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Myeloma Cure Project: Prospective Trial of Indefinite Revlimid Maintenance Versus Observation for Currently Event-Free Patients With Multiple Myeloma

This study is currently recruiting participants. (see Contacts and Locations)
Verified July 2014 by University of Arkansas
Sponsor:
Information provided by (Responsible Party):
University of Arkansas
ClinicalTrials.gov Identifier:
NCT01621672
First received: May 31, 2012
Last updated: July 11, 2014
Last verified: July 2014
  Purpose

The purpose of this study is to determine in a phase II trial, whether further maintenance therapy with Revlimid can extend the duration of progression-free survival and the duration of complete or near complete response compared to no further therapy beyond the TT3 protocol-prescribed 3 years of maintenance with 1 year of VTD plus 2 years with TD, 3 years with VTD (2003-33) or VRD (2006-66).


Condition Intervention Phase
Multiple Myeloma
Drug: Revlimid
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Myeloma Cure Project: Prospective, Randomized Trial of Indefinite Revlimid Maintenance Versus Observation for Currently Event-Free Patients With Multiple Myeloma Who Have Completed 3 Years of VTD/TD or VTD or VRD Maintenance on Total Therapy 3 (TT3) Trials 2003-33 and 2006-66

Resource links provided by NLM:


Further study details as provided by University of Arkansas:

Primary Outcome Measures:
  • Duration of complete or near complete response w/ Revlimid therapy compared to group with no Revlimid therapy [ Time Frame: 3 years ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Toxicities associated with Revlimid versus no further Revlimid treatment [ Time Frame: 3 years ] [ Designated as safety issue: No ]
    In qualitative and quantitative terms in context of pre-treatment parameters, in terms of platelet count and peripheral neuropathy


Estimated Enrollment: 300
Study Start Date: April 2010
Estimated Study Completion Date: April 2015
Estimated Primary Completion Date: April 2015 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Revlimid
Revlimid dosing will be in the morning at the same time each day
Drug: Revlimid
10 mg/day in the morning same time each day
Other Name: Lenalidomide
No Intervention: No further treatment or observation

Detailed Description:

Determine the associated toxicities in qualitative and quantitative terms using NCI CTCAE(NCI common terminology for adverse events)

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Male and female participants of all races/ethnicities with multiple myeloma previously enrolled on UARK 2003-33 or 2006-66.
  • Participant has completed 3 years of maintenance therapy with one of the three study drugs of VTD or VRD and disease status has remained event free (includes patients who prematurely discontinued maintenance therapy as long as 3 years have elapsed since beginning of maintenance).
  • All patients must be ages 18 years of age or greater at the time of signing the informed consent form.
  • Participant has adequate hematopoietic reserve, defined as platelets > 50,000/μL (in participants with bone marrow hypoplasia, remaining peripheral blood progenitor cells can be infused to boost hematopoietic reserve prior to enrollment).
  • Participant has adequate renal function defined as serum creatinine < 3 mg/dL prior to enrolling on study
  • Total bilirubin ≤ 1.5 mg/dL prior to enrolling on study
  • AST (SGOT) and ALT (SGPT) ≤ 2 x ULN prior to enrolling on study
  • Patient must have signed an IRB-approved informed consent and understand the investigational nature of the study.
  • All study participants must be registered into the mandatory RevAssist® program, and be willing and able to comply with the requirements of RevAssist®
  • Pregnant or nursing women may not participate. Females of childbearing potential (FCBP)† must have a negative serum or urine pregnancy test with a sensitivity of at least 50 mIU/mL within 10 - 14 days prior to and again within
  • 24 hours of prescribing Revlimid® (lenalidomide; prescriptions must be filled within 7 days) and must either commit to continued abstinence from heterosexual intercourse or begin TWO acceptable methods of birth control, one highly effective method and one additional effective method AT THE SAME TIME, at least 28 days before she starts taking Revlimid® (lenalidomide).
  • FCBP must also agree to ongoing pregnancy testing.
  • Lactating females must agree that they will not breastfeed.
  • Men must agree to use a latex condom during sexual contact with a FCBP even if they have had a successful vasectomy. See Appendix: Risks of Fetal Exposure,
  • Pregnancy Testing Guidelines and Acceptable Birth Control Methods † A female of childbearing potential is a sexually mature woman who:

    • has not undergone a hysterectomy or bilateral oophorectomy
    • has not been naturally postmenopausal for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months).

Exclusion Criteria:

  • Any condition that the PI believes, laboratory abnormality, or psychiatric illness that would prevent the subject from being enrolled in the research study.
  • Pregnant or breast feeding females. (Lactating females must agree not to breast feed while taking Revlimid®)
  • Any condition, including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he/she were to participate in the study or confounds the ability to interpret data from the study.
  • Use of any other experimental drug or therapy within 28 days of baseline.
  • Known hypersensitivity to thalidomide.
  • The development of erythema nodosum if characterized by a desquamating rash while taking thalidomide or similar drugs.
  • Concurrent use of other anti-cancer agents or treatments.
  • Known positive for HIV or infectious hepatitis, type B or C.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01621672

Contacts
Contact: Nathan Petty 501-526-6990 ext 2435 pettynathanm@uams.edu

Locations
United States, Arkansas
University of Arkansas for Medical Science-MIRT Recruiting
Little Rock, Arkansas, United States, 72205
Contact: Nathan Petty    501-526-6990 ext 2435    pettynathanm@uams.edu   
Sub-Investigator: Jameel Muzaffar, MD         
Sub-Investigator: Monica Grazziutti, MD         
Sub-Investigator: Senu Apewokin, MD         
Sub-Investigator: Shebli Atrash, MD         
Sub-Investigator: Frits Van Rhee, MD, PhD         
Sub-Investigator: Aziz Bakhous, MD         
Sub-Investigator: Vyjayanthi Ganga, MD         
Sub-Investigator: Maurizio Zangari, MD         
Sub-Investigator: Aasiya Matin, MD         
Sub-Investigator: Yogesh Jethava, MD         
Sub-Investigator: Rashid Khan, MD         
Sponsors and Collaborators
University of Arkansas
Investigators
Principal Investigator: Bart Barlogie, MD, PhD UAMS Myeloma Institute for Research & Therapy
  More Information

No publications provided

Responsible Party: University of Arkansas
ClinicalTrials.gov Identifier: NCT01621672     History of Changes
Other Study ID Numbers: UARK 2009-09
Study First Received: May 31, 2012
Last Updated: July 11, 2014
Health Authority: United States: Institutional Review Board

Keywords provided by University of Arkansas:
Revlimid
progression free
Lenalidomide

Additional relevant MeSH terms:
Multiple Myeloma
Neoplasms, Plasma Cell
Blood Protein Disorders
Cardiovascular Diseases
Hematologic Diseases
Hemorrhagic Disorders
Hemostatic Disorders
Immune System Diseases
Immunoproliferative Disorders
Lymphoproliferative Disorders
Neoplasms
Neoplasms by Histologic Type
Paraproteinemias
Vascular Diseases
Lenalidomide
Angiogenesis Inhibitors
Angiogenesis Modulating Agents
Antineoplastic Agents
Growth Inhibitors
Growth Substances
Immunologic Factors
Pharmacologic Actions
Physiological Effects of Drugs
Therapeutic Uses

ClinicalTrials.gov processed this record on November 25, 2014