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Completed Phase 2 Interventional Results available

Lenalidomide Intensification in Patients With Serologic/Asymptomatic Progression of Multiple Myeloma While on Lenalidomide Maintenance

ClinicalTrials.gov ID: NCT01463670

Public ClinicalTrials.gov record NCT01463670. 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 Sep 25, 2026, 4:53 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 II Clinical Trial of Lenalidomide Intensification in Patients With Serologic/Asymptomatic Progression of Multiple Myeloma While on Lenalidomide Maintenance

Brief summary

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

The purpose of this study is to determine whether this disease will get better if treated with higher doses of Lenalidomide even if the disease returns while taking low doses of Lenalidomide. In patients with multiple myeloma treated with Lenalidomide maintenance, the disease will return. However, the physician currently does not know if the disease would respond to treatment with higher doses of Lenalidomide. This is very important for patients with multiple myeloma because the number of drugs available to treat the disease are limited. It is important to know if Lenalidomide remains still effective and if it can still be used in this situation. This study will try to find out what effects, good and/or bad higher doses of Lenalidomide has on the patient and the disease after it has returned.

Study identification

NCT ID
NCT01463670
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
11 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
Oct 27, 2011
Primary completion
Mar 18, 2021
Completion
Mar 18, 2021
Last update posted
May 5, 2022

2011 – 2021

United States locations

U.S. sites
11
U.S. states
3
U.S. cities
9
Facility City State ZIP Site status
Stamford Hospital Stamford Connecticut 06902 —
Memorial Sloan Kettering at Basking Ridge Basking Ridge New Jersey 07920 —
Memoral Sloan Kettering Cancer Center Basking Ridge New Jersey — —
SUNY Downstate Medical Center Brooklyn New York — —
North Shore LIJ New Hyde Park New York 11040 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
Weill Cornell Medical Center New York New York 10065 —
University of Rochester Medical Center Rochester New York — —
Memorial Sloan Kettering at Mercy Medical Center Rockville Centre New York — —
Memoral Sloan Kettering Cancer Center at Phelps Sleepy Hollow New York 10591 —
Montefiore Medical Center The Bronx New York 10467 —

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 NCT01463670, 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 May 5, 2022 · Synced Sep 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01463670 live on ClinicalTrials.gov.

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