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Search / Trial NCT03391791

Long Term Follow up of Subjects Exposed to Genetically Engineered T Cell Receptors

Launched by ADAPTIMMUNE · Jan 2, 2018

Trial Information

Current as of June 18, 2025

Terminated

Keywords

Cell Therapy T Cell Therapy Spear T Cell Immuno Oncology Metastatic T Cell Receptor Long Term Follow Up Genetically Engineered

ClinConnect Summary

This is a non-therapeutic, multi-center, long-term follow-up (LTFU) study of subjects who have received lentivirus-mediated genetically engineered T Cell Receptors in an Adaptimmune sponsored clinical trial. The study is designed in accordance with FDA and EMA guidance on gene therapy trials.

The study involves up to 15 years post-infusion monitoring of subjects who have been exposed to lentivirus-mediated gene transfer in Adaptimmune clinical studies. The study will include subjects who have received various T cell receptors including but not limited to MAGE-A10ᶜ⁷⁹⁶T and MAGE-A4ᶜ¹º³²T. Su...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Subjects must have received T cell receptor therapy in an Adaptimmune clinical study
  • Subjects who have provided informed consent prior to their study participation
  • Exclusion Criteria:
  • Not applicable

About Adaptimmune

Adaptimmune is a clinical-stage biopharmaceutical company specializing in the development of innovative T-cell therapies for cancer treatment. Leveraging its proprietary SPEAR T-cell platform, Adaptimmune aims to harness the power of the immune system to target and eliminate cancer cells with precision. The company is focused on advancing its pipeline of engineered T-cell therapies through rigorous clinical trials, demonstrating a commitment to improving patient outcomes in oncology. With a strong emphasis on scientific excellence and collaboration, Adaptimmune is dedicated to transforming the landscape of cancer immunotherapy.

Locations

Nashville, Tennessee, United States

Houston, Texas, United States

Toronto, Ontario, Canada

Patients applied

0 patients applied

Trial Officials

Marcus Butler, MD

Principal Investigator

Princess Margaret Cancer Centr

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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