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GT BIOPHARMA ANNOUNCES FDA CLEARANCE OF INVESTIGATIONAL NEW DRUG APPLICATION FOR GTB-3650, AN NK CELL ENGAGER FOR TREATMENT OF CD33+ LEUKEMIA
AQ
GT Biopharma Says FDA Clears Investigational New Drug Application for Cancer Drug GTB-3650
MT
GT Biopharma Shares Rise on FDA Clearance for Cancer-Drug Study
DJ
GT Biopharma Announces FDA Clearance of Investigational New Drug (IND) Application for GTB-3650, an NK Cell Engager for Treatment of CD33+ Leukemia
AQ
GT Biopharma, Inc. Announces FDA Clearance of Investigational New Drug Application for GTB-3650, an NK Cell Engager for Treatment of CD33+ Leukemia
CI
GT Biopharma, Inc. Announces CFO Changes
CI
Top Midday Decliners
MT
GT Biopharma Prices $3.2 Million Registered Direct Offering of Shares, Concurrent Private Placement of Warrants
MT
GT Biopharma, Inc. Announces $3.2 Million Registered Direct Offering Priced At-The-Market Under Nasdaq Rules
AQ
Top Premarket Gainers
MT
GT Biopharma Reports First Quarter 2024 Financial Results and Provides Corporate Update
AQ
GT Biopharma, Inc. Reports Earnings Results for the First Quarter Ended March 31, 2024
CI
GT Biopharma, Inc. Reports Earnings Results for the Full Year Ended December 31, 2023
CI
GT Biopharma Reports Fourth Quarter and Full-Year 2023 Financial Results
AQ
GT Biopharma to Conduct 1-for-30 Reverse Stock Split; Shares Fall
MT
GT Biopharma, Inc. Announces 1-for-30 Reverse Stock Split
AQ
LEADING PROXY ADVISORY FIRMS, ISS AND GLASS LEWIS, RECOMMEND GT BIOPHARMA STOCKHOLDERS VOTE 'FOR' ALL PROPOSED ITEMS AT THE UPCOMING SPECIAL MEETING OF STOCKHOLDERS
AQ
Leading Proxy Advisory Firms, ISS and Glass Lewis, Recommend GT Biopharma Stockholders Vote “FOR” All Proposed Items at the Upcoming Special Meeting of Stockholders
AQ
GT Biopharma Announces IND Submission for GTB-3650 for Treatment of CD33+ Leukemia
AQ
GT Biopharma Announces IND Submission for GTB-3650 for Treatment of CD33+ Leukemia
CI
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