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NCT00179699 · ClinicalTrials.gov registry record · Phase 1

Phase I Open-Label, Dose Escalation Study To Determine The Maximum Tolerated Dose And To Evaluate The Safety Profile Of Lenalidomide (Revlimid®, CC-5013) With Pemetrexed In Subjects With Advanced Non-Small Cell Lung Cancer

A Phase 1 study, sponsored by Celgene Corporation.

Terminated
Registry status
Phase 1
Development phase
40
Enrollment target

NCT00179699: Clinical Trial Phase 1 study, sponsored by Celgene Corporation.

NCT00179699 is a Phase 1 study that was terminated before completion, run by Celgene Corporation. The registered enrollment target is 40 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00179699, a Phase 1 study, was terminated before completion, sponsored by Celgene Corporation.

TERMINATED
Registry status
Phase 1
Development phase
40 participants
Enrollment target

Study Summary

Study will deteremine the MTD and evaluate the safety profile of oral lenalidomide on days 1-14 when combined with pemetrexed on day 1 of a 21 days cycle. Subjects will continue on study until documention of disease progression.

Interventions

  • DRUG pemetrexed
  • DRUG CC-5013

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2005-09
Est. Completion 2006-11
Phase Phase 1
Celgene Corporation

40 total trials

Why NCT00179699 stopped before completion

NCT00179699 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower).

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

NCT00179699 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00179699 about?

NCT00179699 is a clinical study titled "Phase I Open-Label, Dose Escalation Study To Determine The Maximum Tolerated Dose And To Evaluate The Safety Profile Of Lenalidomide (Revlimid®, CC-5013) With Pemetrexed In Subjects With Advanced Non-Small Cell Lung Cancer". Study will deteremine the MTD and evaluate the safety profile of oral lenalidomide on days 1-14 when combined with pemetrexed on day 1 of a 21 days cycle. Subjects will continue on study until documention of disease progression.

What is the current status of trial NCT00179699?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2005-09. Estimated completion is 2006-11.

What interventions are being tested in trial NCT00179699?

The interventions under investigation include: pemetrexed (DRUG), CC-5013 (DRUG).

Who is sponsoring clinical trial NCT00179699?

This trial is sponsored by Celgene Corporation, which has 40 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00179699's enrollment target sits among peer trials

40 1130th of 2000 higher than 810 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 NCT00179699, the US trial registry maintained by the National Library of Medicine. NCT00179699 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.