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NCT02281409 · ClinicalTrials.gov registry record · Phase 1

Safety, Tolerability, and Immunoregulatory Activity of Mogamulizumab (KW-0761) in Subjects With Advanced and/or Metastatic Solid Tumors

A Phase 1 study of Advanced Solid Tumors and Metastatic Solid Tumors, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
Phase 1
Development phase
17
Enrollment target
1
Study location

NCT02281409 is a Phase 1 study of Advanced Solid Tumors and Metastatic Solid Tumors that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 17 participants, below the 199-participant average among 144 other Advanced Solid Tumors trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02281409, a Phase 1 study of Advanced Solid Tumors and Metastatic Solid Tumors, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
Phase 1
Development phase
17 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to find out what effects, good and/or bad, KW-0761, an investigational drug, has on the patient and their cancer.

Interventions

  • BIOLOGICAL Mogamulizumab (KW-0761)

Study Locations (1)

New York

  • Memorial Sloan Kettering Cancer Center - New York

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2014-10
Est. Completion 2020-02
Phase Phase 1

Sponsor

Memorial Sloan Kettering Cancer Center

1,884 total trials

What the Registry Record Tells You About NCT02281409

The ClinicalTrials.gov registry entry for NCT02281409 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 17 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 199-participant average among 144 other Advanced Solid Tumors trials with a reported enrollment target (91% lower). The listed sponsor is Memorial Sloan Kettering Cancer Center, which has 1,884 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Advanced Solid Tumors appearing as the primary indexed condition, and to 1 intervention - of which Mogamulizumab (KW-0761) is the first listed.

NCT02281409 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT02281409 about?

NCT02281409 is a clinical study titled "Safety, Tolerability, and Immunoregulatory Activity of Mogamulizumab (KW-0761) in Subjects With Advanced and/or Metastatic Solid Tumors". The purpose of this study is to find out what effects, good and/or bad, KW-0761, an investigational drug, has on the patient and their cancer.

What is the current status of trial NCT02281409?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 17 participants. The study started on 2014-10. Estimated completion is 2020-02.

What conditions does trial NCT02281409 study?

This clinical trial studies the following conditions: Advanced Solid Tumors, Metastatic Solid Tumors.

What interventions are being tested in trial NCT02281409?

The interventions under investigation include: Mogamulizumab (KW-0761) (BIOLOGICAL).

Who is sponsoring clinical trial NCT02281409?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02281409 being conducted?

This trial has 1 study location across New York. 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.