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Hibsago (bepirovirsen)

Chronic hepatitis B virus infection in adults without cirrhosis

Also known as GSK3228836
Manufacturer
GSK
Last updated
190 sources

Economic information and modeling report

Budget impact model

1 evidence topic · 5 sources

Approach and framework

No evidence found.

Perspective and time frame

No evidence found.

Epidemiology and eligible population inputs

No evidence found.

Cost assumptions

No evidence found.

Model outcomes

No evidence found.

Results

Base case

No evidence found.

Scenario analyses

No evidence found.

Budget impact model discussion

Summary: absence of a published budget impact model

No budget impact model of bepirovirsen has been published, and no U.S. list price is public: GSK states that the “list price will become public once pricing and reimbursement discussions have wrapped with payers”, and the UK horizon-scanning briefing states that the cost “is not yet known”. A plan building its own model would need the eligible population defined by the label (adults without cirrhosis who “have been on NrtI therapy for at least 6 months and have suppressed HBV deoxyribonucleic acid (DNA)” and have HBsAg levels “less than or equal to 3,000 IU/mL”), measured locally with quantitative HBsAg testing. Published U.S. inputs are an estimated 300,000 individuals diagnosed with chronic hepatitis B and 143,500 individuals on antiviral treatment, without restriction to the label population, and GSK states that HBsAg ≤1000 IU/mL represents “approximately 45% of diagnosed CHB cases globally”; no source reports the share of U.S. adults on NrtI therapy with HBsAg ≤3,000 IU/mL. The plan would also need the price, the treatment duration (the label states that “The maximum recommended duration of HIBSAGO treatment is 24 weeks”, given as 300 mg twice weekly in weeks 1 and 2 and once weekly in weeks 3 to 24, each dose as two 150 mg prefilled syringes supplied in cartons of 2), the cost of required laboratory monitoring, and continued NrtI therapy costs.