ClinicalTrials.gov record
Terminated Phase 1Phase 2 Interventional Results available

Pilot Immunotherapy Study With Letetresgene Autoleucel (Lete-cel, GSK3377794)T-cells in New York Esophageal Squamous Cell Carcinoma-1 (NY-ESO-1)/ LAGE-1a-positive Advanced Non-small Cell Lung Cancer (NSCLC) Either Alone or in Combination With Pembrolizumab

ClinicalTrials.gov ID: NCT03709706

Public ClinicalTrials.gov record NCT03709706. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 17, 2026, 3:16 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1b/2a Pilot Study to Evaluate the Safety and Tolerability of Autologous T-Cells Expressing Enhanced TCRs (T Cell Receptors) Specific for NY-ESO-1/LAGE-1a (GSK3377794) Alone, or in Combination With Pembrolizumab in HLA-A2+ Participants With NY-ESO-1- or LAGE-1a-Positive Advanced or Recurrent Non-Small Cell Lung Cancer

Study identification

NCT ID
NCT03709706
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
34 participants

Conditions and interventions

Conditions

Interventions

  • Lete-cel Drug
  • Pembrolizumab Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 30, 2018
Primary completion
Jun 26, 2022
Completion
Nov 3, 2022
Last update posted
Feb 22, 2024

2018 – 2022

United States locations

U.S. sites
20
U.S. states
16
U.S. cities
20
Facility City State ZIP Site status
GSK Investigational Site Duarte California 91010
GSK Investigational Site La Jolla California 92093-0987
GSK Investigational Site Sacramento California 95817
GSK Investigational Site Stanford California 94305
GSK Investigational Site Denver Colorado 80218
GSK Investigational Site Hollywood Florida 33021
GSK Investigational Site Atlanta Georgia 30322
GSK Investigational Site Chicago Illinois 60637
GSK Investigational Site Iowa City Iowa 52242
GSK Investigational Site Lexington Kentucky 40536
GSK Investigational Site Baltimore Maryland 21201
GSK Investigational Site St Louis Missouri 63110
GSK Investigational Site New York New York 10065
GSK Investigational Site Durham North Carolina 27710
GSK Investigational Site Columbus Ohio 43210
GSK Investigational Site Philadelphia Pennsylvania 19111
GSK Investigational Site Pittsburgh Pennsylvania 15232
GSK Investigational Site Nashville Tennessee 37203
GSK Investigational Site Houston Texas 77030
GSK Investigational Site Salt Lake City Utah 84112-5550

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03709706, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 22, 2024 · Synced May 17, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03709706 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →