Daily Newsletter

19 September 2023

Daily Newsletter

19 September 2023

BioNTech and CEPI partner to develop Mpox vaccine

A Phase I/II clinical trial will enrol 196 healthy participants irrespective of their smallpox immunisation status.

Vishnu Priyan September 19 2023

BioNTech has entered a strategic collaboration with the Coalition for Epidemic Preparedness Innovations (CEPI) to develop messenger ribonucleic acid (mRNA)-based vaccine candidates for monkeypox (Mpox) prevention.

Under the deal, CEPI will provide funding of up to $90m to support the mRNA-based vaccine development programme BNT166.

This alliance intends to contribute to the 100 Days Mission of CEPI to expedite the development of well-tolerated vaccines for pandemic viruses arising in the future.

This approach will aid in readying the vaccines for regulatory approvals, as well as production at scale within 100 days of detecting a pathogen.

BNT166 is part of the infectious disease programmes of BioNTech and such vaccine candidates encode for surface antigens expressed in the two infectious Mpox virus types to prevent replication of the virus and infectivity.

BioNTech intends to advance a prophylactic mRNA-based Mpox vaccine possessing an encouraging safety profile that can be produced at scale.

In this regard, two mRNA-based multivalent Mpox vaccine candidates will be analysed for safety, tolerability, reactogenicity and immunogenicity.

A Phase I/II trial will enrol 196 healthy subjects irrespective of their smallpox immunisation status.

BioNTech CEO and co-founder Ugur Sahin said: “The global outbreak, which was declared a public health emergency of international concern, underlines the need for a highly effective, well-tolerated and accessible Mpox vaccine. We initiated our BNT166 programme in May 2022 to help address this need.

“We believe our scientific approach, as well as our mRNA technology, have the potential to significantly contribute to deliver on CEPI’s 100 Days Mission.”

Multiple Myeloma (MM) pipeline dominated by CAR-T cells

The success of CAR-Ts in MM has fueled R&D investment into this class of therapy, with more CAR-Ts in development than all other cell and gene therapy classes combined. The approval of the autologous CAR-T cell therapies Abecma and Carvykti sees the CAR-T pipeline mostly constituted of autologous drugs. However, there are also multiple allogeneic CAR-Ts in the pipeline, with these therapies having an “off-the-shelf” advantage over autologous therapies.

Newsletters by sectors

close

Sign up to the newsletter: In Brief

Visit our Privacy Policy for more information about our services, how we may use, process and share your personal data, including information of your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

Thank you for subscribing

View all newsletters from across the GlobalData Media network.

close