Ninsipapogene sibarnarepvec is under clinical development by Hookipa Pharma and currently in Phase II for Squamous Cell Carcinoma. According to GlobalData, Phase II drugs for Squamous Cell Carcinoma does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Ninsipapogene sibarnarepvec LoA Report. Buy the report here.
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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.
Ninsipapogene sibarnarepvec overview
Ninsipapogene sibarnarepvec (HB-202) is under development for the treatment of human papillomavirus (HPV) associated head and neck cancer squamous cell carcinoma, squamous cell carcinoma and oropharyngeal cancer. It is administered through intravenous route. The therapeutic candidate is a vaccine developed based on TheraT platform technology. The drug candidate acts by targeting human papillomavirus protein E6 and E7. It was under development for the treatment of anal cancer, vulvar cancer, penile cancer, cervical cancer and vaginal cancer.
Hookipa Pharma overview
Hookipa Pharma (Hookipa) is a clinical-stage biopharmaceutical company that develops novel immunotherapies through its arenavirus platform for cancer and chronic infectious diseases using its replicating technology and non-replicating technology. Its pipeline products include HB-200 for the treatment of human papillomavirus 16-positive (HPV16+) cancers; HB-700 for the treatment of Kristen rat sarcoma viral oncogene homolog (KRAS) mutated cancers; HB-300 for the treatment of prostate cancer; HB-400 for hepatitis B (HBV) treatment; and HB-500 for the human immunodeficiency virus (HIV) treatment. Hookipa works in collaboration with other pharmaceutical companies for the development of immunotherapies. Hookipa is headquartered in New York, the US.
For a complete picture of Ninsipapogene sibarnarepvec’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
