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NCT01674842 · ClinicalTrials.gov registry record · Phase 1

Cisplatin + RT for Triple Negative Breast Cancer

A Phase 1 study, sponsored by Dana-Farber Cancer Institute.

Completed
Registry status
Phase 1
Development phase
55
Enrollment target

NCT01674842: Completed Phase 1 study, sponsored by Dana-Farber Cancer Institute.

NCT01674842 is a Phase 1 study that has completed, run by Dana-Farber Cancer Institute. The registered enrollment target is 55 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01674842, a Phase 1 study, has completed, sponsored by Dana-Farber Cancer Institute.

COMPLETED
Registry status
Phase 1
Development phase
55 participants
Enrollment target

Study Summary

This is a Phase I dose escalation study of cisplatin and concurrent radiation in patients with ER negative, PR negative and HER2 negative breast cancer who have undergone breast-conserving surgery or mastectomy. Primary objective: To assess the safety, tolerability, and maximum tolerated dose (MTD) of cisplatin when given concurrently with radiation therapy for participants with Stage II or III breast cancer who have undergone breast conserving surgery or mastectomy

Primary Outcome

To determine the maximum tolerated dose of cisplatin when given concurrently with radiation therapy for participants with Stage II or III breast cancer who have undergone breast conserving surgery or mastectomy.

Interventions

  • DRUG Cisplatin
  • RADIATION Radiation Therapy

Trial Details

FieldValue
Enrollment Target 55 participants
Start Date 2012-10
Est. Completion 2021-06-08
Phase Phase 1
Dana-Farber Cancer Institute

781 total trials

What the finished NCT01674842 record still lists

NCT01674842 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 55 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.

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

NCT01674842 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01674842 about?

NCT01674842 is a clinical study titled "Cisplatin + RT for Triple Negative Breast Cancer". This is a Phase I dose escalation study of cisplatin and concurrent radiation in patients with ER negative, PR negative and HER2 negative breast cancer who have undergone breast-conserving surgery or mastectomy. Primary objective: To assess the safety, tolerability, and maximum tolerated dose (MTD)...

What is the current status of trial NCT01674842?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 55 participants. The study started on 2012-10. Estimated completion is 2021-06-08.

What interventions are being tested in trial NCT01674842?

The interventions under investigation include: Cisplatin (DRUG), Radiation Therapy (RADIATION).

Who is sponsoring clinical trial NCT01674842?

This trial is sponsored by Dana-Farber Cancer Institute, which has 781 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01674842's enrollment target sits among peer trials

55 918th of 2000 higher than 1,070 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 NCT01674842, the US trial registry maintained by the National Library of Medicine. NCT01674842 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.