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NCT03391791
Long Term Follow up of Subjects Exposed to Genetically Engineered T Cell Receptors
trial testing Genetically engineered T Cell Receptors in Solid and Hematological Malignancies in 2 participants. Terminated before completion.
24 July 2018
Quick facts
| Lead sponsor | Adaptimmune |
|---|---|
| Status | Terminated |
| Study type | OBSERVATIONAL |
| Enrollment | 2 |
| Start date | 28 February 2018 |
| Primary completion | 24 July 2018 |
| Estimated completion | 24 July 2018 |
| Sites | 3 locations across Canada, United States |
Drugs / interventions tested
- Genetically engineered T Cell Receptors
Conditions studied
- Solid and Hematological Malignancies — all drugs for Solid and Hematological Malignancies →
Sponsor
Adaptimmune — full company profile →
Who can join
18 and older, any sex, with Solid and Hematological Malignancies. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Subjects who previously took part in an Adaptimmune study and received genetically changed T cells (including but not limited to MAGE-A10ᶜ⁷⁹⁶T and MAGE-A4ᶜ¹º³²T) are asked to take part in this long term follow-up study. Subjects will be asked to join this study once they complete the parent interventional study. The purpose of this study is to find out if the genetically changed T cells that subjects received in the parent study have any long-term side effects. No additional study drug will be given, but subjects can receive other therapies for their cancer while they are being followed for long term safety in this study. For a period of 15 years starting from last administration of the genetically changed T cells, subjects will visit their study doctor for a check-up and to have blood tests to look for any changes that might have happened because of the genetically changed T cells.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Engineered T Cell Therapy for Cancer in the Clinic.
Zhao L, Cao YJ. · · 2019 · cited 275× · PMID 31681259 · DOI 10.3389/fimmu.2019.02250 -
T Cell Receptors for Gene Transfer in Adoptive T Cell Therapy.
Sharma P, Kranz DM. · · 2019 · cited 5× · PMID 31679251 · DOI 10.1615/critrevimmunol.2019030788
Verify or expand the search:
- PubMed search for NCT03391791
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other Adaptimmune trials
Trials by the same sponsor.
- NCT04752358 — ADP-A2M4CD8 in HLA-A2+ Subjects With MAGE-A4 Positive Esophageal or Esophagogastric Junction Cancers (SURPASS-2) · Phase 2 · terminated
- NCT06048705 — Study of GSK3901961 In Previously Treated Advanced (Metastatic OR Unresectable) Synovial Sarcoma/ Myxoid/Round Cell Lipo · Phase 1 · terminated
- NCT04526509 — Master Protocol to Assess Safety and Dose of First Time in Human Next Generation Engineered T Cells in NY-ESO-1 and/or L · Phase 1 · terminated
- NCT05943990 — Study of GSK3845097 in Previously Treated Participants With Advanced Synovial Sarcoma and Myxoid/Round Cell Liposarcoma · Phase 1 · terminated
- NCT03132792 — AFPᶜ³³²T in Advanced HCC · Phase 1 · active not recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03391791 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Adaptimmune
- Last refreshed: 7 January 2021
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03391791.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing