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NCT01648764 · ClinicalTrials.gov registry record · Phase 1

A Study of LY2334737 in Participants With Cancer That is Advanced and/or Has Spread

A Phase 1 study, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 1
Development phase
73
Enrollment target

NCT01648764: Completed Phase 1 study, sponsored by Eli Lilly and Company.

NCT01648764 is a Phase 1 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 73 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (22% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01648764, a Phase 1 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 1
Development phase
73 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate two different dosing regimens of LY2334737 in participants with cancer that is advanced and/or has spread to other parts of the body. Information about side effects will be collected.

Primary Outcome

Recommended Phase 2 dose was determined by maximum tolerated dose (MTD). The MTD was the highest dose level at which \<2 out of 6 participants experienced a dose-limiting toxicity (DLT) in Cycle 1. DLT was an adverse event (AE) during Cycle 1 that was likely related to LY2334737 and fulfilled any of the following criteria: Common Terminology Criteria for Adverse Events (CTCAE) ≥Grade 3 nonhematological (except nausea/vomiting controlled with treatment); Grade 3 neutropenia with fever or any Grad

Interventions

  • DRUG LY2334737

Trial Details

FieldValue
Enrollment Target 73 participants
Start Date 2008-09
Est. Completion 2012-11
Phase Phase 1
Eli Lilly and Company

1,341 total trials

What the finished NCT01648764 record still lists

NCT01648764 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 73 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (22% higher).

The record links to 0 conditions, and to 1 intervention - of which LY2334737 is the first listed.

NCT01648764 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01648764 about?

NCT01648764 is a clinical study titled "A Study of LY2334737 in Participants With Cancer That is Advanced and/or Has Spread". The purpose of this study is to evaluate two different dosing regimens of LY2334737 in participants with cancer that is advanced and/or has spread to other parts of the body. Information about side effects will be collected.

What is the current status of trial NCT01648764?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 73 participants. The study started on 2008-09. Estimated completion is 2012-11.

What interventions are being tested in trial NCT01648764?

The interventions under investigation include: LY2334737 (DRUG).

Who is sponsoring clinical trial NCT01648764?

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 NCT01648764's enrollment target sits among peer trials

73 732nd of 2000 higher than 1,265 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 NCT01648764, the US trial registry maintained by the National Library of Medicine. NCT01648764 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.