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NCT01193881 · ClinicalTrials.gov registry record · Phase 1

RO4929097 and Erlotinib Hydrochloride in Treating Patients With Stage IV or Recurrent Non-small Cell Lung Cancer

A Phase 1 study, sponsored by National Cancer Institute (NCI).

Terminated
Registry status
Phase 1
Development phase
16
Enrollment target

NCT01193881: Clinical Trial Phase 1 study, sponsored by National Cancer Institute (NCI).

NCT01193881 is a Phase 1 study that was terminated before completion, run by National Cancer Institute (NCI). The registered enrollment target is 16 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (73% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT01193881, a Phase 1 study, was terminated before completion, sponsored by National Cancer Institute (NCI).

TERMINATED
Registry status
Phase 1
Development phase
16 participants
Enrollment target

Study Summary

This phase I trial studies the side effects and best dose of gamma-secretase/Notch signalling pathway inhibitor RO4929097 (RO4929097) and erlotinib hydrochloride when given together in treating patients with non-small cell lung cancer that is stage IV or has come back. RO4929097 and erlotinib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

Interventions

  • OTHER Laboratory Biomarker Analysis
  • DRUG Erlotinib Hydrochloride
  • OTHER Pharmacological Study
  • DRUG Gamma-Secretase Inhibitor RO4929097

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2010-08
Est. Completion 2015-08
Phase Phase 1
National Cancer Institute (NCI)

3,257 total trials

Why NCT01193881 stopped before completion

NCT01193881 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 16 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (73% lower).

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

NCT01193881 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01193881 about?

NCT01193881 is a clinical study titled "RO4929097 and Erlotinib Hydrochloride in Treating Patients With Stage IV or Recurrent Non-small Cell Lung Cancer". This phase I trial studies the side effects and best dose of gamma-secretase/Notch signalling pathway inhibitor RO4929097 (RO4929097) and erlotinib hydrochloride when given together in treating patients with non-small cell lung cancer that is stage IV or has come back. RO4929097 and erlotinib hydroc...

What is the current status of trial NCT01193881?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 16 participants. The study started on 2010-08. Estimated completion is 2015-08.

What interventions are being tested in trial NCT01193881?

The interventions under investigation include: Laboratory Biomarker Analysis (OTHER), Erlotinib Hydrochloride (DRUG), Pharmacological Study (OTHER), Gamma-Secretase Inhibitor RO4929097 (DRUG).

Who is sponsoring clinical trial NCT01193881?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01193881's enrollment target sits among peer trials

16 1786th of 2000 higher than 203 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

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Source: ClinicalTrials.gov NCT01193881, the US trial registry maintained by the National Library of Medicine. NCT01193881 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.