GSK Therapeutic - Product Scorecard

Company: GSK

Type: Covid-19 Therapeutic
Product (brand name): Baricitinib (Olumiant)
0%
compliance
with criteria
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Sotrovimab (Xevudy) detailed evaluation

Explore the results of PAF’s research into the behaviour of GSK. Each section is given an overall score; individual criteria are also scored (see icon following the criteria heading).

Click on ‘Explanation about the score’ sign next to each entry to expand and learn more.

Category A: Commitments and Accountability

The company should publicly commit to human rights in relation to product development and marketing, by adopting an official human rights policy statement recognising the right to the highest attainable standard of health. The company should endeavour to integrate human rights into its strategies, policies, programmes, projects, and activities.

The company should also have a publicly available global access plan for their Covid-19 product, based on human rights standards, with measurable targets and lines of accountability.

A1: Does GSK publish a global access plan for its product?

GSK signed the Gates Foundation ‘Commitments to Expanded Access for Covid-19 Diagnostics, Therapeutics and Vaccines’. It also states on its website that GSK is committed to supporting global supply.

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A2: Does GSK commit to comply with human rights standards in relation to product development and marketing?

GSK has published a position statement on human rights, and supports the UN Guiding Principles on Business and Human Rights among other human rights documents. GSK has also stated that they believe that ‘governments are responsible for defining and enforcing a legal human rights framework’, but they ‘recognise that we have a role to play in upholding human rights and in addressing adverse human rights impacts where we are in a position to influence.’

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Category C: International cooperation

The company should constructively engage with international initiatives for the equitable distribution of vaccines and therapeutics, such as the Covid-19 Technology Access Pool (C-TAP) or the Medicines Patent Pool (MPP), and the ACT Accelerator (COVAX). The company should also publicly commit to not enforcing the exclusive rights of Covid-19 related patents, and enter into non-exclusive, transparent licensing agreements for its Covid-19 products with other companies.

C1: Does GSK commit to C-TAP or MPP?

GSK does not commit to C-TAP or the MPP.

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C2: Does GSK commit to not enforcing the exclusive rights of Covid-19 related patents?

GSK does not commit to not enforcing the exclusive rights of Covid-19 related patents.

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C3: Does GSK supply to, or signs agreements with, the vaccines or therapeutics pillar of the ACT Accelerator?

GSK has not committed to supply the ACT Accelerator with its Covid-19 therapeutic.

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C4: Does GSK agree to license its Covid-19 medical products to other companies?

GSK has a contract manufacturing deal with Samsung Biologics. It is unclear whether this licensing goes further than fill-and-finish.

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Category E: Equality, non-discrimination & equity

The company should engage in efforts to further equitable distribution of Covid-19 vaccines/therapeutics, by equitably distributing its supplies globally, devising fair pricing strategies, and making the active ingredient for its product available to other manufacturers. The company should also engage in full technology transfer to other manufacturers, including the necessary transfer of skills, legal components, knowledge and intellectual property. Where applicable, the company should agree to waive rights in regulatory test data, and refrain from enforcing TRIPS+ measures.

E1: Does GSK make the active ingredient available on reasonable grounds? [Only for therapeutics]

There is no evidence that GSK makes the active ingredient for Sotrovimab available to other manufacturers.

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E2: Does GSK commit to full technology transfer to other manufacturers?

GSK has a contract manufacturing deal with Samsung Biologics which does not seem to include technology transfer.

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E3: Does GSK commit to non-profit, ‘fair’, or differential pricing?

Sotrovimab is priced at 2100 US dollars per course in the US. GSK makes claims of ‘responsible pricing’ on its website; but so far there is no evidence of fair or non-profit pricing.

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E4: Does GSK equitably distribute supplies globally? [Only applies to vaccines]

[Only applies to vaccines]

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E5: Does GSK not seek protection beyond the minimum criteria in TRIPS, or not enforce TRIPS+ measures? [where applicable]

There is no evidence of GSK enforcing TRIPS- or not enforcing TRIPS+

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E6: Does GSK agree to waive exclusive rights in regulatory test data? [where applicable]

No information was found on this criterion.

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Category T: Transparency

The company should be as transparent as possible, by publishing its research and development costs, profit margin, average costs of production, and production capacity for its Covid-19 product. It should also disclose the amount of public subsidies received during product development and/or testing. Licensing agreements should also be made publicly available and clinical trials should be registered in public repositories.

T1: Does GSK publish its R&D costs?

GSK publishes its overall research and development costs for 2021, but these are not specific to Sotrovimab.

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T2: Does GSK publish its profit margin?

GSK discloses a total of £958 million of sales for Sotrovimab, but does not mention a margin.

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T3: Does GSK publish the average and/or marginal costs of production?

GSK does not publish the average costs of producing Sotrovimab.

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T4: Does GSK publish its production capacity?

GSK plans to produce 2 million doses in the first half of 2022.

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T5: Does GSK publish the public subsidies it received during product development and/or testing?

Sotrovimab was partially funded by Operation Warp Speed, but this has not been published on GSK’s website.

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T6: Does GSK publish the text of licensing agreements?

GSK has not published the text of a licensing agreement.

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T7: Does GSK register its clinical trials in public repositories?

GSK registers its clinical trials on clinicaltrials.gov.

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