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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

Key Takeaway: 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.
Price reaction · baseline $5.85 (2026-07-06 close) · hit after-hours · clean, no other ALGS news in the window
day 0 close · peak
+4.1%

Market Sentiment Analysis

POSITIVE FACTORS

  • Aligos received a $25M upfront payment from Amoytop.
  • Pevifoscorvir sodium granted Breakthrough Therapy Designation in China.
  • Potential for up to $420M in future milestones and royalties.
  • Aligos retains rights for development in major markets outside Greater China.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+153%
120-day peak, hindsight
Typical move
6.1%
average across 6 past catalysts
Cash runway
~3 mo
High dilution risk
Lead asset
ALG-055009
Phase 2 · NASH

Full Press Release Details

Breakthrough Therapy Designation granted for pevifoscorvir sodium in China
SOUTH SAN FRANCISCO, Calif., July 06, 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 that it has received the upfront payment of $25M USD from the exclusive license deal of pevifoscorvir sodium in Greater China with Xiamen Amoytop Biotech Co., Ltd. (Amoytop). In addition, pevifoscorvir sodium was granted Breakthrough Therapy Designation from the Center for Drug Evaluation (CDE) of China’s National Medical Products Administration (NMPA).
Under the terms of the agreement, Aligos is also 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.
“We are pleased to provide this update on the collaboration with Amoytop,” stated Lawrence Blatt, Ph.D., M.B.A., Chairman, President, and Chief Executive Officer of Aligos Therapeutics. “The joint steering committee has been formed, Breakthrough Therapy Designation has been granted for pevifoscorvir sodium in China, and we look forward to the continued progression of this program. In addition, we are continuing to build on our relationship with Amoytop’s planned entrance of our antisense oligonucleotide (ASO) ALG-170675 into the clinic in China in the third quarter of 2026. These two drug candidates together demonstrate the promise of next-generation therapies that have the potential to meaningfully change clinical outcomes for patients with chronic HBV infection.”
Breakthrough Therapy Designation is granted to new drugs that treat serious diseases with preliminary evidence of efficacy. Under this designation, pevifoscorvir sodium is eligible for priority review of a New Drug Application (NDA) in China.

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 infection, metabolic dysfunction-associated steatohepatitis (MASH), obesity, and coronaviruses.
For more information, please visitwww.aligos.comor follow us on LinkedIn or X.

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 Aligos’ financial results and performance as well as research and development activities, including regulatory status and the timing of announcements and updates relating to our regulatory filings and clinical trials; statements about whether pevifoscorvir sodium development will continue to progress successfully in China or any jurisdiction, whether ALG-170675 will enter clinical trials in the third quarter of 2026, and whether pevifoscorvir sodium and ALG-170675 will change clinical outcomes for patients. 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 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, reliance on collaborators, 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’ Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission on May 7, 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 ContactAligos Therapeutics, Inc.Jordyn TaraziVice President, Investor Relations & Corporate Communications+1 (650) 910-0427jtarazi@aligos.com

Media ContactInizio EvokeJake RobisonVice PresidentJake.Robison@inizioevoke.com

Frequently Asked Questions

What is the significance of the $25M payment?

The $25M upfront payment marks the financial commitment from Xiamen Amoytop for the exclusive license of pevifoscorvir sodium in Greater China.

What does Breakthrough Therapy Designation mean?

Breakthrough Therapy Designation allows for priority review of the New Drug Application, expediting the approval process for promising therapies.

What are the potential future earnings for Aligos?

Aligos could earn up to $420M in clinical, regulatory, and sales milestones from the licensing agreement.

Which markets does Aligos retain rights for?

Aligos retains development and commercialization rights for pevifoscorvir sodium in the U.S., Europe, South Korea, Japan, and other markets.

Last updated: Jul 6, 2026