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Fortress Biotech

2.00
+0.12006.38%
Post-market: 2.00-0.0005-0.02%19:36 EDT
Volume:327.68K
Turnover:634.92K
Market Cap:59.14M
PE:-0.91
High:2.00
Open:1.90
Low:1.89
Close:1.88
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Mustang Bio Inc - to Initiate Clinical Trial With Mb-109 for GBM in H2 2025

THOMSON REUTERS
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28 Feb

Mustang Bio Inc - Exits Lease for Worcester Facility, Divests Assets to Abbvie for $1 Mln

THOMSON REUTERS
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28 Feb

Mustang Bio Announces Sale of Fixed Assets and Exit of Facility

THOMSON REUTERS
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28 Feb

Mustang Bio Announces Sale of Fixed Assets and Exit of Facility

GlobeNewswire
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28 Feb

Mustang Bio Regains Compliance With Nasdaq Minimum Bid Price Requirement

THOMSON REUTERS
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12 Feb

Mustang Bio Announces Closing of $8 Million Public Offering

THOMSON REUTERS
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10 Feb

Mustang Bio Announces Closing of $8 Million Public Offering

GlobeNewswire
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10 Feb

Mustang Bio Announces Pricing of $8 Million Public Offering

THOMSON REUTERS
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06 Feb

Mustang Bio Announces Pricing of $8 Million Public Offering

GlobeNewswire
·
06 Feb

Fortress Biotech announces first patient dosed in Phase 2 trial of Triplex

TipRanks
·
28 Jan

Fortress Biotech Announces First Patient Dosed in Phase 2 Clinical Trial of Triplex Vaccination in Stem Cell Donors to Reduce Cmv Events in Recipients of Hsct

THOMSON REUTERS
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27 Jan

Fortress Biotech Announces First Patient Dosed in Phase 2 Clinical Trial of Triplex Vaccination in Stem Cell Donors to Reduce CMV Events in Recipients of HSCT

GlobeNewswire
·
27 Jan

Fortress Biotech Inc - FDA Extends Target Action Date for Cutx-101 Nda to September 30, 2025

THOMSON REUTERS
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17 Jan

Mustang Bio Inc - Stock to Begin Trading on Split-Adjusted Basis Jan 16, 2025

THOMSON REUTERS
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14 Jan

Mustang Bio Announces Reverse Stock Split

GlobeNewswire
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14 Jan

Fortress Biotech (FBIO) Gets a Buy from Roth MKM

TIPRANKS
·
08 Jan

BRIEF-Fortress Biotech And Cyprium Therapeutics Announce U.S. FDA Acceptance And Priority Review Of NDA For CUTX-101

Reuters
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06 Jan

Fortress Biotech Inc - FDA Sets Pdufa Target Action Date for Cutx-101 on June 30, 2025

THOMSON REUTERS
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06 Jan

Sentynl Therapeutics Announces U.S. FDA Acceptance and Priority Review of New Drug Application for Cutx-101 (Copper Histidinate) Product Candidate for Treatment of Menkes Disease

THOMSON REUTERS
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06 Jan

Fortress Biotech and Cyprium Therapeutics Announce U.S. FDA Acceptance and Priority Review of Nda for Cutx-101 for Treatment of Menkes Disease

THOMSON REUTERS
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06 Jan