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NCT01760252 · ClinicalTrials.gov registry record · Phase 2

Neoadjuvant CAPOXIRI Chemotherapy in the Treatment of Pancreatic Adenocarcinoma Protocol

A Phase 2 study, sponsored by Beth Israel Medical Center.

Terminated
Registry status
Phase 2
Development phase
17
Enrollment target

NCT01760252: Clinical Trial Phase 2 study, sponsored by Beth Israel Medical Center.

NCT01760252 is a Phase 2 study that was terminated before completion, run by Beth Israel Medical Center. The registered enrollment target is 17 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01760252, a Phase 2 study, was terminated before completion, sponsored by Beth Israel Medical Center.

TERMINATED
Registry status
Phase 2
Development phase
17 participants
Enrollment target

Study Summary

The combination of capecitabine, oxaliplatin, and irinotecan (CAPOXIRI) may be better than other combinations used to treat earlier stage pancreatic cancer patients with resectable (able to be cut out), borderline resectable, and locally advanced pancreatic adenocarcinoma. For subjects who can not obtain Capecitabine can be treated with 5-Fluorouracil (5-FU) along with Oxaliplatin and Irinotecan. Though all of the drugs in this study have been approved by the FDA, their combination is investigational. The purpose of this study is to evaluate the effects of CAPOXIRI (good and bad) on you and your cancer.

Primary Outcome

Adherence of subjects with treatment

Interventions

  • DRUG Capecitabine, Oxaliplatin and Irinotecan (CAPOXIRI)

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2011-12
Est. Completion 2018-02-21
Phase Phase 2
Beth Israel Medical Center

44 total trials

Why NCT01760252 stopped before completion

NCT01760252 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 17 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (87% lower).

The record links to 0 conditions, and to 1 intervention - of which Capecitabine, Oxaliplatin and Irinotecan (CAPOXIRI) is the first listed.

NCT01760252 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01760252 about?

NCT01760252 is a clinical study titled "Neoadjuvant CAPOXIRI Chemotherapy in the Treatment of Pancreatic Adenocarcinoma Protocol". The combination of capecitabine, oxaliplatin, and irinotecan (CAPOXIRI) may be better than other combinations used to treat earlier stage pancreatic cancer patients with resectable (able to be cut out), borderline resectable, and locally advanced pancreatic adenocarcinoma. For subjects who can not o...

What is the current status of trial NCT01760252?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 17 participants. The study started on 2011-12. Estimated completion is 2018-02-21.

What interventions are being tested in trial NCT01760252?

The interventions under investigation include: Capecitabine, Oxaliplatin and Irinotecan (CAPOXIRI) (DRUG).

Who is sponsoring clinical trial NCT01760252?

This trial is sponsored by Beth Israel Medical Center, which has 44 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01760252's enrollment target sits among peer trials

17 1903rd of 2000 higher than 93 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 NCT01760252, the US trial registry maintained by the National Library of Medicine. NCT01760252 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.