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Sony Corporation Message Board

repo_man_one 52 posts  |  Last Activity: Aug 18, 2014 9:04 PM Member since: Sep 6, 2012
  • repo_man_one by repo_man_one Aug 18, 2014 9:04 PM Flag

    Hot off the press from the trial today:

    “Anatabloc was not the only product to be feted at the governor’s mansion under Robert F. McDonnell. Even the humble chickpea inspired a breakfast at the 200-year-old home, complete with governor and state university researchers.

    Bob McDonnell’s commerce and trade secretary, Jim Cheng, recalled on the stand just now that the governor once hosted the presidents of Israeli-based Strauss Foods and PepsiCo for breakfast. The two companies had, under a joint venture, produce Sabra hummus. McDonnell hosted them for a mansion breakfast when they opened a plant in Virginia to produce the chickpea dip.”

  • repo_man_one repo_man_one Aug 16, 2014 1:51 AM Flag

    You is We?
    The SEC has rules about such things.

  • Reply to

    Under Oath

    by rockcreekpharma Aug 8, 2014 4:27 AM
    repo_man_one repo_man_one Aug 12, 2014 12:01 AM Flag

    I thought the shorts assured everyone that Johns Hopkins and Dr Ladenson were not involved?
    Were those shorts lying?

  • repo_man_one repo_man_one Aug 11, 2014 9:08 PM Flag

    know what?

  • From the Quotient Clinical web site

    We prepare and submit:
    Clinical Trial Authorisation (CTA) applications to the MHRA, with an average approval time of just 15 days.

    The end of third quarter is only 7 weeks away.

    Looks to me like Dr Mullan must have been working with Quotient Clinical long before they announced it.

  • "the FDA has issued a clinical hold on the application, pending clarification of data from 2010. We are currently reviewing the FDA's comments and intend to respond accordingly."

    So the FDA has responded and is just looking for "clarification of data"?

  • Reply to

    the company does anticipate

    by repo_man_one Aug 11, 2014 5:05 PM
    repo_man_one repo_man_one Aug 11, 2014 5:22 PM Flag

    My take is the company has had conversations with the FDA about the nutritional supplement business and obviously believes that with the filing of the NDIN, along with a temporary suspension, that will lead to resolution of the matter.

    I would have been much more concerned if it was not worded as "voluntarily suspending" as opposed to un-voluntary suspension, or the company anticipates mandatory suspension.

  • Reply to

    News

    by tensurf Aug 11, 2014 4:27 PM
    repo_man_one repo_man_one Aug 11, 2014 5:11 PM Flag

    I don't think there is anything new in the above, that wasn't reported in the previous statements.

    However, what is new is the filing of the NIND back in June for resolution of that issue, and they raised more money to carry on operations thru June 2015.

    Shorts will try to spin this as negative but it looks to me like progress is being made.

  • repo_man_one by repo_man_one Aug 11, 2014 5:05 PM Flag

    From the Press release,

    "However, the company does anticipate these actions will bring the FDA warning letter matter to a close."

    Sounds to me that with the NDIN filing, along with the "voluntarily suspending its sale of CigRx and Anatabloc, the FDA warning letter will be resolved.

  • Ms. Canaan’s extensive experience in the private equity industry will be valuable to the Company’s Board of Directors as the Company develops and implements strategies to finance its expected pharmaceutical development efforts in connection with its ongoing corporate transition.

    I like the sound of that

  • From the Quotient Clinical web site

    We prepare and submit:
    Clinical Trial Authorisation (CTA) applications to the MHRA, with an average approval time of just 15 days.

    The press release indicates the CTA filing should occur sometime in the next two months.
    Doesn't this imply the European trials should be underway long before the end of the year?

  • Reply to

    Consider ~

    by a_brown3 Jul 31, 2014 8:58 PM
    repo_man_one repo_man_one Aug 1, 2014 6:57 AM Flag

    There is no doubt the European CTA track is part of the overall plan. I agree the last SEC 10Q filing said as much. What I want to know now is what disease will the European track focus on?

  • repo_man_one by repo_man_one Jul 29, 2014 1:38 PM Flag

    Looks like Maureen was a true believer in Anatabloc

    "But Burck said Maureen was a true believer in his dietary supplement Anatabloc and had, for years, been sold on the virtues of "nutraceuticals.""

    Goggle
    McDonnell Corruption Trial Bombshell: Couple's Marriage Has Broken Down, Say Maureen's Lawyers

    I wonder what the Governor and Doctors are going to say about Anatabloc?

  • Saw this posted on another board
    Google - Access to Gov. McAuliffe can be bought for $50k, through new PAC

    "Donors giving the largest amount to Common Good VA get regular access to McAuliffe, including a private reception, a round-table discussion with state leaders, a retreat and a private dinner with McAuliffe and his family."

    Wonder if this will come up at the trial for comparison?

  • repo_man_one by repo_man_one Jul 23, 2014 12:02 PM Flag

    Check out this new article
    Google - McDonnell Trial: Was former governor set up?

    In this latest article, the author speculates about whether JW was working with the Feds to trap a Governor?
    What a Circus this is turning into!

  • Reply to

    Holder signed off?

    by repo_man_one Jul 22, 2014 3:22 PM
    repo_man_one repo_man_one Jul 23, 2014 11:51 AM Flag

    Have you seen the latest article?
    Google - McDonnell Trial: Was former governor set up?

  • Reply to

    Holder signed off?

    by repo_man_one Jul 22, 2014 3:22 PM
    repo_man_one repo_man_one Jul 22, 2014 5:12 PM Flag

    Then there is this from the article-

    "The Democratic led DOJ investigation into a sitting Virginia Governor is unprecedented. It occurred during the 2013 gubernatorial year aided and abetted by leaks."

    "Aided and abetted by leaks"?

    I assume the author is talking about the relentless negative press coverage last year which was obviously sourced by leaks and anonymous sources. I hope the source of those press "leaks" get exposed at trial. I think it would go a long way in helping to expose the political motives behind this case.

  • repo_man_one by repo_man_one Jul 22, 2014 3:22 PM Flag

    Goggle - McDonnell Trial: Acquittal could force Obama to replace Holder

    From the article:
    "Fair or not, politics is in good measure perception. The Democratic led DOJ investigation into a sitting Virginia Governor is unprecedented. It occurred during the 2013 gubernatorial year aided and abetted by leaks. Until then, McDonnell reigned as the most popular Republican Governor in Virginia history, a possible 2016 GOP contender."

    "Meaning: If McDonnell gets acquitted, the investigation may strike many voters as political, especially since Holder signed-off on giving Williams a rare form of blanket immunity from past criminal and related activities. Former prosecutors have publicly said they don’t recall such deals in these cases. It could get ugly. Meaning: If McDonnell gets acquitted, the investigation may strike many voters as political, especially since Holder signed-off on giving Williams a rare form of blanket immunity from past criminal and related activities. Former prosecutors have publicly said they don’t recall such deals in these cases. It could get ugly."

    “Holder signed-off on giving Williams a rare from of blanket immunity” - Really?

    This entire thing stinks of politics

  • Reply to

    FDA Comments are forthcoming

    by crooked_analyst Jul 11, 2014 4:33 PM
    repo_man_one repo_man_one Jul 12, 2014 12:59 PM Flag

    I don't think we can conclude the FDA has sent a letter, can we?

    It says " the Food and Drug Administration ("FDA"), has notified the Company that the agency will provide comments on RCP's Investigational New Drug ("IND") application."

    The IND overview of the process that crooked_analyst has posted indicates phone calls are another likely source of contact. In fact, it says be ready to receive an unannounced phone call.

    In any event, whether a phone call or letter, it appears RCP may not even know what the specific topics are the FDA wants to discuss given the following statement from the press release.

    "When we receive the agency's official comments and/or recommendations...."

    "When we receive" implies to me that RCP may not even know the specific topics yet, doesn't it?

  • Reply to

    FDA Comments are forthcoming

    by crooked_analyst Jul 11, 2014 4:33 PM
    repo_man_one repo_man_one Jul 11, 2014 6:29 PM Flag

    If the IND was submitted at the end of June, about the same time as the SEC filing was made, then that would put the process at the start of the 3 to 4 week. According to the above, that would be about the time when questions and specific requests might come from the project manager.

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