Checkpoint Therapeutics reported their Q2 2020 financial results, highlighting the progress of cosibelimab's registration-enabling study in metastatic cutaneous squamous cell carcinoma, which is over 50% enrolled and expected to be fully enrolled by year-end.
Continued to advance the development of cosibelimab, a potential best-in-class anti-PD-L1 antibody product candidate.
The trial for cosibelimab in metastatic cutaneous squamous cell carcinoma is currently over 50% enrolled, with full enrollment anticipated around year-end.
Plan to present updated interim safety and efficacy data from the ongoing mCSCC trial at the European Society for Medical Oncology Virtual Congress 2020.
Previously reported encouraging data, including a 50% objective response rate for cosibelimab by investigator assessment in the first 14 mCSCC patients, including one complete response.
This press release contains forward-looking statements regarding plans to submit Biologics License Applications for cosibelimab, the potential differentiation of cosibelimab, the timing of completion of enrollment and full top-line results, and how long the company believes its cash will fund operations.