ClinicalTrials.gov record
Completed Phase 1 Interventional

Safety and Dose Study of GRN163L and Velcade to Treat Patients With Refractory or Relapsed Myeloma

ClinicalTrials.gov ID: NCT00718601

Public ClinicalTrials.gov record NCT00718601. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 20, 2026, 11:56 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase I Study of GRN163L in Combination With Bortezomib and Dexamethasone in Patients With Relapsed or Refractory Multiple Myeloma

Study identification

NCT ID
NCT00718601
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Geron Corporation
Industry
Enrollment
40 participants

Conditions and interventions

Interventions

  • Imetelstat Sodium (GRN163L) Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 30, 2008
Primary completion
Sep 30, 2011
Completion
Sep 30, 2011
Last update posted
Dec 23, 2015

2008 – 2011

United States locations

U.S. sites
3
U.S. states
3
U.S. cities
3
Facility City State ZIP Site status
Karmanos Cancer Center Detroit Michigan 48201
St. Vincent's Comprehensive Cancer Center New York New York 10011
Fred Hutchinson Cancer Research Center Seattle Washington 98109

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00718601, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 23, 2015 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00718601 live on ClinicalTrials.gov.

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