Immunotherapeutic for prostate cancer treatment
AssigneeHexamer Therapeutics, Inc.
InventorsKeith Douglas Miller, Robert Bogden
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AssigneeHexamer Therapeutics, Inc.
InventorsKeith Douglas Miller, Robert Bogden
Estimating the term…
The present disclosure describes a GnRH therapeutic for neutralizing GnRH levels in subjects which can reduce testosterone levels to attenuate or eliminate prostate cancer cell growth and/or metastasis. The therapeutic is produced synthetically. The GnRH therapeutic includes a hapten carrier (hC) comprising a monomeric peptide (MP), synthesized separately from the GnRH peptide, and following self-assembly of the hC, GnRH is covalently coupled to form a GnRH-hC conjugate which can serve as a therapeutic. The MP includes heptad repeats following a specific pattern. The hC can include a GnRH peptide attached to a monomeric peptide prior to self-assembly to form a therapeutic. Optionally, the GnRH-hC conjugate further includes one or more T-cell epitopes at the N- and/or C-terminus of the one or more amphipathic alpha-helices. The present disclosure also describes compositions including immunogenic compositions including the therapeutics described herein.
A scaffold peptide including one or more Gonadotropin releasing hormone (GnRH) peptides covalently attached to a monomeric peptide,
A GnRH conjugate (GnRH-hC) or a GnRH oligomer (GhC) comprising one or more Gonadotropin releasing hormone (GnRH) peptides covalently attached to a hapten carrier (hC), the hC comprising an oligomer which comprises a monomeric peptide,
Dependencies are inferred from the claim text.