THE BIG PICTURE
The UK government commissioned report published in 2016 by Jim O’Neill, highlights the growing problem of antimicrobial resistance (AMR). This is particularly evident for Gram negative bacteria, where resistance is now emerging to even last resort antibiotics, such as colistin. The report suggests that unless action is taken, the global burden of deaths from AMR could balloon to 10 million lives each year by 2050.
Phico Therapeutics is pioneering a radical approach to antibacterial therapy which it believes could form the basis of a solution. By targeting and inactivating the bacterial DNA directly, irrespective of its sequence, mutations in the bacterial DNA don’t prevent SASP from working. Phico’s SASPject products can directly tackle the genetic cause of antibiotic resistance.
THE COMPANY
Phico Therapeutics is a biotechnology company developing a novel platform technology which it believes could form the basis for a new generation of antibiotics to overcome antibacterial resistance.
The company, founded in Cambridge by Dr Heather Fairhead, is built around the SASPject™ platform, which utilises a unique anti-bacterial protein, SASP, which targets and deactivates bacterial DNA stopping bacteria from metabolising or reproducing. Phico has raised over £22 M from business angels, venture investment, high net-worth individuals, the Wellcome Trust and Government grants. Phico’s goal is to advance the science of antibacterial therapy to help overcome the problem of bacterial resistance.
TECHNOLOGY
Our SASPject™ platform delivers pan-spectrum anti-bacterial proteins called small acid-soluble spore proteins, or SASPs, to selected bacterial species using targetable nano-delivery vehicles (NDVs). SASPject™ works by injecting a gene that encodes SASP directly into the targeted bacteria. The injected gene then produces SASPs, which bind to bacterial DNA and inactivate it. SASPs “turn off” DNA so the targeted bacterial cell cannot metabolise or reproduce. The immune system can then remove the bacteria from the body.
SASPs bind to all bacterial DNA, irrespective of the sequence of that DNA. Spontaneous mutations in DNA, or the import of new DNA that gives new characteristics to the bacterial cell, are key ways in which bacteria develop resistance to antibiotics. Neither of these strategies affects the ability of SASP to bind to and inactivate bacterial DNA.
This approach has the potential to provide a number of significant advantages over traditional antibiotics:
- The unique mode of action of SASP makes it unlikely the bacteria will be able to develop resistance to this anti-bacterial protein
- SASPject technology can be used to target any selected bacteria, individual or multiple bacterial species or genera, including those that are multi-antibiotic resistant.
- Unlike conventional antibiotics, SASPject has no effect on any bacteria other than those at which it is targeted. Normal skin and gut bacteria (“good bacteria”) are unharmed.
- SASPject target specificity prevents the release of toxins and other inflammatory cell components from non-target bacteria thus potentially minimising associated side effects.
- SASPject has the potential to limit the further spread of antibiotic resistance genes and to shrink the current antibiotic resistance pool
PRODUCTS
SASPject™ PT3
SASPject™ PT3 is being developed against Pseudomonas aeruginosa. These infections can involve any part of the human body, but most commonly cause urinary tract, lung, bloodstream, wound/burn, and intra-abdominal infections. P. aeruginosa is responsible for a number of hospital-acquired infections with its incidence in intensive care units having risen sharply and its incidence almost doubling between the mid 1970’s and early 2000’s. The increasing incidence of P. aeruginosa of strains showing multi-drug resistance against commonly used first-line antibiotics has resulted in the U.S. CDC (Centers for Disease Control and Prevention) classifying P. aeruginosa as a serious threat to human health. The PT3 project has been supported by Innovate UK.
SASPject™ PT4 and PT5
SASPject™ PT4 and SASPject™ PT5 are being developed for systemic (intravenous) use against both Klebsiella pneumoniae and Escherichia coli respectively. These bacteria cause a wide range of infections, which can be serious or life threatening as isolates which are resistant to almost all conventional antibiotics continue to spread around the globe, resulting in very poor treatment outcomes. PT4 and PT5 projects are supported by a Wellcome Translation Award.
SASPject™ PT1.2
SASPject™ PT1.2 targets Staphylococcus aureus, including MRSA. MRSA infections are now a global problem in hospitals, with thousands of fatalities recorded as a result of their presence, and their control is vital to many national health systems. SASPject™ PT1.2 will be used for the intra-nasal decolonisation of the bacteria. A Phase I clinical trial has been successfully completed.
TEAM
Dr Heather Fairhead
FOUNDER AND CEO
Dr Fairhead has over 20 years’ experience directing research teams in a variety of disciplines and has led Phico in developing SASPject technology from a concept through a Phase I clinical trial. Prior to her scientific career, Heather worked in sales and marketing in a wide range of industries.
Dr Anthony MartinCHAIRMAN
Dr Martin has more than 25 years' experience in providing life science and biotechnology companies counsel on a range of strategic, management and funding issues, including as Chairman of anti-infectives company, NeuTec Pharma plc, where he played a pivotal role in guiding the company’s sale to Novartis for over £300M.
Allan HirstNON-EXECUTIVE DIRECTOR
Allan spent 24 years with Citigroup, in the last 15 years leading Citibank’s expansion into Central and Eastern Europe, Russia and Central Asia. Allan sits on the Board of the Financial Services Volunteer Corp and will shortly be joining the Board of the Georgia Healthcare Group.
Dr Robert NolanNON-EXECUTIVE DIRECTOR
Robert has over 30 years’ experience in big pharma, including from 1989 to end 2004 as Director of Global Licensing at AstraZeneca. Bob is a non-executive director of Epistem Ltd. He gained his Ph.D. in biochemistry from King’s College, London, and completed two post-doctoral fellowships in the US at Dartmouth Medical School and MIT.
DR JAMES CASSRESEARCH MANAGER
Microbiologist with over 10 years' experience in the biotech and anti-infectives industry; Biocontrol Ltd (Ampliphi Biosciences)
MEDIA AND INVESTORS
MEDIA
SCIENTIFIC PUBLICATIONS
TWITTER FEED
Phico Therapeutics @Phicotx
New study finds that also certain non-antibiotic pharmaceuticals may increase horizontal transfer of bacterial… https://t.co/LJ8Qx0NJHI
Phico Therapeutics @Phicotx
Tomorrow, the #AMRChallenge will be launched at a side event of the 73rd UN General Assembly #UNGA to encourage act… https://t.co/g6S5frZv26
Phico Therapeutics @Phicotx
New study @MonashUni identifies mechanism of how bacteria causing food poisoning share #AntibioticResistance genes
https://t.co/BffSN3OMWj
https://t.co/BffSN3OMWj
CONTACTS
If you are interested in learning more about what we do, or have general enquiries:
+44(0)1954 741040
info@phicotx.co.uk
#phicotx
www.linkedin.com/company/phico-therapeutics-ltd
For media enquiries please contact:
Consilium Strategic Communications
Mary-Jane Elliott: +44(0)203 709 5702
Jessica Hodgson: +44(0)203 709 5703
hodgson@consilium-comms.com
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Copyright © 2012 Phico Therapeutics Limited
Registered Address: Phico Therapeutics Ltd, Bertarelli Building, Bourn Hall, High Street, Bourn ,Cambridgeshire ,CB23 2TN
Registration number 04062313 VAT number 759886742
Registered Address: Phico Therapeutics Ltd, Bertarelli Building, Bourn Hall, High Street, Bourn ,Cambridgeshire ,CB23 2TN
Registration number 04062313 VAT number 759886742