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NCT02409355 · ClinicalTrials.gov registry record · Phase 3

A Study of Atezolizumab Compared With Gemcitabine Plus (+) Cisplatin or Carboplatin for PD-L1-Selected Participants With Stage IV Squamous Non-Small Cell Lung Cancer (NSCLC) (IMpower111)

A Phase 3 study, sponsored by Hoffmann-La Roche.

Terminated
Registry status
Phase 3
Development phase
8
Enrollment target

NCT02409355: Clinical Trial Phase 3 study, sponsored by Hoffmann-La Roche.

NCT02409355 is a Phase 3 study that was terminated before completion, run by Hoffmann-La Roche. The registered enrollment target is 8 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02409355, a Phase 3 study, was terminated before completion, sponsored by Hoffmann-La Roche.

TERMINATED
Registry status
Phase 3
Development phase
8 participants
Enrollment target

Study Summary

This randomized, open-label study was designed to evaluate and compare the safety and efficacy of atezolizumab with gemcitabine + cisplatin or carboplatin in PD-L1 selected participants with chemotherapy-naive, Stage IV squamous NSCLC. The study was closed due to low patient enrollment and the Sponsor's decision to include patients with squamous NSCLC into the GO29431 study, NCT02409342. Therefore the planned objectives of this study are no longer applicable and formal analyses of efficacy or safety have not been performed.

Interventions

  • DRUG Carboplatin
  • DRUG Atezolizumab
  • DRUG Cisplatin
  • DRUG Gemcitabine

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2015-05-07
Est. Completion 2017-12-07
Phase Phase 3
Hoffmann-La Roche

909 total trials

Why NCT02409355 stopped before completion

NCT02409355 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 4 interventions - of which Carboplatin is the first listed.

NCT02409355 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02409355 about?

NCT02409355 is a clinical study titled "A Study of Atezolizumab Compared With Gemcitabine Plus (+) Cisplatin or Carboplatin for PD-L1-Selected Participants With Stage IV Squamous Non-Small Cell Lung Cancer (NSCLC) (IMpower111)". This randomized, open-label study was designed to evaluate and compare the safety and efficacy of atezolizumab with gemcitabine + cisplatin or carboplatin in PD-L1 selected participants with chemotherapy-naive, Stage IV squamous NSCLC. The study was closed due to low patient enrollment and the Spons...

What is the current status of trial NCT02409355?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 8 participants. The study started on 2015-05-07. Estimated completion is 2017-12-07.

What interventions are being tested in trial NCT02409355?

The interventions under investigation include: Carboplatin (DRUG), Atezolizumab (DRUG), Cisplatin (DRUG), Gemcitabine (DRUG).

Who is sponsoring clinical trial NCT02409355?

This trial is sponsored by Hoffmann-La Roche, which has 909 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02409355's enrollment target sits among peer trials

8 1993rd of 2000 higher than 6 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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

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Source: ClinicalTrials.gov NCT02409355, the US trial registry maintained by the National Library of Medicine. NCT02409355 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.