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NCT01308840 · ClinicalTrials.gov registry record · Phase 2

Gemcitabine, Oxaliplatin and Panitumumab in Kras/B-raf Wild-Type Biliary Track and Gallbladder Cancer

A Phase 2 study, sponsored by University of Rochester.

Completed
Registry status
Phase 2
Development phase
31
Enrollment target

NCT01308840: Completed Phase 2 study, sponsored by University of Rochester.

NCT01308840 is a Phase 2 study that has completed, run by University of Rochester. The registered enrollment target is 31 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01308840, a Phase 2 study, has completed, sponsored by University of Rochester.

COMPLETED
Registry status
Phase 2
Development phase
31 participants
Enrollment target

Study Summary

The purpose of this study is to determine disease response of GEMOX-Panitumumab (GEMOX-P) in KRAS/ BRAF wild-type, Stage IV, biliary tract and gallbladder cancer patients who have previously not received chemotherapy. This study will also examine the potential toxicities, progression-free and overall survival in this population.

Primary Outcome

Tumor measurement - same imaging modality used in pre-treatment evaluation - include radiological examination of all areas with affected disease. For pretreatment and at the end of cycle 2 CT scans (chest/abdomen/pelvis) will be used. For all subsequent cycles, CT of chest/abdomen/pelvis will be used every 8 weeks.

Interventions

  • DRUG oxaliplatin
  • DRUG Panitumumab
  • DRUG gemcitabine

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2010-12
Est. Completion 2013-01
Phase Phase 2
University of Rochester

636 total trials

What the finished NCT01308840 record still lists

NCT01308840 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 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (77% lower).

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

NCT01308840 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01308840 about?

NCT01308840 is a clinical study titled "Gemcitabine, Oxaliplatin and Panitumumab in Kras/B-raf Wild-Type Biliary Track and Gallbladder Cancer". The purpose of this study is to determine disease response of GEMOX-Panitumumab (GEMOX-P) in KRAS/ BRAF wild-type, Stage IV, biliary tract and gallbladder cancer patients who have previously not received chemotherapy. This study will also examine the potential toxicities, progression-free and overal...

What is the current status of trial NCT01308840?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 31 participants. The study started on 2010-12. Estimated completion is 2013-01.

What interventions are being tested in trial NCT01308840?

The interventions under investigation include: oxaliplatin (DRUG), Panitumumab (DRUG), gemcitabine (DRUG).

Who is sponsoring clinical trial NCT01308840?

This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01308840's enrollment target sits among peer trials

31 1578th of 2000 higher than 419 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 NCT01308840, the US trial registry maintained by the National Library of Medicine. NCT01308840 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.