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NCT01682187 · ClinicalTrials.gov registry record · Phase 1

A Dose-Escalation Study in Participants With Recurrent Malignant Glioma

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

Completed
Registry status
Phase 1
Development phase
66
Enrollment target
4
Study locations

NCT01682187 is a Phase 1 study of Glioma that has completed, run by Eli Lilly and Company. The registered enrollment target is 66 participants, below the 209-participant average among 87 other Glioma trials with a reported enrollment target (68% lower). The trial reports 4 study locations across 2 states.

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The verdict

NCT01682187, a Phase 1 study of Glioma, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 1
Development phase
66 participants
Enrollment target
4
Study locations

Study Summary

This is a study of oral LY2157299 as monotherapy and in combination with lomustine in participants with recurrent malignant glioma.

Conditions Studied

Interventions

  • DRUG Lomustine
  • DRUG LY2157299

Study Locations (4)

Other

  • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. - Barcelona
  • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. - Madrid
  • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. - Seville

Maryland

  • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. - Baltimore

Trial Details

FieldValue
Enrollment Target 66 participants
Start Date 2005-12-15
Est. Completion 2024-09-30
Phase Phase 1

Sponsor

Eli Lilly and Company

1,341 total trials

What the Registry Record Tells You About NCT01682187

The ClinicalTrials.gov registry entry for NCT01682187 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 66 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 209-participant average among 87 other Glioma trials with a reported enrollment target (68% lower). The listed sponsor is Eli Lilly and Company, which has 1,341 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Glioma appearing as the primary indexed condition, and to 2 interventions - of which Lomustine is the first listed.

NCT01682187 reports 4 study locations spanning 2 distinct geographic areas - top geographies include Other, Maryland.

Frequently Asked Questions

What is clinical trial NCT01682187 about?

NCT01682187 is a clinical study titled "A Dose-Escalation Study in Participants With Recurrent Malignant Glioma". This is a study of oral LY2157299 as monotherapy and in combination with lomustine in participants with recurrent malignant glioma.

What is the current status of trial NCT01682187?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 66 participants. The study started on 2005-12-15. Estimated completion is 2024-09-30.

What conditions does trial NCT01682187 study?

This clinical trial studies the following conditions: Glioma.

What interventions are being tested in trial NCT01682187?

The interventions under investigation include: Lomustine (DRUG), LY2157299 (DRUG).

Who is sponsoring clinical trial NCT01682187?

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

Where is trial NCT01682187 being conducted?

This trial has 4 study locations across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.