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Novartis (NVS)

(Delayed Data from NYSE)

$121.20 USD

121.20
1,087,718

+1.89 (1.58%)

Updated Aug 13, 2025 04:00 PM ET

After-Market: $121.24 +0.04 (0.03%) 4:52 PM ET

Zacks Rank:

This is our short term rating system that serves as a timeliness indicator for stocks over the next 1 to 3 months. How good is it? See rankings and related performance below.

Zacks Rank Definition Annualized Return
1Strong Buy23.75%
2Buy17.82%
3Hold9.58%
4Sell5.28%
5Strong Sell2.61%
S&P50011.30%

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3-Hold of 5     3    

Style Scores:

The Style Scores are a complementary set of indicators to use alongside the Zacks Rank. It allows the user to better focus on the stocks that are the best fit for his or her personal trading style.

The scores are based on the trading styles of Value, Growth, and Momentum. There's also a VGM Score ('V' for Value, 'G' for Growth and 'M' for Momentum), which combines the weighted average of the individual style scores into one score.

  • Value Score A
  • Growth Score A
  • Momentum Score A
  • VGM Score A

Within each Score, stocks are graded into five groups: A, B, C, D and F. As you might remember from your school days, an A, is better than a B; a B is better than a C; a C is better than a D; and a D is better than an F.

As an investor, you want to buy stocks with the highest probability of success. That means you want to buy stocks with a Zacks Rank #1 or #2, Strong Buy or Buy, which also has a Score of an A or a B in your personal trading style.

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B Value B Growth B Momentum A VGM

Industry Rank:

The Zacks Industry Rank assigns a rating to each of the 265 X (Expanded) Industries based on their average Zacks Rank.

An industry with a larger percentage of Zacks Rank #1's and #2's will have a better average Zacks Rank than one with a larger percentage of Zacks Rank #4's and #5's.

The industry with the best average Zacks Rank would be considered the top industry (1 out of 265), which would place it in the top 1% of Zacks Ranked Industries. The industry with the worst average Zacks Rank (265 out of 265) would place in the bottom 1%.

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Zacks Industry Rank Education -- Learn more about the Zacks Industry Rank

Top 35% (85 out of 245)

Industry: Large Cap Pharmaceuticals

Zacks News

Zacks Equity Research

Incyte's (INCY) Q1 Earnings and Revenues Fall Shy of Estimates

Incyte's (INCY) earnings and revenues miss estimates in the first quarter of 2022. The company raises the bottom end of full-year Jakafi net product revenue guidance.

Zacks Equity Research

Alnylam (ALNY) Misses on Q1 Earnings, Lowers '22 Revenue View

Alnylam's (ALNY) earnings and sales fall shy of estimates in the first quarter of 2022. The company cuts 2022 guidance for net product revenues. Shares down.

Kinjel Shah headshot

Pharma Stock Roundup: Q1 Earnings of LLY, MRK & NVS, FDA Updates for AZN & PFE

Eli Lilly (LLY), Merck (MRK), Novartis (NVS) and others announce Q1 results. FDA updates for AstraZeneca (AZN) and Pfizer (PFE) grab headlines in the pharma space.

Zacks Equity Research

Drug/Biotech Stocks Q1 Earnings Due on Apr 29: BMY, ABBV, AZN

Let us take a look at what is in store for BMY, ABBV, and AZN that are scheduled to report on Apr 29.

Zacks Equity Research

Incyte (INCY) to Report Q1 Earnings: What's in the Cards?

Incyte's (INCY) top line is likely to have been driven in the first quarter by the sales of its lead drug, Jakafi.

Zacks Equity Research

Novartis (NVS) Beats on Q1 Earnings, Sandoz Posts Growth

Novartis (NVS) beats on earnings in the first quarter but sales lag expectations. Generic Sandoz business returns to growth.

Zacks Equity Research

Novartis (NVS) Gets Positive CHMP Opinion on Lung Cancer Drug

The CHMP gives a positive opinion on, and recommends approval for Novartis' (NVS) Tabrecta for treating patients with METex14 advanced non-small cell lung cancer.

Zacks Equity Research

KemPharm (KMPH) Starts Early-Stage Cardiovascular Safety Study

KemPharm (KMPH) initiates dosing in a phase I study to evaluate the cardiovascular safety profile of its lead pipeline candidate, KP1077's sole active API, serdexmethylphenidate.

Zacks Equity Research

BioCardia (BCDA) Gains FDA Nod for ARDS Cell Therapy Study

BioCardia (BCDA) gets FDA approval to start a phase I/II study to evaluate its allogenic stem cell therapy candidate, BCDA-04, in patients with ARDS due to COVID-19.

    Zacks Equity Research

    BeiGene (BGNE) Brukinsa Superior to Imbruvica in Leukemia Study

    BeiGene (BGNE) is comparing Brukinsa to AbbVie's Imbruvica as a treatment for R/R CLL or SLL. Brukinsa achieves superior ORR versus Imbruvica in a phase III study.

    Kinjel Shah headshot

    Pharma Stock Roundup: PFE to Buy RSV Drugmaker, FDA Updates for NVS, MRK and RHHBY

    Pfizer (PFE) announces plans to acquire ReViral for up to $525 million. Merck (MRK), Novartis (NVS) and Roche (RHHBY) provide FDA updates.

    Zacks Equity Research

    Regeneron (REGN), Sanofi's Dupixent Gets EU Nod for Asthma in Kids

    Regeneron (REGN) and Sanofi's (SNY) Dupixent receives label expansion in the European Union for severe asthma with type 2 inflammation in children aged between 6 years and 11 years.

    Zacks Equity Research

    Novartis (NVS) Anti-PD-1 Drug Validated by EMA for Lung Cancer

    Novartis (NVS) application seeking approval of tislelizumab in multiple non-small cell lung cancer and esophageal squamous cell carcinoma indications gets EMA's validation.

    Zacks Equity Research

    Novartis (NVS) Gets FDA Nod for Vijoice in Rare Disorder

    The FDA approves Novartis' (NVS) Vijoice (alpelisib) for the treatment of select patients with PIK3CA-related overgrowth spectrum.

    Zacks Equity Research

    Accenture (ACN) Joins Health Data Collaborative, AI4BetterHearts

    Accenture's (ACN) goal behind joining the collaborative is to support and advance cardiovascular disease prevention through integrating innovation and emerging technologies.

    Kinjel Shah headshot

    Pharma Stock Roundup: FDA Nod for 2nd COVID Booster, New Approvals for AZN, GSK, NVS

    FDA authorizes second booster dose of PFE and MRNA COVID-19 vaccines for older adults. RHHBY's late-stage study for ES-SCLC fails.

    Zacks Equity Research

    Novartis (NVS) Beovu Gets Label Expansion for DME in EU

    Novartis (NVS) ophthalmology drug Beovus label gets expanded in EU for diabetic macular edema.

    Zacks Equity Research

    The Zacks Analyst Blog Highlights Visa, Novartis, Deere & Company, Airbnb, and Edwards Lifesciences

    Visa, Novartis, Deere & Company, Airbnb, and Edwards Lifesciences have been included in this Analyst Blog.

    Sheraz Mian headshot

    Top Stock Reports for Visa, Novartis & Deere

    Today's Research Daily features new research reports on 16 major stocks, including Visa Inc. (V), Novartis AG (NVS), and Deere & Company (DE).

    Zacks Equity Research

    Novartis (NVS) Gets Positive CHMP Opinion for Jakafi, Kymriah

    Novartis (NVS) obtains positive CHMP opinion for the label expansion of Jakafi and Kymriah.

    Zacks Equity Research

    The Zacks Analyst Blog Highlights Novartis, Merck and Pfizer

    Novartis, Merck and Pfizer have been included in this Analyst Blog.

    Zacks Equity Research

    Novartis' (NVS) Pluvicto Gets FDA Nod for Advanced Prostate Cancer

    The FDA okays Novartis' (NVS) targeted radioligand therapy Pluvicto to treat PSMA-positive metastatic castration-resistant prostate cancer.

    Kinjel Shah headshot

    Pharma Stock Roundup: NVS, MRK Get FDA Nod, PFE Ulcerative Colitis Study Succeeds

    FDA approves Novartis' (NVS) Pluvicto for a certain type of advanced prostate cancer and Merck's (MRK) Keytruda for expanded use in endometrial carcinoma. Pfizer's (PFE) late-stage ulcerative colitis study on etrasimod meets goal.

    Zacks Equity Research

    Incyte's (INCY) Going Gets Tough Due to Pipeline Setbacks

    The recent pipeline setbacks will weigh on Incyte's (INCY) growth trajectory and jeopardize its plans to diversify its revenue base.

    Zacks Equity Research

    Incyte (INCY) Label Expansion for Ruxolitinib Cream Delayed

    Incyte' s (INCY) sNDA seeking label expansion of ruxolitinib cream gets extended by three months by the FDA for reviewing additional information.