Johnson & Johnson (JNJ)
| Market Cap | 644.82B +49.0% |
| Revenue (ttm) | 97.93B +8.1% |
| Net Income | 21.04B -7.2% |
| EPS | 8.63 -7.6% |
| Shares Out | 2.41B |
| PE Ratio | 31.52 |
| Forward PE | 24.24 |
| Dividend | $5.36 (2.00%) |
| Ex-Dividend Date | Aug 25, 2026 |
| Volume | 5,572,932 |
| Open | 269.11 |
| Previous Close | 271.95 |
| Day's Range | 265.59 - 271.89 |
| 52-Week Range | 179.80 - 281.07 |
| Beta | 0.23 |
| Analysts | Buy |
| Price Target | 277.91 (+3.86%) |
| Earnings Date | Oct 13, 2026 |
About JNJ
Johnson & Johnson, together with its subsidiaries, engages in the research and development, manufacture, and sale of a range of products in the healthcare field worldwide. It operates in two segments, Innovative Medicine and MedTech. The Innovative Medicine segment offers products for various therapeutic areas, such as oncology, immunology, neuroscience, pulmonary hypertension, infectious diseases, and cardiovascular and metabolism distributed through retailers, wholesalers, distributors, hospitals, and healthcare professionals for prescription... [Read more]
Financial Performance
In 2025, Johnson & Johnson's revenue was $94.19 billion, an increase of 6.05% compared to the previous year's $88.82 billion. Earnings were $26.80 billion, an increase of 90.56%.
Financial StatementsAnalyst Summary
According to 23 analysts, the average rating for JNJ stock is "Buy." The 12-month stock price target is $277.91, which is an increase of 3.86% from the latest price.
News
Johnson & Johnson’s Imaavy shows efficacy in gMG Phase 2/3 trial
Johnson & Johnson announced new findings on Imaavy – nipocalimab-aahu – for the treatment of generalized myasthenia gravis, or gMG, across 15 novel abstracts to be presented at the 2026…
Johnson & Johnson presents new data reinforcing sustained disease control and improved daily function achieved with IMAAVY® (nipocalimab-aahu) in generalized myasthenia gravis (gMG)
New two-year findings from the Phase 2/3 long-term extension demonstrate sustained disease control through two years, improvement in daily function and muscle strength, and reductions in corticosteroi...
Johnson & Johnson price target raised to $285 from $270 at JPMorgan
JPMorgan raised the firm’s price target on Johnson & Johnson to $285 from $270 and keeps a Neutral rating on the shares ahead of the earnings report on October 13.
Johnson & Johnson price target raised to $278 from $263 at BofA
BofA raised the firm’s price target on Johnson & Johnson to $278 from $263 and keeps a Neutral rating on the shares. Following a physician dermatology survey, the firm raised…
Johnson & Johnson says Tremfya met endpoints in Phase 4 STAR study
Johnson & Johnson announced that Tremfya met the primary and major secondary endpoints demonstrating both improvement in axial symptoms and reduction in inflammation by MRI assessment in the Phase 4…
Johnson & Johnson announces TREMFYA® (guselkumab) is the first and only IL-23 inhibitor to show significant improvement in spinal pain and stiffness in landmark axial psoriatic arthritis (PsA) study
Topline results show TREMFYA met the primary and major secondary endpoints of axial involvement in PsA - including spinal pain and stiffness - and demonstrated significant improvement in MRI-confirmed...
Johnson & Johnson reports new long-term data from Phase 2 CARTITUDE-2 study
Johnson & Johnson announced new long-term follow-up data from the initial subgroup of cohort A in the Phase 2 CARTITUDE-2 study showing that 50% of patients in early line relapsed…
Single infusion of CARVYKTI® (ciltacabtagene autoleucel) delivered five-year treatment-free remissions in 50% of patients in early line relapsed/refractory multiple myeloma
New results suggest earlier treatment may increase the likelihood of long-term remission Study adds to Johnson & Johnson's overwhelming body of evidence supporting its innovative multiple myeloma the...
Johnson & Johnson: Phase 3 MajesTEC-3 study shows ‘sustained’ disease control
Johnson & Johnson announced new data from the Phase 3 MajesTEC-3 study showing sustained disease control and survival with TECVAYLI plus DARZALEX FASPRO in patients with relapsed or refractory multipl...
New model-based analysis further supports the potential of TECVAYLI® (teclistamab-cqyv) plus DARZALEX FASPRO® (daratumumab and hyaluronidase-fihj) to redefine long-term survival expectations in early line relapsed/refractory multiple myeloma
Analysis shows ~87% of patients treated with TECVAYLI® plus DARZALEX FASPRO® as early as second line were estimated to have comparable mortality risk to the general population A separate analysis show...
J&J's Caplyta meets main goal of bipolar mania study
Johnson & Johnson said on Monday its experimental use of Caplyta for bipolar mania met the main goal of a late-stage study, bringing the drug a step closer to expanding beyond its currently approved...
Johnson & Johnson announces ‘positive’ results from Phase 3 trial of Caplyta
Johnson & Johnson announced positive topline results from the pivotal Phase 3 study evaluating Caplyta for the treatment of manic episodes with or without mixed features in adults with bipolar…
Johnson & Johnson Transcript: Deutsche Bank 2026 Healthcare Summit
The summit highlighted a focus on high-growth markets, robust innovation in oncology and immunology, and a diversified portfolio supporting double-digit growth targets. Med tech and pharma segments are positioned for margin improvement, with disciplined capital allocation and major legal risks resolved.
Johnson & Johnson announces new results from COPERNICUS study
Johnson & Johnson announced new results from the Phase 2b COPERNICUS study evaluating how subcutaneous Rybrevant Faspro plus Lazcluze, with less frequent dosing and prophylactic strategies, can improv...
RYBREVANT FASPRO™ (amivantamab and hyaluronidase-lpuj) plus LAZCLUZE® (lazertinib) with prophylactic strategies shows low rates of treatment-related events at WCLC 2026
Low rates of rash, blood clots and administration-related reactions were observed with subcutaneous treatment and prophylaxis Fewer than 1% of patients discontinued treatment due to treatment-related ...
Contineum, J&J's depression drug fails to meet mid-stage trial goal
Contineum Therapeutics said on Monday an experimental depression drug it developed with Johnson & Johnson failed to meet the main goal of a mid-stage study.
Johnson & Johnson Transcript: Morgan Stanley 24th Annual Global Healthcare Conference
The event highlighted a focused portfolio driving accelerated growth, robust pipeline progress, and strategic capital allocation. Advanced therapies in oncology and immunology, new product launches, and MedTech innovation underpin double-digit growth targets through the decade.
Johnson & Johnson reports PAPILLON study meets primary endpoint
Johnson & Johnson announced results from the final overall survival, or OS, analysis of the Phase 3 PAPILLON study evaluating first-line intravenous Rybrevant plus carboplatin-pemetrexed chemotherapy ...
Johnson & Johnson's RYBREVANT® (amivantamab-vmjw) plus chemotherapy delivers longest reported median overall survival in EGFR exon 20 insertion mutation-positive lung cancer
RYBREVANT plus chemotherapy demonstrates durable benefit with a differentiated approach that dual-targets EGFR and MET Results mark significant progress for a patient population with poor outcomes and...
J&J Is In Talks to Sell Its Hips-and-Knees Business to Apollo for $20 Billion
The health-products company said it planned to hive off its DePuy Synthes unit to focus on higher-growth areas.
Apollo Global in talks to acquire J&J's orthopedics unit, Bloomberg News reports
Apollo Global Management is in discussions to acquire Johnson & Johnson's orthopedics unit in a deal that could value the unit at close to $20 billion, Bloomberg News reported on Friday, c...
Johnson & Johnson receives CE Marking for ACUVUE OASYS MAX
Johnson & Johnson has received CE Marking for ACUVUE OASYS MAX 2-Week, a new reusable contact lens featuring proprietary MAX technologies designed to deliver superior comfort and visual clarity, even…
Johnson & Johnson Receives CE Marking for ACUVUE OASYS MAX Reusable Contact Lenses
LIMERICK, Ireland--(BUSINESS WIRE)--Johnson & Johnson receives CE Marking for ACUVUE OASYS MAX 2-Week, a new reusable contact lens featuring proprietary MAX technologies.
Johnson & Johnson Transcript: Wells Fargo 21st Annual Healthcare Conference
MedTech is on track for high-end growth, driven by a focused shift into cardiovascular, surgery, and vision, with robust innovation and a new operating model. Despite competitive and geopolitical headwinds, confidence remains high for 2026 and beyond, with major contributions expected from OTTAVA and portfolio optimization.
Johnson & Johnson spotlights new neuropsychiatry data across bipolar mania, depression and schizophrenia at Psych Congress 2026
First presentation of pivotal Phase 3 CAPLYTA ® data in adults with bipolar mania underscores the asset's potential across mood disorders New SPRAVATO ® analyses and schizophrenia research emphasize a...