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NCT01074970 · ClinicalTrials.gov registry record · Phase 2

PARP Inhibition for Triple Negative Breast Cancer (ER-/PR-/HER2-)With BRCA1/2 Mutations

A Phase 2 study, sponsored by Hoosier Cancer Research Network.

Completed
Registry status
Phase 2
Development phase
135
Enrollment target

NCT01074970: Completed Phase 2 study, sponsored by Hoosier Cancer Research Network.

NCT01074970 is a Phase 2 study that has completed, run by Hoosier Cancer Research Network. The registered enrollment target is 135 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01074970, a Phase 2 study, has completed, sponsored by Hoosier Cancer Research Network.

COMPLETED
Registry status
Phase 2
Development phase
135 participants
Enrollment target

Study Summary

The purpose of this trial is to evaluate 2-year disease-free survival in this patient population treated with single agent cisplatin and patients treated with cisplatin in combination with Rucaparib following preoperative chemotherapy. Side effects and tolerability of this treatment in patients with residual disease following preoperative chemotherapy will also be observed and characterized.

Primary Outcome

To evaluate 2-year disease-free survival (DFS), in patients with confirmed TNBC or ER/PR + HER2-, known BRCA1/2 mutations treated with single agent cisplatin and patients treated with cisplatin in combination with Rucaparib following preoperative chemotherapy

Interventions

  • DRUG Cisplatin
  • DRUG Rucaparib

Trial Details

FieldValue
Enrollment Target 135 participants
Start Date 2010-02
Est. Completion 2018-12-15
Phase Phase 2
Hoosier Cancer Research Network

26 total trials

What the finished NCT01074970 record still lists

NCT01074970 is an interventional study that assigns participants to a tested intervention. The registered 135 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.

The record links to 0 conditions, and to 2 interventions - of which Cisplatin is the first listed.

NCT01074970 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01074970 about?

NCT01074970 is a clinical study titled "PARP Inhibition for Triple Negative Breast Cancer (ER-/PR-/HER2-)With BRCA1/2 Mutations". The purpose of this trial is to evaluate 2-year disease-free survival in this patient population treated with single agent cisplatin and patients treated with cisplatin in combination with Rucaparib following preoperative chemotherapy. Side effects and tolerability of this treatment in patients with...

What is the current status of trial NCT01074970?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 135 participants. The study started on 2010-02. Estimated completion is 2018-12-15.

What interventions are being tested in trial NCT01074970?

The interventions under investigation include: Cisplatin (DRUG), Rucaparib (DRUG).

Who is sponsoring clinical trial NCT01074970?

This trial is sponsored by Hoosier Cancer Research Network, which has 26 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01074970's enrollment target sits among peer trials

135 532nd of 2000 higher than 1,464 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 NCT01074970, the US trial registry maintained by the National Library of Medicine. NCT01074970 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.