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NCT02147990 · ClinicalTrials.gov registry record · Phase 2

Multicenter Study of Rociletinib Administered to Patients With Previously Treated Mutant EGFR Non-small Cell Lung Cancer

A Phase 2 study, sponsored by Clovis Oncology.

Terminated
Registry status
Phase 2
Development phase
318
Enrollment target

NCT02147990: Clinical Trial Phase 2 study, sponsored by Clovis Oncology.

NCT02147990 is a Phase 2 study that was terminated before completion, run by Clovis Oncology. The registered enrollment target is 318 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (139% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02147990, a Phase 2 study, was terminated before completion, sponsored by Clovis Oncology.

TERMINATED
Registry status
Phase 2
Development phase
318 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety and anti-tumor effect of rociletinib. The trial is open-ended, which means patients will continue to take rociletinib until the study doctor determines it is no longer beneficial for them.

Primary Outcome

ORR is defined as the percentage of patients with a best overall confirmed response of partial response (PR) or complete response (CR) recorded from the start of the treatment until disease progression. For patients who continued treatment post-progression, the first date of progression was used for the analysis. Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1) for target lesions, defined by and assessed as: Complete Response (CR), is disappearance of all target lesions. A

Interventions

  • DRUG Rociletinib

Trial Details

FieldValue
Enrollment Target 318 participants
Start Date 2014-06-16
Est. Completion 2019-08-27
Phase Phase 2
Clovis Oncology

11 total trials

Why NCT02147990 stopped before completion

NCT02147990 is an interventional study that assigns participants to a tested intervention. The registered 318 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (139% higher).

The record links to 0 conditions, and to 1 intervention - of which Rociletinib is the first listed.

NCT02147990 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02147990 about?

NCT02147990 is a clinical study titled "Multicenter Study of Rociletinib Administered to Patients With Previously Treated Mutant EGFR Non-small Cell Lung Cancer". The purpose of this study is to evaluate the safety and anti-tumor effect of rociletinib. The trial is open-ended, which means patients will continue to take rociletinib until the study doctor determines it is no longer beneficial for them.

What is the current status of trial NCT02147990?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 318 participants. The study started on 2014-06-16. Estimated completion is 2019-08-27.

What interventions are being tested in trial NCT02147990?

The interventions under investigation include: Rociletinib (DRUG).

Who is sponsoring clinical trial NCT02147990?

This trial is sponsored by Clovis Oncology, which has 11 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02147990's enrollment target sits among peer trials

318 153rd of 2000 higher than 1,846 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 NCT02147990, the US trial registry maintained by the National Library of Medicine. NCT02147990 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.