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Big Pharma & FDA Collusion?

Discussion in 'The Darkened Sample Closet' started by anonymous, Aug 18, 2020 at 2:05 PM.

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  1. anonymous

    anonymous Guest

    Millions of US citizens are so fed up with our FederalDeathAdministration they are petitionong congress to fire the entore lot of them and start all over (including me).
    This Europen stock message board poster is right on with his/her description:

    "go_wa xx Sunday, 01/23/22 09:07:23 PMRe: TheBigTicket post# 43746 [​IMG]0
    Post # of 43776

    Failure to render assistance to a helplessly injured person commits a crime and is punished with imprisonment for "failure to render assistance". At least that's how it is in Europe. I don't know how this is handled in the US.
    I'm just amazed to read again and again that there is an FDA. who should have their own laws in the event of a pandemic, these just dont acknowledge and people are dying because they dont care about!! This is second class and unworthy!!!
    The FDA simply fails to acknowledge that they are obligated to provide immediate assistance!
    More Americans have been killed by COVID than by all of America’s foreign wars.
    The time will come when the FDA will be held accountable! At least I hope so!

  2. anonymous

    anonymous Guest

    Hidden camera proof that our worthless FDA favors BP over immediate Covid therapeutics from
    small companies ?
  3. anonymous

    anonymous Guest


    Friday, February 25, 2022 7:19:27 AM

    Re: cowtown jay post# 35607

    Post# of 35676
    This is exactly why Humanigen will NEVER Get Approval! Big Pharma Elites Control The FDA. Unfortunately, this is the world we live in today whether or not folks want to accept this.

    Our approval will shut off the Covid revenue streams to Pfizer, Moderna, etc. We know that.

    Big pharma and their sponsored FDA staff have utter disregard for the lives lost in pursuit of their own self-interest.
  4. anonymous

    anonymous Guest


    Tuesday, May 03, 2022 12:44:28 PM

    Re: None

    Post# of 861
    So big pharma... Pfizer received an emergency use authorization for Paxlovid before any real proof that it actually works! The FDA has some serious corruption and it is affecting the health of Americans. Government run agencies are not exactly full of the brightest and best of people. Political influence, graft, corruption and special future employment favors... all influence their decisions.

    Pfizer Inc. slumped after Paxlovid, its pill for treating Covid-19, failed to show benefit as a preventive therapy in a trial.


    "Paxlovid is poised to become one of the fastest-selling drugs of all time, with $24 billion in projected 2022 sales, according to analytics group Airfinity Ltd. Pfizer has also reaped billions in global sales from its Covid-19 vaccine.

    The company said late Friday that the drug failed to hit its main goal of reducing the risk that adults exposed to the coronavirus through contact with a household member would become infected. Compared with those who took a placebo, people who received Paxlovid had about a third less risk of infection, which wasn’t statistically significant.

    The shares fell 2.2% at 9:36 a.m. in New York. They had declined 17% this year through Friday’s close.

    The trial failure, along with reports of rebounding coronavirus levels in some patients who have completed a course of Paxlovid, are unlikely to change the drug’s sales potential, according to Bloomberg Intelligence analysts John Murphy and Sam Fazeli.

    “The trial miss at most takes away a small incremental sales opportunity in future years,” they said Monday in a research note. The reports of rebound infections are “also not surprising as viral dynamics during an infection are unlikely to fit perfectly with a rigid 5-day course.”

    Morgan Stanley analysts, who had estimated the drug’s sales to reach $48 billion in 2022, said the prophylaxis data might affect their forecast."
  5. anonymous

    anonymous Guest

  6. anonymous

    anonymous Guest

    Biden Admin Wasting $10.6 Billion On Pfizer's COVID-19 Paxlovid Flop

    Pfizer Altered its Paxlovid Protocol. . . After Receiving its first $5.3 billion:

    As we can see, FDA Emergency Use Authorizations (EUAs) don’t always work out as they should, but in this case, it was because of some manipulative action by Pfizer and an outrageous and risky bet by the Biden White House.

    That’s because with no public mention, Pfizer had secretly lowered its own bar following its EUA after the White House had committed to purchasing $5.3 billion dollars of product. Pfizer stated:

    “Following the Emergency Use Authorization of Paxlovid for individuals at high risk of progression to severe COVID-19, the protocol was amended to exclude high-risk individuals and allow enrollment of patients without risk factors for progression to severe COVID-19 who were either unvaccinated, or whose last COVID-19 vaccination occurred more than 12 months from enrollment.” (emphasis added)

    This way, Pfizer was able to administer its drug to a less severely ill, and healthier population in hopes of having a superior efficacy signal and a decreased safety signal, but it still failed to show an adequate clinical effect on any of its prospective protocol-established endpoints.
  7. anonymous

    anonymous Guest

    This original post is two years old & our glorious FDA continues its history of letting sick people die because they only approve drugs from their deep pocket "Big Pharms' pals. You know, those companies who contribute millions of dollars a year to FDA. Here is another small biotech with a repurposed drug that has a great previous safety profile and with a Covid possibility but the Mafia at FDA continue their barrage of forcefully making them jump through endless hoops like this one-denying a meeting months ago, making them resubmit & making them wait another THREE MONTHS!
    Revive Therapeutics Announces Type C Meeting Request Granted by FDA for Amended Protocol Agreement of Phase 3 Clinical Study for Bucillamine in the Treatment of COVID-19
    January 05, 2023 09:19 ET | Source: Revive Therapeutics Ltd.

    TORONTO, Jan. 05, 2023 (GLOBE NEWSWIRE) -- Revive Therapeutics Ltd. (“Revive” or the “Company”) (OTCQB: RVVTF) (CSE: RVV) (FRANKFURT: 31R), a specialty life sciences company focused on the research and development of therapeutics for medical needs and rare disorders, announced today that the U.S. Food & Drug Administration (“FDA”) has granted the Company’s Type C meeting request to obtain agreement on the revised protocol endpoints for the Company’s Phase 3 clinical trial (the “Study”) (NCT04504734) to evaluate the safety and efficacy of Bucillamine, an oral drug with anti-inflammatory and antiviral properties, in patients with mild to moderate COVID-19. The goal date for the FDA to provide its written responses is March 7, 2023.

    The Company is not making any express or implied claims that its product has the ability to eliminate or cure COVID-19 (SARS-2 Coronavirus) at this time.

    Wake up Congress peeps and demand the FDA SAVE LIVES vs being a Federal Death Authority!!!