Phylogica is a biotechnology company based in Perth, Australia and Oxford, UK, which provides peptide drug discovery services to the Pharmaceutical industry.
 
Phylogica has discovered and patented a unique proprietary class of targeted peptide therapeutics (Phylomer® peptides). These peptides exhibit competitive therapeutic, manufacturing, and commercial advantages over other more traditional targeted biologics such as proteins, monoclonal antibodies and most current therapeutic peptides. Libraries of billions of Phylomers have been constructed, which constitute the most structurally diverse set of peptides available, resulting in a higher quality and quantity of hits. For example, the hit to target ratios from Phylomer® libraries are high and the proportion of hits which are functional, is also very high, when compared with traditional libraries of random peptides. The value of Phylomer libraries as a rich source of drug-like peptides is demonstrated by Phylogica’s growing list of drug discovery partnerships with big Pharma companies, including Roche, Medimmune/AstraZeneca and Pfizer.
 
Phylogica has created, and validated potential therapeutic Phylomer® drug leads against intracellular and extracellular targets, with high affinities. These peptides can be readily enhanced by focused lead optimization strategies based on the structural information obtained from the parent proteins from which Phylomers are derived. Phylomers have also been obtained which are capable of transporting large biologics into cells.
 
Phylogica has also demonstrated in-vivo efficacy for Phylomer® peptides against intracellular targets in animal models of diverse diseases such as stroke/traumatic brain injury, of burns, wound healing and of acute respiratory distress syndrome. As these peptides are synthetic, chemical manipulation can enhance their stability, improve their solubility, prolong their in-vivo half-lives and minimize their risk of being immunogenic.
 
Phylomer® peptides are suited for targeting a wide range of disease-associated proteins and their interactions and this versatility is ideal for phenotypic screening for target discovery. Phenomica is new spinoff between Phylogica and the prestigious Cambridge University in the UK, which was created to pursue commercial opportunities created by the proven use of Phylomer libraries for target discovery and validation.

Videos

Mar,2013 05:00 PM
Commercialising new classes of..
28 Mar 2013 - Phylogica Limited (ASX:PYC) CFO and VP of corporate development Nick Woolf outlines the drug discovery company’s ongoing collaborations and the pharmaceutical potential of the Phylomer Peptide.

Phylogica (ASX:PYC)

Contact Information

Phone: 08 9382 8888
Email: info@phylogica.com
Website: www.phylogica.com
Address
c/- Australian Heritage Group, Level 22, 77 St Georges Tce, Perth, WA, Australia, 6000

Media Releases see all media releases

Phylogica, Shareholder Newsletter
10 Jul,2012 09:39 AM

In this edition:
• Partnership activities have never been busier
• Pharma industry reorganisations
• Phylogica is not immune to industry dynamics
• Biological drugs are leading the way
• Secure financial position
• Benefitting from the new R&D tax credit legislation
• Progress with Pfizer vaccine collaboration
• Research activities underway with Janssen

More deal opportunities than ever before -
The resilience of the Phylogica team in a challenging environment has been commendable. Recent specialist international meetings have shown that Phylogica’s unique Phylomer libraries of prototype drugs are more in demand than ever before as one potential lifeline for Pharma companies seeking to carve out fresh approaches to drug discovery against challenging targets.

There is considerable interest in the field of drug targeting to the intracellular space, where Phylomers are being considered as a unique approach for delivering other biological payloads across the cell membrane into cells. To date, it has proved challenging for the Pharma industry to get biological payloads into the intracellular space, where the majority of candidate therapeutic targets reside, most of which have proved intractable with both biological approaches or with conventional ‘small molecule’ drugs.


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