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NCT00642941 · ClinicalTrials.gov registry record · Phase 2

A Study of R1507 in Participants With Recurrent or Refractory Sarcoma

A Phase 2 study, sponsored by Hoffmann-La Roche.

Terminated
Registry status
Phase 2
Development phase
317
Enrollment target

NCT00642941: Clinical Trial Phase 2 study, sponsored by Hoffmann-La Roche.

NCT00642941 is a Phase 2 study that was terminated before completion, run by Hoffmann-La Roche. The registered enrollment target is 317 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (138% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00642941, a Phase 2 study, was terminated before completion, sponsored by Hoffmann-La Roche.

TERMINATED
Registry status
Phase 2
Development phase
317 participants
Enrollment target

Study Summary

The study was primarily designed to determine objective response, progression-free survival (PFS), and the safety and tolerability of R1507 in participants with recurrent or refractory Ewing's sarcoma, osteosarcoma, synovial sarcoma, rhabdomyosarcoma and other sarcomas including alveolar soft part sarcoma, desmoplastic small round cell tumor, extraskeletal myxoid chondrosarcoma, clear cell sarcoma, and myxoid liposarcoma.

Primary Outcome

Complete response is the disappearance of all known disease, determined by two consecutive observations not less than 4 weeks apart. Partial response is \>=50% decrease in the total tumor load of the lesions that have been measured to determine the effect of therapy not less than four weeks apart. The observations must be consecutive.

Interventions

  • DRUG RG1507

Trial Details

FieldValue
Enrollment Target 317 participants
Start Date 2007-12-18
Est. Completion 2014-02-19
Phase Phase 2
Hoffmann-La Roche

909 total trials

Why NCT00642941 stopped before completion

NCT00642941 is an interventional study that assigns participants to a tested intervention. The registered 317 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 (138% higher).

The record links to 0 conditions, and to 1 intervention - of which RG1507 is the first listed.

NCT00642941 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00642941 about?

NCT00642941 is a clinical study titled "A Study of R1507 in Participants With Recurrent or Refractory Sarcoma". The study was primarily designed to determine objective response, progression-free survival (PFS), and the safety and tolerability of R1507 in participants with recurrent or refractory Ewing's sarcoma, osteosarcoma, synovial sarcoma, rhabdomyosarcoma and other sarcomas including alveolar soft part s...

What is the current status of trial NCT00642941?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 317 participants. The study started on 2007-12-18. Estimated completion is 2014-02-19.

What interventions are being tested in trial NCT00642941?

The interventions under investigation include: RG1507 (DRUG).

Who is sponsoring clinical trial NCT00642941?

This trial is sponsored by Hoffmann-La Roche, which has 909 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00642941's enrollment target sits among peer trials

317 155th 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 NCT00642941, the US trial registry maintained by the National Library of Medicine. NCT00642941 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.