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Find Clinical Drug Pipeline Developments & Deals by Hookipa Pharma
The financing aims to fund the HOOKIPA investigational product HB-500, which is a 2-vector arenaviral therapeutic vaccine. It is currently under evaluation as a component of a potential curative regimen for HIV infections.
HB-500 is an alternating, 2-vector novel arenaviral therapeutic vaccine which is under clinical development for the treatment of human immunodeficiency virus (HIV).
HB-200 is HOOKIPA’s lead oncology candidate engineered with the its proprietary replicating arenaviral vector platform. HB-200 in combination with pembrolizumab received Fast Track Designation for the treatment of 1st-line recurrent/metastatic HPV16+ head and neck cancers.
HB-400 (GS-2829) is an alternating, 2-vector non-replicating arenaviral therapeutic vaccine which uses the lymphocytic choriomeningitis virus and pichinde virus as arenaviral backbones,for the treatment of chronic hepatitis B.
The collaboration between HOOKIPA and Roche is to license and develop HB-700, a novel arenaviral immunotherapy for KRAS-mutated cancers and an option for a second, undisclosed arenaviral immunotherapy. HOOKIPA is conducting research through Phase 1b for HB-700.
Following the submission of the clinical trial application (IND equivalent) for HB-400, a Hepatitis B therapeutic, in 2022, HOOKIPA expects the first patient to be dosed in a Phase 1 clinical trial during 2023.
HOOKIPA will conduct development, based on its proprietary arenavirus platform, through Phase 1b for HB-700, an arenaviral immunotherapy for treatment of KRAS-mutated cancers and option to license a second undisclosed novel arenaviral immunotherapy.
HB-300 is alternating, 2-vector replicating arenaviral immunotherapy for castration-resistant prostate cancer, uses Lymphocytic Choriomeningitis Virus and Pichinde Virus as arenaviral backbones, with each expressing two well-defined antigens of prostate cancer, PAP and PSA.
HB-200 was generally well tolerated, rapidly induced a high magnitude of tumor-specific T cells and showed early anti-tumor activity in these difficult-to-treat patients.
Novel arenaviral therapeutic HB-200 generates outstanding tumor antigen-specific CD8+ T cell responses (average of 6 percent and up to 40 percent of T cell pool).