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NCT01456325 · ClinicalTrials.gov registry record · Phase 3

A Study of Onartuzumab (MetMAb) in Combination With Tarceva (Erlotinib) in Participants With Met Diagnostic-Positive Non-Small Cell Lung Cancer Who Have Received Chemotherapy For Advanced or Metastatic Disease (MetLung)

A Phase 3 study, sponsored by Genentech.

Completed
Registry status
Phase 3
Development phase
494
Enrollment target

NCT01456325: Completed Phase 3 study, sponsored by Genentech.

NCT01456325 is a Phase 3 study that has completed, run by Genentech. The registered enrollment target is 494 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (36% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01456325, a Phase 3 study, has completed, sponsored by Genentech.

COMPLETED
Registry status
Phase 3
Development phase
494 participants
Enrollment target

Study Summary

This randomized, multicenter, double-blind, placebo-controlled study will evaluate the efficacy and safety of onartuzumab (MetMAb) in combination with Tarceva (erlotinib) in participants with incurable non-small cell lung cancer identified to be Met diagnostic-positive. Participants will be randomized to receive either onartuzumab (MetMAb) or placebo in combination with erlotinib. Anticipated time on study treatment is until disease progression or unacceptable toxicity occurs.

Interventions

  • DRUG Placebo
  • DRUG Erlotinib
  • DRUG Onartuzumab (MetMab)

Trial Details

FieldValue
Enrollment Target 494 participants
Start Date 2012-01
Est. Completion 2016-01
Phase Phase 3
Genentech

332 total trials

What the finished NCT01456325 record still lists

NCT01456325 is an interventional study that assigns participants to a tested intervention. The registered 494 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (36% lower).

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT01456325 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01456325 about?

NCT01456325 is a clinical study titled "A Study of Onartuzumab (MetMAb) in Combination With Tarceva (Erlotinib) in Participants With Met Diagnostic-Positive Non-Small Cell Lung Cancer Who Have Received Chemotherapy For Advanced or Metastatic Disease (MetLung)". This randomized, multicenter, double-blind, placebo-controlled study will evaluate the efficacy and safety of onartuzumab (MetMAb) in combination with Tarceva (erlotinib) in participants with incurable non-small cell lung cancer identified to be Met diagnostic-positive. Participants will be randomiz...

What is the current status of trial NCT01456325?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 494 participants. The study started on 2012-01. Estimated completion is 2016-01.

What interventions are being tested in trial NCT01456325?

The interventions under investigation include: Placebo (DRUG), Erlotinib (DRUG), Onartuzumab (MetMab) (DRUG).

Who is sponsoring clinical trial NCT01456325?

This trial is sponsored by Genentech, which has 332 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01456325's enrollment target sits among peer trials

494 779th of 2000 higher than 1,222 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 NCT01456325, the US trial registry maintained by the National Library of Medicine. NCT01456325 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.