Financials
Cash Data
- Monthly Burn
- Burn Trend
- Dilution Risk
- SEC Filing
Key Stats
Upcoming Catalysts
FDA decisions, readouts and PDUFA dates · scored by probability of approval
ALGS Catalyst Timeline
Dated clinical, regulatory and corporate events for Aligos Therapeutics, Inc.
Catalyst Timeline
Dated clinical, regulatory & corporate events for Aligos Therapeutics, Inc.
Upcoming catalysts 2
Event history 50
Past FDA Catalysts and PDUFA Decisions
How ALGS actually traded into and out of each decision
| Date | Drug | Catalyst | Stage | Reaction | Event Move % | Best Trade % |
|---|---|---|---|---|---|---|
| 2026-05-28 | ALG-093940 | Pre-clinical data readout | Pre-clinical |
Drug Pipeline Intelligence
| Drug | Indication | Phase | PTRS | rNPV | Status | Enroll | Velocity | Design | Est. Completion | ML Signal | Last Change |
|---|---|---|---|---|---|---|---|---|---|---|---|
| ALG-055009 Small moleculeCompletedNCT06342947 | NASH | Phase 2 | COMPLETED | 102 | Sep 9, 2024 |
Clinical Trial Results
Readouts, endpoints and source filings for every ALGS program
| Drug Name | Indication | Phase | Date | Trial Results Summary | Title | Source |
|---|---|---|---|---|---|---|
| pevifoscorvir sodium BreakthroughFast Track | chronic HBV infection | Phase 1 | 2026-05-27 | 40% of HBeAg+ participants achieved significant reductions in HBsAg; 4 (44%) maintained HBV DNA levels below the lower limit of quantification (LLOQ; 10 IU/mL); 40% (4/10) achieved HBsAg <3,000 IU/mL at 48 weeksRead More | Aligos Therapeutics Presents Positive Data at the EASL Congress 2026Read More |
Inside Trades
| Insider | Side | Shares | Price | Value | Date |
|---|---|---|---|---|---|
| Preston HeatherDirector | Grant/Award | 5,860 5,860 held | $0.00 | 06/25/2026 |
Hedge Fund 13F Activity
Hedge Funds invested in ALGS
| Fund | % of Portfolio | Current MV | Shares Owned | Activity |
|---|---|---|---|---|
| Deep Track Capital, LP | 0 % (-100 %) | 2.56 M | 444.11 K |
ALGS Institutional Ownership Trends
Options Data
Option Volume
Option Chain Statistics
| Expiry | Call Vol | Put Vol | Vol P/C | Call OI | Put OI | OI P/C | IV Call | IV Call OI-Wtd | IV Call Vol-Wtd | IV Put | IV Put OI-Wtd | IV Put Vol-Wtd |
|---|
Real-Time Option Chain
| Calls | Strike | Puts | ||||
|---|---|---|---|---|---|---|
| Last | Vol | OI | Last | Vol | OI | |
| No data available | ||||||
Calls vs Puts by Expiry
Competitive positioning
How ALGS ranks across every disease it competes in
ALGS News
Aligos Therapeutics Announces Five Abstracts Accepted for Presentation at The Liver Meeting® 2026
Aligos Therapeutics announced that five abstracts have been accepted for presentation at The Liver Meeting® 2026, scheduled for November 5-9 in Denver, CO. The abstracts highlight the company's innovative therapies targeting chronic hepatitis B virus infection, showcasing promising results from their clinical research. This participation underscores Aligos's commitment to advancing treatment options in liver diseases.
Read more →Aligos Therapeutics to Present at the Cantor Global Healthcare Conference
Aligos Therapeutics, a clinical-stage biopharmaceutical company, will present at the Cantor Global Healthcare Conference on September 9, 2026. The presentation will focus on their pipeline aimed at treating liver and viral diseases. A replay will be available for 30 days post-event, emphasizing their commitment to improving patient outcomes.
Read more →Aligos Therapeutics Announces First Participant Dosed in the Phase 1 Study of its Potentially Best-in-Class Antisense Oligonucleotide ALG-170675 by its Partner Amoytop in China
Aligos Therapeutics has initiated dosing in a Phase 1 study for ALG-170675, an antisense oligonucleotide aimed at treating chronic hepatitis B virus infection. Conducted by Amoytop in China, the study will assess safety, tolerability, and pharmacokinetics. The first participant has been dosed, marking a significant milestone for Aligos in advancing therapies for chronic HBV.
Read more →Aligos Therapeutics Reports Recent Business Progress and Second Quarter 2026 Financial Results
Aligos Therapeutics reported significant progress in its business and financial results for Q2 2026. The company secured a $25 million upfront payment from a licensing agreement and completed enrollment for its Phase 2 B-SUPREME study. Additionally, Aligos received Breakthrough Designation for its drug in China, with topline data expected in late Q3 2027. However, the company also reported a net loss of $1.5 million during the quarter.
Read more →Aligos Therapeutics to Announce 2nd Quarter 2026 Financial Results on August 6, 2026
Aligos Therapeutics, a clinical stage biotechnology company, will announce its second quarter 2026 financial results on August 6, 2026, before U.S. markets open. The company aims to enhance patient outcomes through innovative therapies for liver and viral diseases. Aligos emphasizes its commitment to addressing high unmet medical needs in chronic hepatitis B virus infection.
Read more →Aligos Therapeutics Announces the Completion of Enrollment in the Phase 2 B-SUPREME Study of Pevifoscorvir Sodium Under Development for the Treatment of Chronic HBV Infection
Aligos Therapeutics has announced the completion of enrollment in its Phase 2 B-SUPREME study for pevifoscorvir sodium, targeting chronic HBV infection. The study enrolled 131 HBeAg+ and 114 HBeAg- participants, surpassing initial enrollment goals. Topline data is anticipated in late Q3 2027, marking a crucial step in the development of this potential treatment.
Read more →Aligos Therapeutics Receives Upfront Payment of $25M USD from the Exclusive License Deal of Pevifoscorvir Sodium in Greater China for Chronic Hepatitis B Virus Infection
Aligos Therapeutics has secured a $25 million upfront payment from Xiamen Amoytop Biotech for the exclusive licensing of pevifoscorvir sodium in Greater China. The drug has also received Breakthrough Therapy Designation from China's regulatory authority, facilitating priority review for its New Drug Application. Aligos stands to gain up to $420 million in milestone payments and retains rights in other key markets.
Read more →Aligos Therapeutics Presents Positive Data at the EASL Congress 2026
Aligos Therapeutics presented promising data at the EASL Congress 2026, highlighting the efficacy of pevifoscorvir sodium in reducing the cccDNA reservoir in chronic HBV patients. Notably, 40% of participants achieved significant reductions in HBsAg, suggesting eligibility for functional cure treatments. The combination of pevifoscorvir sodium and antisense oligonucleotide ALG-170675 showed synergistic effects, indicating a potential shift in treatment standards for chronic HBV infection.
Read more →Aligos Therapeutics Announces Ten Abstracts Accepted for Presentation at the EASL Congress 2026
Aligos Therapeutics has announced that ten of its abstracts have been accepted for poster presentations at the EASL Congress 2026 in Barcelona. The presentations will focus on their innovative therapies targeting chronic hepatitis B and metabolic dysfunction-associated steatohepatitis. This recognition highlights Aligos' commitment to advancing treatment options in liver diseases.
Read more →Aligos Therapeutics Reports Recent Business Progress and First Quarter 2026 Financial Results
Aligos Therapeutics has reported its business progress and financial results for Q1 2026, highlighting the Fast Track Designation for its drug, pevifoscorvir sodium, aimed at chronic HBV infection. The interim analysis of the B-SUPREME study indicated positive results, with a recommendation to increase participant numbers to improve the study's success rate. However, the company also reported a significant net loss compared to the previous year due to rising R&D expenditures. Aligos continues to collaborate with Amoytop for developments in Greater China, which could enhance its market presence.
Read more →Aligos Therapeutics to Announce 1st Quarter 2026 Financial Results on May 7, 2026
Aligos Therapeutics, Inc. has announced it will report its first quarter 2026 financial results on May 7, 2026. The company is focused on improving patient outcomes through its development of best-in-class therapies aimed at liver and viral diseases, addressing conditions like chronic hepatitis B and metabolic disorders. However, the press release also emphasizes the inherent risks associated with drug development and clinical trials, which may affect actual results compared to forward-looking statements. Investors are advised to refer to Aligos' annual report for detailed risks.
Read more →Aligos Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Aligos Therapeutics, Inc. has announced the granting of stock options amounting to 10,700 shares to newly hired employees as part of an Inducement Grant under Nasdaq Listing Rule 5635(c)(4). This move aims to attract talent as the company focuses on developing therapies for liver and viral diseases. The stock options will vest over four years, reflecting a commitment to employee retention and growth in the clinical stage biopharmaceutical field. However, the announcement includes forward-looking statements that highlight potential risks and uncertainties related to drug development and regulatory processes.
Read more →Aligos Therapeutics Enters into Exclusive License Deal with Xiamen Amoytop Biotech Co., Ltd. to Develop and Commercialize Pevifoscorvir Sodium in Greater China for Chronic Hepatitis B Virus Infection
Aligos Therapeutics has entered an exclusive licensing agreement with Xiamen Amoytop Biotech to develop and commercialize pevifoscorvir sodium for chronic hepatitis B in Greater China. Aligos will receive an upfront payment of $25 million and could earn up to $420 million in milestones. The partnership aims to leverage Amoytop's established market presence to enhance the drug's development and regulatory success.
Read more →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 Therapeutics announced positive interim results from the Phase 2 B-SUPREME study of pevifoscorvir sodium for chronic hepatitis B virus infection. The independent Data Safety Monitoring Board recommended increasing the sample size for better statistical power. Additionally, the FDA granted Fast Track Designation to the drug, facilitating its development and review process.
Read more →Aligos Therapeutics Reports Recent Business Progress and Fourth Quarter and Full Year 2025 Financial Results
Aligos Therapeutics reported progress in its clinical trials and financial results for 2025. The Phase 2 B-SUPREME study of pevifoscorvir sodium has completed enrollment for the HBeAg- cohort, with ongoing enrollment for HBeAg+ participants. The company also advanced ALG-170675 into IND-enabling studies and appointed James Hassard as Chief Commercial Officer. Financially, Aligos showed reduced net losses compared to 2024.
Read more →Aligos Therapeutics to Announce 4th Quarter 2025 Financial Results on March 5, 2026
Aligos Therapeutics, a clinical-stage biotechnology company, will announce its fourth quarter 2025 financial results on March 5, 2026. The company aims to improve patient outcomes through innovative therapies for liver and viral diseases. Aligos has a pipeline targeting chronic hepatitis B, metabolic dysfunction-associated steatohepatitis, obesity, and coronaviruses.
Read more →Aligos Therapeutics Presents Positive Data at the Conference on Retroviruses and Opportunistic Infections (CROI)
Aligos Therapeutics presented promising data at the Conference on Retroviruses and Opportunistic Infections (CROI), focusing on two key projects. The Phase 1 study of pevifoscorvir sodium demonstrated high viral suppression in chronic hepatitis B virus (HBV) patients. Additionally, data on ALG-097558, a pan-coronavirus protease inhibitor, was showcased, highlighting its pharmacokinetics in patients with renal and hepatic impairment.
Read more →Aligos Therapeutics Provides Phase 2 B-SUPREME Study Progress Updates
Aligos Therapeutics has provided an update on its Phase 2 B-SUPREME study for pevifoscorvir sodium in chronic hepatitis B patients. Currently, 144 subjects are enrolled, with interim analyses planned for 2026. The company remains optimistic about the drug's potential, with topline data expected in 2027. However, a leadership change has occurred with the resignation of the Chief Medical Officer.
Read more →