DF-6215 is under clinical development by Dragonfly Therapeutics and currently in Phase I for Human Papillomavirus (HPV) Associated Cancer. According to GlobalData, Phase I drugs for Human Papillomavirus (HPV) Associated Cancer have a 76% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how DF-6215’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
DF-6215 is under development for the treatment of advanced or metastatic solid tumors including melanoma, ovarian cancer, head and neck cancer, HPV-positive advanced malignancies, non-small cell lung cancer and renal cell carcinoma. The therapeutic candidate is a cytokine. It acts by targeting interleukin 2 receptor.
Dragonfly Therapeutics overview
Dragonfly Therapeutics (Dragonfly) is a bio-technology company that discovers, develops and commercializes novel immunotherapies to treat cancer. It is investigating tri-specific, NK (natural killer) cell engager therapies against solid and hematological cancers. The company utilizes its proprietary NK cell based TriNKET platform technology to develop anticancer drugs. It works in partnership with University of Washington, The University of Chicago, Seattle Children’s hospital, Massachusetts Institute of Technology and other companies. Dragonfly is headquartered in Waltham, Massachusetts, the US.
For a complete picture of DF-6215’s drug-specific PTSR and LoA scores, buy the report here.