Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03709706 · ClinicalTrials.gov registry record · Phase 1

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

A Phase 1 study, sponsored by GlaxoSmithKline.

Terminated
Registry status
Phase 1
Development phase
34
Enrollment target

NCT03709706: Clinical Trial Phase 1 study, sponsored by GlaxoSmithKline.

NCT03709706 is a Phase 1 study that was terminated before completion, run by GlaxoSmithKline. The registered enrollment target is 34 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (43% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03709706, a Phase 1 study, was terminated before completion, sponsored by GlaxoSmithKline.

TERMINATED
Registry status
Phase 1
Development phase
34 participants
Enrollment target

Study Summary

This trial will evaluate safety and tolerability of letetresgene autoleucel (GSK3377794) with or without pembrolizumab in participants with non-small cell lung cancer.

Primary Outcome

An AE is any untoward medical occurrence in a clinical investigation participant, temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product. SAE is defined as any untoward medical occurrence that, at any dose results in death, is life-threatening, requires hospitalization or prolongation of existing hospitalization, results in disability/incapacity, is a congenital anomaly/birth defect, other situations which involve medical or scientif

Interventions

  • DRUG Pembrolizumab
  • DRUG Lete-cel

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2018-12-31
Est. Completion 2022-11-04
Phase Phase 1
GlaxoSmithKline

1,345 total trials

Why NCT03709706 stopped before completion

NCT03709706 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 34 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (43% lower).

The record links to 0 conditions, and to 2 interventions - of which Pembrolizumab is the first listed.

NCT03709706 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03709706 about?

NCT03709706 is a clinical study titled "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". This trial will evaluate safety and tolerability of letetresgene autoleucel (GSK3377794) with or without pembrolizumab in participants with non-small cell lung cancer.

What is the current status of trial NCT03709706?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 34 participants. The study started on 2018-12-31. Estimated completion is 2022-11-04.

What interventions are being tested in trial NCT03709706?

The interventions under investigation include: Pembrolizumab (DRUG), Lete-cel (DRUG).

Who is sponsoring clinical trial NCT03709706?

This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03709706's enrollment target sits among peer trials

34 1273rd of 2000 higher than 721 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02897063 · 34 participants · Phase 1

    Effects of Midodrine and Droxidopa on Splanchnic Capacitance in Autonomic Failure

  • NCT03906617 · 34 participants · Phase 4

    Bupivacaine/Epinephrine +Dexamethasone vs. Liposomal Bupivacaine

  • NCT03992378 · 34 participants · NA

    Neuromodulation to Regulate Inflammation and Autonomic Imbalance in Sepsis

  • NCT04047849 · 34 participants · Phase 4

    Latency Antibiotics in Previable PPROM, 18 0/7- 22 6/7 WGA

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03709706, the US trial registry maintained by the National Library of Medicine. NCT03709706 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.