News
CKPT
3.670
-3.42%
-0.130
FDA Oks Checkpoint Therapeutics' UNLOXCYT For Advanced Cutaneous Squamous Cell Carcinoma treatment
NASDAQ · 3h ago
Checkpoint Therapeutics' Shares Rise After Securing First FDA Approval
Dow Jones · 4h ago
Checkpoint Therapeutics trading resumes
TipRanks · 5h ago
Checkpoint Therapeutics confirms FDA approval of unloxcyt
TipRanks · 5h ago
Checkpoint Therapeutics Gets Its First FDA Approval
Dow Jones · 5h ago
CHECKPOINT THERAPEUTICS ANNOUNCES FDA APPROVAL OF UNLOXCYT™ (COSIBELIMAB-IPDL)
Reuters · 5h ago
US FDA approves Checkpoint's skin cancer drug
Reuters · 5h ago
FDA: APPROVAL OF COSIBELIMAB-IPDL (UNLOXCYT) GRANTED TO CHECKPOINT THERAPEUTICS
Reuters · 5h ago
FDA APPROVES COSIBELIMAB-IPDL FOR METASTATIC OR LOCALLY ADVANCED CUTANEOUS SQUAMOUS CELL CARCINOMA - WEBSITE
Reuters · 5h ago
Checkpoint Therapeutics’ unloxcyt approved by FDA
TipRanks · 5h ago
Checkpoint Therapeutics trading halted, news pending
TipRanks · 6h ago
FDA Decision On Checkpoint Therapeutics' Cosibelimab Due On Dec.28 - Will Second Time Be The Charm?
NASDAQ · 1d ago
Weekly Report: what happened at CKPT last week (1202-1206)?
Weekly Report · 4d ago
Buy Rating for Checkpoint Therapeutics: Anticipated Approval of Cosibelimab and Strategic Growth Opportunities
TipRanks · 12/05 16:07
Checkpoint Therapeutics Price Target Maintained With a $20.00/Share by HC Wainwright & Co.
Dow Jones · 12/04 11:30
HC Wainwright & Co. Reiterates Buy on Checkpoint Therapeutics, Maintains $20 Price Target
Benzinga · 12/04 11:20
Biotech Stocks Facing FDA Decision In December 2024
NASDAQ · 12/02 16:38
Weekly Report: what happened at CKPT last week (1125-1129)?
Weekly Report · 12/02 09:57
Biotech Advances Drive Cancer Research as Global Rates Continue Upward Trend
Barchart · 12/02 09:18
Biotech Alert: Searches spiking for these stocks today
TipRanks · 11/29 16:15
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About CKPT
Checkpoint Therapeutics, Inc. is a clinical-stage immunotherapy and targeted oncology company focused on the acquisition, development and commercialization of novel treatments for patients with solid tumor cancers. The Company is evaluating its lead antibody product candidate, cosibelimab, a potential best-in-class anti-programmed death-ligand 1 (PD-L1) antibody licensed from the Dana-Farber Cancer Institute, as a potential new treatment for patients with selected recurrent or metastatic cancers, including metastatic and locally advanced cutaneous squamous cell carcinoma. The Company is also evaluating its lead small-molecule, targeted anti-cancer agent, olafertinib, a third-generation epidermal growth factor receptor (EGFR) inhibitor, as a potential new treatment for patients with EGFR mutation-positive non-small cell lung cancer. Its anti-GITR monoclonal antibody, CK-302, is a fully human agonistic antibody that is designed to bind to and trigger signaling in GITR expressing cells.