Johnson and Johnson (JNJ)

[IHuser]

imo..... i have toppled bf starting w the evil worthless king flying red bull ace....those paying attention have watched in dismay...next!


JNJ PFE

IHuser

[IHuser]

imo... this ticker is a toxic POS...FOLOW MY GROUP at PFE....


IHuser

[IHuser]

imo...my global following will crash this stock.....and me....JNJ

[IHuser]

imo.... if you are bullish on this ticker i will ruin you and your whole life....f with me JNJ


IHuser

[DewDiligence]

JNJ’s KVUE spin-off now has its own iHub board:

https://investorshub.advfn.com/Kenvue-Inc-KVUE-42070

[1jas]

anyone here, read about enzolytics pharm announcing the now have a cure for hiv/aids called clone 3 yesterday.

[Enterprising Investor]

Johnson & Johnson Announces Preliminary Results of Kenvue Inc. Exchange Offer (8/21/23)

NEW BRUNSWICK, N.J.--(BUSINESS WIRE)--Johnson & Johnson (NYSE: JNJ) today announced that, based on preliminary results, its previously announced offer to its shareholders to exchange their shares of Johnson & Johnson common stock for shares of Kenvue Inc. (NYSE: KVUE) (“Kenvue”) common stock owned by Johnson & Johnson was oversubscribed. The exchange offer expired at 12:00 midnight, New York City time, at the end of the day on August 18, 2023. Under the terms of the exchange offer, 8.0324 shares of Kenvue common stock will be exchanged for each share of Johnson & Johnson common stock accepted in the exchange offer.

According to the exchange agent, Computershare Trust Company, N.A., 802,707,331 shares of Johnson & Johnson common stock were validly tendered and not validly withdrawn, including 250,407,279 shares that were tendered by notice of guaranteed delivery. Johnson & Johnson intends to accept 190,955,436 of the tendered shares in exchange for the 1,533,830,450 shares of Kenvue common stock owned by Johnson & Johnson. Because the exchange offer was oversubscribed, Johnson & Johnson is accepting only a portion of the shares of its common stock that were validly tendered and not validly withdrawn, on a pro rata basis in proportion to the number of shares tendered. Shareholders who owned fewer than 100 shares of Johnson & Johnson common stock, or an "odd-lot," who have validly tendered all of their shares, will not be subject to proration, in accordance with the terms of the exchange offer.

Based on the total number of shares of Johnson & Johnson common stock reported to be tendered prior to the expiration of the exchange offer, it is estimated that approximately 23.8% of the tendered shares of Johnson & Johnson common stock will be exchanged, assuming all shares tendered by guaranteed delivery procedures are delivered under the terms of the exchange offer. This preliminary proration factor is subject to change based on the number of tendered shares that satisfy the guaranteed delivery procedures, as well as the number of "odd-lot" shares that were validly tendered and are not subject to proration. Johnson & Johnson expects to announce the final proration factor on August 23, 2023, promptly following the expiration of the guaranteed delivery period. Shares of Johnson & Johnson common stock tendered but not accepted for exchange will be returned to the tendering shareholders in book-entry form promptly after the final proration factor is announced. Following the completion of the exchange offer, Johnson & Johnson will retain approximately 9.5% of the outstanding shares of Kenvue common stock.

Goldman Sachs & Co. LLC and J.P. Morgan Securities LLC are the dealer managers for the exchange offer.

About Johnson & Johnson

At Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress. That’s why for more than 135 years, we have aimed to keep people well at every age and every stage of life. Today, as the world’s largest, most diversified healthcare products company, we are committed to using our reach and size for good. We strive to improve access and affordability, create healthier communities, and put a healthy mind, body and environment within reach of everyone, everywhere. We are blending our heart, science and ingenuity to profoundly change the trajectory of health for humanity.

https://www.businesswire.com/news/home/20230821033927/en/Johnson-Johnson-Announces-Preliminary-Results-of-Kenvue-Inc.-Exchange-Offer

[Enterprising Investor]

The Final Exchange Ratio is 8.0324 shares of KVUE per JNJ share (unless extended).

https://www.sec.gov/Archives/edgar/data/200406/000162828023029851/vwapday19.htm

[IHuser]

imo... this ticker is culpable as any poisoning people...JNJ

IHuser

[TRUSTUNITS1000000]

Type in a symbol by mistake and came up with this stock

[TRUSTUNITS1000000]

Type in a symbol by mistake and came up with this stock

[TRUSTUNITS1000000]

Nice long run

[fung_derf]

And.....?

[DewDiligence]

Bankruptcy judge tosses JNJ’s proposed talc settlement:

https://www.wsj.com/articles/johnson-johnsons-second-talc-bankruptcy-case-thrown-out-74a63a13

A New Jersey bankruptcy judge threw out the second chapter 11 case that Johnson & Johnson filed to resolve its mass talc liabilities, again shutting down the healthcare-product company’s plan to achieve an $8.9 billion settlement [see #msg-171617699].

Judge Michael Kaplan of the U.S. Bankruptcy Court in Trenton, N.J., said that J&J affiliate LTL Management LLC, created to carry the company’s talc-related liabilities into bankruptcy, wasn’t in sufficient financial distress to warrant granting it the legal protections of chapter 11.

[DewDiligence]

JNJ launches tax-free exchange offer for KVUE:

https://www.businesswire.com/news/home/20230723805654/en

[BottomBounce]

J&J Vaccine and Guillain-Barré Syndrome: Information on the FDA Warning
https://www.yalemedicine.org/news/covid-vaccine-guillain-barre-syndrome $JNJ

[BottomBounce]

Johnson & Johnson $JNJ Total Debt (mrq) $52.91B

[Agoura Guy]

***US FDA Revokes Emergency Use Authorization of J&J COVID-19 Vaccine***

***serious risk of blood clots***

TOO MANY DEAD PEOPLE.... JNJ KILLED TO MANY PATIENTS WITH THIS EXPERIMENTAL VACCINE POISON THAT HAD NO LONG TERM SAFETY TESTING!!!!!!

JNJ IS LIABLE FOR KILLING ALL THOSE INNOCENT PEOPLE!!!!!!

THESE CRIMINALS WILL BE SUED INTO OBLIVION!!!!!!!

SHORT THIS RANCID STOCK!!!!!!!!!

[DewDiligence]

BMY/JNJ—Milvexian—>FDA Fast Track designation for_all_phase-3_indications:

https://finance.yahoo.com/news/milvexian-granted-u-fda-fast-105900364.html

The three Milvexian indications BMY/JNJ are pursuing in phase-3 are: secondary stroke prevention; ACS; and primary stroke prevention in patients with AF—see #msg-171338375.

FDA Fast Track status doesn’t mean much, but it makes a Priority Review of the NDAs somewhat more likely (if one or more of these phase-3 trials pan out).

Please see #msg-169818942 for additional background info.

p.s. This PR was issued yesterday.

[DewDiligence]

JNJ’s talc settlement encounters a hitch:

https://endpts.com/talc-claimants-look-to-sue-jj-over-alleged-fraud-in-bankruptcy-case/

[DewDiligence]

KVUE +22% on_first_day_of_trading, valuing_the_company_at ~$50B.

[DewDiligence]

JNJ consumer spinoff, Kenvue IPOs @$22.00—starts_trading_today_as KVUE:

https://finance.yahoo.com/news/kenvue-begin-trading-york-stock-132500217.html

At the IPO price, KVUE’s market cap is ~$41B. Following the IPO, JNJ still owns about 90% of KVUE and plans to distribute the remainder to JNJ shareholders at some point.

Caution: KVUE bears 100% of JNJ’s talc liability outside of the US and Canada.

[Agoura Guy]

Holding Big Pharma ACCOUNTABLE: J & J To Pay Victims $8.9 Billion For Cancer Causing Baby Powder!!!!!

WHAT KIND OF MONSTERS RUN J & J?????

SMEARING CANCER ON BABIES???????

SHORT THIS CRAP TO OBLIVION!!!!!!!

[DewDiligence]

Addendum—JNJ’s ex-North America talc liabilities are being transferred to the Kenvue spinoff, according to Kenvue’s SEC filings.

[DewDiligence]

JNJ asserts_it_has_settled_North_America talc claims_for_an NPV_of_$8.9B_spread_over_25_years:

https://www.sec.gov/ix?doc=/Archives/edgar/data/0000200406/000020040623000037/jnj-20230404.htm

On April 4, 2023, the Company announced that its wholly owned subsidiary LTL Management LLC (LTL) has re-filed for voluntary Chapter 11 bankruptcy protection to obtain approval of a reorganization plan that will efficiently resolve all current and future claims arising from cosmetic talc litigation against the Company and its affiliates in North America. The Company has agreed to contribute up to the present value of $8.9 billion over 25 years (nominal value approximately $12 billion) to resolve the North America talc claims…

JNJ’s press release (https://www.sec.gov/Archives/edgar/data/200406/000020040623000037/a44238-kexhibit991.htm ) says:

LTL also has secured commitments from over 60,000 current claimants to support a global resolution on these terms.

Notably, the PR doesn’t say how many other ex-North America claimants there are (or will be) and what is meant by the phrase, “these terms.”

[DewDiligence]

JNJ has earmarked $61.5B for talc liability, according to court documents:

https://www.fiercepharma.com/pharma/after-johnson-johnson-loses-again-bankruptcy-case-its-game-talc-lawsuits

[IHuser]

imo...Mr. Putin and the white hat US are dropping these criminals...thank-you..from USA___JNJ

[BottomBounce]

Court Rejects J&J Bankruptcy Petition To End Talc Cancer Lawsuits https://www.rttnews.com/3340418/court-rejects-j-j-bankruptcy-petition-to-end-talc-cancer-lawsuits.aspx $JNJ

[Sesh]

Whoops better start digging in the cushions for some change J&J!

[BottomBounce]

$JNJ Book Value only $28.51

[BottomBounce]

$JNJ has $32.03B DEBT

[IHuser]

imo...no posts....yal want me to post godsmack....ok.......ready____JNJ

[IHuser]

imo...

[IHuser]

imo...

[IHuser]

imo....thank you Mr. Putin for replying to my communication...we American citizens see through these assholes bs....ty. This is our channel now where you can hear directly from the American market and the American people without interference.... subject to ihub rules....imo JNJ

Huser

[IHuser]

imo....all world leaders be warned I now own ihub sentiment with the people and you will have a very hard time getting past me to make war......because that is not what humantity wants........so......try me. JNJ

[IHuser]

imo...DY i se your sentiments in the green room......we are taking this over period no miscellaneous mass poisoning allowed....i hear you DY......JNJ.

Huser

[IHuser]

imo...WW3 is called off.......subliminally.....the trumps cued me to this post....humanity does not naturally fight humanity......we don't......so quit....the bs....JNJ......everybody has money....and thats a good thing.....JNJ

[IHuser]

imo...i can talk directly to putin on this channel....people don't have the problem...speculators are the problem......and blood doesnt spend very well....JNJ...hee sees this post and agrees with me....JNJ.

[IHuser]

imo...my johnson is smaller than this company...JNJ

[DewDiligence]

BMY/JNJ—Milvexian phase-2 data in treatment of acute ischemic stroke…

PR:
https://finance.yahoo.com/news/breaking-results-phase-2-axiomatic-073600645.html

CC slides:
https://s21.q4cdn.com/104148044/files/doc_presentations/2022/Bristol-Myers-Squibb-ESC-IR-2022-Event-Presentation.pdf

Milvexian is an oral inhibitor of Factor XIa being co-developed by BMY and JNJ (#msg-140083631). For BMY specifically, Milvexian is the company’s hope for replacing Eliquis revenue when Eliquis goes off-patent in 2028.

In the trial reported today, Milvexian + Plavix/aspirin was compared to Plavix/aspirin alone at five different Milvexian doses. Despite the lackluster results, which include a flat dose response, BMY/JNJ have committed to a phase-3 program for Milvexian in three indications: secondary stroke prevention; ACS; and primary stroke prevention in patients with AF. The phase-3 trials are slated to start by year-end 2022 (see slide #13). Curiously, the three phase-3 indications do not include either of the indications tested in phase-2, which are treatment of acute ischemic stroke (see above) and VTE prevention (#msg-166773814).

The main competition for Milvexian is Bayer’s Asundexian, another oral FXIa inhibitor that just started phase-3 trials in AF/stroke prevention and treatment of acute ischemic stroke (https://www.businesswire.com/news/home/20220828005030/en ).

BMY has pegged Milvexian is a $5B+ opportunity (not risk adjusted—see slide #20), but this seems optimistic in light of the dataset released today.

[Tamtam]

Johnson and Johnson (JNJ)
179.53 ? -1.56 (-0.86%)
Volume: 16,367,427

[Chrism0000]

PLEASE!! BUY UEEC, but it has to be for at least "8B :)) so I can retire. Lol

[Tamtam]

Johnson and Johnson (JNJ)
180.09 ? -0.57 (-0.32%)
Volume: 6,188,193

[Tamtam]

Johnson and Johnson (JNJ)
174.56 ? -2.24 (-1.27%)
Volume: 13,809,537

[wedman]

You are spot on!

[ofspring]

NEW ?? Johnson & Johnson has suspended production at a key plant manufacturing the Covid-19 vaccine

More: https://cutt.ly/SOVMeXD

[Tamtam]

Possibly

[Chrism0000]

Will J&J buy them down the road? HENDERSON, Nev.--(BUSINESS WIRE)--United Health Products, Inc. (OTC: UEEC) (“UHP” or the “Company”), developer, manufacturer and marketer of HemoStyp, a patented Oxidized Regenerated Cellulose (ORC), today announced that the Journal of Wound Care, headquartered in London, England, has informed the Company that UHP’s submitted article, Efficacy and Safety of HemoStyp as an Adjunct for Management of Secondary Hemostasis in the Operative Setting, has been accepted for publication in the November 2020 edition. This article, which was peer reviewed, was authored by Raymond Schaerf, MD, Sasan Najibi, MD, John Conrad, MD, and Gerard Abate, MD. This journal submission highlights the results of the study showing HemoStyp’s superiority to Surgicel®, an Ethicon Inc. product, a division of Johnson & Johnson.

Dr. Gerard Abate, Chief Medical Officer, United Health Products, stated: “This is the first head-to-head trial of two ORCs. The data demonstrates that HemoStyp consistently achieved hemostasis faster than Surgicel in all surgical classes studied in less than two minutes, whereas Surgicel could not and failed to control bleeding in six (6) patients where the control timed out at 10 minutes. Based on the overall data, upon anticipated PMA approval for class III FDA surgical use, surgeons will have a superior product to utilize for low grade surgical bleeds.”

[BottomBounce]

Omicron Booster -- WE ARE in luck? https://www.cnbc.com/video/2021/12/20/russias-sputnik-light-vaccine-is-a-very-significant-booster-against-omicron-rdif-says.html $JNJ