Register Now: From Clinical to Commercial: Accelerating ADC Late-Stage Development with Technology Innovation and Integrated Platform
|Articles|August 6, 2013

iQur Leads Major European Project to Develop a Universal Influenza Virus Vaccine

iQur announced that it has been granted 5 million EUR ($6.6 million) by the European Union Framework 7 fund to develop a universal influenza vaccine.

iQur, a UK biotechnology company, announced that it has been granted €5 million ($6.6 million) by the European Union Framework 7 fund to develop a universal influenza vaccine based on its proprietary tandem core technology.

iQur will lead a consortium of world-leading scientists from six sites across Europe, which have the complimentary skills and experience to discover and develop a novel flu vaccine. iQur’s technology will enable the design of a vaccine for influenza with the potential to confer long-term protection, removing the need for annual vaccination, the company reports. In addition, iQur’s vaccine can be made using recombinant protein technology and should be more effective and cheaper to manufacture than conventional vaccines, the company says.

The consortium partners include Leeds University and University College London from the UK, CRP Santé from Luxemburg, the Latvijas Medicinal Centre from Latvia, 3P Pharmaceuticals and Institut Catala de la Salut, both from Spain. The consortium will develop an optimal vaccine using preclinical models, manufacture the product to GMP and finally carry out a Phase I clinical trial. It is anticipated that the project will reach completion in 2017.

Source: iQur


Related to this article

The BioPharm Brief: An AI-Designed Multibody ADC Enters the Clinic, Blackstone Backs Pfizer’s Monthly GLP-1, and enGene Readies a Bladder Cancer BLA
FDA clears the IND for Biolojic Design’s BD200, an AI-designed Trop2/Nectin-4 multibody ADC; Blackstone Life Sciences agrees to provide Pfizer up to $1.5 billion to develop its monthly GLP-1 receptor agonist berobenatide; and enGene Therapeutics plans a year-end BLA for detalimogene voraplasmid in BCG-unresponsive non-muscle invasive bladder cancer.
The BioPharm Brief: FDA Designations for a Bispecific CAR-T, a BLA for Friedreich’s Ataxia, and Phase 2b MASH Data for Efinopegdutide
FDA grants RMAT and Fast Track designations to AbelZeta’s CD20/CD19 bispecific CAR-T prizlon-cel in relapsed or refractory large B-cell lymphoma, Larimar Therapeutics completes a BLA seeking accelerated approval of nomlabofusp for Friedreich’s ataxia, and Merck’s GLP-1/glucagon receptor agonist efinopegdutide meets its primary endpoint in a phase 2b MASH trial.