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Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T

Phase 1

Non-Small Cell Lung Cancer | Biologics | Oncology |Adaptimmune Therapeutics PLC|Trials Updated: Dec 9, 2025

Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T target and mechanism

Molecular targetADA
Target classExogenous Gene
ModalityBiologics

Success Probability

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Market & Valuation

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Trial Design

UNCONTROLLEDBiomarker
Total Trials1
Total Enrollment28

FDA Designations

No designations recorded

Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T clinical trials

Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T · 1 trial · 2 indications

Phase 1 1
NCT02592577MAGE A10ᶜ⁷⁹⁶T for Advanced NSCLCNon-Small Cell Lung Cancer
COMPLETED28 Analytics
PHASE1COMPLETED
MAGE A10ᶜ⁷⁹⁶T for Advanced NSCLC
Non-Small Cell Lung CancerUnlock trial analytics

Study Endpoints

Primary Endpoints

Number of subjects with dose-limiting toxicity (DLT) and adverse events (AE), including serious adverse events (SAE)
24 months

Determine if treatment with autologous genetically modified T cells, (MAGE A10ᶜ⁷⁹⁶T ) is safe and tolerable through assessment of DLTs, AEs, including SAEs; laboratory assessments, including chemistry, hematology, and coagulation; cardiac and pulmonary assessments, including ECG and troponin.

Secondary Endpoints

Proportion of subjects with a confirmed Complete Response (CR) or Partial Response (PR)
24 months
Interval between the date of first T cell infusion dose and first documented evidence of CR or PR
24 months
Interval between the date of first documented evidence of CR or PR until first documented disease progression or death due to any cause
24 months
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Study Design & Arms

AllocationNA
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶TEXPERIMENTAL -

Interventions

NameTypeDescription
Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶TBIOLOGICAL -
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites19

Key Inclusion Criteria: 1. Subject has histologically or cytologically confirmed diagnosis of advanced non-small cell lung cancer (stage IIIB or IV) or recurrent disease 2. Subject has received at least one line of prior therapy 3. Subjects with known epidermal growth factor receptor (EGFR) mutatio...

Countries:United StatesCanadaSpainUnited Kingdom
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Competitive Landscape -Non-Small Cell Lung Cancer 547 trials

Top 20 of 87 competitors

CompanyTickerTrialsLead PhaseDrugs
Merck & Co., Inc.MRK37PHASE3Pembrolizumab, Olaparib, Sacituzumab tirumotecan, Intismeran autogene, Pembrolizumab Berahyaluronidase alfa
Revolution Medicines, Inc.RVMD9PHASE3Daraxonrasib, Zoldonrasib, Elironrasib, RMC-5127
Eli Lilly and CompanyLLY19PHASE3Selpercatinib, Pemetrexed, Abemaciclib, Olomorasib, LY3537982
AbbVie, Inc.ABBV12PHASE3Livmoniplimab, Budigalimab, Telisotuzumab Adizutecan, Telisotuzumab vedotin, ABBV-1480
AstraZeneca PLCAZN70PHASE3Datopotamab deruxtecan, Durvalumab, Oleclumab, Monalizumab, Tremelimumab
Gilead Sciences, Inc.GILD7PHASE3Sacituzumab govitecan, Zimberelimab, Domvanalimab, Etrumadenant, TUB-040- Dose escalation
Regeneron Pharmaceuticals, Inc.REGN7PHASE3Fianlimab, Cemiplimab, REGN5093, Marlotamig, REGN10597
Bristol-Myers Squibb CompanyBMY23PHASE3Repotrectinib, Nivolumab, Pumitamig, Iza-bren, Relatlimab
GSK plc Sponsored ADRGSK4PHASE3Cobolimab, Dostarlimab, Belrestotug, Nelistotug
Johnson & JohnsonJNJ19PHASE3Lazertinib, Amivantamab, Cetrelimab, JNJ-90301900, JNJ-86974680
BioNTech SE Sponsored ADRBNTX7PHASE3Gotistobart, Pumitamig, BNT326, BNT116, BNT324
Pfizer Inc.PFE21PHASE3Lorlatinib, Crizotinib, Avelumab, Talazoparib, Axitinib
Amgen Inc.AMGN4PHASE3ABP 234, Sotorasib, Anvumetostat
ArriVent BioPharma, Inc.AVBP5PHASE3Firmonertinib
Summit Therapeutics IncSMMT2PHASE3Ivonescimab
Genmab A/S Sponsored ADRGMAB4PHASE3Acasunlimab, GEN1042, Rina-S
Nuvation Bio, Inc. Class ANUVB4PHASE3Taletrectinib
Eikon Therapeutics, Inc.EIKN3PHASE3EIK1001
Nuvalent, Inc. Class ANUVL1PHASE3Neladalkib
BeOne Medicines Ltd. Sponsored ADRONC5PHASE3Tislelizumab, BGB-43395
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Frequently asked questions about Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T

What is autologous genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T?

Autologous genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T is an investigational cell therapy being developed by Adaptimmune Therapeutics PLC for non-small cell lung cancer. It is a biologic made from a patient's own T cells that have been genetically modified, and it is being studied in biomarker-selected patients with advanced NSCLC.

What is MAGEA10ᶜ⁷⁹⁶T used for in non-small cell lung cancer?

MAGEA10ᶜ⁷⁹⁶T is being studied for the treatment of advanced non-small cell lung cancer, including carcinoma, in adults 18 years and older. The Phase 1 trial enrolled biomarker-selected patients, meaning eligibility depended on a defined biomarker rather than an unselected NSCLC population.

What does MAGEA10ᶜ⁷⁹⁶T target?

MAGEA10ᶜ⁷⁹⁶T is an autologous T-cell product genetically modified to express a T-cell receptor directed at MAGE-A10, a cancer-testis antigen. The target class is an exogenous gene introduced into the patient's T cells, so the therapy's activity depends on that engineered receptor recognizing MAGE-A10-expressing tumor cells.

Who is developing MAGEA10ᶜ⁷⁹⁶T?

MAGEA10ᶜ⁷⁹⁶T is being developed by Adaptimmune Therapeutics PLC, which trades under the ticker ADAPY. The company is the sponsor of the Phase 1 study of this autologous genetically modified T-cell therapy in advanced non-small cell lung cancer.

What phase is MAGEA10ᶜ⁷⁹⁶T in?

MAGEA10ᶜ⁷⁹⁶T is in Phase 1 development and is investigational; it is not an approved therapy. The single Phase 1 trial, NCT02592577, has been completed and enrolled 28 patients. No active trials of this asset are currently listed.

What clinical trials is MAGEA10ᶜ⁷⁹⁶T in?

MAGEA10ᶜ⁷⁹⁶T has been studied in one Phase 1 trial, NCT02592577, titled MAGE A10ᶜ⁷⁹⁶T for Advanced NSCLC. The completed study enrolled 28 patients across the United States, Canada, Spain, and the United Kingdom. It was an uncontrolled, non-randomized, open-label study without double blinding.