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NCT00312975 · ClinicalTrials.gov registry record · Phase 2

Randomized Study Of CP-675,206 or Best Supportive Care Immediately After Platinum-Based Therapy For Non-Small Cell Lung Cancer (NSCLC)

A Phase 2 study, sponsored by AstraZeneca.

Completed
Registry status
Phase 2
Development phase
90
Enrollment target

NCT00312975: Completed Phase 2 study, sponsored by AstraZeneca.

NCT00312975 is a Phase 2 study that has completed, run by AstraZeneca. The registered enrollment target is 90 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (32% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00312975, a Phase 2 study, has completed, sponsored by AstraZeneca.

COMPLETED
Registry status
Phase 2
Development phase
90 participants
Enrollment target

Study Summary

The purpose of this trial is to study how long patients can remain progression free when they receive CP-675,206, compared to how long patients can remain progression free when they receive best supportive care. If you choose to take part, you will be randomized to receive either CP-675,206 as maintenance therapy or best supportive care. Best supportive care means you will not receive any study drug or other treatment for your cancer. Best supportive care could include treatment with antibiotics, analgesic drugs (medicine for pain), blood transfusions or psychosocial and nutritional support, depending on your needs. You have a 50% chance of being randomized to receive CP-675,206.

Interventions

  • DRUG CP-675,206
  • DRUG best supportive care

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2006-05
Est. Completion 2010-02
Phase Phase 2
AstraZeneca

1,285 total trials

What the finished NCT00312975 record still lists

NCT00312975 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 90 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (32% lower).

The record links to 0 conditions, and to 2 interventions - of which CP-675,206 is the first listed.

NCT00312975 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00312975 about?

NCT00312975 is a clinical study titled "Randomized Study Of CP-675,206 or Best Supportive Care Immediately After Platinum-Based Therapy For Non-Small Cell Lung Cancer (NSCLC)". The purpose of this trial is to study how long patients can remain progression free when they receive CP-675,206, compared to how long patients can remain progression free when they receive best supportive care. If you choose to take part, you will be randomized to receive either CP-675,206 as maint...

What is the current status of trial NCT00312975?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 90 participants. The study started on 2006-05. Estimated completion is 2010-02.

What interventions are being tested in trial NCT00312975?

The interventions under investigation include: CP-675,206 (DRUG), best supportive care (DRUG).

Who is sponsoring clinical trial NCT00312975?

This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00312975's enrollment target sits among peer trials

90 772nd of 2000 higher than 1,199 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 NCT00312975, the US trial registry maintained by the National Library of Medicine. NCT00312975 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.