Drugs / ABI-1179
last change Apr 2026 re-read 3 minutes ago

ABI-1179

Developed for
genital herpes simplex type 2 infectious disorder
Investigated by
Assembly Biosciences

Trials 1

20252026
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT06698575 Dec 2024 → Jan 2026 genital herpes simplex type 2 infectious disorder Assembly Biosciences Completed No outcome recorded

News releases announcing trial results or a regulatory action · 4

DateIssuerRelease
2025-12-08 Assembly Biosciences Results Assembly Biosciences Reports Positive Interim Results from Phase 1b Clinical Studies of Long-Acting Helicase-Primase Inhibitor Candidates ABI-1179 and ABI-5366 Showing Reductions in Viral Shedding Rate and Virologically Confirmed Genital Lesion Rate in Recurrent Genital Herpes assemblybio.com ↗
98% reduction in HSV-2 shedding rate, >99% reduction in high viral load shedding rate and 91% reduction in virologically confirmed genital lesion rate observed in 50 mg weekly oral dose of ABI-1179, exceeding expectations for the study
2025-07-26 Assembly Biosciences Results Assembly Biosciences Presents Data Highlighting Recurrent Genital Herpes Program at STI & HIV 2025 World Congress and International Herpesvirus Workshop assemblybio.com ↗
2025-02-20 Assembly Biosciences Results Assembly Biosciences Reports Positive Interim Phase 1a Results from Clinical Trial Evaluating Long-Acting Helicase-Primase Inhibitor ABI-1179 in Development for Recurrent Genital Herpes assemblybio.com ↗
A half-life of approximately four days and high exposure across the dose range evaluated exceeded Assembly Bio’s targets for a once-weekly oral dosing profile.
2024-07-15 Assembly Biosciences Results Assembly Biosciences Presents New Preclinical Data Highlighting Investigational Helicase-Primase Inhibitors at International Herpesvirus Workshop assemblybio.com ↗

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as ABI-1179 ClinicalTrials.gov intervention name — accepted as the source's own label NCT06698575 ↗
Route Oral “Once daily tablet dosing (SAD), or weekly tablet dosing over 29 days (MAD)” NCT06698575 ↗