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JNJNYSE

JOHNSON & JOHNSON

Pharmaceutical preparations·Commercial·New Brunswick, NJ, United States·CEO: Mr. Joaquin Duato
OncologyNeurologyImmunologyOphthalmologyCardiovascularRespiratoryPainDermatologyGastroenterologyPsychiatry

JNJ evidence brief

What we can confirm

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What it means

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BioSniper AIPage evidence connected

Prepared research question

What matters most for JNJ—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · JNJ

Johnson & Johnson is a diversified healthcare company operating in Innovative Medicine and MedTech, with a strong financial profile and a pipeline spanning oncology, immunology, neuroscience, and medical devices.

Key risk: Biosimilar competition for STELARA

4.6/10

BioSniper Score

Based on 4 of 6 signals

Market Cap

$645.95B

Cash Runway

9.7 mo

Lead Asset

Financial data as of Jun 28, 2026.

Tracking 42 clinical trials · 3 catalysts for JOHNSON & JOHNSON.

AI OverviewAI overview is shown in English only.

Johnson & Johnson is a diversified healthcare company operating in Innovative Medicine and MedTech, with a strong financial profile and a pipeline spanning oncology, immunology, neuroscience, and medical devices.

  • Cash & equivalents of $20,422M, total revenue of $25,310M, net income of $5,534M, shareholders' equity of $81,544M, and total debt of $49,036M as of 2026-06-28 [sec].
  • The company has 28 Innovative Medicine products and MedTech platforms with >$1B in annual sales, and has delivered ~$20B in free cash flow [sec · filed 2026-03-11].
  • Johnson & Johnson has 63 consecutive years of dividend increases and has invested ~$50B in R&D and inorganic innovation since January 2024 [sec · filed 2025-03-12].
  • The Innovative Medicine segment focuses on Oncology, Immunology, Neuroscience, Pulmonary Hypertension, Infectious Diseases, and Cardiovascular/Metabolism [sec_mda · as of 2026-02-11].

What works

  • Strong financial foundation with $20.4B cash, $81.5B equity, and consistent free cash flow generation of ~$20B, supporting a 63-year dividend growth streak [sec · filed 2026-03-11] [sec].
  • Diversified portfolio across Innovative Medicine and MedTech with 28 products/platforms exceeding $1B in annual sales, reducing reliance on any single therapeutic area [sec · filed 2026-03-11].
  • Significant R&D investment (~$50B since Jan 2024) and 27 Innovative Medicine regulatory approvals in major markets, indicating a robust innovation pipeline [sec · filed 2025-03-12].
  • Recent acquisition of Intra-Cellular Therapies (CAPLYTA) and growth in Neuroscience (14.6% operational growth) and SPRAVATO show momentum in high-growth segments [sec_mda · as of 2025-10-22].

What to weigh

  • Intense competition across all product lines, requiring substantial R&D investment and facing risks from competitors' more effective or lower-cost products [sec_mda · as of 2026-02-11].
  • Biosimilar competition for STELARA is expected to impact sales, with launches in Europe and the U.S. anticipated in 2025 [sec_mda · as of 2025-07-24].
  • Product development and regulatory approval are inherently uncertain; only a few R&D programs result in commercially viable products [sec_mda · as of 2026-02-11].
  • The company faces ongoing patent litigation and intellectual property challenges that could affect product exclusivity and revenue [sec_mda · as of 2026-02-11].

From the filings

Quoted directly from source documents.

  • The company has 28 products/platforms with >$1B in annual sales.

    28 Innovative Medicine products & MedTech platforms >$1 billion in annual sales

    SEC filings · March 11, 2026

  • Biosimilar competition for STELARA is expected to impact sales.

    the Company expects continued launches of biosimilar versions of STELARA in Europe and the United States in 2025 which will impact the Company's sales of STELARA.

    SEC MD&A · July 24, 2025

  • The company competes intensely on innovation and cost-effectiveness.

    The Company's businesses compete with companies of all sizes on the basis of cost-effectiveness, technological innovations, intellectual property rights, product performance, real or perceived product advantages, pricing and availability and rate of reimbursement.

    SEC MD&A · February 11, 2026

Catalyst timeline

  • 2026-09-30 · Phase2_Topline · nexicart-2 — Phase 2 Readout: nexicart-2Topline data from the Phase 2 study of nexicart-2 will provide early efficacy and safety signals for this cell therapy candidate.
  • 2028-06-30 · Phase3_Topline · nbtxr3 — Phase 3 Topline: A Phase 3 Study of NBTXR3 Activated by Investigator's Choice of Radiotherapy Alone or Radiotherapy iPhase 3 results for NBTXR3, a radioenhancer, will assess its potential to improve outcomes in solid tumors when combined with radiotherapy.
  • 2029-03-31 · Phase3_Topline — Phase 3 Topline: Bumetanide vs. Furosemide for Adults Hospitalized With Cirrhosis: the BUFF TrialTopline data from the BUFF trial will compare bumetanide and furosemide in hospitalized cirrhosis patients, addressing a key unmet need.
Risks & what to watch (4)

Key risks

  • Biosimilar competition for STELARAExpected launches of biosimilars in Europe and U.S. in 2025 will reduce STELARA sales [sec_mda · as of 2025-07-24].
  • Product development uncertaintyOnly a few R&D programs result in commercially viable products; success depends on clinical trials, IP, and regulatory approvals [sec_mda · as of 2026-02-11].
  • Intense competitive environmentCompetition on cost, innovation, and IP across all product lines requires substantial ongoing investment [sec_mda · as of 2026-02-11].
  • Patent litigation risksOngoing legal proceedings regarding patents and IP could affect product exclusivity and revenue [sec_mda · as of 2026-02-11].

What to watch

  • Impact of STELARA biosimilar launches on revenue in 2025 and beyond [sec_mda · as of 2025-07-24].
  • Progress of pipeline candidates, particularly in Oncology and Neuroscience, and upcoming Phase 2/3 readouts [sec_mda · as of 2026-02-11].
  • Integration and sales performance of the Intra-Cellular Therapies acquisition (CAPLYTA) [sec_mda · as of 2025-10-22].
  • Ability to maintain free cash flow and dividend growth amid competitive and regulatory pressures [sec · filed 2026-03-11].

Sources: SEC filings · SEC MD&A · Generated August 28, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 4 of 6 signals · derived from public data

No clinical pipeline tracked — this score reflects financial & catalyst signals only.

Cash Runway2.7

9.7 months

Financial Health7.8

D/E 1.37 · 1% dilution

Pipeline MaturityN/A

No tracked pipeline phase

Pipeline BreadthN/A

No tracked pipeline candidates

Catalyst Momentum8.0

3 upcoming, next in ~31d

Insider Signal0.0

0 buys · 9 sells (180d)

Runway

Catalysts

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

4,593

Total value held

$451.94B

HolderSharesValue
vanguard capital management llc313,210,740$76.56B
blackrock, inc.213,385,546$52.16B
state street corp133,476,288$32.63B
vanguard portfolio management llc63,514,436$15.53B
geode capital management, llc59,164,862$14.42B
morgan stanley44,721,167$10.93B
state farm mutual automobile insurance co31,590,952$7.72B
northern trust corp29,319,669$7.17B
bank of america corp /de/25,516,697$6.24B
fmr llc24,771,828$6.06B

Showing top 10 of 4,593 institutional holders of JOHNSON & JOHNSON. Open the full 13F history after sign-in.

Short Interest

as of May 21, 2026
% of float
1.0%
Days to cover
2.9
Shares short
22,349,005
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

JNJ short interest

Governance

Frequently asked questions

What is the AI investment thesis for JOHNSON & JOHNSON?

Johnson & Johnson is a diversified healthcare company operating in Innovative Medicine and MedTech, with a strong financial profile and a pipeline spanning oncology, immunology, neuroscience, and medical devices.

What is JOHNSON & JOHNSON's next catalyst?

JOHNSON & JOHNSON's next tracked catalyst is a Phase2_Topline event — "Phase 2 Readout: nexicart-2" — expected September 30, 2026.

Who is the CEO of JOHNSON & JOHNSON?

Mr. Joaquin Duato is the chief executive officer of JOHNSON & JOHNSON (JNJ).

Where is JOHNSON & JOHNSON headquartered?

JOHNSON & JOHNSON (JNJ) is headquartered in New Brunswick, NJ, United States.

What therapeutic areas does JOHNSON & JOHNSON focus on?

JOHNSON & JOHNSON develops therapies across Oncology, Neurology, Immunology, Ophthalmology, Cardiovascular, Respiratory, Pain, Dermatology, Gastroenterology, Psychiatry.

925 companies232,681 SEC filings21,417 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.