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

NCT02920476 · ClinicalTrials.gov registry record · Phase 2

TAS-102 in Previously Treated Unresectable or Metastatic Squamous Cell Lung Carcinoma (UF-STO-LUNG-003)

A Phase 2 study, sponsored by University of Florida.

Completed
Registry status
Phase 2
Development phase
4
Enrollment target

NCT02920476: Completed Phase 2 study, sponsored by University of Florida.

NCT02920476 is a Phase 2 study that has completed, run by University of Florida. The registered enrollment target is 4 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02920476, a Phase 2 study, has completed, sponsored by University of Florida.

COMPLETED
Registry status
Phase 2
Development phase
4 participants
Enrollment target

Study Summary

This is a non-randomized, open label, sequentially enrolling phase II study with a Simon two-step enrollment design to evaluate the activity of TAS-102 in previously treated unresectable or metastatic squamous non-small cell cancer after progression through or intolerance to prior systemic therapy. The trial therapy of TAS-102 is to be administered orally at 35 mg/m2 each dose twice daily. The primary objective of the trial is to determine the progression-free survival, in months, of subjects receiving TAS 102 for the treatment of unresectable or metastatic recurrent squamous non-small cell lung cancers.

Primary Outcome

To determine the percentage of subjects who achieve an objective response by RECIST 1.1 criteria. ORR is defined as the number of participants who achieved either a partial or complete response by RECIST 1.1 criteria. By these criteria, Complete Response (CR) is defined as the disappearance of all target lesions and Partial Response (PR) is defined as a decrease of at least 30% in the sum of the longest diameter of the target lesions. Subjects must have received at least 2 cycles of therapy to b

Interventions

  • DRUG TAS-102

Trial Details

FieldValue
Enrollment Target 4 participants
Start Date 2017-07-19
Est. Completion 2021-08-14
Phase Phase 2
University of Florida

1,106 total trials

What the finished NCT02920476 record still lists

NCT02920476 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 4 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 1 intervention - of which TAS-102 is the first listed.

NCT02920476 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02920476 about?

NCT02920476 is a clinical study titled "TAS-102 in Previously Treated Unresectable or Metastatic Squamous Cell Lung Carcinoma (UF-STO-LUNG-003)". This is a non-randomized, open label, sequentially enrolling phase II study with a Simon two-step enrollment design to evaluate the activity of TAS-102 in previously treated unresectable or metastatic squamous non-small cell cancer after progression through or intolerance to prior systemic therapy. ...

What is the current status of trial NCT02920476?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 4 participants. The study started on 2017-07-19. Estimated completion is 2021-08-14.

What interventions are being tested in trial NCT02920476?

The interventions under investigation include: TAS-102 (DRUG).

Who is sponsoring clinical trial NCT02920476?

This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02920476's enrollment target sits among peer trials

4 2001st of 2000 the lowest of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 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 NCT02920476, the US trial registry maintained by the National Library of Medicine. NCT02920476 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.