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ill keep mine for a while
scott gots it .0014 x .002
wow moves good
hope so. maby nice little sleeper
how does L2 look dream
just heard commercial on howard stern with ticker symbol. looks good.
lunch is over here we go again!
Press Release Source: Protherics PLC
Protherics PLC - Rule 2.10 Announcement
Thursday August 14, 4:41 am ET
CHESHIRE, UK--(MARKET WIRE)--Aug 14, 2008 --
Protherics PLC
Rule 2.10 Announcement
London, UK; Brentwood, TN, US; 14 August 2008
In accordance with Rule 2.10 of the City Code on Takeovers and Mergers
(the "Code"), Protherics confirms that at the close of business
on 13 August 2008, it has 342,159,034 ordinary shares of 2 pence each
in issue and admitted to trading on the London Stock Exchange under the
UK ISIN code GB0007029209.
The ISIN number above corrects that cited in the Rule 2.4 announcement
issued by the Company on 13 August 2008.
ENDS
For further information please contact:
Protherics +44 (0)20 7246 9950
Andrew Heath, CEO
Rolf Soderstrom, Finance Director
Nick Staples, Director of Corporate Affairs
Jefferies International Ltd.
Ian Crosbie +44 (0)20 7029 8000
Nomura Code Securities Ltd.
Chris Collins +44 (0) 207 776 1200
Financial Dynamics - press enquiries
Ben Atwell +44 (0) 20 7831 3113
Or visit http://www.Protherics.com
Dealing Disclosure Requirements
Under the provisions of Rule 8.3 of the Code, if any person is, or
becomes, interested" (directly or indirectly) in 1% or more of any
class of "relevant securities" of Protherics, all "dealings" in
any"relevant securities" of that company (including by means of an option
in respect of, or a derivative referenced to, any such "relevant
securities") must be publicly disclosed by no later than 3.30 pm
(London time) on the London business day following the date of the
relevant transaction. This requirement will continue until the date on
which the offer becomes, or is declared, unconditional as to
acceptances, lapses or is otherwise withdrawn or on which the "offer
period" otherwise ends. If two or more persons act together pursuant to
an agreement or understanding, whether formal or informal, to acquire
an "interest" in "relevant securities" of Protherics, they will be
deemed to be a single person for the purpose of Rule 8.3.
Under the provisions of Rule 8.1 of the Code, all "dealings" in"relevant
securities" of Protherics by a potential offeror, or
by Protherics, or by any of their respective "associates", must be
disclosed by no later than 12.00 noon (London time) on the London
business day following the date of the relevant transaction.
A disclosure table, giving details of the companies in whose "relevant
securities""dealings" should be disclosed, and the number of such
securities in issue, can be found on the Takeover Panel's website at
http://www.thetakeoverpanel.org.uk."Interests in securities" arise, in summary,
when a person has long
economic exposure, whether conditional or absolute, to changes in the
price of securities. In particular, a person will be treated as having
an "interest" by virtue of the ownership or control of securities, or
by virtue of any option in respect of, or derivative referenced to,
securities. Terms in quotation marks are defined in the Code, which can
also be found on the Panel's website. If you are in any doubt as to
whether or not you are required to disclose a "dealing" under Rule 8,
you should consult the Panel.
CytoDyn on Target with Target for Electronic FDA Application
GLORIETA, N.M. & NEW YORK, Jul 28, 2008 (BUSINESS WIRE) -- CytoDyn, Inc. (Pink Sheets:CYDY) has selected Target Health, Inc. for the preparation and electronic filing of CytoDyn's upcoming FDA application using Target Health's proprietary e*CRF(R) system. The advantage of Target Health is based on its core expertise in regulatory affairs and clinical research, and its paperless approach to FDA filings, including submission of electronic INDs (eIND) and electronic common technical documents (eCTD). Paperless clinical research and the electronic filing of regulatory documents reflect a growing trend in the pharmaceutical industry. Dow Pharmaceutical Sciences (NYSE:DOW), King Pharmaceuticals (NYSE:KG) and Pain Therapeutics (Nasdaq:PTIE) are among the leading pharmaceutical companies that have helped pioneer this modernization of the industry.
About CytoDyn
CytoDyn, which expects its first electronic application to be submitted to the FDA in about eight weeks, is developing Cytolin(R), a first-in-class drug that uses the human immune system to help control HIV infection. Because a well-functioning immune system can usually control a virus regardless of its subspecies, this could potentially provide a "salvage" therapy for those failing antiretroviral therapy. For the same reason, it might help prevent drug-resistance strains of HIV from ever emerging when used in combination with traditional antiretroviral drugs.
At the height of the AIDS epidemic, community physicians treated about 200 patients experimentally with a generic form of Cytolin(R) to delay the need for antiretroviral therapy, which had not yet become fully available, as previously reported by CBS-TV News. This might also turn out to be a way of using a drug like Cytolin(R) since, despite the great strides that have been made in treating HIV/AIDS, the U.S. Department of Health and Human Services recommends delaying the use of antiretroviral drugs until the disease has progressed to the point where such drugs are indicated.
CytoDyn has not yet decided which of these potential uses for Cytolin(R) it will pursue as an initial indication, pending completion of its upcoming clinical trial. The upcoming trial will re-investigate dosing and is designed to be pristine in order to qualify as a proof-of-principle study. Although not the first clinical trial of Cytolin(R), it will be the first clinical trial sponsored by CytoDyn, whose CEO invented this treatment. The Principal Investigator is Dr. Jay Lalezari, a prominent clinical researcher in San Francisco California specializing in HIV/AIDS. Dr. Lalezari was instrumental in defining the parameters of a proof-of-principle study under the current treatment guidelines.
About Target Health
Target Health, Inc. is a New York City-based full service e*CRO with full-time staff dedicated to all aspects of Regulatory Affairs, Clinical Research, Biostatistics, Data Management, Paperless Clinical Trials (Target e*CRF(R), Target Document(R), Target Encoder(R), Target e*CTMS(TM)), Software Development, Strategic Planning and Drug/Device/Biologic Development. Target Health, Inc. currently represents 28 companies at the FDA and two companies at Health Canada. Target's clients include Fortune 100 companies as well as many smaller companies. A complimentary newsletter, "On Target," is available from Target Health, Inc. for those interested in contemporary drug-development issues.
"We were impressed with the broad experience, rapid response, and flexibility of Target Health, Inc., and gained a sense of security from the positive outcome of an on-site audit of that company conducted by the FDA," said Dr. Nadar Pourhassan, CytoDyn's COO.
Disclaimer
This press release contains forward-looking statements that are not historical facts. CytoDyn's management makes forward-looking statements concerning the Company's expected future operations, performance and other developments. These forward-looking statements are necessarily estimates based upon current information and projections and involve a number of risks and uncertainties, including but not limited to, the failure of preliminary results from clinical studies to reflect the results from more comprehensive studies. There can be no assurance that such risks and uncertainties, or other factors, will not affect the accuracy of such forward-looking statements. It is impossible to identify all the factors that could cause actual results to differ materially from those estimated by CytoDyn. They include, but are not limited to, government regulation, managing and maintaining growth, victimization by white-collar offenders, and the effects of adverse publicity, litigation, competition, and other factors that may be identified from time to time in the Company's announcements.
SOURCE: CytoDyn
CONTACT: CytoDyn, Inc.
Corinne Allen, 505-577-1636
or
Target Health, Inc.
Dr. Jules T. Mitchel, 212-681-2100
Copyright Business Wire 2008
**********************************************************************
CytoDyn on Target with Target for Electronic FDA Application
GLORIETA, N.M. & NEW YORK, Jul 28, 2008 (BUSINESS WIRE) -- CytoDyn, Inc. (Pink Sheets:CYDY) has selected Target Health, Inc. for the preparation and electronic filing of CytoDyn's upcoming FDA application using Target Health's proprietary e*CRF(R) system. The advantage of Target Health is based on its core expertise in regulatory affairs and clinical research, and its paperless approach to FDA filings, including submission of electronic INDs (eIND) and electronic common technical documents (eCTD). Paperless clinical research and the electronic filing of regulatory documents reflect a growing trend in the pharmaceutical industry. Dow Pharmaceutical Sciences (NYSE:DOW), King Pharmaceuticals (NYSE:KG) and Pain Therapeutics (Nasdaq:PTIE) are among the leading pharmaceutical companies that have helped pioneer this modernization of the industry.
About CytoDyn
CytoDyn, which expects its first electronic application to be submitted to the FDA in about eight weeks, is developing Cytolin(R), a first-in-class drug that uses the human immune system to help control HIV infection. Because a well-functioning immune system can usually control a virus regardless of its subspecies, this could potentially provide a "salvage" therapy for those failing antiretroviral therapy. For the same reason, it might help prevent drug-resistance strains of HIV from ever emerging when used in combination with traditional antiretroviral drugs.
At the height of the AIDS epidemic, community physicians treated about 200 patients experimentally with a generic form of Cytolin(R) to delay the need for antiretroviral therapy, which had not yet become fully available, as previously reported by CBS-TV News. This might also turn out to be a way of using a drug like Cytolin(R) since, despite the great strides that have been made in treating HIV/AIDS, the U.S. Department of Health and Human Services recommends delaying the use of antiretroviral drugs until the disease has progressed to the point where such drugs are indicated.
CytoDyn has not yet decided which of these potential uses for Cytolin(R) it will pursue as an initial indication, pending completion of its upcoming clinical trial. The upcoming trial will re-investigate dosing and is designed to be pristine in order to qualify as a proof-of-principle study. Although not the first clinical trial of Cytolin(R), it will be the first clinical trial sponsored by CytoDyn, whose CEO invented this treatment. The Principal Investigator is Dr. Jay Lalezari, a prominent clinical researcher in San Francisco California specializing in HIV/AIDS. Dr. Lalezari was instrumental in defining the parameters of a proof-of-principle study under the current treatment guidelines.
About Target Health
Target Health, Inc. is a New York City-based full service e*CRO with full-time staff dedicated to all aspects of Regulatory Affairs, Clinical Research, Biostatistics, Data Management, Paperless Clinical Trials (Target e*CRF(R), Target Document(R), Target Encoder(R), Target e*CTMS(TM)), Software Development, Strategic Planning and Drug/Device/Biologic Development. Target Health, Inc. currently represents 28 companies at the FDA and two companies at Health Canada. Target's clients include Fortune 100 companies as well as many smaller companies. A complimentary newsletter, "On Target," is available from Target Health, Inc. for those interested in contemporary drug-development issues.
"We were impressed with the broad experience, rapid response, and flexibility of Target Health, Inc., and gained a sense of security from the positive outcome of an on-site audit of that company conducted by the FDA," said Dr. Nadar Pourhassan, CytoDyn's COO.
Disclaimer
This press release contains forward-looking statements that are not historical facts. CytoDyn's management makes forward-looking statements concerning the Company's expected future operations, performance and other developments. These forward-looking statements are necessarily estimates based upon current information and projections and involve a number of risks and uncertainties, including but not limited to, the failure of preliminary results from clinical studies to reflect the results from more comprehensive studies. There can be no assurance that such risks and uncertainties, or other factors, will not affect the accuracy of such forward-looking statements. It is impossible to identify all the factors that could cause actual results to differ materially from those estimated by CytoDyn. They include, but are not limited to, government regulation, managing and maintaining growth, victimization by white-collar offenders, and the effects of adverse publicity, litigation, competition, and other factors that may be identified from time to time in the Company's announcements.
SOURCE: CytoDyn
CONTACT: CytoDyn, Inc.
Corinne Allen, 505-577-1636
or
Target Health, Inc.
Dr. Jules T. Mitchel, 212-681-2100
Copyright Business Wire 2008
**********************************************************************
Hmmm makes you wonder if someone knows something. Like the news is coming out eod today or monday. Just a possibility
Could be lol.
If the director is buying must be a good sign of something.
It popped up to .90 last time pretty easy.
Once it starts moving I think it will hit that level again in a short time.
bid moved up to .60 can't hold her back forever.
WOW!!!
Good news. JAVO is growing and growing.
Some good potential here.
Thanks, I try to drop in from time to time.
That is exactly why I'm here. There is definately some short term and long term potential.
Great news.
I like the fundimentals of the company.
Plus with the price of gas I imagine that more people are looking for cheaper alternatives to Starbucks to get there coffee fix.
Try checking out this link to see what the short status is on this stock
http://shortsqueeze.com/?symbol
The gap is filled now we can move up again.
close above 2 today who knows where we'll open tomorrow.
can't hold it back for long
Took only a little volume to take it down. Should only tak e a little volume to take it back up to HOD for close.
Looks like the volume is picking up a little over here.
Might be time to wake up and pay attention.
I think that the last 5-6 times I wanted to buy anything through scottrade they told me the same thing.
Funny thing is the 3 different stocks I bought have all gone up 60-100% since I bought them. Its a little more of a hassle but I'll make the call to make a little green.
They seem to do that when the volume fluctuates more than they like.
I called yesterday and they placed the trade for me at internet prices.
They have done that on quite a few of the stocks I trade.
Twalk just how short are you?
It's hard for me to believe that if you are in this stock you would post as negatively as you have unless you have shorted the stock.
I bought a few weeks back and continue to pick up more shares today. I personally know how draining a lawsuit is to a company in resources, both financial and time. I also personally know how much a company can strive and recover after that lawsuit is closed.
I eagerly will pick up at these levels there is no reason not to at these levels with the technology ARSC has and the potential of company.
CytoDyn to Meet with Quest Clinical Research to Finalize Phase II Strategy for Novel AIDS Drug
Following a management meeting in San Francisco on June 7, representatives of CytoDyn, Inc. (Pink Sheets: CYDY) will be meeting with Principle Investigator Dr. Jay Lalezari at Quest Clinical Research to finalize the Company’s strategy for a Phase II trial of Cytolin®. An immune therapy that uses the human immune system to control HIV infection, Cytolin® was used for two years before the antiretroviral cocktails became available to delay the progression of AIDS in about 200 patients, as reported by CBS-TV News.
Because the standard for treating HIV/AIDS is rapidly evolving, the Company must decide on the best indication to pursue prior to submitting a protocol to the FDA. On the one hand, patients failing Highly Active Antiretroviral Therapy (HAART) have an urgent need for treatment options. On the other hand, experts recognize a benefit to delaying initiation of antiretroviral therapy until medically necessary because starting treatment may mean a change in the patient’s lifestyle, some antiretroviral drugs have serious side effects, and resistance may develop, which limits future treatment options. Based on previous clinical experience, Cytolin® might also be used to control HIV infection delaying the need for antiretroviral therapy.
About Quest Clinical Research Quest Clinical Research provides clinical research dedicated to the development of new therapies for treating life-threatening viral illnesses, such as HIV/AIDS, Hepatitis B and C, CMV infection and influenza. It has provided access to investigational drugs to over 5,000 individuals throughout Northern California since 1989 at no cost to patients.
About Cytolin® HIV infects other species, such as chimpanzees. But only humans get sick from HIV infection. In the early 1990s, several teams of university-based scientists reported in the peer-review literature that this is because of a flaw in the human immune system. Cytolin®, a monoclonal antibody, is designed to correct that flaw. This is different from "reconstituting" the immune system, which can make patients sick ("immune reconstitution syndrome"). With the human immune system working better, we would expect it to do a better job of controlling HIV infection.
Disclaimer This press release contains forward-looking statements that are not historical facts but only reflect the Company’s estimates and projections. There are many factors, known and unknown, that could cause actual results to differ significantly. These factors include, but are not limited to, unanticipated problems and accidents during the manufacturing process, unexpected regulatory difficulties, unexpected difficulties with patient enrollment, unexpected study results, economic downturns, the effects of adverse publicity, litigation, competition, victimization by white-collar offenders, and other factors that may be identified from time to time in the Company's announcements.
Please visit our web site at www.cytodyn.com.
words out!!!!
looks like a real nice gem you found here!!!
looks good!!!
.34x.35 nice
I bought a few the other day just to play around a little.
Hmmm....the plot thickens.
That is some great DD...lol
thanks
That's what I want to hear.
Nice to see a little perk up the last few days.
Great thanks for the information.
So a specific Gravity of 39 is a GOOD thing to say the least.
That is definately what I'm hoping too.
Welcome to the best stock on the pinksheet. That is of coarse just IMHO
I got to PFUO on Friday at about 4:00.
I saw a few people working in the back away from the front office. Bruce was walking with another gentleman and saw me come in. He came over and welcomed me as we have met before.
I said that I was just there to check in and did explain that for some reason Barbara had not been answering e-mails and investor questions.
Bruce gave me his e-mail address and a different number than is in the ibox to call.
bgrogg@pfuo.com
(800)225-4143
He said that he didn't know why she wasn't returning calls and e-mails but did say he'd be happy to answer questions if people e-mailed him.
I said that some of the current investors including myself are watching closely and can't help but be dissappointed in the current pps. He said that yes as of late they had be hit pretty hard in the stock market along with many others. He did however assure me that they are still working very hard to grow the company and he didn't see any reason for the pps to be where it is at today. They are courting some other big clients and the software is working great making that task even easier.
Bruce also said that they had some exciting prs in the works and to watch for them. He was just as relaxed and upbeat with me on this visit as he has been in the past.
We talked breifly of the sell off of the old prepaid route. He said that it really wasn't bringing in the kind of cashflow they wanted to see so they sold it at a profit.
I asked about the float on pinksheets as it is clearly wrong. He wrote it down and said that he would look into it but that it was probably off by a few 00's.
So the company is still there, people are working, some prs should be out soon, and now everyone has someone else to contact for questions and such.
Everyone that I saw at PFUO was working and seemed busy with something. I'm in for awhile as I think it is still a solid investment.
No worries. I went to visit PFUO and chatted with Bruce for awhile.
I'll post more about it later tonight or tomorrow as I have a family engagement tonight and have to go.
But the company is still there and I saw the employees hard at work.
I can't go until about 2-3 MST
But I'm definately going today.
7001 S 900 East Suite 400
Midvale, UT 84047
They are still in the sam ebuilding just upstairs so the new suite number is 400