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Checkpoint Therapeutics inc   (NASDAQ: CKPT)
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Price: $4.0600 $0.01 0.247%
Day's High: $4.06 Week Perf: -0.25 %
Day's Low: $ 4.05 30 Day Perf: 37.63 %
Volume (M): 1,317 52 Wk High: $ 4.44
Volume (M$): $ 5,348 52 Wk Avg: $2.65
Open: $4.05 52 Wk Low: $1.38



 Market Capitalization (Millions $) 175
 Shares Outstanding (Millions) 43
 Employees 22
 Revenues (TTM) (Millions $) -
 Net Income (TTM) (Millions $) -46
 Cash Flow (TTM) (Millions $) 3
 Capital Exp. (TTM) (Millions $) 0

Checkpoint Therapeutics Inc
Checkpoint Therapeutics Inc. is a clinical stage biopharmaceutical company that focuses on the development of immunotherapy treatments for cancer. The company was founded in 2014 and is headquartered in New York City, USA. Checkpoint Therapeutics is a publicly traded company on the NASDAQ stock exchange with the ticker symbol "CKPT".

The company's primary focus is to develop treatments that enable the immune system to recognize and attack cancer cells by blocking two specific proteins: PD-L1 and VISTA. These proteins are frequently found on the surface of cancer cells, and they help the cancer cells evade detection by the body's immune system. If the immune system can't recognize the cancer cells, it can't attack them effectively, and the cancer cells continue to grow and spread.

Checkpoint Therapeutics is developing two lead drug candidates: CK-301 and CK-10 CK-301 is an anti-PD-L1 antibody that is entering Phase 3 clinical trials for non-small cell lung cancer, and CK-101 is an anti-PD-L1/VISTA bispecific antibody that is currently in Phase 1b clinical trials for advanced solid tumors.

In addition to its lead candidates, Checkpoint Therapeutics has a pipeline of additional immunotherapy treatments in preclinical development, including a bispecific antibody targeting PD-1 and LAG-3, and an agonistic antibody targeting CD40.

The company has a partnership with TG Therapeutics, Inc. for the development and commercialization of CK-301 in combination with TG's anti-CD20 monoclonal antibody, ublituximab, for the treatment of lymphoma.

Overall, Checkpoint Therapeutics' mission is to develop innovative immunotherapy treatments that can improve outcomes for patients with cancer. The company's emphasis on targeting PD-L1 and VISTA makes it well-positioned to continue making progress in the fight against cancer.


   Company Address: 95 Sawyer Road Waltham 2453 MA
   Company Phone Number: 652-4500   Stock Exchange / Ticker: NASDAQ CKPT


   

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Clinical Study

UNLOXCYT A New Horizon in the Management of Advanced Cutaneous Squamous Cell Carcinoma CSIMark...

Published Fri, Dec 13 2024 11:15 PM UTC

UNLOXCYT: A New Horizon in the Management of Advanced Cutaneous Squamous Cell Carcinoma CSIMarket.com Abstract The recent approval of UNLOXCYT (cosibelimab-ipdl) by the U.S. Food and Drug Administration (FDA) marks a significant advancement in the treatment landscape of advanced cutaneous squamous cell carcinoma (cSCC). This novel therapeutic, distinguished as the first ...

Clinical Study

Checkpoint Therapeutics Announces Cosibelimab Longer-Term Results in Advanced Cutaneous Squamous Cell Carcinoma Prese...

Published Mon, Sep 16 2024 11:31 AM UTC

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Contract

A Match Made in Cancer Research Uniting GC Cell and Checkpoint Therapeutics for Powerful Cancer Therapy

Published Mon, Jul 15 2024 12:01 PM UTC

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Shares

Checkpoint Therapeutics Announces $12 Million Capital Boost for Clinical-stage Immunotherapy and Targeted Oncology Pipelines

Published Tue, Jul 2 2024 12:01 PM UTC


Checkpoint Therapeutics Announces $12 Million Registered Direct Offering Priced At-the-Market Under Nasdaq Rules
WALTHAM, Mass., July 02, 2024 - Checkpoint Therapeutics, Inc. (Checkpoint) (Nasdaq: CKPT), a clinical-stage immunotherapy and targeted oncology company, has recently revealed a significant development that will impact its future trajectory. The company ha...

Licensing Agreement

Checkpoint Therapeutics Biologics License Application Resubmission for Cosibelimab Brings New Hope for Advanced cSCC...

Published Tue, Jul 2 2024 11:01 AM UTC

Checkpoint Therapeutics, a clinical-stage immunotherapy and targeted oncology company, has recently announced that it has completed the resubmission of its Biologics License Application (BLA) to the U.S. Food and Drug Administration (FDA) for cosibelimab. Cosibelimab is an anti-programmed death ligand-1 (PD-L1) antibody that shows promise as a potential new treatment for pat...










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