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Novartis

Full company profile

uuid00000js

Namestring
Novartis
Legal namestring
Novartis AG
Websiteurl
novartis.com
Company typeenum
Public
Founded yearint
1996
Descriptiontext

Novartis AG is a Swiss-headquartered global pharmaceutical company (NYSE: NVS; SIX: NOVN) that researches, develops, manufactures, and commercializes innovative prescription medicines across four core therapeutic areas: cardiovascular/renal/metabolic, immunology, neuroscience, and oncology. Headquartered in Basel with operations in over 50 countries, the company maintains an integrated technology platform spanning small molecules, biologics, antibody-oligonucleotide conjugates (AOC), radioligand therapy (RLT) with alpha- and beta-emitting isotopes, CAR-T cell therapy, gene therapy, molecular glue degraders, and AI-driven drug discovery partnerships. The 2025 oncology segment generated $16.8 billion in revenue (18% YoY growth), anchored by the Pluvicto/Lutathera radioligand therapy franchise ($2.8 billion combined in 2025, with Pluvicto projected to reach $5 billion by 2030), and management has guided to 5–6% annual sales growth through 2030.

Novartis's marketed portfolio includes Pluvicto (lutetium-177 PSMA-617 RLT for prostate cancer), Lutathera (lutetium-177 DOTATATE for neuroendocrine tumors), Cosentyx (secukinumab IL-17A inhibitor), Scemblix (asciminib STAMP inhibitor for CML), Vanrafia (atrasentan for IgA nephropathy), Rhapsido (remibrutinib BTK inhibitor for urticaria), Fabhalta (iptacopan complement Factor B inhibitor), ianalumab (anti-BAFF-R antibody in Phase III), and Kymriah (the first FDA-approved CAR-T therapy). The pipeline has been materially expanded by recent acquisitions: Avidity Biosciences ($12 billion, March 2026) added a muscle-directed AOC platform with three late-stage programs including delpacibart braxlosiran for FSHD; Mariana Oncology added RLT candidates for solid tumors including actinium-225 programs; MorphoSys (€2.7 billion, 2024) contributed pelabresib and tulmimetostat; Pikavation/Synnovation ($3 billion) added the PI3Kα inhibitor SNV4818; and Excellergy ($2 billion) added the anti-IgE antibody Exl-111.

The company generates revenue primarily through direct sales of branded prescription medicines to healthcare providers, hospitals, and patients via an enterprise field sales motion across global markets, supplemented by upfront and milestone payments from biotech licensing collaborations (Antares up to $1.9 billion; Orionis up to $1.4 billion; Monte Rosa up to $5.7 billion; Isomorphic Labs strategic agreement) and tiered royalties on approved products. Pricing is value-based and not publicly disclosed, with Novartis having committed to Most-Favored-Nation pricing for US medicines as part of a Swiss-US framework agreement. The company is investing $50 billion in US manufacturing and R&D, anchored by a new 10,000-square-foot radioligand therapy facility in Carlsbad, California opened in May 2026. Notable headwinds include US generic erosion on Entresto and Promacta, a complete loss in the Curium patent dispute affecting Lutathera, a Supreme Court denial regarding Medicare drug-price negotiation, and a state-level whistleblower lawsuit concerning Xolair, partially offset by the launch momentum in radioligand therapy and immunology. Management is led by CEO Vasant (Vas) Narasimhan with a 13-member Executive Committee and a 13-member Board chaired by Giovanni Caforio.

Short descriptiontext

Novartis AG is a Swiss-headquartered global pharmaceutical company that researches, develops, and commercializes innovative prescription medicines across oncology, immunology, cardiovascular/renal, and neuroscience, serving patients in over 50 countries.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
5,001–10,000
akta.pro rankint
HeadquartersBasel, Switzerland
HQ citystring
Basel
HQ countrystring
Switzerland
HQ regionstring
Europe
Markets served

Serves global market

Keyword5 values
prescription pharmaceuticals, radioligand therapy, oncology treatments, immunology biologics, rare disease therapies
Industry2 codes
1Neurology & Psychiatry (CNS) Pharmaceuticals
CodeHLAIAAAFPrimaryYes
2Neurology & CNS Specialty Pharmaceuticals
CodeHLAIACACPrimaryNo
NAICS code2 codes
  • Pharmaceutical and Medicine Manufacturing32541
  • Pharmaceutical Preparation Manufacturing325412
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
Product category
Prescription Pharmaceuticals
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model5 records
1Pharmaceutical Product Sales
TypeTransaction Fee
Description

Direct sales of innovative medicines (prescription drugs) to healthcare providers, hospitals, and patients; major revenue drivers include Pluvicto and Lutathera (radioligand therapy franchise generating $2.8 billion in 2025 net sales), oncology segment generated $16.8 billion in 2025 sales (18% growth), with Pluvicto projected to reach $5 billion in sales by 2030.

finance.yahoo.com
2Strategic Collaboration Upfront and Milestone Payments
TypeLicensing Royalties
Description

Upfront cash payments and milestone-based payments from licensing/co-development deals with smaller biotech partners. Recent examples include $105M upfront to Antares Therapeutics (up to $1.9B total), $40M upfront to Orionis Biosciences (up to $1.4B), and $105M upfront to Monte Rosa (up to $5.7B).

fiercebiotech.com
3Royalty and Tiered Royalty Income
TypeLicensing Royalties
Description

Tiered royalties on global net sales from collaboration products. Example: Novartis will pay tiered royalties to Antares, Orionis, and Monte Rosa on net sales of approved drugs emerging from these collaborations.

fool.com
4M&A-Driven Portfolio Revenue
TypeOne Time License
Description

Acquired product revenue streams integrated post-acquisition. Novartis has completed 43 acquisitions spanning 7 countries and 23 sectors, with peak activity in 2024 and 2016 (5 deals each); most recent being Excellergy in March 2026 ($2B), Avidity ($12B), and Pikavation/Synnovation ($3B).

novartis.com
5Geographic Market Expansion Revenue
TypeTransaction Fee
Description

Country-specific market expansion including India launch of Pluvicto as first regulatory-approved radioligand therapy for advanced prostate cancer, in collaboration with select hospitals and nuclear medicine centres, despite having sold 70.68% stake in Novartis India to ChrysCapital for ₹1,446 crore ($159M).

expansion.mx
Cost components6 values
Personnel, Technology or R&D, Marketing or Sales, Supply Chain, Operations, Infrastructure
Pricing details1 tier
1Value-based pricing for innovative medicines across therapeutic areas
ModelOutcome Based/ PerformanceBilling cadenceOther
Notes

Pricing is quote-based / not publicly disclosed. Novartis employs value-based pricing per its access principles and engages in Most-Favored-Nation pricing for US markets per Swiss-US framework deal. Patient assistance programs and Novartis Access portfolio for lower-income countries available; rare disease pricing reflected in launches like Vanrafia (atrasentan), Pluvicto, and gene therapies.

novartis.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 2 records shown
1Novartis Gene Therapies
Description

Distinct Novartis business unit dedicated to gene therapy development and manufacturing (referenced on About menu of Novartis.com).

novartis.com
+1 more record
Core offering1 text field

Novartis researches, develops, manufactures, and commercializes innovative prescription medicines across four therapeutic areas: Cardiovascular/Renal/Metabolic, Immunology, Neuroscience, and Oncology. Its marketed-product portfolio includes the radioligand therapy franchise (Pluvicto, Lutathera), immunology biologics (Cosentyx, ianalumab), oncology targeted therapies (Scemblix, Vanrafia, Kymriah), and antisense/RNA therapies (del-brax), with a pipeline supplemented by technology platforms in CAR-T, gene therapy, antibody-oligonucleotide conjugates, and AI-driven drug discovery.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Novartis operates as an integrated platform of innovative medicines plus dedicated technology platforms, organized around four therapeutic areas (Cardiovascular/Renal/Metabolic, Immunology, Neuroscience, Oncology). The marketed-product core spans multiple high-value franchises: the radioligand-therapy (RLT) franchise (Pluvicto and Lutathera, together generating ~USD 2.8B in 2025 sales) anchors a growing actinium-225 program (225Ac-PSMA-617); immunology is led by Cosentyx, Rhapsido and ianalumab; oncology by Scemblix, Vanrafia, Kisqali and the Kymriah CAR-T platform; renal by Vanrafia and Fabhalta; and the del-brax antisense program (acquired with Avidity) addresses FSHD. Novartis augments its in-house pipeline through targeted acquisitions (Avidity Biosciences USD 12B, Pikavation/SNV4818 USD 3B, Excellergy USD 2B, Mariana Oncology, Kedalion, Gyroscope, Arctos, MorphoSys, Tourmaline) and discovery collaborations (Antares, Orionis, Monte Rosa, Isomorphic Labs), all running on technology platforms that include CAR-T cell therapy manufacturing, gene therapy manufacturing, a USD 50B U.S. R&D and manufacturing expansion, and a deep genomic-research dataset (Pakistan Genome Resource). Together, these named products, technology platforms, and partnerships form the modular architecture of Novartis's medicines business.

Product and service12 records
1Pluvicto (177Lu vipivotide tetraxetan / 177Lu-PSMA-617)
CategoryRadioligand therapy (RLT) — proprietary branded pharmaceutical
Description

First-in-class PSMA-targeted radioligand therapy delivering lutetium-177 radiation directly to PSMA-positive prostate cancer cells; FDA-approved March 2022 for PSMA-positive metastatic castration-resistant prostate cancer; combined Pluvicto+Lutathera generated $2.8B in 2025 net sales; projected to reach $5B by 2030.

2Lutathera (177Lu-DOTATATE)
CategoryRadioligand therapy (RLT) — proprietary branded pharmaceutical
Description

FDA-approved radioligand therapy for gastroenteropancreatic neuroendocrine tumors (GEP-NETs) marketed by Novartis subsidiary Advanced Accelerator Applications (AAA); combined with Pluvicto, generated $2.8B in 2025 net sales.

3Cosentyx (secukinumab)
CategoryImmunology biologic (IL-17A inhibitor)
Description

Anti-IL-17A monoclonal antibody for autoimmune diseases including psoriasis, psoriatic arthritis, ankylosing spondylitis, hidradenitis suppurativa, and (per 2026 REPLENISH Phase III data) polymyalgia rheumatica.

4Scemblix (asciminib)
CategoryOncology targeted therapy (BCR-ABL / STAMP inhibitor)
Description

First-in-class STAMP (Specifically Targeting the ABL Myristoyl Pocket) inhibitor for chronic myeloid leukemia; 144-week ASC4FIRST Phase III data showed ~24% higher major molecular response vs standard-of-care TKIs and >50% lower discontinuation rates.

5Vanrafia (atrasentan)
CategoryRenal / cardiovascular targeted therapy (endothelin receptor antagonist)
Description

Endothelin receptor antagonist for IgA nephropathy; final 2.5-year ALIGN Phase III results showed ~34% slowing of kidney function decline vs placebo with sustained 38.3% proteinuria reduction at 9 months.

6Rhapsido (remibrutinib)
CategoryImmunology small molecule (BTK inhibitor)
Description

Oral BTK inhibitor for chronic spontaneous urticaria, chronic inducible urticaria (CIndU) and IgE-mediated peanut allergy; first treatment to demonstrate efficacy in a global Phase III CIndU trial (RemIND); supplemental NDA submitted to FDA.

7Kymriah (tisagenlecleucel)
8Fabhalta (iptacopan)
9ianalumab
10del-brax (delpacibart braxlosiran)
CategoryAntisense / RNA therapy (antibody-oligonucleotide conjugate)
Description

Investigational antibody-oligonucleotide conjugate for facioscapulohumeral muscular dystrophy (FSHD); FORTITUDE Phase I/II biomarker cohort met primary endpoint (KHDC1L reduction) and key secondary endpoint (CK reduction); acquired via $12B purchase of Avidity Biosciences.

11Exl-111 (anti-IgE antibody)
CategoryBiologic — anti-IgE antibody (acquired)
Description

Half-life extended, high-affinity anti-IgE antibody in Phase 1 development (DISARM trial) for food allergy and IgE-driven diseases; designed to dissociate receptor-bound IgE for faster, deeper pathway suppression than conventional anti-IgE approaches; acquired via $2B Excellergy deal.

12SNV4818
CategorySmall molecule — PI3Kα inhibitor (acquired)
Description

Pan-mutant-selective PI3Kα inhibitor in Phase 1/2 development for HR+/HER2- breast cancer, designed to selectively target mutated PI3Kα (in ~40% of HR+/HER2- breast cancer patients) while sparing healthy cells.

Recent move11 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Swiss-headquartered global pharmaceutical company with comparable oncology (including radioligand therapy) and immunology franchises, similar therapeutic-area breadth, and a similarly large innovative-medicines R&D platform.

TypeDirect peer
Description

Top-tier U.S. pharma with overlapping oncology, immunology, and rare-disease franchises and a similarly active M&A strategy (Seagen $43B). Direct peer across innovative branded pharmaceuticals and large-cap R&D scale.

TypeDirect peer
Description

U.S. major pharma with leading oncology franchise (Keytruda) and similar exposure to IRA pricing pressure and patent-cliff dynamics; competes in immuno-oncology, renal cell carcinoma, and antibody-drug conjugates that overlap Novartis's AOC ambitions.

TypeDirect peer
Description

Global pharma with parallel oncology, renal/cardiovascular, and rare-disease franchises; AZ also has a leading radioligand therapy program (Lumakras, Pluvicto competitor efforts, and its own Ac-225 supply agreement with Niowave) — directly comparable in RLT pipeline and oncology focus.

TypeDirect peer
Description

U.S. major pharma with comparable oncology, immunology, and cardiovascular franchises, similar IRA exposure, and parallel late-stage pipeline investments in cell therapy, ADCs, and immunology — directly comparable revenue scale and therapeutic-area mix.

TypeDirect peer
Description

European-headquartered pharma with overlapping immunology, rare-disease, and oncology ambitions; Sanofi's CEO co-authored an April 2025 FT op-ed with Vas Narasimhan on European pharma competitiveness. Highly comparable in geographic and therapeutic profile.

TypeDirect peer
Description

U.S. major pharma with comparable innovative-medicines franchise, recent Isomorphic Labs AI drug-design partnership, and active expansion in oncology and rare diseases — Lilly is Novartis's AI-discovery partner co-counterparty and a direct therapeutic-area peer.

TypeDirect peer
Description

U.K.-headquartered pharma with comparable immunology (JAKs, BTK, IL-pathway agents) and oncology R&D pipelines; competes with Rhapsido in chronic urticaria and with Cosentyx in autoimmune diseases — directly comparable in targeted-therapy and immunology.

TypeBroad incumbent
Description

Diversified healthcare giant with an Innovative Medicine pharma segment that overlaps Novartis's oncology, immunology, and pulmonary hypertension portfolios; large-cap peer with similar M&A scale and IRA exposure.

TypeRegional player
Description

European-headquartered pharma with oncology and cardiovascular franchises that overlap Novartis's CRM therapeutic area; comparable in European geographic footprint though with weaker U.S. presence in radioligand therapy.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat7 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Ideal customer profile1 record

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

Integration3 records

Each record includes

Title, Type, Description, Source

AI capability14 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature8 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles28 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries9 records

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance4 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds3 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors1 record

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A44 records

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment86 records

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Novartis

Prescription Pharmaceuticalsnovartis.com

Novartis AG is a Swiss-headquartered global pharmaceutical company that researches, develops, and commercializes innovative prescription medicines across oncology, immunology, cardiovascular/renal, and neuroscience, serving patients in over 50 countries.

What Novartis does

Novartis AG is a Swiss-headquartered global pharmaceutical company (NYSE: NVS; SIX: NOVN) that researches, develops, manufactures, and commercializes innovative prescription medicines across four core therapeutic areas: cardiovascular/renal/metabolic, immunology, neuroscience, and oncology. Headquartered in Basel with operations in over 50 countries, the company maintains an integrated technology platform spanning small molecules, biologics, antibody-oligonucleotide conjugates (AOC), radioligand therapy (RLT) with alpha- and beta-emitting isotopes, CAR-T cell therapy, gene therapy, molecular glue degraders, and AI-driven drug discovery partnerships. The 2025 oncology segment generated $16.8 billion in revenue (18% YoY growth), anchored by the Pluvicto/Lutathera radioligand therapy franchise ($2.8 billion combined in 2025, with Pluvicto projected to reach $5 billion by 2030), and management has guided to 5–6% annual sales growth through 2030.

Novartis's marketed portfolio includes Pluvicto (lutetium-177 PSMA-617 RLT for prostate cancer), Lutathera (lutetium-177 DOTATATE for neuroendocrine tumors), Cosentyx (secukinumab IL-17A inhibitor), Scemblix (asciminib STAMP inhibitor for CML), Vanrafia (atrasentan for IgA nephropathy), Rhapsido (remibrutinib BTK inhibitor for urticaria), Fabhalta (iptacopan complement Factor B inhibitor), ianalumab (anti-BAFF-R antibody in Phase III), and Kymriah (the first FDA-approved CAR-T therapy). The pipeline has been materially expanded by recent acquisitions: Avidity Biosciences ($12 billion, March 2026) added a muscle-directed AOC platform with three late-stage programs including delpacibart braxlosiran for FSHD; Mariana Oncology added RLT candidates for solid tumors including actinium-225 programs; MorphoSys (€2.7 billion, 2024) contributed pelabresib and tulmimetostat; Pikavation/Synnovation ($3 billion) added the PI3Kα inhibitor SNV4818; and Excellergy ($2 billion) added the anti-IgE antibody Exl-111.

The company generates revenue primarily through direct sales of branded prescription medicines to healthcare providers, hospitals, and patients via an enterprise field sales motion across global markets, supplemented by upfront and milestone payments from biotech licensing collaborations (Antares up to $1.9 billion; Orionis up to $1.4 billion; Monte Rosa up to $5.7 billion; Isomorphic Labs strategic agreement) and tiered royalties on approved products. Pricing is value-based and not publicly disclosed, with Novartis having committed to Most-Favored-Nation pricing for US medicines as part of a Swiss-US framework agreement. The company is investing $50 billion in US manufacturing and R&D, anchored by a new 10,000-square-foot radioligand therapy facility in Carlsbad, California opened in May 2026. Notable headwinds include US generic erosion on Entresto and Promacta, a complete loss in the Curium patent dispute affecting Lutathera, a Supreme Court denial regarding Medicare drug-price negotiation, and a state-level whistleblower lawsuit concerning Xolair, partially offset by the launch momentum in radioligand therapy and immunology. Management is led by CEO Vasant (Vas) Narasimhan with a 13-member Executive Committee and a 13-member Board chaired by Giovanni Caforio.

Novartis firmographics

Firmographics
Name
Novartis
Legal name
Novartis AG
Website
https://novartis.com
Company type
Public
Founded year
1996
Operating status
Operating
Headcount range
5,001–10,000 employees
Short description
Novartis AG is a Swiss-headquartered global pharmaceutical company that researches, develops, and commercializes innovative prescription medicines across oncology, immunology, cardiovascular/renal, and neuroscience, serving patients in over 50 countries.
Ownership category
akta.pro rank

Novartis industry classification

Industry
Product category
Prescription Pharmaceuticals
NAICS
Pharmaceutical and Medicine Manufacturing (32541), Pharmaceutical Preparation Manufacturing (325412)
SIC
Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834)
akta.pro primary industry
Neurology & Psychiatry (CNS) Pharmaceuticals (HLAIAAAF)
akta.pro secondary industry
Neurology & CNS Specialty Pharmaceuticals (HLAIACAC)

Keywords

  • Prescription pharmaceuticals
  • Radioligand therapy
  • Oncology treatments
  • Immunology biologics
  • Rare disease therapies

Where Novartis is headquartered

Location

Headquarters

HQ city
Basel
HQ country
Switzerland
HQ region
Europe

Markets served

Novartis business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Personnel, Technology or R&D, Marketing or Sales, Supply Chain, Operations, Infrastructure

Revenue model

  1. Pharmaceutical Product Sales: Direct sales of innovative medicines (prescription drugs) to healthcare providers, hospitals, and patients; major revenue drivers include Pluvicto and Lutathera (radioligand therapy franchise generating $2.8 billion in 2025 net sales), oncology segment generated $16.8 billion in 2025 sales (18% growth), with Pluvicto projected to reach $5 billion in sales by 2030.
  2. Strategic Collaboration Upfront and Milestone Payments: Upfront cash payments and milestone-based payments from licensing/co-development deals with smaller biotech partners. Recent examples include $105M upfront to Antares Therapeutics (up to $1.9B total), $40M upfront to Orionis Biosciences (up to $1.4B), and $105M upfront to Monte Rosa (up to $5.7B).
  3. Royalty and Tiered Royalty Income: Tiered royalties on global net sales from collaboration products. Example: Novartis will pay tiered royalties to Antares, Orionis, and Monte Rosa on net sales of approved drugs emerging from these collaborations.
  4. M&A-Driven Portfolio Revenue: Acquired product revenue streams integrated post-acquisition. Novartis has completed 43 acquisitions spanning 7 countries and 23 sectors, with peak activity in 2024 and 2016 (5 deals each); most recent being Excellergy in March 2026 ($2B), Avidity ($12B), and Pikavation/Synnovation ($3B).
  5. Geographic Market Expansion Revenue: Country-specific market expansion including India launch of Pluvicto as first regulatory-approved radioligand therapy for advanced prostate cancer, in collaboration with select hospitals and nuclear medicine centres, despite having sold 70.68% stake in Novartis India to ChrysCapital for ₹1,446 crore ($159M).

Pricing tiers

ModelBillingPrice
Outcome Based/ PerformanceOtherValue-based pricing for innovative medicines across therapeutic areas

Go-to-market motion1 record

Novartis product offering

Product offering

Core offering

Novartis researches, develops, manufactures, and commercializes innovative prescription medicines across four therapeutic areas: Cardiovascular/Renal/Metabolic, Immunology, Neuroscience, and Oncology. Its marketed-product portfolio includes the radioligand therapy franchise (Pluvicto, Lutathera), immunology biologics (Cosentyx, ianalumab), oncology targeted therapies (Scemblix, Vanrafia, Kymriah), and antisense/RNA therapies (del-brax), with a pipeline supplemented by technology platforms in CAR-T, gene therapy, antibody-oligonucleotide conjugates, and AI-driven drug discovery.

Product overview

Novartis operates as an integrated platform of innovative medicines plus dedicated technology platforms, organized around four therapeutic areas (Cardiovascular/Renal/Metabolic, Immunology, Neuroscience, Oncology). The marketed-product core spans multiple high-value franchises: the radioligand-therapy (RLT) franchise (Pluvicto and Lutathera, together generating ~USD 2.8B in 2025 sales) anchors a growing actinium-225 program (225Ac-PSMA-617); immunology is led by Cosentyx, Rhapsido and ianalumab; oncology by Scemblix, Vanrafia, Kisqali and the Kymriah CAR-T platform; renal by Vanrafia and Fabhalta; and the del-brax antisense program (acquired with Avidity) addresses FSHD. Novartis augments its in-house pipeline through targeted acquisitions (Avidity Biosciences USD 12B, Pikavation/SNV4818 USD 3B, Excellergy USD 2B, Mariana Oncology, Kedalion, Gyroscope, Arctos, MorphoSys, Tourmaline) and discovery collaborations (Antares, Orionis, Monte Rosa, Isomorphic Labs), all running on technology platforms that include CAR-T cell therapy manufacturing, gene therapy manufacturing, a USD 50B U.S. R&D and manufacturing expansion, and a deep genomic-research dataset (Pakistan Genome Resource). Together, these named products, technology platforms, and partnerships form the modular architecture of Novartis's medicines business.

Differentiator

Problem solved

Functional benefit

Brands

  • Novartis Gene Therapies: Distinct Novartis business unit dedicated to gene therapy development and manufacturing (referenced on About menu of Novartis.com).
  • Novartis Pharmaceuticals

Products and services

  • Pluvicto (177Lu vipivotide tetraxetan / 177Lu-PSMA-617) First-in-class PSMA-targeted radioligand therapy delivering lutetium-177 radiation directly to PSMA-positive prostate cancer cells; FDA-approved March 2022 for PSMA-positive metastatic castration-resistant prostate cancer; combined Pluvicto+Lutathera generated $2.8B in 2025 net sales; projected to reach $5B by 2030.
  • Lutathera (177Lu-DOTATATE) FDA-approved radioligand therapy for gastroenteropancreatic neuroendocrine tumors (GEP-NETs) marketed by Novartis subsidiary Advanced Accelerator Applications (AAA); combined with Pluvicto, generated $2.8B in 2025 net sales.
  • Cosentyx (secukinumab) Anti-IL-17A monoclonal antibody for autoimmune diseases including psoriasis, psoriatic arthritis, ankylosing spondylitis, hidradenitis suppurativa, and (per 2026 REPLENISH Phase III data) polymyalgia rheumatica.
  • Scemblix (asciminib) First-in-class STAMP (Specifically Targeting the ABL Myristoyl Pocket) inhibitor for chronic myeloid leukemia; 144-week ASC4FIRST Phase III data showed ~24% higher major molecular response vs standard-of-care TKIs and >50% lower discontinuation rates.
  • Vanrafia (atrasentan) Endothelin receptor antagonist for IgA nephropathy; final 2.5-year ALIGN Phase III results showed ~34% slowing of kidney function decline vs placebo with sustained 38.3% proteinuria reduction at 9 months.
  • Rhapsido (remibrutinib) Oral BTK inhibitor for chronic spontaneous urticaria, chronic inducible urticaria (CIndU) and IgE-mediated peanut allergy; first treatment to demonstrate efficacy in a global Phase III CIndU trial (RemIND); supplemental NDA submitted to FDA.
  • Kymriah (tisagenlecleucel)
  • Fabhalta (iptacopan)
  • ianalumab
  • del-brax (delpacibart braxlosiran) Investigational antibody-oligonucleotide conjugate for facioscapulohumeral muscular dystrophy (FSHD); FORTITUDE Phase I/II biomarker cohort met primary endpoint (KHDC1L reduction) and key secondary endpoint (CK reduction); acquired via $12B purchase of Avidity Biosciences.
  • Exl-111 (anti-IgE antibody) Half-life extended, high-affinity anti-IgE antibody in Phase 1 development (DISARM trial) for food allergy and IgE-driven diseases; designed to dissociate receptor-bound IgE for faster, deeper pathway suppression than conventional anti-IgE approaches; acquired via $2B Excellergy deal.
  • SNV4818 Pan-mutant-selective PI3Kα inhibitor in Phase 1/2 development for HR+/HER2- breast cancer, designed to selectively target mutated PI3Kα (in ~40% of HR+/HER2- breast cancer patients) while sparing healthy cells.

Companies that use Novartis

Customer profile

Ideal customer profiles1 record

Novartis technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Integration3 records

AI capability14 records

Feature8 records

Novartis partnerships and signals

Strategic signal

Recent moves11 records

Expansion highlights6 records

Novartis competitors and assessment

Company assessment

Direct peers

  • Roche: Swiss-headquartered global pharmaceutical company with comparable oncology (including radioligand therapy) and immunology franchises, similar therapeutic-area breadth, and a similarly large innovative-medicines R&D platform.
  • Pfizer: Top-tier U.S. pharma with overlapping oncology, immunology, and rare-disease franchises and a similarly active M&A strategy (Seagen $43B). Direct peer across innovative branded pharmaceuticals and large-cap R&D scale.
  • Merck & Co. U.S. major pharma with leading oncology franchise (Keytruda) and similar exposure to IRA pricing pressure and patent-cliff dynamics; competes in immuno-oncology, renal cell carcinoma, and antibody-drug conjugates that overlap Novartis's AOC ambitions.
  • AstraZeneca: Global pharma with parallel oncology, renal/cardiovascular, and rare-disease franchises; AZ also has a leading radioligand therapy program (Lumakras, Pluvicto competitor efforts, and its own Ac-225 supply agreement with Niowave) — directly comparable in RLT pipeline and oncology focus.
  • Bristol-Myers Squibb: U.S. major pharma with comparable oncology, immunology, and cardiovascular franchises, similar IRA exposure, and parallel late-stage pipeline investments in cell therapy, ADCs, and immunology — directly comparable revenue scale and therapeutic-area mix.
  • Sanofi: European-headquartered pharma with overlapping immunology, rare-disease, and oncology ambitions; Sanofi's CEO co-authored an April 2025 FT op-ed with Vas Narasimhan on European pharma competitiveness. Highly comparable in geographic and therapeutic profile.
  • Eli Lilly: U.S. major pharma with comparable innovative-medicines franchise, recent Isomorphic Labs AI drug-design partnership, and active expansion in oncology and rare diseases — Lilly is Novartis's AI-discovery partner co-counterparty and a direct therapeutic-area peer.
  • GSK: U.K.-headquartered pharma with comparable immunology (JAKs, BTK, IL-pathway agents) and oncology R&D pipelines; competes with Rhapsido in chronic urticaria and with Cosentyx in autoimmune diseases — directly comparable in targeted-therapy and immunology.

Broad incumbents

  • Johnson & Johnson (Innovative Medicine): Diversified healthcare giant with an Innovative Medicine pharma segment that overlaps Novartis's oncology, immunology, and pulmonary hypertension portfolios; large-cap peer with similar M&A scale and IRA exposure.

Regional players

  • Bayer (Pharmaceuticals): European-headquartered pharma with oncology and cardiovascular franchises that overlap Novartis's CRM therapeutic area; comparable in European geographic footprint though with weaker U.S. presence in radioligand therapy.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat7 records

Key risks6 records

Key highlights7 records

Customer concentration

Novartis social profiles

Digital presence

Novartis compliance and trust

Trust signal

Compliance4 records

Novartis financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Novartis leadership team

Management profile

Number of profiles

Profiles28 records

Novartis subsidiaries and ownership

Company hierarchy

Subsidiaries9 records

Novartis funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors1 record

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Novartis M&A and investment

M&A and investment

M&A44 records

Investments86 records

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Novartis

What does Novartis do?

Novartis researches, develops, manufactures, and commercializes innovative prescription medicines across four therapeutic areas: Cardiovascular/Renal/Metabolic, Immunology, Neuroscience, and Oncology. Its marketed-product portfolio includes the radioligand therapy franchise (Pluvicto, Lutathera), immunology biologics (Cosentyx, ianalumab), oncology targeted therapies (Scemblix, Vanrafia, Kymriah), and antisense/RNA therapies (del-brax), with a pipeline supplemented by technology platforms in CAR-T, gene therapy, antibody-oligonucleotide conjugates, and AI-driven drug discovery.

Is Novartis a public or private company?

Novartis is a public company. It is classified as public and is currently operating.

When was Novartis founded?

Novartis was founded in 1996. It employs 5,001 to 10,000 people.

Where is Novartis based?

Novartis is headquartered in Basel, Switzerland, in the Europe region.

How does Novartis make money?

Five revenue lines are on record. Pharmaceutical Product Sales are the primary driver. The others are strategic Collaboration Upfront and Milestone Payments, royalty and Tiered Royalty Income, M&A-Driven Portfolio Revenue and geographic Market Expansion Revenue.

Who are Novartis's main competitors?

Direct peers on record are Roche, Pfizer, Merck & Co., AstraZeneca, Bristol-Myers Squibb, Sanofi, Eli Lilly and GSK. Johnson & Johnson (Innovative Medicine) is listed as a broad incumbent. Bayer (Pharmaceuticals) is listed as a regional player.

Does Novartis have an API?

No public API is recorded for Novartis.

What industry is Novartis in?

Novartis's product category is Prescription Pharmaceuticals. Its primary akta.pro industry code is HLAIAAAF, Neurology & Psychiatry (CNS) Pharmaceuticals, with a secondary code of HLAIACAC, Neurology & CNS Specialty Pharmaceuticals. Its NAICS code is 32541 and its SIC code is 2836.

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FinanzNachrichten.deNovartis setzt bis zu 7,8 Milliarden Dollar auf Immuntherapie - warum Eli Lilly und Co. die Zelltherapie neu erfinden wollenNovartis signed a licensing and option deal with Abogen Biosciences for an mRNA-encoded T-cell engager, with total value up to $7.8 billion. Eli Lilly agreed to acquire Kelonia Therapeutics for up to $7 billion. Both companies pursue in vivo cell therapies, while Mesoblast advances allogeneic products like Ryoncil.Channel NewsAsiaCommentary: Keep medicine out of the US-China tech warThe author argues that the US should not restrict access to Chinese biotech innovations, citing recent licensing deals like Novo Nordisk's $2.6 billion deal with Jiangsu Hengrui and Novartis's $7.8 billion deal with Abogen. The piece contends that medicine is inherently collaborative and that Washington should outdo China rather than ignore its innovations.FinancialContent Business PageINVESTOR ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of Novartis AG - NVSPomerantz LLP is investigating claims on behalf of Novartis AG investors over potential securities fraud. The investigation follows a September 8, 2026 study failure that caused Novartis's stock to fall 13.93% to $137.70 per ADS.YahooSAP Puts the Autonomous Enterprise to WorkSAP showcased its Autonomous Enterprise at SAP Connect, featuring Joule Work and Joule Assistants across finance, supply chain, HR, and procurement. Joule Work is live with 110,000 SAP employees, delivering 20% productivity gains, while customers like Novartis and Nestlé are piloting AI agents. SAP also announced SAP Pay and partnerships with Moody's and ORO Labs.PR NewswireSAP Puts the Autonomous Enterprise to WorkSAP showcased its Autonomous Enterprise at SAP Connect, featuring Joule Work and Joule Assistants across finance, supply chain, HR, and procurement. The company reported 20% productivity gains for its 110,000 employees using Joule Work, and customers like Novartis and Nestlé are piloting AI agents. SAP also announced SAP Pay for embedded payments and partnerships with Moody's and ORO Labs.NJBIZNovartis signs $7.8B mRNA deal with Chinese biotechNovartis signed a licensing deal worth up to $7.8 billion with Chinese biotech Abogen Biosciences for an mRNA-based autoimmune disease treatment. The deal includes $575 million upfront and up to $7.2 billion in milestone payments, with Novartis gaining exclusive worldwide rights to ABO2203.BioSpaceWeighing the risks of CAR T in autoimmune disease as Kyverna nears marketKyverna Therapeutics reported one-year durability data for its CAR T therapy miv-cel in stiff person syndrome, showing improved mobility and no high-grade safety events. Novartis and BMS paused autoimmune CAR T trials after deaths and inflammatory events, but Kyverna's safety profile is attributed to its design and manufacturing process. The company plans to file a biologics license application by year-end.PR NewswireAHN Cardiology Department at Allegheny General Hospital Launches Clinical Trial Investigating New Therapy for Pulmonary Arterial HypertensionAllegheny General Hospital joined a Novartis-sponsored clinical trial for pulmonary arterial hypertension, enrolling patients in a double-blind, placebo-controlled study of investigational drug LTP001. The trial, led by Dr. Hayah Kassis-George, aims to assess safety, tolerability, and effectiveness of the drug, which targets a protein believed to cause PAH. AHN AGH is the only tri-state area health system participating.YahooClinical trial experts turn to AI and new partnerships to tackle growing trial complexityThe Outsourcing in Clinical Trials DACH conference will be held on 3-4 November in Basel, featuring speakers from Roche, AstraZeneca, Novartis, and biotechs. It will cover AI governance, CRO partnerships, patient engagement, and site capacity, with a focus on Europe's clinical trial competitiveness.YahooCarrie Ann Inaba opens up about her journey with Sjögren’s diseaseCarrie Ann Inaba, a judge on Dancing With the Stars, opened up about her Sjögren's disease diagnosis in 2013. The autoimmune disorder affects about 4 million Americans and causes dry eyes, mouth, and joint pain. She is partnering with Novartis on the SJÖUT campaign to help patients connect the dots and share their experiences.