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Completed Phase 2 Interventional

Efficacy of Perifosine Alone and in Combination With Dexamethasone for Patients With Multiple Myeloma

ClinicalTrials.gov ID: NCT00375791

Public ClinicalTrials.gov record NCT00375791. 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 Oct 19, 2026, 10:29 AM EDT

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

Official title

An Open-Label Phase II Study of the Safety and Efficacy of Perifosine Alone and in Combination With Dexamethasone for Patients With Relapsed or Relapsed/Refractory Multiple Myeloma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a phase 2 study of perifosine in patients with multiple myeloma. Patients will receive perifosine 150 mg at bedtime (qhs) daily. Patients will be assessed by serum and/or urine-electrophoresis at least every 3 weeks.

Study identification

NCT ID
NCT00375791
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AEterna Zentaris
Industry
Enrollment
67 participants

Conditions and interventions

Interventions

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
Dec 2005 (Type not available)
Primary completion
Dec 2010 (Actual)
Completion
Oct 2011 (Actual)
Last update posted
Feb 28, 2018

2005 – 2011

United States locations

U.S. sites
7
U.S. states
6
U.S. cities
7
Facility City State ZIP Site status
Investigative Site Berkeley California 94704 —
Investigative Site Duarte California 91010 —
Investigative Site Atlanta Georgia 30322 —
Investigative Site Chicago Illinois 60611 —
Investigative Site Boston Massachusetts 02115 —
Investigative Site Ann Arbor Michigan 48103 —
Investigative Site Charlottesville Virginia 22908 —

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 NCT00375791, 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 Feb 28, 2018 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00375791 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →