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NCT01154426 · ClinicalTrials.gov registry record · Phase 1

ABT-888 and Gemcitabine Hydrochloride in Treating Patients With Advanced Solid Tumors

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

Completed
Registry status
Phase 1
Development phase
31
Enrollment target

NCT01154426: Completed Phase 1 study, sponsored by National Cancer Institute (NCI).

NCT01154426 is a Phase 1 study that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 31 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (48% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT01154426, a Phase 1 study, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 1
Development phase
31 participants
Enrollment target

Study Summary

This phase I trial is studying the side effects and best dose of giving ABT-888 together with gemcitabine hydrochloride in treating patients with advanced solid tumors. ABT-888 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as gemcitabine hydrochloride, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving ABT-888 together with gemcitabine hydrochloride may kill more tumor cells.

Interventions

  • DRUG Gemcitabine Hydrochloride
  • OTHER Diagnostic Laboratory Biomarker Analysis
  • OTHER Pharmacological Study
  • DRUG Veliparib

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2010-05
Est. Completion 2013-10
Phase Phase 1
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT01154426 record still lists

NCT01154426 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 31 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (48% lower).

The record links to 0 conditions, and to 4 interventions - of which Gemcitabine Hydrochloride is the first listed.

NCT01154426 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01154426 about?

NCT01154426 is a clinical study titled "ABT-888 and Gemcitabine Hydrochloride in Treating Patients With Advanced Solid Tumors". This phase I trial is studying the side effects and best dose of giving ABT-888 together with gemcitabine hydrochloride in treating patients with advanced solid tumors. ABT-888 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such...

What is the current status of trial NCT01154426?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 31 participants. The study started on 2010-05. Estimated completion is 2013-10.

What interventions are being tested in trial NCT01154426?

The interventions under investigation include: Gemcitabine Hydrochloride (DRUG), Diagnostic Laboratory Biomarker Analysis (OTHER), Pharmacological Study (OTHER), Veliparib (DRUG).

Who is sponsoring clinical trial NCT01154426?

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 NCT01154426's enrollment target sits among peer trials

31 1322nd of 2000 higher than 669 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 NCT01154426, the US trial registry maintained by the National Library of Medicine. NCT01154426 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.