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NCT02550743 · ClinicalTrials.gov registry record · Phase 1

BrUOG 302:BYL719, Capecitabine and Radiation for Rectal Cancer: A Brown University Oncology Research Group Study

A Phase 1 study, sponsored by howard safran.

Terminated
Registry status
Phase 1
Development phase
7
Enrollment target

NCT02550743: Clinical Trial Phase 1 study, sponsored by howard safran.

NCT02550743 is a Phase 1 study that was terminated before completion, run by howard safran. The registered enrollment target is 7 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02550743, a Phase 1 study, was terminated before completion, sponsored by howard safran.

TERMINATED
Registry status
Phase 1
Development phase
7 participants
Enrollment target

Study Summary

The primary goal of this Brown University Oncology Research Group is to determine that a safe dose of BYL719 can be administered with capecitabine and radiation in patients with rectal cancer. Therefore, the threshold of success for this phase I study is to establish safety.

Interventions

  • DRUG Capecitabine
  • RADIATION Radiation
  • DRUG BYL719

Trial Details

FieldValue
Enrollment Target 7 participants
Start Date 2016-06-03
Est. Completion 2018-11-16
Phase Phase 1
howard safran

6 total trials

Why NCT02550743 stopped before completion

NCT02550743 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 7 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (88% lower).

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

NCT02550743 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02550743 about?

NCT02550743 is a clinical study titled "BrUOG 302:BYL719, Capecitabine and Radiation for Rectal Cancer: A Brown University Oncology Research Group Study". The primary goal of this Brown University Oncology Research Group is to determine that a safe dose of BYL719 can be administered with capecitabine and radiation in patients with rectal cancer. Therefore, the threshold of success for this phase I study is to establish safety.

What is the current status of trial NCT02550743?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 7 participants. The study started on 2016-06-03. Estimated completion is 2018-11-16.

What interventions are being tested in trial NCT02550743?

The interventions under investigation include: Capecitabine (DRUG), Radiation (RADIATION), BYL719 (DRUG).

Who is sponsoring clinical trial NCT02550743?

This trial is sponsored by howard safran, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02550743's enrollment target sits among peer trials

7 1972nd of 2000 higher than 27 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 NCT02550743, the US trial registry maintained by the National Library of Medicine. NCT02550743 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.