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Study of Lenalidomide as a Treatment for Neuropathy Associated With Monoclonal Gammopathy of Undetermined Significance (MGUS)
This study is currently recruiting participants.
Study NCT00665652   Information provided by Dartmouth-Hitchcock Medical Center
First Received: April 22, 2008   Last Updated: August 26, 2009   History of Changes

April 22, 2008
August 26, 2009
April 2008
April 2010   (final data collection date for primary outcome measure)
The primary objective is to evaluate the change in neuropathy in subjects with MGUS associated neuropathy after treatment with lenalidomide. [ Time Frame: Once 15 participants have been treated with three cycles of lenalidomide. ] [ Designated as safety issue: Yes ]
Same as current
Complete list of historical versions of study NCT00665652 on ClinicalTrials.gov Archive Site
 
 
 
Study of Lenalidomide as a Treatment for Neuropathy Associated With Monoclonal Gammopathy of Undetermined Significance
A Phase II Trial of Lenalidomide as a Treatment for Neuropathy Associated With Nonmalignant Monoclonal Gammopathy of Undetermined Significance (MGUS)

The purpose of the study is to learn about the effects of the drug, lenalidomide (Revlimid®), on neuropathy (damage to the nerves that affect feelings and strength) associated with Nonmalignant Monoclonal Gammopathy of Undetermined Significance (MGUS).

 
Phase II
Interventional
Supportive Care, Open Label, Single Group Assignment, Efficacy Study
  • Neuropathy
  • Nonmalignant Monoclonal Gammopathy of Undetermined Significance (MGUS)
Drug: Lenalidomide
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
30
April 2010
April 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Clinically proven MGUS associated neuropathy with a Total Neuropathy Score (TNS) ≥5 (determined by exam, history and confirmatory EDX testing in association with MGUS (IgM,IgG,IgA))
  • Disease duration less than or equal to 8 years
  • Able to take Plavix 75mg/day or aspirin 325 mg daily as prophylactic anticoagulation. (patients currently taking warfarin with a stable INR may stay on current dose)

Exclusion Criteria:

  • Patients previously treated with thalidomide
  • Patients previously treated with lenalidomide
  • Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form.
  • The development of erythema nodosum if characterized by a desquamating rash while taking thalidomide or similar drugs
  • Known positive for HIV or infectious hepatitis, type A, B or C
  • Medical history of deep venous thrombosis or hyper-coagulable state
  • Gastrointestinal abnormalities including: inability to take oral medication, requirement for intravenous alimentation, prior surgical procedures affecting absorption, or active peptic ulcer disease
  • Patients with dementia, other serious neurological diseases, uncompensated medical illness, substance abuse and debilitating psychiatric illness.
  • A serious uncontrolled medical disorder or active infection that would impair the patient's ability to receive study treatment. Significant cardiac disease, including uncontrolled high blood pressure, unstable angina, congestive heart failure, myocardial infarction within the previous 6 months or serious cardiac arrhythmias will be excluded.
  • Medical conditions associated with neuropathy such as active thyroid disease, diabetes mellitus, and lupus, nutritional deficiencies, malignancy, human immunodeficiency virus infection, alcohol dependence, amyloidosis, or connective tissue diseases and Guillain-Barre Syndrome. Medications or toxic exposures known to cause neuropathy, or a family history of neuropathy will also be grounds for exclusion.
  • Pregnant or breast feeding females. (Lactating females must agree not to breast feed while taking lenalidomide).
  • Subjects who are allergic to aspirin or Plavix (clopidogrel)
Both
18 Years and older
No
Contact: Jessica Johnson 603-650-4145 Jessica.Johnson@Hitchcock.ORG
United States
 
NCT00665652
Elijah Stommel, MD, PhD, Dartmouth-Hitchcock Medical Center
RV-PN-PI-235
Dartmouth-Hitchcock Medical Center
Celgene Corporation
Principal Investigator: Elijah W. Stommel, MD, PhD Dartmouth-Hitchcock Medical Center
Dartmouth-Hitchcock Medical Center
August 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP