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NCT01220271 · ClinicalTrials.gov registry record · Phase 1

A Study Combining LY2157299 With Temozolomide-based Radiochemotherapy in Patients With Newly Diagnosed Malignant Glioma

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

Completed
Registry status
Phase 1
Development phase
75
Enrollment target

NCT01220271: Completed Phase 1 study, sponsored by Eli Lilly and Company.

NCT01220271 is a Phase 1 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 75 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (25% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01220271, a Phase 1 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 1
Development phase
75 participants
Enrollment target

Study Summary

The purpose of this trial is to show proof of concept that by blocking the Transforming Growth Factor-beta signaling pathway in patients with Glioblastoma, there will be clinical benefit. Phase 1b: To determine the safe and tolerable dose of LY2157299 in combination with radiochemotherapy with temozolomide for Phase 2 in patients with glioma eligible to receive radiochemotherapy with temozolomide (e.g. newly diagnosed malignant glioma World Health Organization Grade III and IV). Phase 2a: To confirm the tolerability and evaluate the pharmacodynamic effect of LY2157299 in combination with standard radiochemotherapy in patients with newly diagnosed glioblastoma.

Interventions

  • DRUG Temozolomide
  • DRUG Radiation
  • DRUG LY2157299

Trial Details

FieldValue
Enrollment Target 75 participants
Start Date 2011-04
Est. Completion 2016-11
Phase Phase 1
Eli Lilly and Company

1,341 total trials

What the finished NCT01220271 record still lists

NCT01220271 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 75 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (25% higher).

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

NCT01220271 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01220271 about?

NCT01220271 is a clinical study titled "A Study Combining LY2157299 With Temozolomide-based Radiochemotherapy in Patients With Newly Diagnosed Malignant Glioma". The purpose of this trial is to show proof of concept that by blocking the Transforming Growth Factor-beta signaling pathway in patients with Glioblastoma, there will be clinical benefit. Phase 1b: To determine the safe and tolerable dose of LY2157299 in combination with radiochemotherapy with temo...

What is the current status of trial NCT01220271?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 75 participants. The study started on 2011-04. Estimated completion is 2016-11.

What interventions are being tested in trial NCT01220271?

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

Who is sponsoring clinical trial NCT01220271?

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 NCT01220271's enrollment target sits among peer trials

75 711th of 2000 higher than 1,276 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 NCT01220271, the US trial registry maintained by the National Library of Medicine. NCT01220271 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.