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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

(Very Positive)
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Aligos Therapeutics (Nasdaq: ALGS) entered an exclusive license with Xiamen Amoytop to develop and commercialize pevifoscorvir sodium in Greater China for chronic HBV. Aligos will receive a $25M upfront, up to $420M in milestones, plus tiered high single-digit royalties.

Amoytop will fund development in the region; Aligos retains rights outside Greater China and expects current cash runway to extend into Q4 2026.

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Positive

  • Upfront payment of $25M
  • Up to $420M in clinical, regulatory, and sales milestones
  • Tiered, high single-digit royalties on net sales
  • Amoytop funds development in Greater China
  • Aligos retains ex-Greater China global rights to pevifoscorvir sodium
  • Expected cash runway extended into Q4 2026

Negative

  • Transaction closing is conditional on Amoytop shareholder approval within ~30 days
  • License grants Greater China rights, limiting Aligos’ direct commercial upside in that market
  • Cash runway extended only to Q4 2026, indicating near-term funding sensitivity

News Market Reaction – ALGS

+3.23% 6.5x vol
20 alerts
+3.23% Session close to close
+30.9% Peak Tracked
-28.0% Trough Tracked
$47.40M Market Cap
6.5x Rel. Volume

In the Apr 16 session, ALGS gained 3.23%, reflecting a moderate positive market reaction. Argus tracked a peak move of +30.9% during that session. Argus tracked a trough of -28.0% from its starting point during tracking. Our momentum scanner triggered 20 alerts that day, indicating elevated trading interest and price volatility. Trading volume was exceptionally heavy at 6.5x the daily average, suggesting very strong buying interest.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement adds a significant regional partnership for pevifoscorvir sodium, combining a $25M...
Analysis

This announcement adds a significant regional partnership for pevifoscorvir sodium, combining a $25M upfront payment, up to $420M in milestones, and extended cash runway into Q4 2026. It leverages Amoytop’s chronic HBV franchise in a market of more than 90 million patients, while B-SUPREME Phase 2 data are expected through 2026–2027. Investors may track execution milestones, clinical readouts, and cash usage against the newly guided runway.

Key Figures

Upfront payment: $25M Milestone potential: Up to $420M HBV patients: More than 90 million +5 more
8 metrics
Upfront payment $25M Exclusive Greater China license for pevifoscorvir sodium
Milestone potential Up to $420M Clinical, regulatory, and sales milestones under Amoytop agreement
HBV patients More than 90 million People living with HBV in Greater China
Trial phase Phase 2 B-SUPREME study of pevifoscorvir sodium vs TDF
Second interim timing 2H 2026 Planned second interim analysis for B-SUPREME
Topline timing 2027 Planned topline data readout for B-SUPREME
Cash runway extension Into Q4 2026 Company guidance based on current plan and license economics
Deal closing condition Within 30 days Effectiveness conditional on Amoytop shareholder approval

Historical Context

5 past events · Latest: Apr 14 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Apr 14 Phase 2 interim data Positive -15.1% Interim B-SUPREME results and FDA Fast Track for pevifoscorvir sodium.
Mar 05 Earnings and pipeline Positive -2.9% Q4/FY2025 results, HBV trial progress, and cash runway disclosure.
Feb 26 Earnings date notice Neutral +8.1% Scheduling announcement for Q4 2025 financial results release.
Feb 23 Conference data Positive +2.1% Positive HBV and PK data presented at CROI for pipeline programs.
Jan 30 Inducement grants Neutral -0.6% Equity inducement option grants to newly hired employees.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent positive clinical and financial updates have sometimes coincided with negative price reactions, indicating a pattern of divergence between news tone and near-term trading.

Recent Company History

Over the last few months, Aligos has reported several key milestones tied to its HBV program and finances. On Apr 14, 2026, interim Phase 2 B-SUPREME results and FDA Fast Track Designation for pevifoscorvir sodium were followed by a -15.1% move. Q4 and full-year 2025 results on Mar 5, 2026 highlighted $77.8M in cash and narrowed losses, yet shares fell 2.92%. Earlier, positive CROI data and routine corporate updates produced smaller, mixed reactions. Today’s licensing deal fits into this ongoing HBV-focused development trajectory with partner Amoytop already referenced historically.

Key Terms

antisense oligonucleotide, pegylated interferon, capsid assembly modulator, cccDNA, +4 more
8 terms
antisense oligonucleotide medical
"preclinical antisense oligonucleotide (ASO) program, ALG-170675, for chronic HBV"
An antisense oligonucleotide is a small piece of synthetic genetic material designed to attach to specific molecules in the body’s cells, effectively blocking or modifying how genes are expressed. This technology is important because it can be used to develop targeted treatments for certain diseases, which may influence the value of biotech companies and the broader healthcare sector. Its development reflects advances in personalized medicine and gene-based therapies.
pegylated interferon medical
"As the leading provider of pegylated interferon for chronic HBV infection"
A pegylated interferon is an immune-signaling drug chemically linked to a small, protective molecule so it stays in the body longer and needs less frequent dosing—think of adding a slow-release coating to a pill. For investors, this matters because longer-acting formulations can improve patient convenience, reduce healthcare visits, and offer a competitive edge in pricing, market share, regulatory review and long-term revenue potential compared with shorter-acting versions.
capsid assembly modulator medical
"potential first and best-in-class capsid assembly modulator (CAM-E) under development"
A capsid assembly modulator is a drug that disrupts the construction or stability of a virus’s protein shell (the capsid), stopping the virus from forming infectious particles or from releasing its genetic material. For investors, these drugs matter because they represent a targeted antiviral approach that can create new treatment markets or licensing value if clinical trials succeed, but they also carry the usual high development and regulatory risks of experimental therapies.
cccDNA medical
"but also reduce the cccDNA reservoir, all clinically relevant markers"
cccDNA is a stable, circular form of viral genetic material that can hide inside infected cells and act like a permanent backup copy the virus uses to keep making new virus particles. For investors, cccDNA matters because treatments that reduce or eliminate this hidden template are more likely to produce long-lasting cures, shape clinical trial success and regulatory decisions, and therefore affect a drug’s commercial value and a company’s prospects.
nucleoside analog medical
"compared to the nucleoside analog, tenofovir disoproxil fumarate (TDF)"
A nucleoside analog is a lab-made molecule that mimics the natural building blocks of DNA or RNA and can be mistaken for them when cells or viruses copy their genetic material. Once incorporated, it can block or corrupt copying, stopping viral replication or killing rapidly dividing cells. Investors care because these compounds are common drug candidates whose clinical trial results, patents and approvals strongly affect a company’s future revenue and risk profile.
tenofovir disoproxil fumarate medical
"study (NCT06963710) compared to the nucleoside analog, tenofovir disoproxil fumarate (TDF)"
An oral antiviral medication used to treat HIV and chronic hepatitis B by blocking a key step viruses use to copy their genetic material; it is an inactive formulation that the body converts into the active drug, like a packaged cargo that is opened on delivery. It matters to investors because sales, patent status, safety concerns, and regulatory approvals for this widely prescribed therapy can drive drugmakers’ revenue, affect generic competition, and influence stock valuations and clinical-program risk.
phase 2 medical
"Pevifoscorvir sodium is currently being evaluated in the Phase 2 B-SUPREME study"
Phase 2 is the mid-stage clinical trial where a new drug or treatment is tested in a larger group of patients to see if it works and to keep checking safety after initial human testing. Think of it as a field test that proves whether a product actually delivers its promised benefit. Investors watch Phase 2 closely because its results strongly influence a medicine’s chances of reaching the market, the size of its potential sales, and the company’s valuation.
royalties financial
"milestones along with tiered, high single-digit royalties on net sales"
Payments made to the owner of an asset or intellectual property each time that asset is used or a product is sold, often calculated as a percentage of sales or a set amount per unit. Royalties matter to investors because they create predictable, ongoing income streams and affect a company’s cash flow and valuation—like a landlord collecting rent or an author getting a steady cut whenever a book is sold.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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  • Aligos to receive an upfront payment of $25M USD
  • Up to $420M USD in clinical, regulatory, and sales milestones along with tiered, high single-digit royalties
  • Amoytop to fund its development program in Greater China
  • Amoytop is a leading Chinese pharmaceutical company with commercially approved therapeutics, including PEGBING®, to treat chronic HBV infection

SOUTH SAN FRANCISCO, Calif., April 16, 2026 (GLOBE NEWSWIRE) -- Aligos Therapeutics, Inc. (Nasdaq: ALGS, “Aligos”), a clinical stage biopharmaceutical company focused on developing novel therapeutics to address unmet medical needs in liver and viral diseases, today announced that it has entered into an exclusive license agreement to develop and commercialize pevifoscorvir sodium with Xiamen Amoytop Biotech Co., Ltd. (“Amoytop”) in Greater China, which includes Mainland China, Taiwan, Hong Kong, and Macau for chronic hepatitis B virus (HBV) infection.

Under the terms of the agreement, Aligos will receive an upfront milestone of $25M USD and is eligible to receive up to $420M USD in clinical, regulatory, and sales milestones along with tiered, high single-digit royalties on net sales in Amoytop’s licensed territories. Aligos retains all development and commercialization rights for pevifoscorvir sodium in the United States, Europe, South Korea, Japan, and all other markets. In addition, Aligos will retain the right to conduct clinical trials in Greater China. With more than 90 million people living with HBV in Greater China, and given Amoytop’s leadership in the Mainland China hepatology market, this agreement is expected to position pevifoscorvir sodium for greater development and regulatory success in the region. As a result of this agreement, Aligos expects that current cash, cash equivalents and investments will be extended into the fourth quarter of 2026 based on the current operating plan.

“We are pleased to build on our established relationship with Amoytop, a trusted partner through our preclinical antisense oligonucleotide (ASO) program, ALG-170675, for chronic HBV infection,” said Lawrence Blatt, Ph.D., MBA, Chairman, President, and Chief Executive Officer of Aligos Therapeutics. “As the leading provider of pegylated interferon for chronic HBV infection in Mainland China, Amoytop is well positioned to commercialize pevifoscorvir sodium across the licensed territories. With a robust commercial organization comprised of sales representatives focused on the hepatology field, Amoytop has the scale and expertise to support broad adoption. Amoytop’s strong reach in the Mainland China hepatology market is expected to accelerate the development of pevifoscorvir sodium for chronic HBV suppression compared to Aligos developing in the region. Additionally, we believe that combining pevifoscorvir sodium with Amoytop’s drug PEGBING®, along with our ongoing ASO collaboration, will enable differentiated combination regimens and more personalized treatment approaches for patients with chronic HBV infection across Greater China. Aligos currently intends to pursue similar strategies, along with the chronic suppression pathway for monotherapy, in the United States, Europe, Japan, South Korea, and other global markets.”

Pevifoscorvir sodium is a potential first and best-in-class capsid assembly modulator (CAM-E) under development for chronic HBV infection, a novel drug designed to improve clinical outcomes by affecting the entire HBV lifecycle. Through its dual mechanisms of action, pevifoscorvir sodium not only has the potential to block HBV replication and prevent HBV DNA integration, but also reduce the cccDNA reservoir, all clinically relevant markers that improve outcomes in chronic HBV infection. Pevifoscorvir sodium is currently being evaluated in the Phase 2 B-SUPREME study (NCT06963710) compared to the nucleoside analog, tenofovir disoproxil fumarate (TDF), with the second interim analysis expected in the second half of 2026 and topline data planned for 2027.

“Aligos is at the forefront of HBV innovation, and we are pleased to deepen our partnership with this outstanding team,” said Sun Li, Chairman and Chief Executive Officer at Amoytop. “We believe pevifoscorvir sodium has the potential to transform chronic HBV suppression, and we are proud to license this important program for Greater China. As we continue to build our portfolio—including the Aligos-partnered ASO and approved PEGBING® therapy—we look forward to exploring combination approaches that deliver meaningful benefits to patients across the region.”

The closing of this transaction is conditional and automatically effective upon Amoytop receiving approval at a Shareholders’ Meeting, which is anticipated within 30 days.

About pevifoscorvir sodium

Pevifoscorvir sodium (formerly known as ALG-000184) was derived from initial IP licensed from the laboratory of Dr. Raymond Schinazi at Emory University, which was further optimized by Aligos. Pevifoscorvir sodium is a potent potential best/first-in-class oral small molecule capsid assembly modulator (CAM-E) being developed for chronic hepatitis B virus (HBV) infection. Phase 1 studies have demonstrated after single and multiple daily doses that pevifoscorvir sodium was well-tolerated by study participants, with no safety signals observed, and demonstrated linear PK and promising antiviral activity. In longer term Phase 1 studies, pevifoscorvir sodium 300mg QD for 96 weeks monotherapy has demonstrated potent viral suppression in HBV DNA and RNA and substantial reductions in HBsAg, HBeAg, and HBcrAg. Pevifoscorvir sodium has a regulatory path, as acknowledged by the FDA, EMA, and NMPA (China), for subsequent studies utilizing the chronic suppressive pathway.

About Aligos

Aligos Therapeutics, Inc. (NASDAQ: ALGS) is a clinical stage biotechnology company founded with the mission to improve patient outcomes by developing best-in-class therapies for the treatment of liver and viral diseases. Aligos applies its science driven approach and deep R&D expertise to advance its purpose-built pipeline of therapeutics for high unmet medical needs such as chronic hepatitis B virus (HBV) infection, metabolic dysfunction-associated steatohepatitis (MASH), obesity, and coronaviruses.

For more information, please visit www.aligos.com or follow us on LinkedIn or X.

About Xiamen Amoytop Biotech Co., Ltd.
Xiamen Amoytop Biotech Co., Ltd. is an innovative biopharmaceutical company and a listed company on the Science and Technology Innovation Board (SSE STAR Market) in China, specializing in R&D, manufacturing and marketing of regular and long-acting recombinant protein drugs. Focusing on the R&D of immune-related cytokine medicines, Amoytop is committed to becoming a leader in solving cytokine medicine-based systemic immune problems, providing better solutions for major diseases (such as viral hepatitis, malignant tumors) and immunotherapy.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the U.S. Private Securities Litigation Reform Act of 1995. Any statements in this press release that are not historical facts may be considered “forward-looking statements,” including without limitation, statements regarding potential financial milestones being met and future royalties being earned by Aligos under the Amoytop license; timing of transaction closing; timing of a meeting of shareholders of Amoytop and potential approval; Aligos’ expectation of Amoytop’s ability to successfully develop, obtain regulatory approval for, and commercialize pevifoscorvir sodium in Greater China; Aligos’ financial results and performance, including cash runway; and Aligos’ research and development activities, including regulatory status and the timing of announcements and updates relating to our regulatory filings and clinical trials. Such forward looking statements are subject to substantial risks and uncertainties that could cause our development programs, future results, performance, or achievements to differ materially from those anticipated in the forward-looking statements. Such risks and uncertainties include, without limitation, risks that Amoytop does not approve the transaction or that the transaction does not close for any other reason, risks and uncertainties inherent in the drug development process, including Aligos’ clinical-stage of development, the process of designing and conducting clinical trials, the regulatory approval processes, risks related to Amoytop's ability to maintain its commercial organization and market position in Greater China; regulatory and geopolitical risks in the licensed territories, including actions by the NMPA, risks that combination regimens may not demonstrate favorable safety, efficacy, or regulatory profiles, risks from competing therapies, risks related to intellectual property protection in Greater China, risks related to foreign currency fluctuations and cross-border payment constraints, and other matters that could affect the sufficiency of Aligos’ capital resources to fund operations. For a further description of the risks and uncertainties that could cause actual results to differ from those anticipated in these forward-looking statements, as well as risks relating to the business of Aligos in general, see Aligos’ Annual Report on Form 10-K filed with the Securities and Exchange Commission on March 5, 2026 and its future periodic reports to be filed or submitted with the Securities and Exchange Commission. Except as required by law, Aligos undertakes no obligation to update any forward-looking statements to reflect new information, events or circumstances, or to reflect the occurrence of unanticipated events.

Investor Contact
Aligos Therapeutics, Inc.
Jordyn Tarazi
Vice President, Investor Relations & Corporate Communications
+1 (650) 910-0427
jtarazi@aligos.com

Media Contact
Inizio Evoke
Jake Robison
Vice President
Jake.Robison@inizioevoke.com

Xiamen Amoytop Biotech Co., Ltd.

Investor Contact
Liu Peiyu
联系电话:86592-6889118
邮箱:ir@amoytop.com

Media Contact

Wu Xueyan
联系电话:86592-6889127
邮箱:wxy@amoytop.com


FAQ

What did Aligos (ALGS) announce about pevifoscorvir sodium in Greater China on April 16, 2026?

Aligos announced an exclusive Greater China license to Amoytop with a $25M upfront payment. According to the company, the deal includes up to $420M in milestones and tiered high single-digit royalties, while Aligos retains rights outside Greater China and can still run trials there.

How much upfront and milestone money will ALGS receive from the Amoytop license?

Aligos will receive a $25M upfront payment and is eligible for up to $420M in milestones. According to the company, additional economics include tiered high single-digit royalties on net sales in Amoytop’s licensed territories.

How does the Amoytop deal affect Aligos’ cash runway and financial timing?

Aligos expects current cash, cash equivalents and investments to be extended into the fourth quarter of 2026. According to the company, this projection is based on the current operating plan and the upfront payment from the Amoytop agreement.

What development and commercialization rights does Aligos retain after the ALGS–Amoytop agreement?

Aligos retains development and commercialization rights for pevifoscorvir sodium outside Greater China. According to the company, Aligos keeps rights in the U.S., Europe, Japan, South Korea and all other markets while Amoytop covers Greater China.

What clinical milestones and trial timeline for pevifoscorvir sodium did Aligos disclose for 2026–2027?

Aligos reported a Phase 2 B-SUPREME study with a second interim analysis expected in H2 2026 and topline data planned for 2027. According to the company, the study compares pevifoscorvir sodium to tenofovir disoproxil fumarate (TDF).

What strategic benefits does Amoytop claim the ALGS license provides for HBV treatment in Greater China?

Amoytop says the license positions pevifoscorvir sodium for broader development and regulatory success across Greater China. According to the company, Amoytop’s hepatology commercial scale and PEGBING® portfolio support combination and adoption strategies in the region.