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NCT01629758 · ClinicalTrials.gov registry record · Phase 1

Safety Study of IL-21/Anti-PD-1 Combination in the Treatment of Solid Tumors

A Phase 1 study of Neoplasms by Site, sponsored by Bristol-Myers Squibb.

Completed
Registry status
Phase 1
Development phase
33
Enrollment target
5
Study locations

NCT01629758 is a Phase 1 study of Neoplasms by Site that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 33 participants, below the 509-participant average among 11 other Neoplasms by Site trials with a reported enrollment target (94% lower). The trial reports 5 study locations across 5 states.

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The verdict

NCT01629758, a Phase 1 study of Neoplasms by Site, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
33 participants
Enrollment target
5
Study locations

Study Summary

The purpose of this study is to determine whether the combination of the 2 drugs being investigated (IL-21 and anti-PD-1) is safe, and provide preliminary information on the clinical benefits of two different schedules of the combination.

Conditions Studied

Interventions

  • BIOLOGICAL Nivolumab
  • BIOLOGICAL Denenicokin

Study Locations (5)

Arizona

  • Oncology Research Associates, Pllc D/B/A - Scottsdale

Connecticut

  • Yale University School Of Medicine - New Haven

Florida

  • Moffitt Cancer Center - Tampa

Maryland

  • Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins - Baltimore

Washington

  • Seattle Cancer Care Alliance - Seattle

Trial Details

FieldValue
Enrollment Target 33 participants
Start Date 2012-06
Est. Completion 2014-12
Phase Phase 1

Sponsor

Bristol-Myers Squibb

1,025 total trials

What the Registry Record Tells You About NCT01629758

The ClinicalTrials.gov registry entry for NCT01629758 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 33 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 509-participant average among 11 other Neoplasms by Site trials with a reported enrollment target (94% lower). The listed sponsor is Bristol-Myers Squibb, which has 1,025 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Neoplasms by Site appearing as the primary indexed condition, and to 2 interventions - of which Nivolumab is the first listed.

NCT01629758 reports 5 study locations spanning 5 distinct geographic areas - top geographies include Arizona, Connecticut, Florida.

Frequently Asked Questions

What is clinical trial NCT01629758 about?

NCT01629758 is a clinical study titled "Safety Study of IL-21/Anti-PD-1 Combination in the Treatment of Solid Tumors". The purpose of this study is to determine whether the combination of the 2 drugs being investigated (IL-21 and anti-PD-1) is safe, and provide preliminary information on the clinical benefits of two different schedules of the combination.

What is the current status of trial NCT01629758?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 33 participants. The study started on 2012-06. Estimated completion is 2014-12.

What conditions does trial NCT01629758 study?

This clinical trial studies the following conditions: Neoplasms by Site.

What interventions are being tested in trial NCT01629758?

The interventions under investigation include: Nivolumab (BIOLOGICAL), Denenicokin (BIOLOGICAL).

Who is sponsoring clinical trial NCT01629758?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01629758 being conducted?

This trial has 5 study locations across Arizona, Connecticut, Florida, Maryland, Washington. 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.