HOOKIPA Pharma Announces FDA Clearance of its Investigational New Drug Application for HB-500 for the Treatment of Human Immunodeficiency Virus
HOOKIPA is responsible for advancing the HIV program through the completion of a Phase 1b clinical trial.
- HOOKIPA is responsible for advancing the HIV program through the completion of a Phase 1b clinical trial.
- The analyses published were conducted with a simian immunodeficiency virus (SIV) model, commonly used in a preclinical setting as a surrogate to HIV.
- One vector is based on lymphocytic choriomeningitis virus (LCMV) as its arenaviral backbone; another vector is based on Pichinde virus (PICV).
- HB-500 is one of two separate development programs in HOOKIPA’s collaboration and license agreement with Gilead.