Cell therapies with the potential to save lives.

A focused pipeline of late-stage assets.

A focused pipeline of late-stage assets.

Redefining cancer treatment demands a robust and focused pipeline paving the way for successful outcomes.

Our engineered T-cell therapies offer specificity and are administered in a single dose. We are guided 
by rigorous scientific principles and a strategically focused development pipeline that prioritizes late-stage assets like  afamitresgene autoleucel (“afami-cel”) and letetresgene autoleucel (“lete-cel”).

Our Clinical Pipeline

Adaptimmune is developing an industry-leading T cell therapy pipeline in solid tumors and has a deep pipeline of identified and proprietary targets for further product development.

Program [Target] Trial Name(s) / Indications / Design Ind-Enabling Phase 1 Phase 2/3 Registration
afami-cel [MAGE-A4] SPEARHEAD-1 pivotal trial synovial sarcoma
Ind-Enabling complete
Phase 1 complete
Phase 2/3 complete
Registration in progress
U.S. FDA Accelerated Approval
SPEARHEAD-3 pediatric study in tumors that express MAGE-A4 (synovial sarcoma, malignant peripheral nerve sheath tumor (MPNST), neuroblastoma or osteosarcoma)
Ind-Enabling complete
Phase 1 in progress
Phase 2/3 not started
Registration not started
lete-cel [NY-ESO] IGNYTE-ESO synovial sarcoma and MRCLS
Ind-Enabling complete
Phase 1 complete
Phase 2/3 in progress
Registration not started
uza-cel
(ADP-A2M4CD8*) [MAGE-A4]
Collaboration with Galapagos head & neck cancer and potential future solid tumor indications
Ind-Enabling in progress
Phase 1 not started
Phase 2/3 not started
Registration not started
ADP-600 [PRAME] Indications that express PRAME including synovial sarcoma, breast, NSCLC, gastroesophageal, melanoma, endometrial, ovarian and head & neck cancers. Clinical Indications TBD
Ind-Enabling in progress
Phase 1 not started
Phase 2/3 not started
Registration not started
ADP-520 [CD70] Indications that express CD70 including hematological, malignancies, acute myeloid leukemia (AML), lymphoma and renal cell carcinoma (RCC). Clinical Indications TBD
Ind-Enabling in progress
Phase 1 not started
Phase 2/3 not started
Registration not started

--The safety and efficacy of investigational products have not been established.

† Temporary suspension of enrollment as per protocol in SPEARHEAD-3 trial

* Enrollment in uza-cel SURPASS and SURPASS-3 trials has been discontinued.

Promising preclinical allogeneic therapies

We have built one of the leading allogeneic T-cell platforms using human-induced pluripotent stem cell lines (hlPSCs). This platform is flexible and produces functional T-cells that kill tumor cells in vitro. We will combine this platform with everything we have learned from decades of autologous T-cell therapy research and development into a pipeline for Adaptimmune and its partners for off-the-shelf cell or allogeneic T-cell therapies.

Allogeneic Preclinical
Program [Target] Trial Name(s) / Indications / Design Discovery Ind-Enabling Phase 1 Phase 2/3 Registration
Off-the-shelf TCR therapy target 1 TBA
Discovery in progress
Ind-Enabling not started
Phase 1 not started
Phase 2/3 not started
Registration not started
Personalized cell therapy platform TBA
Discovery in progress
Ind-Enabling not started
Phase 1 not started
Phase 2/3 not started
Registration not started