JNJ - Johnson & Johnson

NYSE - Nasdaq Real Time Price. Currency in USD
141.55
-1.71 (-1.19%)
As of 2:34PM EDT. Market open.
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Performance Outlook
  • Short Term
    2W - 6W
  • Mid Term
    6W - 9M
  • Long Term
    9M+
Previous Close143.26
Open144.01
Bid141.43 x 800
Ask141.50 x 800
Day's Range140.82 - 145.39
52 Week Range109.16 - 154.50
Volume6,880,989
Avg. Volume10,984,498
Market Cap373.188B
Beta (5Y Monthly)0.66
PE Ratio (TTM)25.14
EPS (TTM)5.63
Earnings DateApr 13, 2020
Forward Dividend & Yield3.80 (2.76%)
Ex-Dividend DateFeb 23, 2020
1y Target Est156.18
Fair Value is the appropriate price for the shares of a company, based on its earnings and growth rate also interpreted as when P/E Ratio = Growth Rate. Estimated return represents the projected annual return you might expect after purchasing shares in the company and holding them over the default time horizon of 5 years, based on the EPS growth rate that we have projected.
Fair Value
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Overvalued
-9% Est. Return
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As for the total opportunity, Stewart doesn’t dispute that Abbott’s manufacturing capacity, which she thinks would be the rate limiting factor as there is significant demand for the test, remains unclear. “The pricing would likely be under the non-CDC pricing ~$51 level, perhaps in the $35-$45 range. We hope Abbott would supply these details when it announces approval,” the analyst noted. That being said, 4 million of its molecular tests can be conducted each month on its m2000 systems, with ABT charging about $30 per test. As a result, Stewart kept an Overweight call and $98 price target on the stock. Should this target be met, a twelve-month gain of 23% could be in the cards. (To watch Stewart’s track record, click here) Turning now to other Wall Street analysts, the bulls have it. With 8 Buy ratings and 3 Holds assigned in the last three months, the consensus rating comes in as a Moderate Buy. The $97.89 average price target implies only slightly less upside potential than Stewart’s forecast. (See Abbott stock analysis on TipRanks)Johnson & Johnson (JNJ) Next up is a consumer goods and healthcare heavyweight, Johnson & Johnson, which is developing a vaccine against COVID-19. After the company identified a lead candidate, one analyst thinks JNJ is one of the names capable of fueling the stock market’s turnaround. With a lead experimental vaccine candidate selected, Kristen Stewart, who also covers ABT, points out that at the latest, JNJ can kick off Phase 1 human clinical studies by September 2020. According to management, the first doses of the vaccine could be available under Emergency Use Authorization (EUA) in early 2021. Adding to the good news, JNJ has significantly expanded its partnership with the Biomedical Advanced Research and Development Authority (BARDA), with both entities pledging more than $1 billion to co-fund the vaccine’s development and clinical testing. If that wasn’t enough, Stewart notes “BARDA and JNJ have provided additional funding to allow expansion of ongoing work to identify anti-viral treatments against COVID-19.” However, while JNJ has ramped up the scaling of manufacturing capacity and has a target of supplying more than 1 billion vaccine doses, there is a risk that the candidate won’t eventually receive approval. Having said that, Stewart argues the real goal is to develop an affordable vaccine “on a not-for-profit basis for emergency pandemic use.” She added, “Thus we would anticipate the cost it would charge for the vaccine would recoup the cost of development, cost of scaling up the manufacturing, and cost of production. Thus, we would not look at the vaccine as being a windfall or major positive from a financial perspective. 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Yee already thinks that the pbo-adjusted remission rates imply that filgotinib is “competitive with other UC drugs.” Expounding on this, he stated, “While we expect investors to make cross-trial comparisons, we caution comparing directly to other UC datasets is imprecise due to differing baseline characteristics such as proportion of biologic naive/experienced and slightly different endpoints of the Mayo score. However -- recent commentary from GILD suggests positive confidence around results and good activity in both biologic naive and experienced.” With an August PDUFA date for filgotinib in RA, Yee does, however, acknowledge that a class label Black Box could be given as a result of uncertainty related to degree of bleeding difference between various JAK drugs. It’s also still unclear if filgotinib will be approved at the 200mg dose. Commenting on the second issue, Yee said, “In any case, it's reasonable to approve 200mg particularly if the MANTA interim look is OK but FDA is a conservative bunch. Also, even if not, we point out ABBV was only approved at the low dose in RA as well so it would not be a totally critical issue.” To this end, Yee reiterated a Buy recommendation and $89 price target, indicating 14% upside potential. (To watch Yee’s track record, click here) Looking at the consensus breakdown, 10 Buys, 9 Holds and 2 Sells add up to a Moderate Buy consensus rating. At $76.88, the average price target puts the downside potential at 2%. (See Gilead stock analysis on TipRanks)To find good ideas for coronavirus stocks trading at attractive valuations, visit TipRanks’ Best Stocks to Buy, a newly launched tool that unites all of TipRanks’ equity insights.

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(NASDAQ: OPK) * PDS Biotechnology Corp (NASDAQ: PDSB) * Phio Pharmaceuticals Corp (NASDAQ: PHIO) * Precipio Inc (NASDAQ: PRPO) * Seelos Therapeutics Inc (NASDAQ: SEEL) * Sellas Life Sciences Group Inc (NASDAQ: SLS) * Chanticleer Holdings Common Stock (NASDAQ: SONN) * Vaccinex Inc (NASDAQ: VCNX)Stocks In Focus Fate Announces CAR T-cell Therapy Licensing Deal With J&J's Janssen Unit Fate Therapeutics Inc (NASDAQ: FATE) said it has entered into a global collaboration and option agreement with Johnson & Johnson (NYSE: JNJ)'s Janssen unit, under which it will apply its iPSC product platform to research and preclinically develop new iPSC-derived chimeric antigen receptor, or CAR, NK and CAR T-cell product candidates.Janssen will contribute proprietary antigen-binding domains for up to four tumor-associated antigen targets, and pay Fate $50 million in cash and also subscribe to $50 million in the latter's common shares at $31 per share.Fate will be responsible for developing candidate until IND filing after which Janssen has the right to exercise options to license these.Fate is eligible to receive payments of up to $1.8 billion upon the achievement of development and regulatory milestones and up to $1.2 billion upon the achievement of commercial milestones, plus double-digit royalties on worldwide commercial sales of products targeting the antigens.Fate shares jumped 23.40% to $26 in after-hours trading.Sanofi, Regeneron Announces Positive Latestage Data For Dupixent-SoC Combo In Eczema In Kids Sanofi SA (NASDAQ: SNY) and Regeneron Pharmaceuticals Inc (NASDAQ: REGN) announced data from pivotal Phase 3 study of Dupixent combined with standard-of-care topical corticosteroidsin children aged 6-11 years with uncontrolled severe atopic dermatitis, which showed significantly improved disease signs, symptoms and health-related quality of life.The company said detailed results will be presented during a session at the 2020 Revolutionizing Atopic Dermatitis Virtual Conference on Sunday.See Also: Attention Biotech Investors: Mark Your Calendar For These April PDUFA DatesNovartis, Incyte to Study Ruxolitinib For COVID-19 Related Cytokine Storm Novartis AG (NYSE: NVS) said it a plans to initiate a Phase 3 clinical trial in collaboration with Incyte Corporation (NASDAQ: INCY) to evaluate the use of ruxolitinib for the treatment of a type of severe immune overreaction called cytokine storm that can lead to life-threatening respiratory complications in patients with COVID-19.Novartis said it is taking steps to manage the anticipated increase in COVID-19 related requests for Jakavi - trade name of ruxolitinib in territories outside of the U.S. - without interrupting access for patients taking the drug for its licensed indications.Novartis has licensed Jakavi from Incyte to commercialize in regions outside of the U.S., while Incyte markets it in the U.S. under the name Jakafi.Novartis shares gained 1.18% to $84.59 in after-hours trading, while Incyte stock rose 1% to 1.86% to $78.50 in after-hours trading.Immucell Pre-announces Q1 Net Product Sales Growth of 11.3% ImmuCell Corporation (NASDAQ: ICCC) announced preliminary first-quarter results, expecting product sales of $4.9 million, up 11.3% year-over-year.Savara Licenses Latestage Inhaled Antibiotic Asset From Grifols Savara Inc (NASDAQ: SVRA) said it has entered into an exclusive license and collaboration agreement with Grifols SA - ADR ADR Class B (NASDAQ: GRFS) for Apulmiq - inhaled liposomal ciprofloxacin. Apulmiq is a late-stage investigational inhaled antibiotic in Phase 3 development for the treatment of non-cystic fibrosis bronchiectasis.The agreement provides for Savara obtaining worldwide rights to develop and commercialize Apulmiq for an upfront payment. if regulatory approval is obtained, Grifols will be eligible for regulatory milestone payments as well as royalties and potential tiered sales milestones upon commercialization.Savara said it expects to work with regulatory agencies to plan a confirmatory Phase 3 study.The stock rallied 11.83% to $2.08 in after-hours trading.Emergent Biosolutions Gets $14.5M Grant For COVID-19 Therapy Development Emergent Biosolutions Inc (NYSE: EBS) said it has entered into a formal partnership with the U.S. government to expedite development of plasma-derived therapy for patients with COVID-19. The company said it has received $14.5 million from the BARDA for its COVID-HIG program - one of the hyperimmune development programs announced by the company in March.Announcements On COVID-related Impacts Updating on COVID-19 impact, Denali Therapeutics Inc (NASDAQ: DNLI), a neurodegenerative diseases-focused biopharma, said it does not expect delays to its clinical trials due to manufacturing or supply-chain issues. The company, however, said it has paused enrollment of new patients into some of its trials.The company also said it has sufficient cash to fund business operations through 2022.The stock slipped 2.41% to $17.02 in after-hours trading.Dynavax Technologies Corporation (NASDAQ: DVAX) announced withdrawal of its 2020 guidance, citing uncertainties about the duration and effect of the COVID-19 pandemic and the potential impact on hepatitis B vaccine - Heplisav-B - product sales.The company also said it has already exceeded the Heplisav-B minimum product revenue covenant in its term loan agreement of $30 million for the annual measurement period ending June 30.On The Radar Clinical Readout Prothena Corporation PLC (NASDAQ: PRTA) said its development partner Roche Holdings AG Basel ADR (OTC: RHHBY) will present baseline data from the Phase 2 PASADENA study of prasinezumab in patients with early Parkinson's disease in an oral presentation at the Advances in Alzheimer's and Parkinson's Therapies AAT-AD/PD Focus Meeting being held virtually.IPO Zentalis Pharma, a biopharma focused on developing small molecule therapeutics targeting fundamental pathways of cancer, said it has priced its initial public offering of 9.18 million shares at $18 per share for raising gross proceeds of $165.2 million. The company expects the offering to close April 7. The shares are to be listed on the Nasdaq under the ticker symbol ZNTL.See more from Benzinga * The Daily Biotech Pulse: Milestone Pharma Flunks Late-Stage Study, CytomX Strikes Cancer Drug Collaboration, BARDA Grant For GenMark's COVID-19 Test * The Daily Biotech Pulse: Pfizer's Eczema Drug Aces Latestage Study, Orphan Drug Designation For Dicerna, Dyadic's COVID-19 Connection * The Daily Biotech Pulse: NY State Endorses Mallinckrodt's Opioid Settlement, Kamada To Work On COVID-19 Treatment(C) 2020 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.

  • Financial Times

    Johnson & Johnson chief looks to the greater good

    Since the start of the crisis, Alex Gorsky, Johnson & Johnson chief executive, has started every video call by asking his colleagues to talk about something positive in their lives. With a half billion dollar investment from Mr Gorsky, matched by the same amount from the US government to speed up the process, J&J’s researchers had come up with a drug they believed could be ready for human trials by September. The vaccine, Johnson & Johnson said, would be available on a not-for-profit basis.

  • Bull of the Day: Regeneron Pharmaceuticals, Inc. (REGN)
    Zacks

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