Drugs / ALG-000184
last change Jul 2026 re-read 9 days ago

ALG-000184

Other / unclassified

Developed for
chronic hepatitis B virus infection
Investigated by
Aligos Therapeutics

Trials 5

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 14 trials
Phase 1 NCT07342881 Feb → Jun 2026 overdue chronic hepatitis B virus infection Aligos Therapeutics Recruiting No outcome recorded
Phase 1 NCT07342868 Jan → Apr 2026 overdue chronic hepatitis B virus infection Aligos Therapeutics Recruiting No outcome recorded
Phase 1 NCT06672900 Jan → Jul 2025 overdue — Aligos Therapeutics Active not recruiting No outcome recorded
Phase 1 NCT04536337 Oct 2020 → Jun 2025 chronic hepatitis B virus infection Aligos Therapeutics Completed No outcome recorded
Phase 21 trial
Phase 2 NCT06963710 Jul 2025 → Mar 2027 expected chronic hepatitis B virus infection Aligos Therapeutics Active not recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 36

DateIssuerRelease
2026-05-27 Xiamen Amoytop Biotech Co., Ltd. Regulatory 百年儿科匠心 助力健康中国建设 | 院企合作,共同开启儿童罕见病防治新篇章 amoytop.com ↗
5月26日,国 家 药 品 监 督 管 理 局 药 品 审 评 中 心(CDE)官 网 显 示,特 宝 生 物 引 进 的 慢 性 乙 肝 新 药ALG-000184片(Pevifoscorvir sodium)拟 纳 入 突 破 性 疗 法,用 于 治 疗 初 治 或 目 前 未 治 疗 的 慢 性 乙 型 肝 炎 病 毒 感 染 者 以 达 到 长 期 病 毒 学 抑 制 的 目 标.
2026-05-27 Aligos Therapeutics Results Aligos Therapeutics Presents Positive Data at the EASL Congress 2026 aligos.com ↗
Long-term follow up data from the Phase 1 study of pevifoscorvir sodium continues to suggest a reduction in the cccDNA reservoir
2026-05-13 Aligos Therapeutics Results Aligos Therapeutics Announces Ten Abstracts Accepted for Presentation at the EASL Congress 2026 aligos.com ↗
Sustained reduction of HBV antigen levels at ≥6 months follow-up in HBeAg-positive participants with chronic hepatitis B infection after 96 weeks of 300 mg pevifoscorvir sodium monotherapy
2026-05-07 Aligos Therapeutics Results Aligos Therapeutics Reports Recent Business Progress and First Quarter 2026 Financial Results aligos.com ↗
In addition, we completed the first interim analysis for the B-SUPREME HBeAg- cohort with a positive outcome reflecting that the study will continue, the futility criteria were not met, and study drugs were well tolerated.
2026-04-14 Aligos Therapeutics Results Aligos Therapeutics Announces First Interim Analysis Results from the Phase 2 B-SUPREME Study of Pevifoscorvir Sodium in Participants with Chronic Hepatitis B Virus Infection and Grant of FDA Fast Track Designation aligos.com ↗
2026-02-23 Aligos Therapeutics Results Aligos Therapeutics Presents Positive Data at the Conference on Retroviruses and Opportunistic Infections (CROI) aligos.com ↗
SOUTH SAN FRANCISCO, Calif., Feb. 23, 2026 (GLOBE NEWSWIRE) -- Aligos Therapeutics, Inc. (Nasdaq: ALGS), a clinical stage biopharmaceutical company focused on improving patient outcomes through best-in-class therapies for liver and viral diseases, today announced positive data from two presentations at the Conference on Retroviruses and Opportunistic Infections (CROI), being held February 22 – 25, 2026 in Denver, Colorado.
2025-12-11 Aligos Therapeutics Results Aligos Therapeutics Presents Positive Data at HEP-DART 2025 aligos.com ↗
The complete 96-week and post-treatment follow up data from the Phase 1 monotherapy (NCT04536337) cohorts in subjects with chronic HBV infection show the continued potential of pevifoscorvir sodium to become a first-line therapy for chronic suppression.
2025-11-10 Aligos Therapeutics Results Aligos Therapeutics Presents Positive Data at The Liver Meeting® 2025 aligos.com ↗
In the HBeAg- subjects, 8 of 9 subjects switched to NA monotherapy, and all 8 (100%) subjects maintained HBV DNA < LLOQ (10 IU/mL, TD or TND) throughout the NA only 8-week follow-up period.
2025-10-07 Aligos Therapeutics Results Aligos Therapeutics Announces Eight Abstracts Accepted at The Liver Meeting® 2025 aligos.com ↗
Oral Once -Daily 300 mg ALG-000184, a Novel Capsid Assembly Modulator Demonstrates potent suppression of HBV DNA in Treatment-Naive or Currently-not-treated Subjects with Chronic HBV
2025-09-03 Aligos Therapeutics Results Aligos Therapeutics Announces Six Preclinical Presentations at the 2025 International HBV Meeting aligos.com ↗
With the Phase 2 B-Supreme study progressing nicely, we are pleased to present, for the first time, the direct effects of ALG-000184 in reducing HBV cccDNA in a preclinical setting.
2025-05-08 Aligos Therapeutics Results Aligos Therapeutics Presents Positive Data at the EASL Congress 2025 aligos.com ↗
All subjects in both the HBeAg+ and HBeAg- cohorts have achieved HBV DNA viral suppression < LLOQ (10 IU/mL) and continue to demonstrate sustained log10 reductions in viral antigens such as HBcrAg.
2025-04-23 Aligos Therapeutics Results Aligos Therapeutics Announces Eight Abstracts Accepted for Presentation at the EASL Congress 2025 aligos.com ↗
Monotherapy with the Novel Capsid Assembly Modulator ALG-000184 for up to 96 Weeks Results in Profound and Sustained HBV DNA Suppression in Untreated Subjects with Chronic HBV Infection

All press releases naming this drug 49 releases

DateIssuerRelease

Evidence & citations 6 cited values

Every value below carries the sentence it was read from. 6 sources stand behind the page.

FieldValueCited text
Known as ALG-000184 “Pevifoscorvir Sodium (ALG-000184) Single oral doses of 100 mg pevifoscorvir sodium” NCT07342868 ↗
4

“Pevifoscorvir Sodium (ALG-000184)” NCT07342881 ↗

NCT04536337 ↗

NCT06672900 ↗

NCT06963710 ↗

Known as Pevifoscorvir ClinicalTrials.gov intervention name — accepted as the source's own label NCT07342868 ↗
1

NCT07342881 ↗

Known as pevifoscorvir sodium “Pevifoscorvir Sodium (ALG-000184) Single oral doses of 100 mg pevifoscorvir sodium” NCT07342868 ↗
2

“ALG-000184 (pevifoscorvir sodium) is a prodrug of the class-E” PMID 41554267 ↗ Jan 2026

“Pevifoscorvir Sodium (ALG-000184)” NCT07342881 ↗

Action Inhibit “ALG-000184 is a prodrug that is converted to ALG-001075, a Class E CAM that inhibits HBV replication through two mechanisms:” NCT04536337 ↗
Modality Other / unclassified “ALG-000184 is a prodrug that is converted to ALG-001075, a Class E CAM” NCT04536337 ↗
Route Oral “Eligible patients were randomly assigned (4:1) to receive 28 days of oral ALG-000184 (10 mg, 50 mg, 100 mg, or 300 mg) or matching placebo once per day.” PMID 41554267 ↗ Jan 2026