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NCT01049893 · ClinicalTrials.gov registry record · Phase 1

Dose Finding, Safety and Tolerability Study for AC220 to Treat Advanced Solid Tumors

A Phase 1 study of Solid Tumors, sponsored by Daiichi Sankyo.

Completed
Registry status
Phase 1
Development phase
45
Enrollment target
2
Study locations

NCT01049893 is a Phase 1 study of Solid Tumors that has completed, run by Daiichi Sankyo. The registered enrollment target is 45 participants, below the 284-participant average among 125 other Solid Tumors trials with a reported enrollment target (84% lower). The trial reports 2 study locations across 2 states.

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The verdict

NCT01049893, a Phase 1 study of Solid Tumors, has completed, sponsored by Daiichi Sankyo.

COMPLETED
Registry status
Phase 1
Development phase
45 participants
Enrollment target
2
Study locations

Study Summary

AC220 will be administered as a once daily oral solution given continuously as 28-day treatment cycles, without food and without any rest periods, as long as there is no evidence of disease progression or unacceptably severe adverse events (AEs) related to the study drug.

Conditions Studied

Solid Tumors

Interventions

  • DRUG Compound AC220

Study Locations (2)

Massachusetts

  • Dana Farber Cancer Institute - Boston

Texas

  • South Texas Accelerated Research Therapeutics (START) - San Antonio

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2010-01
Est. Completion 2011-11
Phase Phase 1

Sponsor

Daiichi Sankyo

236 total trials

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What the Registry Record Tells You About NCT01049893

The ClinicalTrials.gov registry entry for NCT01049893 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 284-participant average among 125 other Solid Tumors trials with a reported enrollment target (84% lower). The listed sponsor is Daiichi Sankyo, which has 236 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Solid Tumors appearing as the primary indexed condition, and to 1 intervention - of which Compound AC220 is the first listed.

NCT01049893 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Massachusetts, Texas.

Frequently Asked Questions

What is clinical trial NCT01049893 about?

NCT01049893 is a clinical study titled "Dose Finding, Safety and Tolerability Study for AC220 to Treat Advanced Solid Tumors". AC220 will be administered as a once daily oral solution given continuously as 28-day treatment cycles, without food and without any rest periods, as long as there is no evidence of disease progression or unacceptably severe adverse events (AEs) related to the study drug.

What is the current status of trial NCT01049893?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 45 participants. The study started on 2010-01. Estimated completion is 2011-11.

What conditions does trial NCT01049893 study?

This clinical trial studies the following conditions: Solid Tumors.

What interventions are being tested in trial NCT01049893?

The interventions under investigation include: Compound AC220 (DRUG).

Who is sponsoring clinical trial NCT01049893?

This trial is sponsored by Daiichi Sankyo, which has 236 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01049893 being conducted?

This trial has 2 study locations across Massachusetts, Texas. 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 Editorial

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.