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Aligos hands pevifoscorvir license to Xiamen Amoytop in USD 445m deal

Aligos Therapeutics (Nasdaq: ALGS) has entered an exclusive license agreement with Xiamen Amoytop Biotech Co., Ltd. The deal focuses on Aligos's pevifoscorvir sodium, an oral small molecule capsid assembly modulator in Phase II development for chronic hepatitis B virus infection.

Under the deal, Amoytop gains exclusive rights to develop and commercialize the compound across Mainland China, Taiwan, Hong Kong, and Macau. Aligos retains all rights in the US, Europe, Japan, South Korea, and other markets, and also retains the right to run clinical trials in Greater China independently. Aligos will receive a USD 25 million upfront payment and is eligible for up to USD 420 million in clinical, regulatory, and commercial sales milestones, plus tiered high single-digit royalties on net sales. Amoytop will fund its own development program within the licensed territory. The transaction closes upon Amoytop shareholder approval, anticipated within 30 days of the April 16 announcement.

Deal context

Pevifoscorvir sodium, formerly known as ALG-000184, originated from intellectual property licensed from the laboratory of Dr. Raymond Schinazi at Emory University and was further optimized by Aligos. The company describes it as a capsid assembly modulator of the "E" class, or CAM-E, a mechanistic designation referring to compounds that misdirect HBV capsid protein assembly, producing structurally aberrant core particles that cannot package viral pregenomic RNA. According to Aligos' press materials, the compound acts through dual mechanisms: blocking HBV DNA replication and integration, and reducing the covalently closed circular DNA, or cccDNA, reservoir — the nuclear form of the viral genome that persists in infected hepatocytes and underlies chronic infection.

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Phase I studies showed the compound was well-tolerated across single and multiple doses, with linear pharmacokinetics. In longer-term Phase I work, 300 mg once-daily dosing for 96 weeks produced reductions in HBV DNA, HBV RNA, hepatitis B surface antigen, hepatitis B e antigen, and hepatitis B core-related antigen. Pevifoscorvir sodium is currently being evaluated in the Phase II B-SUPREME study (NCT06963710), which compares it against tenofovir disoproxil fumarate. A second interim analysis is expected in H2 2026, with topline data planned for 2027. The US FDA, European Medicines Agency, and China's National Medical Products Administration have each acknowledged a regulatory path for pevifoscorvir sodium using a chronic suppression endpoint.

The deal deepens a relationship that predates this transaction. Aligos and Amoytop formed a research collaboration in 2023, and were already partnered on development of ALG-170675, a preclinical antisense oligonucleotide program targeting chronic HBV. The two companies have now aligned their HBV portfolios across both a small molecule and an oligonucleotide modality within the same geography, positioning Amoytop to pursue combination regimens using its commercially approved pegylated interferon product, PEGBING, alongside both licensed Aligos compounds.


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