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WKN: A2PYCP | ISIN: US34960Q2084 | Ticker-Symbol: CNB0
Frankfurt
15.05.26 | 15:25
12,000 Euro
+10,09 % +1,100
Branche
Biotechnologie
Aktienmarkt
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FORTRESS BIOTECH INC PREF Chart 1 Jahr
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DoFortress Biotech, Inc. - 10-Q, Quarterly Report1
DoFortress Biotech GAAP EPS of $2.82, revenue of $16.04M misses by $0.3M3
DoFortress Biotech, Inc. - 8-K, Current Report1
DoFortress Biotech, Inc.: Fortress Biotech Reports First Quarter 2026 Financial Results and Recent Corporate Highlights400ZYCUBO approved by FDA to treat Menkes disease in the United States; Fortress subsidiary Cyprium Therapeutics closed the sale of its Rare Pediatric Disease Priority Review Voucher (PRV) for $205 million...
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31.03.Fortress Biotech GAAP EPS of -$0.07 misses by $0.39, revenue of $63.26M misses by $10.08M6
FORTRESS BIOTECH INC PREF Aktie jetzt für 0€ handeln
31.03.Fortress Biotech, Inc.: Fortress Biotech Reports 2025 Financial Results and Recent Corporate Highlights723ZYCUBOapproved by FDA to treat Menkes disease in the United States; Fortress subsidiary Cyprium Therapeutics sold its Rare Pediatric Disease Priority Review Voucher (PRV) for gross proceeds of $205...
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31.03.Fortress Biotech, Inc. - 10-K, Annual Report-
30.03.Fortress Biotech, Inc.: Fortress Biotech's Subsidiary Cyprium Therapeutics Closes Sale of Rare Pediatric Disease Priority Review Voucher for $205 Million345MIAMI, March 30, 2026 (GLOBE NEWSWIRE) -- Fortress Biotech, Inc. (Nasdaq: FBIO) ("Fortress") and its majority-owned subsidiary, Cyprium Therapeutics, Inc. ("Cyprium"), today announced the closing...
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23.02.Fortress Biotech, Inc. - 8-K, Current Report5
23.02.Fortress Biotech, Inc.: Fortress Biotech's Subsidiary Cyprium Therapeutics Enters into Agreement to Sell Rare Pediatric Disease Priority Review Voucher for $205 Million448MIAMI, Feb. 23, 2026 (GLOBE NEWSWIRE) -- Fortress Biotech, Inc. (Nasdaq: FBIO) ("Fortress") and its majority-owned subsidiary, Cyprium Therapeutics, Inc. ("Cyprium"), today announced that Cyprium...
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16.01.Weekly Buzz: Lyra Therapeutics Slashes Jobs; FDA Okays Fortress Biotech's ZYCUBO; Boston Scientific To Acquire Penumbra; BriaCell Therapeutics On Watch813NEW BRUNSWICK (dpa-AFX) - This week, the biotech sector saw a steady stream of high-impact news, including a major workforce reduction and a fresh round of regulatory clearances spanning diabetes...
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14.01.Fortress Biotech receives FDA approval for Zycubo to treat Menkes disease13
13.01.Fortress Bio gains on FDA approval of copper replacement therapy6
13.01.Fortress Biotech, Inc. - 8-K, Current Report2
13.01.Fortress 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 States871Rare 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 Highlights759Total 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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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 Gout346MIAMI, 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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01.10.25Fortress Biotech, Inc.: Fortress Biotech and Subsidiary Urica Therapeutics Announce Crystalys Therapeutics' $205 Million Series A Financing205Dotinurad 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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