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GSK, CureVac partnership eyes COVID-19 vaccine against multiple variants

FRANKFURT: Britain’s GlaxoSmithKline and German biotech firm CureVac struck a 150 million euro ($180 million) deal to develop next-generation vaccines against COVID-19 that target several variants in one product.

In a joint statement on Wednesday, the partners said they were targeting a possible launch in 2022.

GSK, which holds a stake in CureVac, will also support the production of up to 100 million doses of CureVac’s first generation COVID-19 vaccine candidate in 2021, they said.

For GSK, the world’s largest vaccine maker by sales, it marks a fresh attempt to play a relevant role in fighting the pandemic after a COVID-19 alliance with Sanofi was hobbled by development delays and after a similar collaboration with China’s Clover Biopharmaceuticals was ended.

Curevac says May approval for COVID-19 vaccine possible: Newspaper

German biotech firm Curevac believes the European Union might give approval for its COVID-19 vaccine in May or June, a spokesman was quoted as saying in the Augsburger Allgemeine newspaper on Saturday.

“We are already very advanced in Phase Three clinical trials and are expecting the data for the final approval package,” spokesman Thorsten Schueller told the paper.

Previously, approval was expected in June.

Curevac still plans to produce up to 300 million vaccine doses this year, the spokesman was quoted as saying.

EU regulator does not expect approval for CureVac vaccine before August

The European Medicines Agency (EMA) does not expect to make a decision on the approval of German biotech group CureVac‘s COVID-19 vaccine before August, an official at Germany’s health ministry familiar with the matter told Reuters.

The source said German health minister Jens Spahn had provided the update on the EMA’s view on the timing of the review on Monday in a call with his regional state counterparts.

The health ministry declined to comment. CureVac did not immediately respond to a request for comment, while the EMA said it would not comment on the timing of ongoing reviews.

In what has so far been CureVac’s only major confirmed supply deal, the European Union secured up to 405 million doses of the vaccine in November last year, of which 180 million are optional.

That was followed by a memorandum of understanding with Germany for another 20 million doses. Both deals are dependent on EMA approval.

CureVac has previously had to climb down from a more optimistic outlook on the speed at which its vaccine is being developed, pushing out to June its guidance on the timing of initial results from a late-stage trial from as early as May previously.

The company said on May 28 that the late-stage trial involving about 40,000 volunteers in Europe and Latin America had reached a first interim analysis at 59 COVID-19 cases, but that more data would be necessary for statistically reliable efficacy numbers.

The stakes for CureVac and its prospective European customers rose after age limits were imposed on the use of Johnson & Johnson and


‘s vaccines.

Shortfalls in AstraZeneca’s and J&J’s supply chains have also knocked the European vaccination campaign.

But with EU vaccinations nonetheless picking up speed, mainly thanks to higher deliveries from BioNTech and Pfizer, the focus could turn to how CureVac’s product can help in low and middle-income countries, which have fallen behind in the global immunisation drive.