Innovation Passport granted to Pfizer's MM candidate by MHRA
Elranatamab, an investigational B-cell maturation antigen (BCMA) CD3-targeted bispecific antibody in development for the treatment of multiple myeloma (MM) by US pharma giant Pfizer (NYSE: PFE), has been granted an ‘Innovation Passport’ from the UK’s Medicines and Healthcare Products Regulatory Agency (MHRA).
The Innovation Passport is the entry point to the MHRA’s new Innovative Licensing and Access Pathway (ILAP), intended to offer regulatory support and flexibilities to bring new medicines to UK patients more quickly. In June this year, the MHRA granted the same ‘passport’ for GSK’s (LSE: GSK) Blenrep (belantamab mafodotin) for the treatment of multiple myeloma.
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