PYC 0.00% 12.5¢ pyc therapeutics limited

another positive ann......

  1. 169 Posts.
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    FYI - $0.30 i don't think so........ time to get it cheap while you still can.

    Phylogica Ltd, PO Box 8207, Subiaco East, Western Australia 6008
    ACN 098 391 961
    PHYLOGICA GENERATES MULTIPLE DRUG CANDIDATES FOR
    TREATMENT OF RHEUMATOID ATHRITIS
    Key Points
    • Multiple Phylomer® drug candidates proven to successfully bind to major
    Rheumatoid Arthritis (RA) disease targets
    • Progresses major technical target for Commercial Ready Grant program
    ($2.3 m)
    • Phylomer® peptides libraries proven to be as effective as antibody libraries in
    identifying drug candidates for RA
    • Phylogica’s extends its competitive advantage of generating Phylomer® drug
    candidates that bind disease targets wherever they reside – both outside and
    inside the cell
    Perth, Tuesday 15th May, 2007: Phylogica Limited (ASX: PYC) announced today that
    it has achieved a key aim of its Commercial Ready Grant funded Rheumatoid
    Arthritis (RA) program, by generating multiple Phylomer® drug candidates with high
    binding strength to several key targets in inflammatory diseases such as RA.
    The $2.3 million Commercial Ready Grant awarded to Phylogica in October 2005 is
    aimed at identifying Phylomer® drug candidates for RA by scanning Phylogica’s
    exclusive libraries of Phylomer® peptides.
    Phylogica’s scientists have now generated more than 30 Phylomer® drug candidates
    that are able to tightly bind to their targets and potentially block critical interactions at
    the onset of RA and also as the disease progresses.
    RA is a chronic autoimmune inflammatory disease that affects approximately 1% of
    the world's population. The RA biological therapeutics market is currently dominated
    by antibody-based drugs, against which Phylogica believes Phylomer® technology
    can establish a strong competitive position.
    Phylogica’s Vice President Drug Discovery, Dr Paul Watt, said: “We were thrilled with
    the large number of high quality drug candidates generated from our Phylomer®
    libraries.”
    Each of the Phylomer® drug candidates is able to bind very strongly to the disease
    target (refer to Figure 1). “The stronger the binding the better the drug candidate
    should perform in preclinical tests, and the lower the dose that may be required for
    therapy” he explained.
    “We are pleased to report that our Phylomer® peptide libraries were as effective as
    antibody libraries in generating multiple strong binding drug candidates for RA,” he
    added.
    Phylogica Ltd, PO Box 8207, Subiaco East, Western Australia 6008
    ACN 098 391 961
    More specifically, the Phylomer® drug candidates were shown to bind strongly to two
    RA disease targets that lie outside of the cell, including the classical target Tumour
    Necrosis Factor (TNF) and CD40 ligand.
    “Considering one of the current antibody drugs used to target TNF (Remicade -
    Johnson & Johnson) has annual sales of approximately $2.5 billion, we’re very
    excited by the potential of pursuing these Phylomer® drug candidates and delivering
    on Phylogica’s vision of more targeted, more affordable drugs” said Phylogica CEO
    Dr Stewart Washer.
    “Our new drug candidates for targeting RA from outside the cell build on our existing
    drug candidates for inflammatory targets inside the cell, so that we have now proved
    that we can block disease targets wherever they reside – both inside and outside the
    cell” he said. “Regardless of where the target resides, we are getting the quantity
    and quality of candidates we are looking for, demonstrating the versatility and
    efficiency of our Phylomer library approach”.
    “This demonstrates yet again the power of the Phylomer® drug discovery engine and
    gives us major competitive advantages against other drug discovery engines.” said
    Dr Washer.
    Phylogica Ltd (ASX: PYC) (www.phylogica.com) is a drug discovery company utilizing its
    proprietary Phylomer® technology to develop revolutionary new drugs for stroke, burns injury,
    and other anti-inflammatory diseases including rheumatoid arthritis and diabetes. The
    Company is preparing to commercialise its lead drugs through licensing deals. Phylogica was
    founded by the Telethon Institute for Child Health Research in Perth (www.ichr.uwa.edu.au)
    and the Fox Chase Cancer Center in Philadelphia, United States (www.fccc.edu).
    About Phylomer® peptides
    Phylomer® peptides are stable fragments of naturally-occurring proteins with the ability to bind
    tightly to target proteins and inactivate them as a result. Phylomer® peptides can be selected
    for activity against specific disease target proteins. The properties of Phylomer® peptides
    make them attractive as cost-effective alternatives to antibodies - a proven multi-billion drug
    class. Phylogica's proprietary Phylomer® libraries are collections of millions of Phylomer®
    peptides that represent a rich source of drug leads which can be used for multiple diseases.
    For further information, please contact:
    Corporate Advisor - Cygnet Capital
    Sam Willis
    + 618 9226 5511
    [email protected]
    [email protected]
    Media
    Daniella Goldberg
    +61 2 9237 2803
    [email protected]
    Phylogica
    Stewart Washer
    Chief Executive Officer
    + 618 9423 8800 / 0418 288 212
    [email protected]
    Phylogica Ltd, PO Box 8207, Subiaco East, Western Australia 6008
    ACN 098 391 961
    FIGURE 1
    Assessment of binding of a Phylomer peptide to its RA disease target
    (CD40 Ligand competition ELISA assay)
    IC50
    22±5 nM (free target)
    68±5 nM (free peptide)
    LEGEND
    Phylomer® peptides were shown to bind tightly to RA disease targets (eg CD40 Ligand and TNF). Strong
    binding Phylomers® are able to block the disease target more efficiently than weak binding Phylomers®.
    (This figure shows a low IC50 value indicating high target affinity for one of the CD40 ligand Phylomer
    candidates. More than 30 such hits were identified with IC50 constants in the nanomolar range, which were
    also demonstrated to be specific for their target).
 
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