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Adaptimmune

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uuid0002o4t

Namestring
Adaptimmune
Legal namestring
Adaptimmune Limited
Websiteurl
adaptimmune.com
Company typeenum
Public
Founded yearint
2015
Descriptiontext

Adaptimmune is a clinical-stage biotechnology company headquartered in Oxford, United Kingdom, that engineers T-cell receptor (TCR) therapies to treat solid tumors. Founded in 2008 and previously listed on Nasdaq under the ticker ADAP, the company built a pipeline of autologous cell therapies targeting tumor-associated antigens including MAGE-A4, PRAME, and CD70. Its lead product, Tecelra (afamitresgene autoleucel), received FDA approval in August 2024 for synovial sarcoma, becoming the first engineered TCR T-cell therapy approved for a solid tumor indication. The company also developed an allogeneic T-cell platform, which became the basis of a September 2021 collaboration with Genentech that included $150 million upfront and more than $3 billion in potential milestones.

Operationally, Adaptimmune served specialty oncology centers treating small solid tumor patient populations through a personalized autologous cell therapy model. In July 2025 the company divested its commercial cell therapy assets (Tecelra, lete-cel, afami-cel, and uza-cel) to US WorldMeds for $55 million cash plus up to $30 million in milestones, exiting commercial product ownership. In November 2025 the company voluntarily delisted from Nasdaq, consolidated leadership under a combined CEO/CFO (Christopher Hill) and a new Chairman (Lawrence Alleva), and retained only preclinical assets (PRAME, CD70, allogeneic platform) plus the Genentech collaboration economics. Funding has historically come through public equity, a 2023 merger with TCR2 Therapeutics, and a May 2024 $125 million debt facility with Hercules Capital (initial $25 million tranche). Post-divestiture, the entity operates as a focused R&D organization without a marketed product.

Short descriptiontext

Adaptimmune is an Oxford-based biotechnology company developing engineered T-cell receptor therapies for solid tumors. Following FDA approval of Tecelra in 2024, it divested its commercial cell therapy assets to US WorldMeds in 2025 and now operates as a preclinical R&D entity retaining PRAME, CD70, and allogeneic platform programs.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersOxford, United Kingdom
HQ citystring
Oxford
HQ countrystring
United Kingdom
HQ regionstring
Europe
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
engineered T-cell therapy, cell therapy platform, solid tumor immunotherapy, TCR cell therapy, cancer immunotherapy
Industry4 codes
1Cell Therapy Developers (Autologous)
CodeHLAAABAAPrimaryYes
2CAR-T & TCR-T Therapies
CodeHLAAABACPrimaryNo
3Cell Therapy Developers (Allogeneic/Off-the-shelf)
CodeHLAAABABPrimaryNo
4Cell Therapy Enabling Technologies (gene editing, cell engineering, delivery methods)
CodeHLAAABALPrimaryNo
NAICS code2 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Pharmaceutical Preparation Manufacturing325412
SIC code1 code
  • Biological Products, (No Disgnostic Substances)2836
Product category
Cancer Immunotherapy / Engineered Cell Therapy
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model5 records
1Product Sales (Tecelra)
TypeOne Time License
Description

Following FDA accelerated approval in 2024, Adaptimmune commercialized afamitresgene autoleucel (Tecelra) for adults with unresectable or metastatic synovial sarcoma. The company sold these commercial assets to US WorldMeds in July 2025 for $55 million cash plus up to $30 million in milestone payments.

adaptimmune.com
2Lete-cel (future)
TypeOne Time License
Description

Lete-cel cell therapy received anticipated FDA approval in 2026. This product was included in the asset sale to US WorldMeds, with US WorldMeds planning to bring it to market.

adaptimmune.com
3Strategic Partnerships and Milestones
TypeLicensing Royalties
Description

Collaboration with Genentech announced September 2021 included $150 million upfront payment with potential milestones exceeding $3 billion for developing allogeneic T-cell therapies.

adaptimmune.com
4Debt Financing
TypeLicensing Royalties
Description

$125 million five-year term loan facility with Hercules Capital, with initial $25 million tranche available at closing and additional tranches contingent on product approvals and conditions. This represents financing rather than operational revenue.

adaptimmune.com
5Asset Sale Proceeds
TypeTransaction Fee
Description

Sale of TECELRA, lete-cel, afami-cel, and uza-cel cell therapy assets to US WorldMeds for $55 million cash plus up to $30 million in milestone payments. Adaptimmune retains rights to preclinical assets including PRAME, CD70, and allogeneic programs.

adaptimmune.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

Each record includes

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

Cost components4 values
Technology or R&D, Personnel, Operations, Supply Chain
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 4 records shown
1Tecelra
Description

FDA-approved engineered TCR T-cell therapy for adults with unresectable or metastatic synovial sarcoma - sold to US WorldMeds in July 2025

adaptimmune.com
+3 more records
Core offering1 text field

Adaptimmune develops engineered T-cell receptor (TCR) T-cell therapies designed to recognize and destroy solid tumor cancer cells expressing specific antigens. Its commercial product Tecelra (afamitresgene autoleucel) became the first FDA-approved engineered TCR T-cell therapy for a solid tumor (synovial sarcoma) in August 2024. Following the July 2025 sale of Tecelra, lete-cel, afami-cel, and uza-cel to US WorldMeds, the company retains preclinical assets (PRAME and CD70 programs) and an allogeneic T-cell therapy platform developed in partnership with Genentech.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 value
  • FDA accelerated approval of Tecelra in August 2024 for synovial sarcoma
Product overview1 text field

Adaptimmune is a biotechnology company focused on developing engineered T-cell therapies for solid tumor cancers. The company's product portfolio includes FDA-approved and investigational cell therapies. Tecelra (afamitresgene autoleucel) is the company's FDA-approved flagship product for synovial sarcoma, representing the first engineered TCR T-cell therapy approved for a solid tumor. The pipeline also includes afami-cel, lete-cel, and uza-cel (all sold to US WorldMeds in 2025), as well as retained preclinical programs targeting PRAME and CD70 antigens. The company operates a technology platform for allogeneic T-cell therapy development.

Product and service3 records
1PRAME-directed T-cell therapy
CategoryPreclinical Cell Therapy
Description

Preclinical engineered TCR T-cell therapy targeting the PRAME antigen for solid tumors. Adaptimmune retained rights to this program following the July 2025 sale of commercial cell therapy assets to US WorldMeds.

2CD70-directed T-cell therapy
CategoryPreclinical Allogeneic Cell Therapy
Description

Preclinical allogeneic T-cell therapy program targeting the CD70 antigen. Adaptimmune retained rights to this program following the July 2025 sale of commercial cell therapy assets to US WorldMeds.

3Allogeneic T-cell therapy platform
CategoryCell Therapy Platform Technology
Description

Technology platform for developing personalized off-the-shelf (allogeneic) T-cell therapies for cancer patients. Developed and validated under the Genentech strategic collaboration (September 2021) with $150 million upfront and over $3 billion in potential milestones. Platform rights retained by Adaptimmune following the 2025 asset sales.

Scale indicator7 records

Each record includes

Type, Value, Description, Source

Partnership5 partners
Strategic tierMinorTypeOthersAnnounced on2025-10-27
Description

Dr. Helen Tayton-Martin, who previously co-founded and served as COO and Chief Business & Strategy Officer at Adaptimmune, was appointed CEO of Evaxion. Dr. Tayton-Martin oversaw strategic partnerships and transatlantic growth at Adaptimmune through to its Nasdaq IPO.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2025-07-28
Description

Sale of TECELRA, lete-cel, afami-cel, and uza-cel cell therapy assets to US WorldMeds for $55 million cash plus up to $30 million in milestone payments. US WorldMeds plans to bring lete-cel to market and continue development of uza-cel in collaboration with Galapagos. Transaction financed by debt led by Oaktree Capital Management with participation from Athyrium Capital Management.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-07-28
Description

Collaboration with Galapagos on continued development of uza-cel following the asset sale to US WorldMeds. Galapagos will work with US WorldMeds on the uza-cel program.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2023-06-01
Description

Strategic all-stock combination with TCR2 Therapeutics completed in June 2023 to create a leading cellular therapy company focused on solid tumors. The merger combined complementary technologies and clinical assets including TCR T-cell therapy programs and allogeneic approaches. The combined entity planned to advance a pipeline with BLA submission for afami-cel in mid-2023.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2021-09-07
Description

Strategic collaboration with Genentech (member of Roche group) to develop and commercialize cancer-targeted allogeneic T-cell therapies. The partnership involves extensive research and development efforts with an upfront payment of $150 million and potential milestones exceeding $3 billion. Adaptimmune aims to leverage its platform for personalized allogeneic cell therapies for cancer patients.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Iovance is a leading cell therapy company developing tumor-infiltrating lymphocyte (TIL) therapies for solid tumors. Both companies are approved autologous cell therapy developers in solid tumor oncology, with similar commercial infrastructure needs and patient identification challenges.

TypeDirect peer
Description

Allogene is a clinical-stage biotechnology company pioneering allogeneic ("off-the-shelf") CAR-T cell therapies. Both companies are pursuing engineered T-cell therapies for cancer with allogeneic platforms, addressing the manufacturing scalability challenge that limits autologous approaches.

3Adaptimmune's TCR-T direct competitors
TypeDirect peer
Description

Tessa Therapeutics and other TCR-T developers for solid tumors compete directly with Adaptimmune's engineered TCR-T platform, particularly for indications like sarcoma and other solid tumors.

TypeBroad incumbent
Description

Kite, a Gilead company, is an established leader in CAR-T cell therapy with approved products (Yescarta, Tecartus). While primarily focused on CAR-T rather than TCR-T, Kite operates in adjacent cell therapy space with deeper commercialization experience and broader solid tumor ambitions.

TypeBroad incumbent
Description

Novartis pioneered the first FDA-approved CAR-T therapy (Kymriah) and has significant R&D investments in next-generation cell therapies for solid tumors, making it a broad peer with larger resources pursuing adjacent technologies.

TypeBroad incumbent
Description

BMS has multiple approved cell therapies (Breyanzi, Abecma) and is actively expanding into solid tumor cell therapy through internal development and partnerships. As a large pharma with established commercial cell therapy infrastructure, BMS represents both a competitor and potential partner.

TypeEmerging player
Description

CRISPR Therapeutics pioneers gene-edited cell therapies, including allogeneic CAR-T approaches. It is a partial competitor in next-generation cell engineering, sharing the platform innovation ethos that defines Adaptimmune's TCR-T work.

TypeEmerging player
Description

Fate Therapeutics is developing iPSC-derived off-the-shelf cell therapies for cancer and immune disorders. Its focus on iPSC-derived NK and T-cell therapies represents an alternative allogeneic approach to Adaptimmune's engineered TCR-T platform.

TypeEmerging player
Description

Cellectis is a clinical-stage biotech developing allogeneic CAR-T therapies using gene editing. It shares with Adaptimmune a focus on overcoming the manufacturing and accessibility limitations of autologous cell therapies through next-generation engineering.

TypeEmerging player
Description

Lyell Immunopharma develops next-generation T-cell therapies for solid tumors, focusing on technologies to overcome T-cell exhaustion and improve persistence. It is a peer in the engineered T-cell space targeting solid tumor indications with similar technical challenges.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers2 records

Each record includes

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

Segment1 record

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 maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles10 records

Each record includes

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

Subsidiaries3 records

Each record includes

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

No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds9 records

Each record includes

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

Investors17 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&A1 record

Each record includes

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

Investment

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 →

Adaptimmune

Cancer Immunotherapy / Engineered Cell Therapyadaptimmune.com

Adaptimmune is an Oxford-based biotechnology company developing engineered T-cell receptor therapies for solid tumors. Following FDA approval of Tecelra in 2024, it divested its commercial cell therapy assets to US WorldMeds in 2025 and now operates as a preclinical R&D entity retaining PRAME, CD70, and allogeneic platform programs.

What Adaptimmune does

Adaptimmune is a clinical-stage biotechnology company headquartered in Oxford, United Kingdom, that engineers T-cell receptor (TCR) therapies to treat solid tumors. Founded in 2008 and previously listed on Nasdaq under the ticker ADAP, the company built a pipeline of autologous cell therapies targeting tumor-associated antigens including MAGE-A4, PRAME, and CD70. Its lead product, Tecelra (afamitresgene autoleucel), received FDA approval in August 2024 for synovial sarcoma, becoming the first engineered TCR T-cell therapy approved for a solid tumor indication. The company also developed an allogeneic T-cell platform, which became the basis of a September 2021 collaboration with Genentech that included $150 million upfront and more than $3 billion in potential milestones.

Operationally, Adaptimmune served specialty oncology centers treating small solid tumor patient populations through a personalized autologous cell therapy model. In July 2025 the company divested its commercial cell therapy assets (Tecelra, lete-cel, afami-cel, and uza-cel) to US WorldMeds for $55 million cash plus up to $30 million in milestones, exiting commercial product ownership. In November 2025 the company voluntarily delisted from Nasdaq, consolidated leadership under a combined CEO/CFO (Christopher Hill) and a new Chairman (Lawrence Alleva), and retained only preclinical assets (PRAME, CD70, allogeneic platform) plus the Genentech collaboration economics. Funding has historically come through public equity, a 2023 merger with TCR2 Therapeutics, and a May 2024 $125 million debt facility with Hercules Capital (initial $25 million tranche). Post-divestiture, the entity operates as a focused R&D organization without a marketed product.

Adaptimmune firmographics

Firmographics
Name
Adaptimmune
Legal name
Adaptimmune Limited
Website
https://adaptimmune.com
Company type
Public
Founded year
2015
Operating status
Operating
Headcount range
101–250 employees
Short description
Adaptimmune is an Oxford-based biotechnology company developing engineered T-cell receptor therapies for solid tumors. Following FDA approval of Tecelra in 2024, it divested its commercial cell therapy assets to US WorldMeds in 2025 and now operates as a preclinical R&D entity retaining PRAME, CD70, and allogeneic platform programs.
Ownership category
akta.pro rank

Adaptimmune industry classification

Industry
Product category
Cancer Immunotherapy / Engineered Cell Therapy
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Pharmaceutical Preparation Manufacturing (325412)
SIC
Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Cell Therapy Developers (Autologous) (HLAAABAA)
akta.pro secondary industries
CAR-T & TCR-T Therapies (HLAAABAC), Cell Therapy Developers (Allogeneic/Off-the-shelf) (HLAAABAB), Cell Therapy Enabling Technologies (gene editing, cell engineering, delivery methods) (HLAAABAL)

Keywords

  • Engineered T-cell therapy
  • Cell therapy platform
  • Solid tumor immunotherapy
  • TCR cell therapy
  • Cancer immunotherapy

Where Adaptimmune is headquartered

Location

Headquarters

HQ city
Oxford
HQ country
United Kingdom
HQ region
Europe

Offices2 records

Markets served

Adaptimmune business model

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

Revenue model

  1. Product Sales (Tecelra): Following FDA accelerated approval in 2024, Adaptimmune commercialized afamitresgene autoleucel (Tecelra) for adults with unresectable or metastatic synovial sarcoma. The company sold these commercial assets to US WorldMeds in July 2025 for $55 million cash plus up to $30 million in milestone payments.
  2. Lete-cel (future): Lete-cel cell therapy received anticipated FDA approval in 2026. This product was included in the asset sale to US WorldMeds, with US WorldMeds planning to bring it to market.
  3. Strategic Partnerships and Milestones: Collaboration with Genentech announced September 2021 included $150 million upfront payment with potential milestones exceeding $3 billion for developing allogeneic T-cell therapies.
  4. Debt Financing: $125 million five-year term loan facility with Hercules Capital, with initial $25 million tranche available at closing and additional tranches contingent on product approvals and conditions. This represents financing rather than operational revenue.
  5. Asset Sale Proceeds: Sale of TECELRA, lete-cel, afami-cel, and uza-cel cell therapy assets to US WorldMeds for $55 million cash plus up to $30 million in milestone payments. Adaptimmune retains rights to preclinical assets including PRAME, CD70, and allogeneic programs.

Go-to-market motion1 record

Distribution channels2 records

Marketing channels6 records

Adaptimmune product offering

Product offering

Core offering

Adaptimmune develops engineered T-cell receptor (TCR) T-cell therapies designed to recognize and destroy solid tumor cancer cells expressing specific antigens. Its commercial product Tecelra (afamitresgene autoleucel) became the first FDA-approved engineered TCR T-cell therapy for a solid tumor (synovial sarcoma) in August 2024. Following the July 2025 sale of Tecelra, lete-cel, afami-cel, and uza-cel to US WorldMeds, the company retains preclinical assets (PRAME and CD70 programs) and an allogeneic T-cell therapy platform developed in partnership with Genentech.

Product overview

Adaptimmune is a biotechnology company focused on developing engineered T-cell therapies for solid tumor cancers. The company's product portfolio includes FDA-approved and investigational cell therapies. Tecelra (afamitresgene autoleucel) is the company's FDA-approved flagship product for synovial sarcoma, representing the first engineered TCR T-cell therapy approved for a solid tumor. The pipeline also includes afami-cel, lete-cel, and uza-cel (all sold to US WorldMeds in 2025), as well as retained preclinical programs targeting PRAME and CD70 antigens. The company operates a technology platform for allogeneic T-cell therapy development.

Differentiator

Problem solved

Functional benefit

Brands

  • Tecelra: FDA-approved engineered TCR T-cell therapy for adults with unresectable or metastatic synovial sarcoma - sold to US WorldMeds in July 2025
  • lete-cel
  • afami-cel
  • uza-cel

Products and services

  • PRAME-directed T-cell therapy Preclinical engineered TCR T-cell therapy targeting the PRAME antigen for solid tumors. Adaptimmune retained rights to this program following the July 2025 sale of commercial cell therapy assets to US WorldMeds.
  • CD70-directed T-cell therapy Preclinical allogeneic T-cell therapy program targeting the CD70 antigen. Adaptimmune retained rights to this program following the July 2025 sale of commercial cell therapy assets to US WorldMeds.
  • Allogeneic T-cell therapy platform Technology platform for developing personalized off-the-shelf (allogeneic) T-cell therapies for cancer patients. Developed and validated under the Genentech strategic collaboration (September 2021) with $150 million upfront and over $3 billion in potential milestones. Platform rights retained by Adaptimmune following the 2025 asset sales.

Quantifiable outcome

  • FDA accelerated approval of Tecelra in August 2024 for synovial sarcoma

Companies that use Adaptimmune

Customer profile

Named customers2 records

Segments1 record

Ideal customer profiles2 records

Adaptimmune technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Adaptimmune partnerships and signals

Strategic signal

Partnerships

Five partnerships are on record, tiered minor and core.

  • EvaxionminorOthers · 27 October 2025Dr. Helen Tayton-Martin, who previously co-founded and served as COO and Chief Business & Strategy Officer at Adaptimmune, was appointed CEO of Evaxion. Dr. Tayton-Martin oversaw strategic partnerships and transatlantic growth at Adaptimmune through to its Nasdaq IPO.
  • US WorldMedscoreChannel Partner/ Reseller/ Distributor · 28 July 2025Sale of TECELRA, lete-cel, afami-cel, and uza-cel cell therapy assets to US WorldMeds for $55 million cash plus up to $30 million in milestone payments. US WorldMeds plans to bring lete-cel to market and continue development of uza-cel in collaboration with Galapagos. Transaction financed by debt led by Oaktree Capital Management with participation from Athyrium Capital Management.
  • GalapagoscoreStrategic or Co-development Partner · 28 July 2025Collaboration with Galapagos on continued development of uza-cel following the asset sale to US WorldMeds. Galapagos will work with US WorldMeds on the uza-cel program.
  • TCR2 TherapeuticscoreStrategic or Co-development Partner · 1 June 2023Strategic all-stock combination with TCR2 Therapeutics completed in June 2023 to create a leading cellular therapy company focused on solid tumors. The merger combined complementary technologies and clinical assets including TCR T-cell therapy programs and allogeneic approaches. The combined entity planned to advance a pipeline with BLA submission for afami-cel in mid-2023.
  • Genentech (Roche)coreStrategic or Co-development Partner · 7 September 2021Strategic collaboration with Genentech (member of Roche group) to develop and commercialize cancer-targeted allogeneic T-cell therapies. The partnership involves extensive research and development efforts with an upfront payment of $150 million and potential milestones exceeding $3 billion. Adaptimmune aims to leverage its platform for personalized allogeneic cell therapies for cancer patients.

Scale indicators7 records

Recent moves7 records

Expansion highlights4 records

Adaptimmune competitors and assessment

Company assessment

Direct peers

  • Iovance Biotherapeutics: Iovance is a leading cell therapy company developing tumor-infiltrating lymphocyte (TIL) therapies for solid tumors. Both companies are approved autologous cell therapy developers in solid tumor oncology, with similar commercial infrastructure needs and patient identification challenges.
  • Allogene Therapeutics: Allogene is a clinical-stage biotechnology company pioneering allogeneic ("off-the-shelf") CAR-T cell therapies. Both companies are pursuing engineered T-cell therapies for cancer with allogeneic platforms, addressing the manufacturing scalability challenge that limits autologous approaches.
  • Adaptimmune's TCR-T direct competitors: Tessa Therapeutics and other TCR-T developers for solid tumors compete directly with Adaptimmune's engineered TCR-T platform, particularly for indications like sarcoma and other solid tumors.

Broad incumbents

  • Kite Pharma (Gilead): Kite, a Gilead company, is an established leader in CAR-T cell therapy with approved products (Yescarta, Tecartus). While primarily focused on CAR-T rather than TCR-T, Kite operates in adjacent cell therapy space with deeper commercialization experience and broader solid tumor ambitions.
  • Novartis: Novartis pioneered the first FDA-approved CAR-T therapy (Kymriah) and has significant R&D investments in next-generation cell therapies for solid tumors, making it a broad peer with larger resources pursuing adjacent technologies.
  • Bristol Myers Squibb: BMS has multiple approved cell therapies (Breyanzi, Abecma) and is actively expanding into solid tumor cell therapy through internal development and partnerships. As a large pharma with established commercial cell therapy infrastructure, BMS represents both a competitor and potential partner.

Emerging players

  • CRISPR Therapeutics: CRISPR Therapeutics pioneers gene-edited cell therapies, including allogeneic CAR-T approaches. It is a partial competitor in next-generation cell engineering, sharing the platform innovation ethos that defines Adaptimmune's TCR-T work.
  • Fate Therapeutics: Fate Therapeutics is developing iPSC-derived off-the-shelf cell therapies for cancer and immune disorders. Its focus on iPSC-derived NK and T-cell therapies represents an alternative allogeneic approach to Adaptimmune's engineered TCR-T platform.
  • Cellectis: Cellectis is a clinical-stage biotech developing allogeneic CAR-T therapies using gene editing. It shares with Adaptimmune a focus on overcoming the manufacturing and accessibility limitations of autologous cell therapies through next-generation engineering.
  • Lyell Immunopharma: Lyell Immunopharma develops next-generation T-cell therapies for solid tumors, focusing on technologies to overcome T-cell exhaustion and improve persistence. It is a peer in the engineered T-cell space targeting solid tumor indications with similar technical challenges.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights6 records

Customer concentration

Adaptimmune social profiles

Digital presence

Adaptimmune financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Adaptimmune leadership team

Management profile

Number of profiles

Profiles10 records

Adaptimmune subsidiaries and ownership

Company hierarchy

Subsidiaries3 records

Adaptimmune funding detail

Funding detail

Funding overview

Funding rounds9 records

Investors17 records

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

Adaptimmune M&A and investment

M&A and investment

M&A1 record

Investments

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

Frequently asked questions about Adaptimmune

What does Adaptimmune do?

Adaptimmune develops engineered T-cell receptor (TCR) T-cell therapies designed to recognize and destroy solid tumor cancer cells expressing specific antigens. Its commercial product Tecelra (afamitresgene autoleucel) became the first FDA-approved engineered TCR T-cell therapy for a solid tumor (synovial sarcoma) in August 2024. Following the July 2025 sale of Tecelra, lete-cel, afami-cel, and uza-cel to US WorldMeds, the company retains preclinical assets (PRAME and CD70 programs) and an allogeneic T-cell therapy platform developed in partnership with Genentech.

Is Adaptimmune a public or private company?

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

When was Adaptimmune founded?

Adaptimmune was founded in 2015. It employs 101 to 250 people.

Where is Adaptimmune based?

Adaptimmune is headquartered in Oxford, United Kingdom, in the Europe region.

How does Adaptimmune make money?

Five revenue lines are on record. Product Sales (Tecelra) is the primary driver. The others are lete-cel (future), strategic Partnerships and Milestones, debt Financing and asset Sale Proceeds.

Who are Adaptimmune's main competitors?

Direct peers on record are Iovance Biotherapeutics, Allogene Therapeutics and Adaptimmune's TCR-T direct competitors. Broad incumbents are Kite Pharma (Gilead), Novartis and Bristol Myers Squibb. Emerging players are CRISPR Therapeutics, Fate Therapeutics, Cellectis and Lyell Immunopharma.

Does Adaptimmune have an API?

No public API is recorded for Adaptimmune.

What industry is Adaptimmune in?

Adaptimmune's product category is Cancer Immunotherapy / Engineered Cell Therapy. 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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Live signals
MorningstarImmunoScape Appoints Peter Olagunju as Chief Executive OfficerImmunoScape appointed Peter Olagunju as CEO to guide its TCR-based cancer immunotherapy platform toward the clinic. Olagunju brings over 20 years of experience, including leading a Catalio Capital-backed company through a $14 million seed round. He will work with partners to advance the platform into clinical trials.European BiotechnologyCell therapies: breaking ­barriers in ­solid tumoursThe FDA approved Iovance's Amtagvi (lifileucel) for advanced melanoma in 2024 and Adaptimmune's Tecelra for synovial sarcoma in August 2025, both engineered cell therapies for solid tumours. Response rates were modest, with confirmatory trials required. Next-generation approaches like CAR-NKs and T-cell engagers are advancing, aiming to overcome barriers in solid tumours.BioXconomyUS WorldMeds takes over quartet of Adaptimmune cell therapies in $55m dealUS WorldMeds has acquired four cell therapies from Adaptimmune for an initial $55 million, with potential additional milestone payments of up to $30 million. The deal includes the FDA-approved Tecelra and three pipeline candidates, allowing US WorldMeds to continue their development while Adaptimmune uses proceeds to settle debt with Hercules Capital.Pharmacy TimesNovel Treatments and Operational Innovations Shape the Future of OncologyThis editorial introduction highlights three peer-reviewed articles in an oncology journal covering advances in cancer treatment and pharmacy operations. A study describes a technician-led workflow at a hospital specialty pharmacy designed to reduce oral oncology drug waste through proactive refill coordination. The FDA granted accelerated approval in 2024 to afamitresgene autoleucel (Tecelra, Adaptimmune, LLC) for adults with unresectable or metastatic synovial sarcoma, representing a meaningful advance in a disease with historically poor outcomes. The articles also review evolving treatment strategies for hepatocellular carcinoma, including immunotherapy and anti-VEGF monoclonal antibodies, which have expanded options for patients with advanced disease.NewsfileAdaptimmune Announces Changes to Board and Executive Leadership TeamAdaptimmune Therapeutics announced leadership changes effective November 14, 2025, appointing CFO Christopher Hill as CEO while retaining his CFO role, following the departure of Adrian Rawcliffe and COO William Bertrand in connection with restructuring. Lawrence Alleva was appointed Chairman, succeeding David Mott, and multiple board members resigned as the board was reduced to three members. The changes follow the company's voluntary delisting from Nasdaq on October 28, 2025, and the initiation of deregistration from SEC reporting obligations.American City Business JournalsAdaptimmune delists from Nasdaq after asset sale to US WorldMedsAdaptimmune has delisted from Nasdaq following the sale of its assets to US WorldMeds. The company's board cited the decision as a measure to eliminate significant costs associated with maintaining its status as a public company.NewsfileAdaptimmune Announces Delisting from NasdaqAdaptimmune Therapeutics plc announced its Board of Directors has decided to voluntarily delist the company's American Depositary Shares from The Nasdaq Capital Market and deregister under the Securities Exchange Act of 1934, with trading expected to be suspended on or around October 27, 2025. The decision follows the company's failure to regain compliance with Nasdaq's minimum $1.00 bid price rule and is intended to reduce costs associated with being a public reporting company. After delisting, the ADSs will transition to trading on the OTC Pink Limited Market, and the company expects to suspend SEC reporting obligations within 90 days of filing Form 25.BioSpaceAdaptimmune Announces Delisting from NasdaqAdaptimmune Therapeutics plc announced its Board of Directors has decided to delist the company's American Depositary Shares from The Nasdaq Capital Market and deregister under the Securities Exchange Act, with trading expected to be suspended on or about October 27, 2025, following a Form 25 filing with the SEC. The delisting comes after the company failed to regain compliance with Nasdaq's minimum bid price rule of $1.00 per share, having received a notice from the Nasdaq Hearings Panel in September 2025. Following delisting, ADSs will trade on the OTC Pink Limited Market, and the company expects to reduce costs associated with operating as a public reporting company.WHYYCentury Therapeutics and Adaptimmune layoffs in PhillyCentury Therapeutics laid off 72 workers, 54 of whom are Pennsylvania residents, while Adaptimmune sold cell therapy divisions for $55 million. Century's layoffs cost $3.7 million, and both companies reported losses, with Century's net income improving to $76 million in Q1 2025.BioPharma DiveAdaptimmune, seeking to stay afloat, sells off cell therapiesAdaptimmune agreed to sell its approved cell therapy Tecelra and two late-stage assets to US WorldMeds for up to $85 million. The deal includes $55 million upfront and potential $30 million in milestone payments, with Adaptimmune cutting its workforce by 62%.