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NCT01359657 · ClinicalTrials.gov registry record · Phase 1

Anti-CXCR4 (BMS-936564) Alone and in Combination With Lenalidomide/Dexamethasone or Bortezomib/Dexamethasone in Relapsed/Refractory Multiple Myeloma

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

Completed
Registry status
Phase 1
Development phase
46
Enrollment target

NCT01359657 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 46 participants.

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The verdict

NCT01359657, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
46 participants
Enrollment target

Study Summary

The purpose of this study is to determine 1) the safety and tolerability of multiple intravenous doses of anti-CXCR4 (BMS-936564) as monotherapy and as combination, and 2) the maximum tolerated dose (MTD) of BMS-936564 in combination with Lenalidomide/Dexamethasone or Bortezomib/Dexamethasone in subjects with relapsed or refractory multiple myeloma.

Interventions

  • BIOLOGICAL Bortezomib
  • BIOLOGICAL Anti-CXCR4 (BMS-936564)
  • BIOLOGICAL Lenalidomide
  • BIOLOGICAL Dexamethasone

Trial Details

FieldValue
Enrollment Target 46 participants
Start Date 2011-09
Est. Completion 2016-03
Phase Phase 1

Sponsor

Bristol-Myers Squibb

1,025 total trials

What the Registry Record Tells You About NCT01359657

The ClinicalTrials.gov registry entry for NCT01359657 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 46 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bristol-Myers Squibb, which has 1,025 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 4 interventions - of which Bortezomib is the first listed.

NCT01359657 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01359657 about?

NCT01359657 is a clinical study titled "Anti-CXCR4 (BMS-936564) Alone and in Combination With Lenalidomide/Dexamethasone or Bortezomib/Dexamethasone in Relapsed/Refractory Multiple Myeloma". The purpose of this study is to determine 1) the safety and tolerability of multiple intravenous doses of anti-CXCR4 (BMS-936564) as monotherapy and as combination, and 2) the maximum tolerated dose (MTD) of BMS-936564 in combination with Lenalidomide/Dexamethasone or Bortezomib/Dexamethasone in sub...

What is the current status of trial NCT01359657?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 46 participants. The study started on 2011-09. Estimated completion is 2016-03.

What interventions are being tested in trial NCT01359657?

The interventions under investigation include: Bortezomib (BIOLOGICAL), Anti-CXCR4 (BMS-936564) (BIOLOGICAL), Lenalidomide (BIOLOGICAL), Dexamethasone (BIOLOGICAL).

Who is sponsoring clinical trial NCT01359657?

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

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.