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Genentech

Full company profile

uuid0002n27

Namestring
Genentech
Legal namestring
Genentech, Inc.
Websiteurl
gene.com
Company typeenum
Private
Founded yearint
1976
Descriptiontext

Genentech, Inc. is a US-based biotechnology research and biopharmaceutical company founded in 1976 in South San Francisco, California. It operates as a wholly-owned subsidiary of Roche Holding AG following Roche's 2009 acquisition for approximately $46.8 billion, serving as the primary US-based research, development, and commercialization vehicle for the Roche Group. The company develops, manufactures, and commercializes a broad portfolio of biologic and small-molecule medicines across five therapeutic areas: oncology (Tecentriq, Vabysmo, Hemlibra, Herceptin, Avastin, Polivy, Lunsumio, Columvi, Venclexta, Itovebi, Kadcyla, Perjeta, Phesgo, Rozlytrek, Alecensa, Zelboraf), immunology (Actemra, Rituxan, Gazyva, Xolair), neuroscience (Ocrevus, Enspryng, Evrysdi), ophthalmology (Vabysmo, Susvimo, Lucentis, Luxturna), and emerging areas including metabolic disease and obesity (enicepatide, petrelintide in Phase III). It maintains additional franchises in hematology (PiaSky) and infectious disease (Xofluza, Tamiflu).

Genentech's underlying technology combines established biologics manufacturing with AI/ML-augmented drug discovery. The Prescient Design platform provides machine learning-based protein design; a partnership with Recursion Pharmaceuticals extends AI-driven discovery into the clinic; and Roche's Galileo platform supports enterprise agentic AI for scientific discovery. Novel drug delivery technology includes the FDA-approved Port Delivery System (Susvimo), a refillable reservoir for continuous ranibizumab delivery in retinal disease, plus a growing set of subcutaneous reformulations (Phesgo, Ocrevus Zunovo, Tecentriq Hybreza, Rituxan Hycela, Lunsumio Velo) that improve convenience. Manufacturing scale is being expanded via a $700 million Holly Springs, North Carolina facility.

The business model centers on biopharmaceutical product sales through enterprise field sales, medical science liaisons, and specialty pharmacy distribution, complemented by Genentech Access Solutions for coverage support and the Genentech Patient Foundation, which provides free medicines to qualifying uninsured or underinsured patients. Revenue also includes co-commercialization economics, notably the joint U.S. commercialization of Venclexta with AbbVie. The company serves hospitals, oncology practices, neurology clinics, ophthalmology specialists, specialty pharmacies, and patients with serious and life-threatening diseases, with a 10,000+ employee base concentrated in South San Francisco and expanding US manufacturing operations.

Short descriptiontext

Genentech is a US-based biotechnology subsidiary of Roche Holding AG that develops and commercializes biologic and small-molecule medicines across oncology, immunology, neuroscience, ophthalmology, and metabolic disease, serving patients, hospitals, and specialty pharmacies worldwide.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
5,001–10,000
akta.pro rankint
HeadquartersSouth San Francisco, United States
HQ citystring
South San Francisco
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
biopharmaceutical medicines, oncology therapeutics, immunology treatments, ophthalmology drugs, gene therapy
Industry5 codes
1Specialty Care Pharmaceuticals
CodeHLAIAAABPrimaryYes
2Neurology & CNS Specialty Pharmaceuticals
CodeHLAIACACPrimaryNo
3Immunology & Inflammation Pharmaceuticals
CodeHLAIAAADPrimaryNo
4Cardiometabolic Pharmaceuticals (Cardiovascular/Diabetes/Obesity)
CodeHLAIAAAEPrimaryNo
5Gene Therapy Regulatory, Pharmacovigilance & Clinical Operations Services
CodeHLAAACAMPrimaryNo
NAICS code2 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Pharmaceutical Preparation Manufacturing325412
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
Product category
Biopharmaceuticals
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1Pharmaceutical Product Sales
TypeOne Time License
Description

Genentech generates revenue through sales of its portfolio of approved biopharmaceutical medicines across oncology, immunology, neuroscience, ophthalmology, and metabolic diseases. Products include Vabysmo, Tecentriq, Hemlibra, Ocrevus, Lucentis, Avastin, Herceptin, Rituxan, Actemra, Xolair, and others. Revenue flows through specialty pharmacies, hospital sales, and direct patient distribution channels.

gene.com
2Co-commercialization Revenue
TypeLicensing Royalties
Description

Venclexta (venetoclax) is jointly commercialized by AbbVie and Genentech in the U.S., representing a co-commercialization partnership revenue stream.

investing.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels4 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components6 values
Technology or R&D, Supply Chain, Personnel, Marketing or Sales, Operations, Infrastructure
Pricing details2 tiers
1TrumpRx discounted pricing for Xofluza
ModelOtherBilling cadencePay-as-you-go
Notes

Xofluza offered at approximately $50 through TrumpRx program versus standard price of $168

usnews.com
2Patient assistance programs
ModelOtherBilling cadencePay-as-you-go
Notes

Genentech Patient Foundation provides free medicine to qualifying patients without insurance coverage or who cannot afford their medicine

cbsnews.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 3 records shown
1Genentech Patient Foundation
Description

A patient assistance program providing free Genentech medicines to people who don't have insurance coverage or who have financial concerns.

gene.com
+2 more records
Core offering1 text field

Genentech develops, manufactures, and commercializes a broad portfolio of biopharmaceutical medicines across oncology, immunology, neuroscience, ophthalmology, and metabolic diseases. Its products include monoclonal antibodies, bispecific antibodies, antibody-drug conjugates, gene therapies, and small molecule drugs such as Tecentriq, Herceptin, Avastin, Ocrevus, Vabysmo, Hemlibra, Venclexta, Polivy, and Susvimo. The company distributes these medicines through specialty pharmacies, hospital channels, and direct patient assistance programs, while also operating a patient foundation providing free medicines to uninsured individuals.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • 59% reduction in risk of disease progression or death with Lunsumio VELO + Polivy combination vs comparator in relapsed/refractory large B-cell lymphoma (Phase III SUNMO study)
+3 more records
Product overview1 text field

Genentech's product portfolio is a diverse platform of biotechnology medicines spanning multiple therapeutic areas including oncology (Avastin, Herceptin, Tecentriq, Venclexta, Polivy, Lunsumio, Columvi, Alecensa, Kadcyla, Perjeta, Phesgo, Rozlytrek, Itovebi), immunology (Rituxan, Gazyva, Ocrevus, Xolair, Actemra), ophthalmology (Lucentis, Vabysmo, Susvimo), rare blood disorders (Hemlibra, PiaSky), neuroscience (Ocrevus, Enspryng), and infectious disease (Xofluza, Tamiflu). The portfolio includes both intravenous and subcutaneous formulations, with several products having received new indications or regulatory approvals recently, including expanded uses for Tecentriq in muscle-invasive bladder cancer and colon cancer, and Venclexta for chronic lymphocytic leukemia. The company also offers gene therapy (Luxturna) and has an advancing obesity portfolio including enicepatide and petrelintide in Phase III development. Genentech provides these medicines through patient support services including the Genentech Patient Foundation for those without insurance coverage.

Product and service28 records
1Actemra (tocilizumab)
CategoryImmunology
2Alecensa (alectinib)
CategoryOncology
3Avastin (bevacizumab)
CategoryOncology
4Columvi (glofitamab-gxbm)
CategoryOncology
5Enspryng (satralizumab-mwge)
CategoryNeuroscience
6Evrysdi (risdiplam)
CategoryNeuroscience
7Gazyva (obinutuzumab)
CategoryOncology/Immunology
8Hemlibra (emicizumab-kxwh)
CategoryHematology
9Herceptin (trastuzumab)
CategoryOncology
10Itovebi (inavolisib)
CategoryOncology
11Kadcyla (ado-trastuzumab emtansine)
CategoryOncology
12Lucentis (ranibizumab injection)
CategoryOphthalmology
13Lunsumio (mosunetuzumab-axgb)
CategoryOncology
14Luxturna (voretigene neparvovec-rzyl)
CategoryGene Therapy/Ophthalmology
15Ocrevus (ocrelizumab)
CategoryNeuroscience
16Perjeta (pertuzumab)
CategoryOncology
17Phesgo
CategoryOncology
18PiaSky (crovalimab-akkz)
CategoryHematology
19Polivy (polatuzumab vedotin-piiq)
CategoryOncology
20Rituxan (rituximab)
CategoryOncology/Immunology
21Rozlytrek (entrectinib)
CategoryOncology
22Susvimo
CategoryOphthalmology
23Tecentriq (atezolizumab)
CategoryOncology
24Vabysmo (faricimab-svoa)
CategoryOphthalmology
25Venclexta (venetoclax)
CategoryOncology
26Xofluza (baloxavir marboxil)
CategoryAnti-Infectives
27Xolair (omalizumab)
CategoryImmunology
28Zelboraf (vemurafenib)
CategoryOncology
Scale indicator3 records

Each record includes

Type, Value, Description, Source

Partnership11 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2021-11-02
Description

Genentech acquired Prescient Design to enhance antibody discovery capabilities through machine learning-based protein design. The acquisition was motivated by Prescient Design's unique platform and talented team, aiming to improve efficiency and effectiveness in identifying therapeutic antibodies.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Sangamo's proprietary STAC-BBB capsid has been licensed to Genentech for up to $4.6 billion in potential milestones. The capsid enables brain-targeting gene therapies.

Strategic tierCoreTypeTechnology or Integration
Description

FDA approved Signatera CDx as companion diagnostic for Tecentriq in muscle-invasive bladder cancer. First blood-based MRD companion diagnostic approved, identifying patients who may benefit from Tecentriq after cystectomy.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Worldwide collaboration for OpRegen (RG6501) cell therapy for geographic atrophy secondary to age-related macular degeneration. Patients showed +9.0 ETDRS letters gain at 36 months with partial restoration of outer retinal structure.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

AI-powered drug development partnership advancing clinical candidates including REC-1245 and REC-4881. Genentech continues as partnered program collaborator following Recursion's partnership with Sanofi.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

December partnership with Genentech for molecular profiling services. Described as the largest pharma deal in Caris' history for precision oncology diagnostics.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Co-commercialization of Venclexta (venetoclax) in the U.S. Venetoclax is co-developed by AbbVie and Roche/Genentech, with positive Phase III CLL14 trial data showing 6.4-year median PFS.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Collaborative research program funding CAR-T cell therapy research for lupus. Inaugural recipients of Lupus Research Alliance-Genentech Award on Immune Resetting Therapies for Lupus each receive $150,000 per year for up to two years.

Strategic tierCoreTypeGTM or Marketing Partner
Description

Funding MS Care Desert Initiative in South Carolina - Genentech's largest corporate sponsorship to date for the Society's healthcare access programs. Part of three-state pilot including Wisconsin and Mississippi.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Collaboration at AACR 2026 for Precede Bio Insight liquid biopsy product enabling genome-wide inference of gene expression from 1mL plasma for predicting therapeutic response.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Co-development of personalized mRNA cancer vaccine (autogene cevumeran) for pancreatic cancer. 87.5% of patients with strong T cell responses remain alive 4-6 years post-surgery vs median survival of 3.4 years for non-responders.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Market position
Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat6 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers5 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment5 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

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
Yes
API detail
Has APIbool
No

Docs URL, Description

AI capability8 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature5 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles5 records

Each record includes

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

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds1 record

Each record includes

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

Investors2 records

Each record includes

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

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

M&A6 records

Each record includes

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

Investment17 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 →

Genentech

Biopharmaceuticalsgene.com

Genentech is a US-based biotechnology subsidiary of Roche Holding AG that develops and commercializes biologic and small-molecule medicines across oncology, immunology, neuroscience, ophthalmology, and metabolic disease, serving patients, hospitals, and specialty pharmacies worldwide.

What Genentech does

Genentech, Inc. is a US-based biotechnology research and biopharmaceutical company founded in 1976 in South San Francisco, California. It operates as a wholly-owned subsidiary of Roche Holding AG following Roche's 2009 acquisition for approximately $46.8 billion, serving as the primary US-based research, development, and commercialization vehicle for the Roche Group. The company develops, manufactures, and commercializes a broad portfolio of biologic and small-molecule medicines across five therapeutic areas: oncology (Tecentriq, Vabysmo, Hemlibra, Herceptin, Avastin, Polivy, Lunsumio, Columvi, Venclexta, Itovebi, Kadcyla, Perjeta, Phesgo, Rozlytrek, Alecensa, Zelboraf), immunology (Actemra, Rituxan, Gazyva, Xolair), neuroscience (Ocrevus, Enspryng, Evrysdi), ophthalmology (Vabysmo, Susvimo, Lucentis, Luxturna), and emerging areas including metabolic disease and obesity (enicepatide, petrelintide in Phase III). It maintains additional franchises in hematology (PiaSky) and infectious disease (Xofluza, Tamiflu).

Genentech's underlying technology combines established biologics manufacturing with AI/ML-augmented drug discovery. The Prescient Design platform provides machine learning-based protein design; a partnership with Recursion Pharmaceuticals extends AI-driven discovery into the clinic; and Roche's Galileo platform supports enterprise agentic AI for scientific discovery. Novel drug delivery technology includes the FDA-approved Port Delivery System (Susvimo), a refillable reservoir for continuous ranibizumab delivery in retinal disease, plus a growing set of subcutaneous reformulations (Phesgo, Ocrevus Zunovo, Tecentriq Hybreza, Rituxan Hycela, Lunsumio Velo) that improve convenience. Manufacturing scale is being expanded via a $700 million Holly Springs, North Carolina facility.

The business model centers on biopharmaceutical product sales through enterprise field sales, medical science liaisons, and specialty pharmacy distribution, complemented by Genentech Access Solutions for coverage support and the Genentech Patient Foundation, which provides free medicines to qualifying uninsured or underinsured patients. Revenue also includes co-commercialization economics, notably the joint U.S. commercialization of Venclexta with AbbVie. The company serves hospitals, oncology practices, neurology clinics, ophthalmology specialists, specialty pharmacies, and patients with serious and life-threatening diseases, with a 10,000+ employee base concentrated in South San Francisco and expanding US manufacturing operations.

Genentech firmographics

Firmographics
Name
Genentech
Legal name
Genentech, Inc.
Website
https://gene.com
Company type
Private
Founded year
1976
Operating status
Operating
Headcount range
5,001–10,000 employees
Short description
Genentech is a US-based biotechnology subsidiary of Roche Holding AG that develops and commercializes biologic and small-molecule medicines across oncology, immunology, neuroscience, ophthalmology, and metabolic disease, serving patients, hospitals, and specialty pharmacies worldwide.
Ownership category
akta.pro rank

Genentech industry classification

Industry
Product category
Biopharmaceuticals
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Pharmaceutical Preparation Manufacturing (325412)
SIC
Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834)
akta.pro primary industry
Specialty Care Pharmaceuticals (HLAIAAAB)
akta.pro secondary industries
Neurology & CNS Specialty Pharmaceuticals (HLAIACAC), Immunology & Inflammation Pharmaceuticals (HLAIAAAD), Cardiometabolic Pharmaceuticals (Cardiovascular/Diabetes/Obesity) (HLAIAAAE), Gene Therapy Regulatory, Pharmacovigilance & Clinical Operations Services (HLAAACAM)

Keywords

  • Biopharmaceutical medicines
  • Oncology therapeutics
  • Immunology treatments
  • Ophthalmology drugs
  • Gene therapy

Where Genentech is headquartered

Location

Headquarters

HQ city
South San Francisco
HQ country
United States
HQ region
North America

Offices2 records

Markets served

Genentech business model

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

Revenue model

  1. Pharmaceutical Product Sales: Genentech generates revenue through sales of its portfolio of approved biopharmaceutical medicines across oncology, immunology, neuroscience, ophthalmology, and metabolic diseases. Products include Vabysmo, Tecentriq, Hemlibra, Ocrevus, Lucentis, Avastin, Herceptin, Rituxan, Actemra, Xolair, and others. Revenue flows through specialty pharmacies, hospital sales, and direct patient distribution channels.
  2. Co-commercialization Revenue: Venclexta (venetoclax) is jointly commercialized by AbbVie and Genentech in the U.S., representing a co-commercialization partnership revenue stream.

Pricing tiers

ModelBillingPrice
OtherPay-as-you-goTrumpRx discounted pricing for Xofluza
OtherPay-as-you-goPatient assistance programs

Go-to-market motion1 record

Distribution channels4 records

Marketing channels5 records

Genentech product offering

Product offering

Core offering

Genentech develops, manufactures, and commercializes a broad portfolio of biopharmaceutical medicines across oncology, immunology, neuroscience, ophthalmology, and metabolic diseases. Its products include monoclonal antibodies, bispecific antibodies, antibody-drug conjugates, gene therapies, and small molecule drugs such as Tecentriq, Herceptin, Avastin, Ocrevus, Vabysmo, Hemlibra, Venclexta, Polivy, and Susvimo. The company distributes these medicines through specialty pharmacies, hospital channels, and direct patient assistance programs, while also operating a patient foundation providing free medicines to uninsured individuals.

Product overview

Genentech's product portfolio is a diverse platform of biotechnology medicines spanning multiple therapeutic areas including oncology (Avastin, Herceptin, Tecentriq, Venclexta, Polivy, Lunsumio, Columvi, Alecensa, Kadcyla, Perjeta, Phesgo, Rozlytrek, Itovebi), immunology (Rituxan, Gazyva, Ocrevus, Xolair, Actemra), ophthalmology (Lucentis, Vabysmo, Susvimo), rare blood disorders (Hemlibra, PiaSky), neuroscience (Ocrevus, Enspryng), and infectious disease (Xofluza, Tamiflu). The portfolio includes both intravenous and subcutaneous formulations, with several products having received new indications or regulatory approvals recently, including expanded uses for Tecentriq in muscle-invasive bladder cancer and colon cancer, and Venclexta for chronic lymphocytic leukemia. The company also offers gene therapy (Luxturna) and has an advancing obesity portfolio including enicepatide and petrelintide in Phase III development. Genentech provides these medicines through patient support services including the Genentech Patient Foundation for those without insurance coverage.

Differentiator

Problem solved

Functional benefit

Brands

  • Genentech Patient Foundation: A patient assistance program providing free Genentech medicines to people who don't have insurance coverage or who have financial concerns.
  • Genentech Access Solutions
  • MEDICALLY

Products and services

  • Actemra (tocilizumab)
  • Alecensa (alectinib)
  • Avastin (bevacizumab)
  • Columvi (glofitamab-gxbm)
  • Enspryng (satralizumab-mwge)
  • Evrysdi (risdiplam)
  • Gazyva (obinutuzumab)
  • Hemlibra (emicizumab-kxwh)
  • Herceptin (trastuzumab)
  • Itovebi (inavolisib)
  • Kadcyla (ado-trastuzumab emtansine)
  • Lucentis (ranibizumab injection)
  • Lunsumio (mosunetuzumab-axgb)
  • Luxturna (voretigene neparvovec-rzyl)
  • Ocrevus (ocrelizumab)
  • Perjeta (pertuzumab)
  • Phesgo
  • PiaSky (crovalimab-akkz)
  • Polivy (polatuzumab vedotin-piiq)
  • Rituxan (rituximab)
  • Rozlytrek (entrectinib)
  • Susvimo
  • Tecentriq (atezolizumab)
  • Vabysmo (faricimab-svoa)
  • Venclexta (venetoclax)
  • Xofluza (baloxavir marboxil)
  • Xolair (omalizumab)
  • Zelboraf (vemurafenib)

Quantifiable outcome

  • 59% reduction in risk of disease progression or death with Lunsumio VELO + Polivy combination vs comparator in relapsed/refractory large B-cell lymphoma (Phase III SUNMO study)
  • +3 more outcomes

Companies that use Genentech

Customer profile

Named customers5 records

Segments5 records

Ideal customer profiles2 records

Genentech technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability8 records

Feature5 records

Genentech partnerships and signals

Strategic signal

Partnerships

Eleven partnerships are on record, tiered core and minor.

  • Prescient DesigncoreStrategic or Co-development Partner · 2 November 2021Genentech acquired Prescient Design to enhance antibody discovery capabilities through machine learning-based protein design. The acquisition was motivated by Prescient Design's unique platform and talented team, aiming to improve efficiency and effectiveness in identifying therapeutic antibodies.
  • Sangamo TherapeuticscoreStrategic or Co-development PartnerSangamo's proprietary STAC-BBB capsid has been licensed to Genentech for up to $4.6 billion in potential milestones. The capsid enables brain-targeting gene therapies.
  • NateracoreTechnology or IntegrationFDA approved Signatera CDx as companion diagnostic for Tecentriq in muscle-invasive bladder cancer. First blood-based MRD companion diagnostic approved, identifying patients who may benefit from Tecentriq after cystectomy.
  • Lineage Cell TherapeuticscoreStrategic or Co-development PartnerWorldwide collaboration for OpRegen (RG6501) cell therapy for geographic atrophy secondary to age-related macular degeneration. Patients showed +9.0 ETDRS letters gain at 36 months with partial restoration of outer retinal structure.
  • Recursion PharmaceuticalscoreStrategic or Co-development PartnerAI-powered drug development partnership advancing clinical candidates including REC-1245 and REC-4881. Genentech continues as partnered program collaborator following Recursion's partnership with Sanofi.
  • Caris Life SciencesminorStrategic or Co-development PartnerDecember partnership with Genentech for molecular profiling services. Described as the largest pharma deal in Caris' history for precision oncology diagnostics.
  • AbbViecoreStrategic or Co-development PartnerCo-commercialization of Venclexta (venetoclax) in the U.S. Venetoclax is co-developed by AbbVie and Roche/Genentech, with positive Phase III CLL14 trial data showing 6.4-year median PFS.
  • Lupus Research AlliancecoreStrategic or Co-development PartnerCollaborative research program funding CAR-T cell therapy research for lupus. Inaugural recipients of Lupus Research Alliance-Genentech Award on Immune Resetting Therapies for Lupus each receive $150,000 per year for up to two years.
  • National Multiple Sclerosis SocietycoreGTM or Marketing PartnerFunding MS Care Desert Initiative in South Carolina - Genentech's largest corporate sponsorship to date for the Society's healthcare access programs. Part of three-state pilot including Wisconsin and Mississippi.
  • Precede BiosciencesminorStrategic or Co-development PartnerCollaboration at AACR 2026 for Precede Bio Insight liquid biopsy product enabling genome-wide inference of gene expression from 1mL plasma for predicting therapeutic response.
  • BioNTechcoreStrategic or Co-development PartnerCo-development of personalized mRNA cancer vaccine (autogene cevumeran) for pancreatic cancer. 87.5% of patients with strong T cell responses remain alive 4-6 years post-surgery vs median survival of 3.4 years for non-responders.

Scale indicators3 records

Recent moves7 records

Expansion highlights6 records

Genentech competitors and assessment

Company assessment

Market position

Weaknesses4 records

Competitive moat6 records

Key risks5 records

Key highlights7 records

Customer concentration

Genentech social profiles

Digital presence

Genentech financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Genentech leadership team

Management profile

Number of profiles

Profiles5 records

Genentech funding detail

Funding detail

Funding overview

Funding rounds1 record

Investors2 records

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

Genentech M&A and investment

M&A and investment

M&A6 records

Investments17 records

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

Frequently asked questions about Genentech

What does Genentech do?

Genentech develops, manufactures, and commercializes a broad portfolio of biopharmaceutical medicines across oncology, immunology, neuroscience, ophthalmology, and metabolic diseases. Its products include monoclonal antibodies, bispecific antibodies, antibody-drug conjugates, gene therapies, and small molecule drugs such as Tecentriq, Herceptin, Avastin, Ocrevus, Vabysmo, Hemlibra, Venclexta, Polivy, and Susvimo. The company distributes these medicines through specialty pharmacies, hospital channels, and direct patient assistance programs, while also operating a patient foundation providing free medicines to uninsured individuals.

Is Genentech a public or private company?

Genentech is a private company. It is classified as corporate owned and is currently operating.

When was Genentech founded?

Genentech was founded in 1976. It employs 5,001 to 10,000 people.

Where is Genentech based?

Genentech is headquartered in South San Francisco, United States, in the North America region.

How does Genentech make money?

Two revenue lines are on record. Pharmaceutical Product Sales are the primary driver. The others are co-commercialization Revenue.

Does Genentech have an API?

No public API is recorded for Genentech.

What industry is Genentech in?

Genentech's product category is Biopharmaceuticals. Its primary akta.pro industry code is HLAIAAAB, Specialty Care Pharmaceuticals, with a secondary code of HLAIACAC, Neurology & CNS Specialty Pharmaceuticals. Its NAICS code is 325414 and its SIC code is 2836.

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Business Wire BlogGenentech Presents New Phase III One-Year Data for Vamikibart in Uveitic Macular Edema (UME), a Serious Cause of Vision LossGenentech presented one-year data from Phase III MEERKAT and SANDCAT studies showing sustained vision and macular thickness improvements with vamikibart in uveitic macular edema. The FDA accepted the Biologics License Application, with an approval decision expected by July 2027. If approved, vamikibart would be the first non-steroid targeted treatment for UME.FinancialContent Business PageGenentech Presents New Phase III One-Year Data for Vamikibart in Uveitic Macular Edema (UME), a Serious Cause of Vision LossGenentech presented one-year data from Phase III MEERKAT and SANDCAT studies showing sustained vision and macular thickness improvements with vamikibart in uveitic macular edema. The FDA accepted the BLA, with an approval decision expected by July 2027. Vamikibart would be the first non-steroid targeted treatment for UME.Stock TitanGenentech vamikibart FDA application acceptedGenentech announced the FDA accepted its Biologics License Application for vamikibart to treat uveitic macular edema, with an approval decision expected by July 2027. The decision follows Phase III MEERKAT and SANDCAT studies showing sustained vision and macular thickness improvements at 52 weeks. The drug would be the first non-steroid targeted therapy for this condition.Longevity.TechnologyGenentech pays $100m upfront for Alector’s AL050Genentech agreed to pay Alector $100 million upfront for Parkinson's drug AL050, with exclusive worldwide rights. The deal can grow to $1.17 billion in milestone payments and tiered royalties. Alector retains ownership of its brain carrier technology and will use the funds to advance its Alzheimer's and gene-silencing programs.YahooFDA Approves Genentech’s Tecentriq in Combination With a Fluoropyrimidine and Oxaliplatin for the Adjuvant Treatment of a Certain Type of Stage III Colon CancerThe FDA approved Tecentriq plus chemotherapy for adjuvant treatment of stage III dMMR colon cancer, based on the ATOMIC study showing a 50% reduction in recurrence or death. This is the first approved adjuvant immunotherapy regimen for this setting, marking the twelfth indication for Tecentriq in the U.S.FinancialContent Business PageFDA Approves Genentech’s Tecentriq in Combination With a Fluoropyrimidine and Oxaliplatin for the Adjuvant Treatment of a Certain Type of Stage III Colon CancerThe FDA approved Tecentriq plus chemotherapy for adjuvant treatment of stage III dMMR colon cancer, based on the ATOMIC study. The regimen reduced recurrence or death risk by 50% and is the first approved adjuvant immunotherapy for this setting.Stock TitanGenentech wins FDA approval for Tecentriq in colon cancerThe FDA approved Genentech's Tecentriq combined with fluoropyrimidine and oxaliplatin for adjuvant treatment of stage III dMMR colon cancer. The approval, based on the ATOMIC study, reduced recurrence or death risk by 50% and marks the twelfth U.S. indication for Tecentriq.Business Wire BlogFDA Approves Genentech’s Tecentriq in Combination With a Fluoropyrimidine and Oxaliplatin for the Adjuvant Treatment of a Certain Type of Stage III Colon CancerThe FDA approved Genentech's Tecentriq plus chemotherapy for adjuvant treatment of stage III dMMR colon cancer, based on the ATOMIC study. The regimen reduced recurrence or death risk by 50% compared to chemotherapy alone, with 36-month disease-free survival of 86% versus 76%. This is the first approved adjuvant immunotherapy for this setting.Seeking AlphaGenentech's Tecentriq gains new indication for colon cancerThe US FDA approved Genentech's Tecentriq as an adjuvant treatment for Stage III mismatch repair deficient colon cancer in adults and children two years and older. The approval is for Tecentriq plus a fluoropyrimidine and oxaliplatin, based on the phase 3 ATOMIC/ML39057 trial, which showed improved disease-free survival. The review was conducted under Project Orbis with regulators from Australia, Canada, Israel, and Switzerland.MediaPostGenentech Marks 50 Years Of Biotech: 'The Impossible Bet'Genentech premiered a documentary marking its 50th anniversary, featuring patient stories and co-founder Herb Boyer's daughter. The company, owned by Roche since 2009, is expanding into obesity treatments and targeting a broader consumer audience.