- Trials showed 47% efficacy for original vaccine
- Move means vaccine supply deal with EU ends
- CureVac shares sink almost 14% on news
BERLIN, Oct 12 (Reuters) – CureVac (5CV.DE) will withdraw its first-generation COVID-19 vaccine candidate and focus on collaborating with GSK (GSK.L) to develop second-generation mRNA vaccine technology instead, the Germany-based biotechnology company said on Tuesday.
The company’s shares plunged almost 14% in afternoon trading, hitting their lowest since listing last August.
CureVac said it would abandon its application for regulatory approval from the European Medicines Agency for its first-generation vaccine candidate CVnCoV after late-stage trials delivered disappointing results in June with 47% efficacy. read more
There would be a potential overlap with approval timelines for a second-generation candidate.
The earliest potential approval of CVnCoV would have come in the second quarter of 2022 when candidates from the second-generation vaccine program were expected to progress to late-stage clinical development by that time, CureVac said.
As a result, the advance purchase agreement the German firm signed to sell shots to the European Union will end, it said.
It said it expected to start human trials for its second-generation shot in coming months, aiming for regulatory approval in 2022. Results from early-stage animal trials have shown the strong potential of the shot compared with the original, it said.
The German firm cancelled contract manufacturing deals last month for CVnCoV with two prospective partners. read more
The shot is the latest casualty in the drug industry’s race to develop a vaccine against the virus, which has killed more than 5 million people and infected more than 238 million.
Instead, it would pursue the technology, acquired as part of its takeover of Translate Bio , in potential vaccines against influenza and other diseases.
Reporting by Zuzanna Szymanska and Josephine Mason; Editing by Louise Heavens and Edmund Blair
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