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NCT01017640 · ClinicalTrials.gov registry record · Phase 1

Veliparib With or Without Mitomycin C in Treating Patients With Metastatic, Unresectable, or Recurrent Solid Tumors

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

Completed
Registry status
Phase 1
Development phase
20
Enrollment target

NCT01017640: Completed Phase 1 study, sponsored by National Cancer Institute (NCI).

NCT01017640 is a Phase 1 study that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 20 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01017640, a Phase 1 study, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 1
Development phase
20 participants
Enrollment target

Study Summary

This phase I trial studies the side effects and best dose of veliparib when given with or without mitomycin C in treating patients with solid tumors that have spread to other places in the body, cannot be removed by surgery or have come back. Veliparib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as mitomycin C, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving veliparib together with mitomycin C may kill more tumor cells.

Interventions

  • OTHER Laboratory Biomarker Analysis
  • DRUG Mitomycin
  • DRUG Veliparib

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2009-10
Phase Phase 1
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT01017640 record still lists

NCT01017640 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower).

The record links to 0 conditions, and to 3 interventions - of which Laboratory Biomarker Analysis is the first listed.

NCT01017640 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01017640 about?

NCT01017640 is a clinical study titled "Veliparib With or Without Mitomycin C in Treating Patients With Metastatic, Unresectable, or Recurrent Solid Tumors". This phase I trial studies the side effects and best dose of veliparib when given with or without mitomycin C in treating patients with solid tumors that have spread to other places in the body, cannot be removed by surgery or have come back. Veliparib may stop the growth of tumor cells by blocking ...

What is the current status of trial NCT01017640?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2009-10.

What interventions are being tested in trial NCT01017640?

The interventions under investigation include: Laboratory Biomarker Analysis (OTHER), Mitomycin (DRUG), Veliparib (DRUG).

Who is sponsoring clinical trial NCT01017640?

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 NCT01017640's enrollment target sits among peer trials

20 1629th of 2000 higher than 285 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 NCT01017640, the US trial registry maintained by the National Library of Medicine. NCT01017640 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.