Randomized Trial Comparing Lenalidomide With Low Dose Dexamethasone Versus Lenalidomide in Second Line Multiple Myeloma

Phase 2

Completed

• Conditions: Multiple Myeloma
• Interventions: Drug: Revlimid

• Registration Number: NCT01450215
• Lead Sponsor: Karolinska University Hospital

Brief Summary

This is:

* A prospective, randomized, open, phase II, multi-centre, interventional study. Patients who are in at least PR and have received lenalidomide as 2nd line treatment for MM will be recruited.

* The patients will be randomized into two groups. Group R will receive lenalidomide 25 mg/day p.o. continuously for 21 days and group Rb will receive a similar dose of lenalidomide with the addition of 40 mg of dexamethasone p.o. on days 1, 8, 15 and 22 of every 28 day treatment cycle. Study includes a maximum of 24 cycles including two consolidating cycles per patients.

Detailed Description

Not available

Study Timeline

• Study Start: 2011-03
• Study First Submitted: 2011-09-07
• Study First Submitted QC: 2011-10-09
• Study First Posted: 2011-10-12
• Primary Completion: 2016-01
• Status Verified: 2016-03
• Last Update Submitted: 2016-03-24
• Last Update Posted: 2016-03-25

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 62

Inclusion Criteria

Inclusion Criteria - all subjects must:

1. Be at least 18 years of age

2. Subjects must have a documented diagnosis of MM and have either refractory or relapsed and refractory after first line treatment disease defined as:

   • Primary refractory
   • Refractory
   • Relapsed and Refractory

3. Subjects must have undergone prior treatment with one treatment line of anti-myeloma therapy. Induction therapy followed by ASCT and consolidation/maintenance will be considered as one line.Have a confirmed diagnosis of MM

4. Have received lenalidomide after one prior treatment for MM and have reached at least a partial response (PR), according to IMWG criteria, including two consolidating cycles. Subjects have experienced a response at least PR after starting treatment with lenalidomide and cortisone cycles.

5. Have personally signed and dated a legally effective written informed consent form prior to admission to the study.

6. Must be willing and able to understand and comply with the study requirements.

7. Females of childbearing potential must agree to ongoing pregnancy testing and to practice contraception.

8. Male must agree to practice contraception

Exclusion Criteria

1. Any of the following laboratory abnormalities:

   • Absolute neutrophil count (ANC) < 1,000/µL
   • Platelet count < 75,000/ µL
   • Creatinine Clearance < 45 mL/min according to Cockcroft-Gault formula
   • Serum SGOT/AST or SGPT/ALT > 3.0 x upper limit of normal (ULN)
   • Serum total bilirubin > 2.0 mg/dL

2. ECOG performance status <4.

3. Individuals who have had a stem-cell transplant as a 2nd line treatment for MM

4. Individuals who have taken any experimental drugs or participated in a clinical trial within 30 days prior to screening.

5. Individuals with significant psychiatric illness or a clinically significant acute/chronic uncontrolled medical condition that might affect their experience of myeloma symptoms or their ability to describe them.

6. Pregnant or lactating females.

7. Any other clinically significant medical disease or condition that, in the Investigator´s opinion, may interfere with protocol adherence or a subject´s ability to give informed consent.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Revlimid	Revlimid	-

Primary Outcome Measures

Name	Time	Method
Time to progression	24 months

Secondary Outcome Measures

Name	Time	Method
Number of Participants with Adverse Events	participants will be followed for the duration of hospital stay, an expected average of 2 years	Number of Participants with Adverse Events

Trial Locations

Locations (2)

Karolinska Institute; 🇸🇪 Stockholm, Sweden

Karolinska Inst.; 🇸🇪 Stockholm, Sweden