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NCT01059643 · ClinicalTrials.gov registry record · Phase 2

A Study in Ovarian, Non-Small Cell Lung, Prostate, Colorectal, Gastroesophageal Cancers, and Squamous Cell Carcinoma of the Head and Neck

A Phase 2 study, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 2
Development phase
103
Enrollment target

NCT01059643: Completed Phase 2 study, sponsored by Eli Lilly and Company.

NCT01059643 is a Phase 2 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 103 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (23% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01059643, a Phase 2 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 2
Development phase
103 participants
Enrollment target

Study Summary

The purpose of the study is to estimate the rate of response for patients with ovarian, non-small cell lung, prostate, colorectal, gastroesophageal, and head and neck cancers who are administered LY2523355.

Primary Outcome

The percentage of participants who achieved a best response of either CR or PR, as determined by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 guidelines. CR was defined as the disappearance of all target and non-target lesions and any pathological lymph nodes (whether target or non-target) must have reduction in short axis to \<10 millimeter (mm) and normalization of tumor marker level of non-target lesions. PR was defined as at least a 30% decrease in sum of longest diameter of tar

Interventions

  • DRUG pegfilgrastim
  • DRUG LY2523355

Trial Details

FieldValue
Enrollment Target 103 participants
Start Date 2011-04
Est. Completion 2012-12
Phase Phase 2
Eli Lilly and Company

1,341 total trials

What the finished NCT01059643 record still lists

NCT01059643 is an interventional study that assigns participants to a tested intervention. The registered 103 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (23% lower).

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

NCT01059643 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01059643 about?

NCT01059643 is a clinical study titled "A Study in Ovarian, Non-Small Cell Lung, Prostate, Colorectal, Gastroesophageal Cancers, and Squamous Cell Carcinoma of the Head and Neck". The purpose of the study is to estimate the rate of response for patients with ovarian, non-small cell lung, prostate, colorectal, gastroesophageal, and head and neck cancers who are administered LY2523355.

What is the current status of trial NCT01059643?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 103 participants. The study started on 2011-04. Estimated completion is 2012-12.

What interventions are being tested in trial NCT01059643?

The interventions under investigation include: pegfilgrastim (DRUG), LY2523355 (DRUG).

Who is sponsoring clinical trial NCT01059643?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01059643's enrollment target sits among peer trials

103 664th of 2000 higher than 1,333 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 NCT01059643, the US trial registry maintained by the National Library of Medicine. NCT01059643 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.