Pfizer Inc (PFE) Options

Mark. $27

Bearish 100%

Imagine being dumb enough to own this stock knowing that rfk and kash will rescind their liability clause!! Can’t wait till these fuckers pay for what they have done

Winning no matter what
Will be short lived

Time is at hand

Nothing says unbiased better, am I right? leavening the the istitution that regulates for a company that it regulates. Hot garbage 🗑️ humans with no morals. 

PFE hires former head of FDA/CDER as CMO:

https://e.endpointsnews.com/t/t-l-skthrhy-pktjidrih-t/ Patrizia Cavazzoni, the FDA’s for­mer head of drug regula­tion, will become Pfizer’s new chief medical officer, End­points News has learned. Cavazzoni led the FDA’s Cen­ter for Drug Evaluation and Research (CDER), which oversees all drug applications, for about four years during the Biden administration. Cavazzoni resigned from the FDA immediately prior to Trump’s inauguration.

Summit Therapeutics Announces Clinical Trial Collaboration with Pfizer to Evaluate Ivonescimab in Combination with Pfizer Antibody Drug Conjugates (ADCs)

https://www.biospace.com/press-releases/summit-therapeutics-announces-clinical-trial-collaboration-with-pfizer-to-evaluate-ivonescimab-in-combination-with-pfizer-antibody-drug-conjugates-adcs

-they were born winners-

"They win no matter what.."
Excellent synopsis..

Key word there is at the end with establishment in the line. The Media is on the payroll, it harmed way more than it helped. Folks need to go to jail. But hay how about them dividends. Folks supporting this company is insane. The aMount of mental gymnastics to avoid acknowledging Al the dirty stuff that they have done in the past even before the Jab is wild. In every instance they made more than they lost in the lawsuits. There is no incentive to be honest with the customer because they win no matter what. 

This time around though things will be different. The "unintentional lab leaks" won't be tolerated.
Think about it. Toying with mother nature to create a deadly virus on purpose is insanity and pure evil.
More of this will be dealt with so harshly that no one in the Chinese Communist Party will be
enjoying any more Wonton Batshit Soup.

-history repeats itself - New coronavirus with potential to cause pandemic discovered in China

The new virus is even closer related to MERS, a deadlier type of coronavirus that kills up to a third of people it infects.

HKU5-CoV-2 is strikingly similar to the pandemic virus, sparking fears that history could repeat itself just two years after the worst was declared over.



https://www.dailymail.co.uk/health/article-14421599/coronavirus-potential-cause-pandemic-discovered-china.html

great choice!

wow. now cutting off that gravy bowl will hurt. let's see what develops from this.
and how much mulah came back around from Pfizer into Falsi's pocket and to others in congress and media who gave their all to support the killer jabs? Investigations ongoing. This could get really nasty.

Yes, but the Pfizer is being laid bare and it is not what it appeared to be in the past.
I do agree though it is getting cheap. If it returns to around 22 I will go from short to long.

Another company is about to enter that market with a much better product.
What hurts even much more is the mRNA stuff being put on hold.
Add that to growing call for liability issues could put the nail in the coffin.

How does one know
Not true (eom).

Trump to pull covid vaccines off market

For reassessment

Click on "For reassessment" Trump may BAN COVID VACCINES

- Trump's Potential Ban on COVID Vaccines (0:01)
- Criticism of Operation Warp Speed (0:54)
- Media Narratives and Vaccine Criticism (2:11)
- Breaking the Collusion Between Media and Big Pharma (3:48)
- Future Actions and Accountability (7:09)
- Health Ranger Store Promotions (8:41)
- Final Thoughts and Closing (11:43)

For more updates, visit: http://www.brighteon.com/channel/hrreport

PFE discontinues commercialization of Beqvez due_to_low_demand:

https://finance.yahoo.com/news/pfizer-shelves-haemophilia-gene-therapy-172523645.html

Conventional therapies for hemophilia, including PFE’s Hympavzi (#msg-175217202), are sufficiently safe, effective, and convenient that gene-therapy solutions are a tough sell—for the entire industry, not just PFE.

The discontinuation of Beqvez will have a near-zero effect on PFE's financials since hardly anyone was using the product.

Not true (eom).

Trump to pull covid vaccines off market

For reassessment

-history repeats itself-Covid vaccines saved almost 20million lives during the first year of their existence, according to estimates.

British grandmother Maggie Keenan became the first person in the world to get an approved jab on December 8, 2020.

The mRNA vaccines made by Moderna and Pfizer are estimated to have saved tens of millions of lives globally from Covid, including 3million in the US.

https://www.dailymail.co.uk/health/article-10944873/Covid-vaccines-saved-nearly-20MILLION-lives-year-worlds-roll-out.html

Good perspective

~~~ When facts are laid forth ~~~
(51:18)

Open for discussion

Dr. Tom Cowan

Pfizer is trading at a considerable discount:

Currently, Pfizer's stock is trading at just 18 times trailing earnings
All this negativity, however, does open up an opportunity for investors to buy the stock at a discount. Despite being a top company in the healthcare industry, investors are treating Pfizer as a highly risky business to invest in, and that could be a huge mistake
There's a significant discount here, as the average stock in the Health Care Select Sector SPDR Fund trades at more than 18 times its future profits.

And its high-yielding dividend, which pays 6.6%, can give investors plenty of incentive to be patient.

Agree

Prophetic indeed

Another angle

On the chopping block finally...let the guillotine find it's target.
https://www.fiercehealthcare.com/regulatory/mass-layoffs-hhs-cdc-cuts-1300-probationary-workers-reports-say?oly_enc_id=4924G0643390I0A

Those illegal immigrants from all over the world... the poorest of the poor that their countries neglected came pouring across the border with all the infections and other hitchhikers attached. Kennedy was posted to the world by MSM to be an anti vaxxer which was never the case.
When I go to buy moonshine, do I buy from a mountain family that has been producing it for generations or do I buy from some yaahoo off the street?
Details matter.
https://www.investors.com/news/technology/rfk-jr-senate-confirmation-hhs-secretary/

It was DARPA money that supported the mRNA research for covid jabs and others. Hence, as court records revealed and as CDC and Fizzer admitted to .... that it is a bioweapon... and the court ruled against the suitors because of this. So folks, you have the facts. Get in line and take those bioweapons for God's sake!! Now, yes now, the hatchet is falling: https://www.fiercebiotech.com/research/director-advanced-research-projects-agency-health-fired-trump-administration?oly_enc_id=4924G0643390I0A

The Wall Street Journal’s editorial board published an op-ed Monday calling on Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. to set aside his anti-vaccine activist positions in light of the nearly 50 measles cases that have been confirmed among mostly unvaccinated children in Texas.
history repeats itself-------------------------------

https://thehill.com/policy/healthcare/5149761-wsj-kennedy-antivax-texas-measles-outbreak/

Kennedy has downplayed concerns about his anti-vaccine sentiments, saying in a Senate hearing that “all of my kids are vaccinated, and I believe vaccines have a critical role in healthcare.”

FDA Issues Back-to-Back Vaccine Approvals as RFK Jr. Takes HHS Seat

As they say, history repeats itself
https://www.biospace.com/fda/fda-issues-back-to-back-vaccine-approvals-as-rfk-jr-takes-hhs-seat

thanks for that! Great story and great song. Amazing he wrote that in 2011.

https://rumble.com/v6l6jc7-rumble-mrna-ban.html
Oh Fizzer. They helped with their conspiracy with the FDA to do what?? To make us sicker than sick and blow up the narrative so to scare hell out of people with a protocol that kills ...then use those kills to hype the "cure" Jab. Oh then look now at the numbers of cancers.. It is cancer gone wild... even in children like never seen before... but oh fizzer bring us a super bowl commercial of a boxing cancer kid who gets his fizzer cancer cure... I would like to laugh but the crime here is two fold sad. First the crime of citizens still duped and stupid who are so enamored by the fizzer behavior ... oh they are our saviours!! Secondly, the create deadly jabs with mRna that changes the DNA the core of our being. Thank God we have RFK Jr. who is especially fond of children being poisoned by our Pig Pharma FDA mafia.
https://rumble.com/v6l6jc7-rumble-mrna-ban.html

Written in 2011

~~~ Prophetic indeed ~~~
(4:13)

Video recently added to lyrics

NaturalNews

PFE independent director bought $500K of stock on the open market yesterday:

https://www.sec.gov/Archives/edgar/data/78003/000122520825001778/xslF345X05/doc4.xml

TALZENNA + XTANDI is the first PARP inhibitor plus ARPI combination to demonstrate statistically significant and clinically meaningful improvement in overall survival (OS) in patients with metastatic castration-resistant prostate cancer (mCRPC) regardless of HRR mutation status
TALZENNA + XTANDI improved median OS by almost 9 months in unselected patients (Cohort 1) and by 14 months in patients selected for HRR mutations (Cohort 2) versus standard of care XTANDI
NEW YORK--(BUSINESS WIRE)--Pfizer Inc. (NYSE: PFE) today announced positive results from the Phase 3 TALAPRO-2 study of TALZENNA® (talazoparib), an oral poly ADP-ribose polymerase (PARP) inhibitor, in combination with XTANDI® (enzalutamide), an androgen receptor pathway inhibitor (ARPI), demonstrating a statistically significant and clinically meaningful improvement in overall survival (OS) compared to placebo plus XTANDI in patients with metastatic castration-resistant prostate cancer (mCRPC), with or without homologous recombination repair (HRR) gene mutations. The TALAPRO-2 results will be presented at the American Society of Clinical Oncology Genitourinary (ASCO GU) Cancers Symposium in San Francisco and featured in the ASCO GU official Press Program.




The TALAPRO-2 study evaluated two sets of patients, unselected (cohort 1) and selected for HRR gene-mutations (cohort 2). Overall survival was a prespecified, alpha-protected key secondary endpoint. After more than four years of median follow-up (52.5 months), the median OS in cohort 1 was 45.8 months with TALZENNA in combination with XTANDI, and 37.0 months with XTANDI and placebo (Hazard Ratio [HR] of 0.80; 95% Confidence Interval [CI], 0.66-0.96; p=0.015), representing a 20% reduction in the risk of death. This represents a nearly 9-month gain in median OS versus standard of care XTANDI. Data from cohort 1 will be presented today at ASCO GU in an oral presentation (Abstract LBA18) by Dr. Neeraj Agarwal, global lead investigator for TALAPRO-2.

In Cohort 2, a statistically significant and clinically meaningful improvement in OS was observed in patients with HRR-mutated mCRPC. At a median follow-up of 44.2 months, the median OS was 45.1 months with TALZENNA in combination with XTANDI, and 31.1 months with XTANDI and placebo (HR of 0.62; 95% CI, 0.48-0.81; p=0.0005), a 38% reduction in the risk of death. This result represents a 14-month gain in median OS versus standard of care XTANDI in a patient population with a historically poor prognosis. The OS improvement in the HRR-mutated population was observed in patients in both BRCA and non-BRCA gene alterations. Dr. Karim Fizazi, Institut Gustave Roussy, University of Paris-Saclay will share data from Cohort 2 at ASCO GU today (Abstract LBA141).

“Since its approval, TALZENNA in combination with XTANDI has redefined the standard of care for those living with homologous recombination repair gene-mutated mCRPC. These latest data from TALAPRO-2 are extremely compelling, demonstrating that the combination significantly extended overall survival, in patients selected and unselected for HRR gene alterations, potentially shifting the treatment paradigm for all men living with mCRPC,” said Roger Dansey, M.D., Chief Oncology Officer, Pfizer. “Although definitive conclusions cannot be drawn across studies, these results appear to represent the longest median overall survival reported in a randomized, controlled Phase 3 trial in mCRPC. We look forward to continuing to work with global authorities to potentially update the TALZENNA label with these results.”

“TALAPRO-2 is the first study demonstrating a significant and clinically meaningful survival benefit using a combination of PARP and androgen receptor inhibitors in mCRPC,” said Neeraj Agarwal, M.D., FASCO, Professor and Presidential Endowed Chair of Cancer Research at Huntsman Cancer Institute, University of Utah, and global lead investigator for TALAPRO-2. “Survival rates in metastatic castration-resistant prostate cancer are poor due to the advanced and aggressive stage of the disease. Today’s results demonstrate the potential for TALZENNA in combination with XTANDI to be a practice-changing treatment to help improve patient survival in mCRPC.”

At the time of the final analysis, updated radiographic progression free survival (rPFS) and other secondary efficacy endpoints demonstrated maintained clinical benefit in both cohorts and were consistent with the primary analyses previously reported and published in The Lancet and Nature Medicine.

In addition to the FDA, these data have been shared with the European Medicines Agency (EMA) and other global health authorities to support potential updates of the approved labels for TALZENNA.

The safety profile of TALZENNA plus XTANDI was generally consistent with the known safety profile of each medicine. The most common all-cause adverse events in the TALZENNA group (=30% of patients) were anemia, neutropenia, and fatigue, and the most common (=10% of patients) grade 3–4 adverse events were anemia (49%) and neutropenia (19.3%). Adverse events were generally manageable with dose modification and supportive care.





https://www.biospace.com/press-releases/pfizers-talzenna-in-combination-with-xtandi-improves-survival-outcomes-in-metastatic-castration-resistant-prostate-cancer

What does the confirmation of RFK Jr. mean

~~~ For FDA and Big pharma ~~~
(23:50)

Follow the data

This is historic - RFK Jr. Confirmed as HHS Head: A Pivotal Moment (0:01)

- Censorship and Corruption in Government Agencies (1:34)

- Proposed Reforms and Legal Actions Against the FDA (2:24)

- Impact on the Nutrition Industry and Big Pharma (7:56)

- Concerns About Heavy Metals and GMOs (12:03)

- Calls for Criminal Prosecutions and Systemic Reform (17:16)

For more updates, visit: http://www.brighteon.com/channel/hrreport NaturalNews

Senate confirms RFK Jr. as HHS secretary in 52-48 vote

https://www.foxnews.com/politics/senate-confirms-robert-f-kennedy-jr-serve-trumps-health-secretary

Currently, Pfizer's stock is trading at just 18 times trailing earnings. And based on analyst projections, it's at a forward price-to-earnings multiple of less than 9

FDA approves PFE’s Adcetris for third-line DLBCL as addend to Revlimid/Rituxan:

https://www.businesswire.com/news/home/20250207460554/en DLBCL is the most common and aggressive type of LBCL and is difficult to treat. More than 25,000 cases of DLBCL are diagnosed each year in the United States, accounting for more than 25% of all lymphoma cases. In the phase-3 trial supporting approval, the HR for OS was an impressive 0.63.

A paper inadvertently published on the website of an ASCO conference revealed good results for mevrometostat in treating castration-resistant prostate cancer.
Pfizer’s experimental drug mevrometostat cut disease progression rates in half in combination with standard hormone therapy, according to an article describing data from a Phase I trial of metastatic castration-resistant prostate cancer that appeared on Monday morning on the website for the ASCO Genitourinary Cancers Symposium.

The only issue is that the team from Pfizer wasn’t going to speak about the data until Thursday. Later in the day Monday, the conference published a full study abstract.

In addition to reducing disease progression rates, mevrometostat cut the risk of death by 49% in trial participants, all of whom had already received hormone treatment and one round of chemotherapy, according to reporting from Endpoints News.

Adverse effects were diarrhea (78% of patients), decreased appetite (58.5%) and dysgeusia (58.5%).

Pfizer is currently recruiting for two Phase III trials, MEVPRO-1 and MEVPRO-2, testing mevrometostat, an inhibitor of the oncoprotein EZH2, in prostate cancer as well.

Castration-resistant prostate cancer is a common form of prostate cancer, often treated with androgen deprivation therapy and chemotherapy.

The results, although announced prematurely, should be welcome news for Pfizer. Analysts were already buoyant on the company, with Guggenheim analysts writing in an investor note early Monday morning, before the leak, that Pfizer beat their fourth quarter 2024 expectations as well as consensus estimates.

Pfizer has a number of critical updates from its oncology pipeline coming down the pike this year. Phase III data for vepdegestrant in treating breast cancer and danuglipron for obesity are expected later this quarter, as well as Padcev in combination with pembrolizumab for bladder cancer sometime this year. On Monday, Pfizer announced data showing that Padcev in combination with Merck’s Keytruda reduced the risk of death by 49% in urothelial cancer compared to chemotherapy.

https://www.biospace.com/drug-development/leaked-conference-article-shows-pfizers-positive-phase-i-prostate-cancer-data

https://meetings.asco.org/abstracts-presentations/243221

https://www.biospace.com/press-releases/pfizer-and-astellas-padcev-enfortumab-vedotin-ejfv-plus-keytruda-pembrolizumab-shows-long-term-efficacy-in-first-line-treatment-of-locally-advanced-or-metastatic-urothelial-cancer-la-muc

The turn is in...

As Pfizer's CEO Albert Bourla said about the acquisition of Seagen, "We are not buying the golden eggs. We are acquiring the goose that is laying the golden eggs."

This smaller, cancer-focused drugmaker was already developing an impressive number of products for its size. With the backing of the much larger Pfizer, that innovative wheel should spin even faster.

https://www.fool.com/investing/2025/02/09/is-now-a-good-time-to-buy-the-dip-on-pfizer/

Pfizer is the 2nd largest recipient of USAID

Don't call it a comeback: Pfizer returns to Super Bowl with ad pledging to 'knock out' cancer

https://www.fiercepharma.com/marketing/pfizer-returns-super-bowl-ad-pledging-knock-out-cancer

Open to debate

Facts don't lie

From Pfizer documents

Excellent breakdown

And explanation

Of adverse reactions

has an attractive dividend yield of 6.3%, higher than most blue-chip stocks

PHMPT submitted a Freedom of Information Act Request

To the FDA

For all of the data within Pfizer’s COVID-19 vaccine biological product file

PHMPT has now sued the FDA for not releasing the data

Dividend secured...

Pfizer says it has at least $10B available for deals in 2025, with a focus on pipeline!