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Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T

Phase 1

Non-Small Cell Lung Cancer | Monoclonal antibody | Oncology |Adaptimmune Therapeutics PLC Sponsored ADR|Last Updated: Dec 9, 2025

Target and mechanism

Molecular targetADA
Target classExogenous Gene
ModalityMonoclonal antibody

Success Probability

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Market & Valuation

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Trial Design

UNCONTROLLEDBiomarker
Total Trials1
Total Enrollment28

FDA Designations

No designations recorded

Clinical trial landscape

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 387 trials

Top 20 of 79 competitors

CompanyTickerTrialsLead PhaseDrugs
Merck & Co., Inc.MRK24PHASE3Pembrolizumab, Olaparib, Sacituzumab tirumotecan, Intismeran autogene, Pembrolizumab Berahyaluronidase alfa
AstraZeneca PLCAZN62PHASE3Datopotamab deruxtecan, Durvalumab, Oleclumab, Monalizumab, Tremelimumab
Revolution Medicines, Inc.RVMD8PHASE3Daraxonrasib, Elironrasib, Zoldonrasib, RMC-5127
Eli Lilly and CompanyLLY18PHASE3Selpercatinib, Pemetrexed, Abemaciclib, Olomorasib, LY3537982
AbbVie, Inc.ABBV10PHASE3Telisotuzumab vedotin, Telisotuzumab Adizutecan, Livmoniplimab, Budigalimab, ABBV-927
Bristol-Myers Squibb CompanyBMY18PHASE3Repotrectinib, Nivolumab, Pumitamig, Relatlimab, Adagrasib
BioNTech SE Sponsored ADRBNTX7PHASE3Gotistobart, Pumitamig, BNT326, BNT116, BNT324
Gilead Sciences, Inc.GILD4PHASE3Sacituzumab govitecan, Zimberelimab, Domvanalimab, Etrumadenant
Pfizer Inc.PFE16PHASE3Lorlatinib, Crizotinib, Avelumab, Talazoparib, Axitinib
Johnson & JohnsonJNJ17PHASE3Lazertinib, Amivantamab, JNJ-90301900, JNJ-86974680, Cetrelimab
ArriVent BioPharma, Inc.AVBP9PHASE3Firmonertinib
Amgen Inc.AMGN4PHASE3ABP 234, Sotorasib, Anvumetostat
Novartis AG Sponsored ADRNVS9PHASE3Opnurasib, TNO155, DKY709, Spartalizumab, trametinib
GSK plc Sponsored ADRGSK3PHASE3Dostarlimab, Belrestotug, Nelistotug, Cobolimab
Summit Therapeutics IncSMMT2PHASE3Ivonescimab
Nuvation Bio, Inc. Class ANUVB4PHASE3Taletrectinib
Genmab A/S Sponsored ADRGMAB4PHASE3Acasunlimab, Rina-S, GEN1042
Regeneron Pharmaceuticals, Inc.REGN6PHASE2Cemiplimab, Marlotamig, Fianlimab, REGN5093
BeOne Medicines Ltd. Sponsored ADRONC6PHASE3Tislelizumab, BGB-A445, LBL-007, BGB-15025, BGB-43395
BeyondSpring Inc.BYSI1PHASE3Plinabulin
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Frequently asked questions about Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T

What is Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T used for?

Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T is being studied for the treatment of non-small cell lung cancer (NSCLC). It is an investigational therapy being developed by Adaptimmune Therapeutics PLC (ticker: ADAP). The therapy is designed for patients with advanced NSCLC whose tumors express the MAGE-A10 antigen, as it is a biomarker-selected treatment.

What does Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T target?

Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T targets the MAGE-A10 antigen, which is a cancer-testis antigen expressed in certain tumors. The target class is an exogenous gene, meaning the T cells are genetically modified to express a T-cell receptor that recognizes MAGE-A10. This allows the modified T cells to specifically attack cancer cells presenting the MAGE-A10 antigen.

Who is developing Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T?

Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T is being developed by Adaptimmune Therapeutics PLC, which trades on the Nasdaq under the ticker ADAP. Adaptimmune is a clinical-stage biopharmaceutical company focused on T-cell therapies for cancer.

What phase is Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T in?

Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T is in Phase 1 clinical development. The only trial conducted for this therapy was a Phase 1 study that has been completed. As a Phase 1 investigational therapy, it has not been approved by the FDA for any indication.

What clinical trials is Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T in?

Autologous Genetically modified T cells, MAGEA10ᶜ⁷⁹⁶T has been evaluated in one clinical trial: NCT02592577, titled "MAGE A10ᶜ⁷⁹⁶T for Advanced NSCLC." This Phase 1 trial enrolled 28 patients with non-small cell lung cancer and was conducted in the United States, Canada, Spain, and the United Kingdom. The trial is now completed.