It is true that there are hundreds of small biotech companies like MBP.
If you read through their future drug pipeline.....all of these small caps read like the next CSL, however fast forward three years - and really nothing has changed. They are trying to make it big...but they usually never do.
Many investors considered MBP had their one chance at the making it into the big time also....with the weight loss drug. (We know what happened there. )
Exactly my views after after news of the obesity drug failure.......just as I was about sell at a big loss......decided to have a look at what other drugs they may have.
The more research that I did....the more interesting (the pain drug) seemed to become. Typical of the info that is out there on MBP's pain drug ACV1 is this from the inventor of the drug, before MBP secured the rights to it.
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http://www.listserv.uga.edu/cgi-bin/wa?A2=ind0703b&L=conch-l&F=&S=&P=2759
Date: Sun, 11 Mar 2007 09:03:31 -0400
Reply-To: Conchologists List <CONCH-L@LISTSERV.UGA.EDU>
Sender: Conchologists List <CONCH-L@LISTSERV.UGA.EDU>
From: Livett Family <blivett@BIGPOND.NET.AU>
Subject: Update on Conus victoriae analgesic "ACV1"
Clincal trials (Phase 2A) of conotoxin Vc1.1 (ACV1) from Conus victoriae
were begun by Metabolic Pharmaceuticals, Melbourne, (
www.metabolic.com.au)
ACV1 is a synthetic 16 amino acid peptide drug designed from a component
of the venom of the Australian marine cone snail, Conus victoriae, a
mollusc hunting cone shell.
In laboratory animals, ACV1 has profound, direct effects on pain sensing
nerves in the peripheral nervous system called C-fibres, which are
hypersensitive in neuropathic pain. It blocks a subtype of a broad class
of receptors called neuronal nicotinic acetylcholine receptors (nAChR)
which reside on the C-fibres. ACV1 has been shown to directly reduce the
sensitivity of sensitised C-fibres. It is the first drug to utilise this
biochemical mechanism.
ACV1 has been tested in several well-established animal pain models and
shows efficacy in relieving the characteristic pain symptoms of
neuropathy, allodynia and hyperalgesia, following subcutaneous or
intramuscular dosing. In addition, evidence suggests that ACV1 accelerates
the recovery of injured nerves and tissues.
On 24 November 2006, Metabolic Pharmaceuticals announced that the Phase 2A programme for ACV1, for neuropathic pain is progressing well. This
programme involves two human clinical trials targeting specific
neuropathies. The first group of patients (with painful sciatica) in the
first of two trials in this Phase 2A programme have been treated and the
second trial (involving patients with painful shingles and others with
painful diabetic neuropathy) is due to commence in Q107. Additionally, a
separate trial to test safety of a higher dose level of ACV1 commenced in
Q406.
Enjoy !
Bruce Livett
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As you can see from Dr Livett email....results are due soon for the phase trial 2 that started in Nov 2006. Little exclusive here where Dr Levitt reports that this trial is progressing well (this is a March email).
World market for this type of pain is increasing towards $5 billion. If successful....the drug will go a long way to replace morphine.