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Find Clinical Drug Pipeline Developments & Deals by Assembly Biosciences
The partnership aims to advance the R&D of Assembly Bio’s portfolio of small molecule antiviral therapeutics, including next-generation core inhibitor ABI-4334 for the treatment of HBV, long-acting helicase-primase inhibitor ABI-5366 for herpes simplex virus.
ABI-6250, an orally bioavailable small molecule entry inhibitor, is the first development candidate nominated by the company for the treatment of chronic hepatitis D virus (HDV) infection.
ABI-4334 is a investigational next-generation, highly potent hepatitis B virus (HBV) core inhibitor, which is currently being investegated in phase I for Hepatitis B.
ABI-5366 is a long-acting herpes simplex virus type 2 (HSV-2) helicase inhibitor program. It has low clearance, will enhance both adherence and antiviral activity
The observed PK for the new tablet formulation of ABI-H3733 was consistent with predictions from preclinical studies, providing exposure equivalent to the liquid formulation evaluated in the Phase 1a study for 3733.
ABI-4334 is an investigational next-generation core inhibitor that is optimized for significantly increased potency against covalently closed circular DNA (cccDNA) formation and new virus production versus first-generation core inhibitors.
ABI-4334, novel hepatitis B core inhibitor, accelerates capsid assembly and inhibits cccDNA formation via multiple pathways, in preclinical data it demonstrate the core inhibitor activity of ABI-4334 against pgRNA encapsidation and covalently closed circular DNA formation.
AB-729 is a subcutaneously-delivered RNAi therapeutic specifically designed to reduce all HBV viral antigens, which is thought to be a key prerequisite to enable reawakening of a patient’s immune system to respond to virus.
AB-729 is an RNA interference (RNAi) therapeutic specifically designed to reduce all HBV viral proteins and antigens, including hepatitis B surface antigen, which is thought to be a key prerequisite to enable reawakening of a patient’s immune system to respond to the virus.
Preclinical data presented for ABI-H3733, with its best-in-class potential, demonstrates the candidate's potent activity against both cccDNA formation and pre-genomic RNA (pgRNA) encapsidation.
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