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NCT00855894 · ClinicalTrials.gov registry record · Phase 2

A Study of the Combination of Erlotinib and Pertuzumab in Patients With Relapsed Non-small Cell Lung Cancer

A Phase 2 study, sponsored by Genentech.

Completed
Registry status
Phase 2
Development phase
41
Enrollment target

NCT00855894: Completed Phase 2 study, sponsored by Genentech.

NCT00855894 is a Phase 2 study that has completed, run by Genentech. The registered enrollment target is 41 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (69% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00855894, a Phase 2 study, has completed, sponsored by Genentech.

COMPLETED
Registry status
Phase 2
Development phase
41 participants
Enrollment target

Study Summary

This was a Phase II, open-label, single-arm, single-stage, multicenter trial in patients with relapsed non-small cell lung cancer (NSCLC), with the objective of assessing the activity of the combination of erlotinib and pertuzumab on the basis of the endpoint of FDG-PET response rate.

Primary Outcome

The assessment of FDG-PET response was performed by a central reading site. PET response was based on the maximum standard uptake value (SUVmax) of up to 5 regions of interest (ROI). The tumor ROIs were identified for each patient on pretreatment FDG-PET scans and corresponded to a subset of the target lesions identified for Response Evaluation Criteria for Solid Tumors (RECIST) analysis. Specifically, the SUVmax of each ROI on the on-treatment scans was compared with the SUVmax on the correspon

Interventions

  • DRUG Pertuzumab
  • DRUG Erlotinib

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2009-03
Est. Completion 2012-03
Phase Phase 2
Genentech

332 total trials

What the finished NCT00855894 record still lists

NCT00855894 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 41 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (69% lower).

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

NCT00855894 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00855894 about?

NCT00855894 is a clinical study titled "A Study of the Combination of Erlotinib and Pertuzumab in Patients With Relapsed Non-small Cell Lung Cancer". This was a Phase II, open-label, single-arm, single-stage, multicenter trial in patients with relapsed non-small cell lung cancer (NSCLC), with the objective of assessing the activity of the combination of erlotinib and pertuzumab on the basis of the endpoint of FDG-PET response rate.

What is the current status of trial NCT00855894?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 41 participants. The study started on 2009-03. Estimated completion is 2012-03.

What interventions are being tested in trial NCT00855894?

The interventions under investigation include: Pertuzumab (DRUG), Erlotinib (DRUG).

Who is sponsoring clinical trial NCT00855894?

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

How this trial's enrollment target compares

Where NCT00855894's enrollment target sits among peer trials

41 1352nd of 2000 higher than 639 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

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Source: ClinicalTrials.gov NCT00855894, the US trial registry maintained by the National Library of Medicine. NCT00855894 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.