetzt für 0€ handeln
DiFortress Biotech, Inc.: Fortress Biotech and Cyprium Therapeutics Announce U.S. FDA Approval of ZYCUBO (copper histidinate), the First and Only Approved Treatment for Menkes Disease in the United States512Rare Pediatric Disease Priority Review Voucher (PRV) granted by FDA at approval to be transferred from Sentynl Therapeutics to Cyprium Cyprium eligible to receive tiered royalties and up to $129 million...
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15.12.25FDA sets new PDUFA date for Fortress Biotech's Menkes disease therapy31
15.12.25Fortress Biotech, Inc. - 8-K, Current Report3
14.11.25Fortress Biotech, Inc.: Fortress Biotech Reports Third Quarter 2025 Financial Results and Recent Corporate Highlights585Total net revenue increased 20.5% to $17.6 million for third quarter of 2025 compared to the third quarter of 2024 Fortress subsidiary Checkpoint Therapeutics acquired by Sun Pharma; Fortress received...
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14.11.25Fortress Biotech, Inc. - 10-Q, Quarterly Report3
14.11.25Fortress Biotech, Inc. - 8-K, Current Report-
11.11.25Fortress Biotech Q3 Earnings Preview5
21.10.25Fortress Biotech: Aktie legt zu - Gichtmittel der Tochtergesellschaft erreicht Phase-3-Studie16
21.10.25Fortress Biotech stock rises after subsidiary's gout treatment enters Phase 3 trials2
21.10.25Fortress Biotech, Inc.: Fortress Biotech and Subsidiary Urica Therapeutics Announce First Patients Dosed in Crystalys Therapeutics' Global Phase 3 Trials of Dotinurad for the Treatment of Gout239MIAMI, Oct. 21, 2025 (GLOBE NEWSWIRE) -- Urica Therapeutics, Inc. ("Urica" or the "Company"), a Fortress Biotech, Inc. (Nasdaq: FBIO) ("Fortress") subsidiary, today announced that Crystalys Therapeutics...
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02.10.25FDA verweigert Zulassung für Medikament von Fortress Biotech wegen Produktionsmängeln20
02.10.25Fortress Biotech stock faces setback as FDA issues CRL for CUTX-1013
01.10.25Fortress Biotech stock plummets after FDA rejects Menkes disease drug13
01.10.25Fortress Biotech plunges as FDA rejects rare disease drug20
01.10.25Fortress Biotech, Inc. - 8-K, Current Report5
01.10.25Fortress Biotech, Inc.: Fortress Biotech and Subsidiary Urica Therapeutics Announce Crystalys Therapeutics' $205 Million Series A Financing129Dotinurad is a next-generation URAT1 inhibitor in two Phase 3 clinical trials with potential for best-in-class safety and efficacy Urica sold dotinurad to Crystalys Therapeutics in 2024 in exchange...
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01.10.25Fortress Biotech, Inc.: Fortress Biotech and Cyprium Therapeutics Announce an Update on the NDA for CUTX-101182MIAMI, Oct. 01, 2025 (GLOBE NEWSWIRE) -- Fortress Biotech, Inc. (Nasdaq: FBIO) ("Fortress") and its majority-owned subsidiary, Cyprium Therapeutics, Inc. ("Cyprium"), today announced that the U.S....
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