Please login to the form below

Not currently logged in

CureVac and Bayer partner on mRNA-based COVID-19 vaccine

German pharma giant will support further development of CVnCoV

CureVac and Bayer have entered into an agreement for CureVac’s COVID-19 vaccine candidate CVnCoV, which is currently in development.

Under the terms of the agreement, German pharma company Bayer will support the further development, supply and key territory operations of CVnCoV.

This includes contributing its expertise and established infrastructure in areas such as clinical operations, regulatory affairs, pharmacovigilance, medical information and supply chain performance.

CureVac will remain the marketing authorisation holder for the product, while Bayer will support the company with specific country operations in the EU and ‘additional market’.

“We are very happy to join forces with Bayer, whose expertise and infrastructure will help us make our vaccine candidate CVnCoV even more rapidly available to as many people as possible,” said Franz-Werner Haas, chief executive officer of CureVac.

“Building on the positive data we have seen so far with CVnCoV, we now also have another strong partner on our side to get the vaccine to the people who need it following the receipt of the requisite regulatory approvals,” he added.

In November 2020, CureVac announced that CVnCoV, which uses mRNA-based technology, has up to 24 hours of stability when stored at room temperature.

CureVac also said that data for its potential COVID-19 vaccine suggests the vaccine remains stable and within defined specifications for at least three months when stored at a standard refrigerator temperature +2 °- +5 °C (+41°F).

The stability of CVnCoV was tested at the anticipated storage concentration and also stored at +5°C (+41°F) as well as below -60°C (-76°F), with the vaccine fulfilling all set release specifications at both temperatures after three months.

In a phase 1 study of CVnCoV, the investigational mRNA-based vaccine candidate induced strong binding and neutralising antibody responses.

The vaccine also demonstrated early indications of functional T cells, confirming activation of cellular immune response according to the German biotech company.

The European Commission (EC) has already secured 405 million doses of CVnCoV which will be delivered ‘if the vaccine has proven safe and effective against COVID-19’.

According to Reuters, the deal includes access to an initial 225 million doses of CureVac's vaccine, with the EC eligible to purchase a further 180 million.

Article by
Lucy Parsons

7th January 2021

From: Research



PMEA Awards 2020

COVID-19 Updates and Daily News

Featured jobs


Add my company Events and Exhibition Stands is one of the UK’s leading exhibition stand and event agencies, specialising in healthcare. We understand your communication goals,...

Latest intelligence

#DemandDiversity: For International Women's Day, we ask... why do women often suffer from more side effects than men?
Women are largely prescribed exactly the same treatment regimens as men, with no account for the underlying differences in physiology and drug metabolism between the sexes....
Good design saves lives
Good design and creative thinking are essential if we are to improve on existing problems in new ways, which is why design and creativity within healthcare is vital. Health is...
Why you must understand the pricing of patient recruitment companies
Recruiting a diverse range of patients and engaging with them for your clinical trial isn’t an easy task, which means you might turn to patient recruitment companies, like us, who...