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Kite Pharma

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uuid00025m3

Namestring
Kite Pharma
Legal namestring
Kite Pharma, Inc.
Websiteurl
kitepharma.com
Company typeenum
Private
Founded yearint
2017
Descriptiontext

Kite Pharma, Inc. is a clinical-stage and commercial-stage biotechnology company focused exclusively on autologous CAR T-cell therapies for the treatment of relapsed or refractory blood cancers. The company engineers a patient's own T cells ex vivo to express chimeric antigen receptors targeting tumor-associated antigens including CD19, CD20, BCMA, and CLL-1, and operates as a wholly-owned subsidiary of Gilead Sciences following its 2017 acquisition for approximately $11.9 billion. Its core technology is autologous CAR T-cell therapy, with each dose custom-manufactured per patient through a five-step process of collection, isolation, engineering with a CAR gene, expansion, and reinfusion.

Kite's commercial portfolio is anchored by Yescarta (axicabtagene ciloleucel), a CD19-directed CAR T-cell therapy approved for large B-cell lymphoma, follicular lymphoma, and (as of February 2026) primary central nervous system lymphoma, which generated approximately $1.6 billion in 2024 revenue. Tecartus (brexucabtagene autoleucel) is a second approved product for relapsed/refractory mantle cell lymphoma and B-cell acute lymphoblastic leukemia. The clinical pipeline comprises anito-cel (BCMA-directed CAR-T for multiple myeloma, co-developed with Arcellx and now fully owned by Gilead following its $7.8 billion acquisition completed April 2026, with a December 23, 2026 PDUFA date), KITE-363 (dual CD19/CD20 CAR-T for LBCL), KITE-222 (CLL-1 CAR-T for AML, FDA Orphan Drug Designation), and KITE-753 (next-generation bicistronic CAR-T). The company has additionally moved into in vivo CAR-T through the $350 million Interius BioTherapeutics acquisition (announced August 2025) and the $1.64 billion Pregene Biopharma licensing deal (October 2025).

The business model is the sale of one-time, high-cost individualized treatments (U.S. market pricing in the $373,000-$475,000 range) reimbursed through a mix of private insurance, Medicare, and national health systems. Distribution runs through a network of 300+ qualified treatment centers across the U.S., Canada, Australia, Europe, Brazil, Singapore, Saudi Arabia, a joint venture in China, and a licensing partner in Japan. Kite operates what it describes as the world's largest dedicated in-house cell therapy manufacturing network, with facilities in Santa Monica (headquarters), Frederick, Maryland (manufacturing, 500+ jobs by end of 2026), and Hoofddorp, Netherlands (a EUR 185 million facility producing over 4,000 cell therapies annually). Gilead/Kite led global cell and gene therapy sales with 15% market share in 2024, and together with Bristol Myers Squibb accounts for over 70% of the CAR-T market.

Short descriptiontext

Kite Pharma is a Gilead Sciences subsidiary that develops and commercializes autologous CAR T-cell therapies for relapsed or refractory blood cancers, distributing Yescarta and Tecartus through 300+ qualified treatment centers worldwide while advancing a pipeline of next-generation and in vivo cell therapies.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1,001–5,000
akta.pro rankint
HeadquartersLos Angeles, United States
HQ citystring
Los Angeles
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices4 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
CAR T-cell therapy, cell therapy products, autologous immunotherapy, cancer cell therapy, oncology biologics manufacturing
Industry4 codes
1Cell Therapy Developers (Autologous)
CodeHLAAABAAPrimaryYes
2CAR-T & TCR-T Therapies
CodeHLAAABACPrimaryNo
3Rare Oncology & Hematologic Malignancy Therapies
CodeHLAIAIACPrimaryNo
4Oncology & Hematology Pharmaceuticals
CodeHLAIAAACPrimaryNo
NAICS code3 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Pharmaceutical Preparation Manufacturing325412
  • Pharmaceutical and Medicine Manufacturing32541
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
Product category
Cell Therapy / CAR T-cell Biologics
Social media profiles2 records
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Commercial CAR T-cell therapies
TypeOne Time License
Description

Revenue from sale of approved CAR T-cell therapy products including Yescarta and Tecartus. Yescarta generated approximately $1.6 billion in 2024. Therapies are one-time treatments customized for each patient.

dcatvci.org
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

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

Cost components6 values
Technology or R&D, Operations, Personnel, Infrastructure, Marketing or Sales, Supply Chain
Pricing details1 tier
1Yescarta commercial therapy
ModelOne time/ perpetual licenseBilling cadencePay-as-you-go
Notes

High-cost one-time cancer treatment; exact pricing not publicly disclosed but market reports indicate CAR-T therapies range from $373,000 to $475,000 in the U.S. market

dcatvci.org
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Kite Pharma designs, develops, and manufactures autologous CAR T-cell therapies that harness a patient's own immune system to treat relapsed or refractory blood cancers. Its commercial products include Yescarta for large B-cell lymphoma, follicular lymphoma, and primary central nervous system lymphoma, and Tecartus for mantle cell lymphoma and B-cell acute lymphoblastic leukemia. Each dose is individually manufactured per patient through a five-step cell engineering process and delivered through qualified oncology treatment centers worldwide.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 6 values shown
  • 74% overall response rate in ZUMA-1 trial for aggressive non-Hodgkin lymphoma
+5 more records
Product overview1 text field

Kite Pharma is a biopharmaceutical company focused exclusively on cell therapy to treat and potentially cure cancer. The company's core offerings include Yescarta (axicabtagene ciloleucel), a CD19-directed CAR T-cell therapy for large B-cell lymphoma and follicular lymphoma, and its pipeline includes investigational therapies such as anito-cel (BCMA-directed CAR T for multiple myeloma), KITE-363 (dual-targeting CD19/CD20 CAR T), KITE-222 (CLL-1 targeted for AML), and KITE-753 (bicistronic CAR T). Kite operates the world's largest dedicated in-house cell therapy manufacturing network with facilities in the U.S. (California, Maryland), Netherlands, and distribution in Japan, serving over 300 treatment centers globally.

Product and service3 records
1Yescarta (axicabtagene ciloleucel)
CategoryCommercial CAR T-cell therapy
Description

CD19-directed genetically modified autologous T cell immunotherapy (CAR T-cell therapy) indicated for adult patients with relapsed/refractory large B-cell lymphoma and follicular lymphoma, manufactured individually for each patient using their own T cells.

2Tecartus (brexucabtagene autoleucel)
CategoryCommercial CAR T-cell therapy
Description

Autologous CAR T-cell therapy directed at CD19 for adult patients with relapsed/refractory mantle cell lymphoma and B-cell acute lymphoblastic leukemia, manufactured individually for each patient.

3Anito-cel (anitocabtagene autoleucel)
CategoryPipeline CAR T-cell therapy
Description

Investigational BCMA-directed CAR T-cell therapy using proprietary D-Domain binder technology for adult patients with relapsed/refractory multiple myeloma, co-developed with Arcellx, with planned U.S. launch in 2026.

Scale indicator6 records

Each record includes

Type, Value, Description, Source

Partnership7 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-10-17
Description

Global licensing agreement with Chinese biotech Pregene involving $120 million upfront payment and potential milestones up to $1.52 billion ($1.64 billion total deal value) to accelerate development of in vivo CAR-T therapies for oncology and autoimmune diseases.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-08-21
Description

Kite Pharma agreed to acquire Interius BioTherapeutics for $350 million in cash. Interius develops in vivo CAR-T cell therapies that could make cancer treatments more accessible by programming T cells directly inside the patient's body.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2023-02-22
Description

Strategic research and licensing agreement with University of Pennsylvania as part of Kite's acquisition of Tmunity Therapeutics, enhancing cell therapy research and pipeline assets. Involves further funding and potential future financial benefits for Penn researchers.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Co-development and co-commercialization partnership for anito-cel, a BCMA-directed CAR T-cell therapy for relapsed/refractory multiple myeloma. Gilead Sciences acquired Arcellx for $7.8 billion in 2026, gaining full control of the therapy. PDUFA date December 23, 2026.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Partnership agreement signed at Global Health Exhibition 2025 to improve local access to advanced treatments, develop innovative therapies, and build local healthcare talent in Saudi Arabia.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Investigator-sponsored study conducted by Dana-Farber supporting FDA label update for Yescarta in relapsed/refractory primary central nervous system lymphoma, demonstrating manageable safety profile with no new safety signals.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Strategic collaboration with Seattle biotech Accipiter Biosciences for development of de novo protein therapeutics. Kite Pharma collaboration alongside Pfizer as part of company's $12.7 million seed funding round.

Recent move9 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight7 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Novartis commercializes Kymriah, the first FDA-approved CAR-T therapy, targeting pediatric ALL and diffuse large B-cell lymphoma. It is a foundational direct peer with overlapping indications and similar autologous manufacturing model.

TypeEmerging player
Description

Sana Biotechnology is developing in vivo cell engineering platforms (including in vivo CAR-T) that could potentially disrupt Kite's autologous manufacturing model. It is an early-stage peer with thematic overlap on Kite's newly acquired Interius/Pregene in vivo CAR-T programs.

TypeEmerging player
Description

Caribou is developing allogeneic CAR-T cell therapies using CRISPR gene editing for hematologic cancers. It is an emerging peer with partial overlap on CAR-T modality and indication space, targeting similar patient populations as Kite.

TypeEmerging player
Description

Allogene is a leading allogeneic (off-the-shelf) CAR-T developer targeting the same hematologic malignancies as Kite. Its platform aims to disrupt Kite's autologous manufacturing model with ready-to-use cell therapies.

TypeEmerging player
Description

Adaptimmune commercializes Tecelra, a TCR-T cell therapy for synovial sarcoma, and is developing next-generation cell therapies for solid tumors. It is an adjacent cell therapy peer in the engineered T-cell category that overlaps with Kite's CAR-T pipeline.

TypeEmerging player
Description

CRISPR Therapeutics (partnered with Vertex) developed Casgevy, the first CRISPR-based cell therapy, for sickle cell disease and beta thalassemia. It is an adjacent cell therapy player leveraging gene editing in the same autologous cell engineering paradigm as Kite.

TypeOthers
Description

Iovance commercializes Amtagvi, the first FDA-approved tumor-infiltrating lymphocyte (TIL) therapy for melanoma, representing an adjacent cell therapy modality. It expands the engineered cell therapy category that Kite operates in, though TIL and CAR-T are distinct platforms.

TypeDirect peer
Description

BMS commercializes Brexu-cel (mantle cell lymphoma) and Abecma (BCMA CAR-T for multiple myeloma), making it the closest direct CAR-T competitor to Kite's Tecartus and anito-cel. Together Kite and BMS control 70%+ of the CAR-T market across overlapping indications.

TypeEmerging player
Description

Autolus commercializes Aucatzyl, a CD19 CAR-T therapy for adult ALL, directly competing with Kite's Tecartus in the B-ALL indication. It is a focused CAR-T peer with overlapping hematologic malignancy targets.

TypeDirect peer
Description

Legend Biotech (partnered with Johnson & Johnson) commercializes Carvykti, a BCMA-directed CAR-T therapy for multiple myeloma. It directly competes with Kite's anito-cel in the same relapsed/refractory multiple myeloma indication.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 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

Named customers4 records

Each record includes

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

Segment2 records

Each record includes

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

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
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature6 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 rounds5 records

Each record includes

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

Investors4 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&A2 records

Each record includes

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

Investment16 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 →

Kite Pharma

Cell Therapy / CAR T-cell Biologicskitepharma.com

Kite Pharma is a Gilead Sciences subsidiary that develops and commercializes autologous CAR T-cell therapies for relapsed or refractory blood cancers, distributing Yescarta and Tecartus through 300+ qualified treatment centers worldwide while advancing a pipeline of next-generation and in vivo cell therapies.

What Kite Pharma does

Kite Pharma, Inc. is a clinical-stage and commercial-stage biotechnology company focused exclusively on autologous CAR T-cell therapies for the treatment of relapsed or refractory blood cancers. The company engineers a patient's own T cells ex vivo to express chimeric antigen receptors targeting tumor-associated antigens including CD19, CD20, BCMA, and CLL-1, and operates as a wholly-owned subsidiary of Gilead Sciences following its 2017 acquisition for approximately $11.9 billion. Its core technology is autologous CAR T-cell therapy, with each dose custom-manufactured per patient through a five-step process of collection, isolation, engineering with a CAR gene, expansion, and reinfusion.

Kite's commercial portfolio is anchored by Yescarta (axicabtagene ciloleucel), a CD19-directed CAR T-cell therapy approved for large B-cell lymphoma, follicular lymphoma, and (as of February 2026) primary central nervous system lymphoma, which generated approximately $1.6 billion in 2024 revenue. Tecartus (brexucabtagene autoleucel) is a second approved product for relapsed/refractory mantle cell lymphoma and B-cell acute lymphoblastic leukemia. The clinical pipeline comprises anito-cel (BCMA-directed CAR-T for multiple myeloma, co-developed with Arcellx and now fully owned by Gilead following its $7.8 billion acquisition completed April 2026, with a December 23, 2026 PDUFA date), KITE-363 (dual CD19/CD20 CAR-T for LBCL), KITE-222 (CLL-1 CAR-T for AML, FDA Orphan Drug Designation), and KITE-753 (next-generation bicistronic CAR-T). The company has additionally moved into in vivo CAR-T through the $350 million Interius BioTherapeutics acquisition (announced August 2025) and the $1.64 billion Pregene Biopharma licensing deal (October 2025).

The business model is the sale of one-time, high-cost individualized treatments (U.S. market pricing in the $373,000-$475,000 range) reimbursed through a mix of private insurance, Medicare, and national health systems. Distribution runs through a network of 300+ qualified treatment centers across the U.S., Canada, Australia, Europe, Brazil, Singapore, Saudi Arabia, a joint venture in China, and a licensing partner in Japan. Kite operates what it describes as the world's largest dedicated in-house cell therapy manufacturing network, with facilities in Santa Monica (headquarters), Frederick, Maryland (manufacturing, 500+ jobs by end of 2026), and Hoofddorp, Netherlands (a EUR 185 million facility producing over 4,000 cell therapies annually). Gilead/Kite led global cell and gene therapy sales with 15% market share in 2024, and together with Bristol Myers Squibb accounts for over 70% of the CAR-T market.

Kite Pharma firmographics

Firmographics
Name
Kite Pharma
Legal name
Kite Pharma, Inc.
Website
https://kitepharma.com
Company type
Private
Founded year
2017
Operating status
Operating
Headcount range
1,001–5,000 employees
Short description
Kite Pharma is a Gilead Sciences subsidiary that develops and commercializes autologous CAR T-cell therapies for relapsed or refractory blood cancers, distributing Yescarta and Tecartus through 300+ qualified treatment centers worldwide while advancing a pipeline of next-generation and in vivo cell therapies.
Ownership category
akta.pro rank

Kite Pharma industry classification

Industry
Product category
Cell Therapy / CAR T-cell Biologics
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Pharmaceutical Preparation Manufacturing (325412), Pharmaceutical and Medicine Manufacturing (32541)
SIC
Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834)
akta.pro primary industry
Cell Therapy Developers (Autologous) (HLAAABAA)
akta.pro secondary industries
CAR-T & TCR-T Therapies (HLAAABAC), Rare Oncology & Hematologic Malignancy Therapies (HLAIAIAC), Oncology & Hematology Pharmaceuticals (HLAIAAAC)

Keywords

  • CAR T-cell therapy
  • Cell therapy products
  • Autologous immunotherapy
  • Cancer cell therapy
  • Oncology biologics manufacturing

Where Kite Pharma is headquartered

Location

Headquarters

HQ city
Los Angeles
HQ country
United States
HQ region
North America

Offices4 records

Markets served

Kite Pharma business model

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

Revenue model

  1. Commercial CAR T-cell therapies: Revenue from sale of approved CAR T-cell therapy products including Yescarta and Tecartus. Yescarta generated approximately $1.6 billion in 2024. Therapies are one-time treatments customized for each patient.

Pricing tiers

ModelBillingPrice
One time/ perpetual licensePay-as-you-goYescarta commercial therapy

Go-to-market motion1 record

Distribution channels3 records

Marketing channels6 records

Kite Pharma product offering

Product offering

Core offering

Kite Pharma designs, develops, and manufactures autologous CAR T-cell therapies that harness a patient's own immune system to treat relapsed or refractory blood cancers. Its commercial products include Yescarta for large B-cell lymphoma, follicular lymphoma, and primary central nervous system lymphoma, and Tecartus for mantle cell lymphoma and B-cell acute lymphoblastic leukemia. Each dose is individually manufactured per patient through a five-step cell engineering process and delivered through qualified oncology treatment centers worldwide.

Product overview

Kite Pharma is a biopharmaceutical company focused exclusively on cell therapy to treat and potentially cure cancer. The company's core offerings include Yescarta (axicabtagene ciloleucel), a CD19-directed CAR T-cell therapy for large B-cell lymphoma and follicular lymphoma, and its pipeline includes investigational therapies such as anito-cel (BCMA-directed CAR T for multiple myeloma), KITE-363 (dual-targeting CD19/CD20 CAR T), KITE-222 (CLL-1 targeted for AML), and KITE-753 (bicistronic CAR T). Kite operates the world's largest dedicated in-house cell therapy manufacturing network with facilities in the U.S. (California, Maryland), Netherlands, and distribution in Japan, serving over 300 treatment centers globally.

Differentiator

Problem solved

Functional benefit

Products and services

  • Yescarta (axicabtagene ciloleucel) CD19-directed genetically modified autologous T cell immunotherapy (CAR T-cell therapy) indicated for adult patients with relapsed/refractory large B-cell lymphoma and follicular lymphoma, manufactured individually for each patient using their own T cells.
  • Tecartus (brexucabtagene autoleucel) Autologous CAR T-cell therapy directed at CD19 for adult patients with relapsed/refractory mantle cell lymphoma and B-cell acute lymphoblastic leukemia, manufactured individually for each patient.
  • Anito-cel (anitocabtagene autoleucel) Investigational BCMA-directed CAR T-cell therapy using proprietary D-Domain binder technology for adult patients with relapsed/refractory multiple myeloma, co-developed with Arcellx, with planned U.S. launch in 2026.

Quantifiable outcome

  • 74% overall response rate in ZUMA-1 trial for aggressive non-Hodgkin lymphoma
  • +5 more outcomes

Companies that use Kite Pharma

Customer profile

Named customers4 records

Segments2 records

Ideal customer profiles1 record

Kite Pharma technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature6 records

Kite Pharma partnerships and signals

Strategic signal

Partnerships

Seven partnerships are on record, tiered core and minor.

  • Pregene BiopharmacoreStrategic or Co-development Partner · 17 October 2025Global licensing agreement with Chinese biotech Pregene involving $120 million upfront payment and potential milestones up to $1.52 billion ($1.64 billion total deal value) to accelerate development of in vivo CAR-T therapies for oncology and autoimmune diseases.
  • Interius BioTherapeuticscoreStrategic or Co-development Partner · 21 August 2025Kite Pharma agreed to acquire Interius BioTherapeutics for $350 million in cash. Interius develops in vivo CAR-T cell therapies that could make cancer treatments more accessible by programming T cells directly inside the patient's body.
  • University of PennsylvaniacoreStrategic or Co-development Partner · 22 February 2023Strategic research and licensing agreement with University of Pennsylvania as part of Kite's acquisition of Tmunity Therapeutics, enhancing cell therapy research and pipeline assets. Involves further funding and potential future financial benefits for Penn researchers.
  • ArcellxcoreStrategic or Co-development PartnerCo-development and co-commercialization partnership for anito-cel, a BCMA-directed CAR T-cell therapy for relapsed/refractory multiple myeloma. Gilead Sciences acquired Arcellx for $7.8 billion in 2026, gaining full control of the therapy. PDUFA date December 23, 2026.
  • King Faisal Specialist Hospital and Research Centre (KFSHRC)minorStrategic or Co-development PartnerPartnership agreement signed at Global Health Exhibition 2025 to improve local access to advanced treatments, develop innovative therapies, and build local healthcare talent in Saudi Arabia.
  • Dana-Farber Cancer InstituteminorStrategic or Co-development PartnerInvestigator-sponsored study conducted by Dana-Farber supporting FDA label update for Yescarta in relapsed/refractory primary central nervous system lymphoma, demonstrating manageable safety profile with no new safety signals.
  • Accipiter BiosciencesminorStrategic or Co-development PartnerStrategic collaboration with Seattle biotech Accipiter Biosciences for development of de novo protein therapeutics. Kite Pharma collaboration alongside Pfizer as part of company's $12.7 million seed funding round.

Scale indicators6 records

Recent moves9 records

Expansion highlights7 records

Kite Pharma competitors and assessment

Company assessment

Direct peers

  • Novartis: Novartis commercializes Kymriah, the first FDA-approved CAR-T therapy, targeting pediatric ALL and diffuse large B-cell lymphoma. It is a foundational direct peer with overlapping indications and similar autologous manufacturing model.
  • Bristol Myers Squibb: BMS commercializes Brexu-cel (mantle cell lymphoma) and Abecma (BCMA CAR-T for multiple myeloma), making it the closest direct CAR-T competitor to Kite's Tecartus and anito-cel. Together Kite and BMS control 70%+ of the CAR-T market across overlapping indications.
  • Legend Biotech: Legend Biotech (partnered with Johnson & Johnson) commercializes Carvykti, a BCMA-directed CAR-T therapy for multiple myeloma. It directly competes with Kite's anito-cel in the same relapsed/refractory multiple myeloma indication.

Emerging players

  • Sana Biotechnology: Sana Biotechnology is developing in vivo cell engineering platforms (including in vivo CAR-T) that could potentially disrupt Kite's autologous manufacturing model. It is an early-stage peer with thematic overlap on Kite's newly acquired Interius/Pregene in vivo CAR-T programs.
  • Caribou Biosciences: Caribou is developing allogeneic CAR-T cell therapies using CRISPR gene editing for hematologic cancers. It is an emerging peer with partial overlap on CAR-T modality and indication space, targeting similar patient populations as Kite.
  • Allogene Therapeutics: Allogene is a leading allogeneic (off-the-shelf) CAR-T developer targeting the same hematologic malignancies as Kite. Its platform aims to disrupt Kite's autologous manufacturing model with ready-to-use cell therapies.
  • Adaptimmune Therapeutics: Adaptimmune commercializes Tecelra, a TCR-T cell therapy for synovial sarcoma, and is developing next-generation cell therapies for solid tumors. It is an adjacent cell therapy peer in the engineered T-cell category that overlaps with Kite's CAR-T pipeline.
  • CRISPR Therapeutics: CRISPR Therapeutics (partnered with Vertex) developed Casgevy, the first CRISPR-based cell therapy, for sickle cell disease and beta thalassemia. It is an adjacent cell therapy player leveraging gene editing in the same autologous cell engineering paradigm as Kite.
  • Autolus Therapeutics: Autolus commercializes Aucatzyl, a CD19 CAR-T therapy for adult ALL, directly competing with Kite's Tecartus in the B-ALL indication. It is a focused CAR-T peer with overlapping hematologic malignancy targets.

Others

  • Iovance Biotherapeutics: Iovance commercializes Amtagvi, the first FDA-approved tumor-infiltrating lymphocyte (TIL) therapy for melanoma, representing an adjacent cell therapy modality. It expands the engineered cell therapy category that Kite operates in, though TIL and CAR-T are distinct platforms.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

Kite Pharma social profiles

Digital presence

Kite Pharma financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Kite Pharma leadership team

Management profile

Number of profiles

Profiles5 records

Kite Pharma funding detail

Funding detail

Funding overview

Funding rounds5 records

Investors4 records

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

Kite Pharma M&A and investment

M&A and investment

M&A2 records

Investments16 records

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

Frequently asked questions about Kite Pharma

What does Kite Pharma do?

Kite Pharma designs, develops, and manufactures autologous CAR T-cell therapies that harness a patient's own immune system to treat relapsed or refractory blood cancers. Its commercial products include Yescarta for large B-cell lymphoma, follicular lymphoma, and primary central nervous system lymphoma, and Tecartus for mantle cell lymphoma and B-cell acute lymphoblastic leukemia. Each dose is individually manufactured per patient through a five-step cell engineering process and delivered through qualified oncology treatment centers worldwide.

Is Kite Pharma a public or private company?

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

When was Kite Pharma founded?

Kite Pharma was founded in 2017. It employs 1,001 to 5,000 people.

Where is Kite Pharma based?

Kite Pharma is headquartered in Los Angeles, United States, in the North America region.

How does Kite Pharma make money?

One revenue line is on record: commercial CAR T-cell therapies.

Who are Kite Pharma's main competitors?

Direct peers on record are Novartis, Bristol Myers Squibb and Legend Biotech. Emerging players are Sana Biotechnology, Caribou Biosciences, Allogene Therapeutics, Adaptimmune Therapeutics, CRISPR Therapeutics and Autolus Therapeutics. Iovance Biotherapeutics is listed as an others.

Does Kite Pharma have an API?

No public API is recorded for Kite Pharma.

What industry is Kite Pharma in?

Kite Pharma's product category is Cell Therapy / CAR T-cell Biologics. Its primary akta.pro industry code is HLAAABAA, Cell Therapy Developers (Autologous), with a secondary code of HLAAABAC, CAR-T & TCR-T Therapies. Its NAICS code is 325414 and its SIC code is 2836.

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Phirda双靶点 CAR-T:细胞疗法的下一个价值周期CD20/CD19 dual-target CAR-T therapies are advancing to address antigen escape, with Miltenyi's zamto-cel seeking EMA approval and C-CAR039 showing 5-year PFS of 60.1 months. Global MNCs and Chinese firms are investing, and regulatory policies support these products.GenengnewsNew Cytometry Technique for Characterizing Viral VectorsKite Pharma, a Gilead Company, has developed a flow virometry technique to analyze individual lentiviral vector particles, measuring attributes such as size and surface proteins. The method preserves differences between particles that Western blotting averages out, and Kite plans to apply it throughout development, including batch-to-batch consistency checks.OncoDailyThe Next Frontier in R/R ALL: CAR-T, Bispecifics, and Emerging StrategiesThe article outlines the evolving treatment landscape for relapsed or refractory acute lymphoblastic leukemia (R/R ALL), highlighting the shift from conventional chemotherapy to immunotherapies such as CAR-T cells, bispecific antibodies like blinatumomab, and targeted agents including menin inhibitors. It details clinical trial data for products from Kite Pharma (brexucabtagene autoleucel) and Pfizer (blinatumomab, inotuzumab ozogamicin), emphasizing strategies to overcome antigen escape and resistance mechanisms. The piece concludes by promoting the LeukO 2026 congress organized by OncoDaily, where experts will discuss these emerging therapeutic strategies.FierceBiotechStudy of Yescarta patients reveals genetic red flags for CAR-T therapy side effectsResearchers led by Mark Leick at Massachusetts General Hospital analyzed data from Kite Pharma's Zuma-1 and Zuma-7 clinical trials of Yescarta (axi-cel), a CAR-T cell therapy for lymphoma, and identified genetic markers including STXBP2, ADAMTSL3, and PTPN22 associated with toxicity risk and CAR-T cell proliferation. The study, published in Science Immunology, found that patients with STXBP2 mutations all experienced treatment toxicity, while ADAMTSL3 variants showed protective effects and PTPN22 gene variants were linked to CAR-T cell expansion ability. The findings suggest that intentional modifications of genes like PTPN22 could be incorporated into CAR-T manufacturing protocols to improve cell expansion and reduce required doses.BioSpaceKite Helps Fund American Cancer Society’s Expanded Efforts to Advance Innovation and Improve Support for People Facing Blood CancersKite, a Gilead company, announced an expanded sponsorship of American Cancer Society programs to improve access to CAR T-cell therapy for blood cancer patients. The initiative, launched in 2025, provided grants in 16 states and identified caregiver support gaps. The next phase will close remaining gaps across the care continuum.U.S. Food and Drug AdministrationYESCARTAThe article provides product information for the drug YESCARTA (axicabtagene ciloleucel), manufactured by Kite Pharma Inc. It details the approved indications for treating various forms of large B-cell lymphoma and follicular lymphoma in adult patients who have received prior systemic therapies. The text notes that continued approval is contingent upon verification of clinical benefit in confirmatory trials.Labiotech.euEight in vivo CAR T biotechs to follow closelyEight in vivo CAR-T biotechs are profiled, including Umoja Biopharma, Vyriad, CPTx, Legend, Strand, Alaya.bio, AAVivo, and Create Medicines. Their lead candidates target CD19, BCMA, or other antigens, with some in clinical trials. Big pharma is acquiring these companies for billions.Business Wire BlogCencora to Support U.S. Distribution of Kite’s CAR T-Cell TherapiesCencora announced an agreement with Kite to support U.S. distribution of Kite's FDA-approved CAR T-cell therapies Yescarta and Tecartus. The collaboration aims to facilitate efficient access at expanding treatment centers, including health systems and community oncology practices.Labiotech.euIn vivo CAR-T gains momentum as big pharma bets billionsBig pharma is shifting toward in vivo CAR-T therapies, with Lilly planning a $7B acquisition of Kelonia Therapeutics. Other deals include AstraZeneca's $1B purchase of EsoBiotec and Gilead's $350M buy of Interius BioTherapeutics. The shift aims to overcome manufacturing and cost barriers of ex vivo CAR-T.The Pharma LetterUpdated EU safety info for Yescarta and TecartusGilead Sciences and its Kite Oncology subsidiary announced that the European Medicines Agency approved a Type II variation to the Summary of Product Characteristics for Yescarta and Tecartus. The change supports a more flexible, evidence-based post-infusion management approach.