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NCT01589419 · ClinicalTrials.gov registry record · Phase 1

A Clinical Study Conducted in Multiple Centers Evaluating Escalating Doses of Veliparib in Combination With Capecitabine and Radiation in Patients With Locally Advanced Rectal Cancer

A Phase 1 study, sponsored by AbbVie (prior sponsor, Abbott).

Completed
Registry status
Phase 1
Development phase
32
Enrollment target

NCT01589419 is a Phase 1 study that has completed, run by AbbVie (prior sponsor, Abbott). The registered enrollment target is 32 participants.

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The verdict

NCT01589419, a Phase 1 study, has completed, sponsored by AbbVie (prior sponsor, Abbott).

COMPLETED
Registry status
Phase 1
Development phase
32 participants
Enrollment target

Study Summary

An open-label, Phase 1b, dose escalation study evaluating the safety and tolerability of the PARP inhibitor Veliparib in combination with capecitabine and radiation in subjects with locally advanced rectal cancer (LARC).

Interventions

  • DRUG capecitabine
  • RADIATION radiation
  • DRUG veliparib

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 2012-06
Est. Completion 2015-01
Phase Phase 1

Sponsor

AbbVie (prior sponsor, Abbott)

88 total trials

What the Registry Record Tells You About NCT01589419

The ClinicalTrials.gov registry entry for NCT01589419 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 32 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AbbVie (prior sponsor, Abbott), which has 88 total studies on file at ClinicalTrials.gov.

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

NCT01589419 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01589419 about?

NCT01589419 is a clinical study titled "A Clinical Study Conducted in Multiple Centers Evaluating Escalating Doses of Veliparib in Combination With Capecitabine and Radiation in Patients With Locally Advanced Rectal Cancer". An open-label, Phase 1b, dose escalation study evaluating the safety and tolerability of the PARP inhibitor Veliparib in combination with capecitabine and radiation in subjects with locally advanced rectal cancer (LARC).

What is the current status of trial NCT01589419?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 2012-06. Estimated completion is 2015-01.

What interventions are being tested in trial NCT01589419?

The interventions under investigation include: capecitabine (DRUG), radiation (RADIATION), veliparib (DRUG).

Who is sponsoring clinical trial NCT01589419?

This trial is sponsored by AbbVie (prior sponsor, Abbott), which has 88 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.