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NCT01240538 · ClinicalTrials.gov registry record · Phase 1

Viral Therapy in Treating Young Patients With Relapsed or Refractory Solid Tumors

A Phase 1 study, sponsored by National Cancer Institute (NCI).

Completed
Registry status
Phase 1
Development phase
26
Enrollment target

NCT01240538: Completed Phase 1 study, sponsored by National Cancer Institute (NCI).

NCT01240538 is a Phase 1 study that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 26 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (57% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01240538, a Phase 1 study, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 1
Development phase
26 participants
Enrollment target

Study Summary

This phase I trial studies the side effects and the best dose of viral therapy in treating young patients with solid tumors that have come back or that have not responded to standard therapy. Some tumors have cells with a genetic weakness that makes them unable to fight off a virus called wild-type reovirus. The virus causes cells with this weakness to die, and may therefore be able to kill tumor cells without damaging normal cells. Cyclophosphamide is a drug used in chemotherapy that stops tumor cells from dividing and causes them to die. Giving wild-type reovirus together with cyclophosphamide may kill more tumor cells.

Interventions

  • OTHER laboratory biomarker analysis
  • DRUG cyclophosphamide
  • OTHER pharmacological study
  • BIOLOGICAL wild-type reovirus

Trial Details

FieldValue
Enrollment Target 26 participants
Start Date 2010-12
Phase Phase 1
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT01240538 record still lists

NCT01240538 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 26 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (57% lower).

The record links to 0 conditions, and to 4 interventions - of which laboratory biomarker analysis is the first listed.

NCT01240538 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01240538 about?

NCT01240538 is a clinical study titled "Viral Therapy in Treating Young Patients With Relapsed or Refractory Solid Tumors". This phase I trial studies the side effects and the best dose of viral therapy in treating young patients with solid tumors that have come back or that have not responded to standard therapy. Some tumors have cells with a genetic weakness that makes them unable to fight off a virus called wild-type ...

What is the current status of trial NCT01240538?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 26 participants. The study started on 2010-12.

What interventions are being tested in trial NCT01240538?

The interventions under investigation include: laboratory biomarker analysis (OTHER), cyclophosphamide (DRUG), pharmacological study (OTHER), wild-type reovirus (BIOLOGICAL).

Who is sponsoring clinical trial NCT01240538?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01240538's enrollment target sits among peer trials

26 1482nd of 2000 higher than 506 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 NCT01240538, the US trial registry maintained by the National Library of Medicine. NCT01240538 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.