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Thalidomide to Patients With Previously Untreated Multiple Myeloma

Primary Purpose

Multiple Myeloma

Status
Completed
Phase
Phase 3
Locations
Norway
Study Type
Interventional
Intervention
thalidomide
placebo
Sponsored by
Norwegian University of Science and Technology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Myeloma focused on measuring Multiple Myeloma, Phase 3, randomised, double blind study, thalidomide

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients with multiple myeloma in need of treatment Exclusion Criteria: Previous treatment against multiple myeloma Need of high dose chemotherapy with autologous stem cell support Women in fertile age Psychiatric disease or mental reduction leading to lack of cooperation Lack of consent Life expectancy below 3 months Active cancer of other etiology

Sites / Locations

  • Department of Haematology, St. Olavs hospital/NTNU

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

A

B

Arm Description

Outcomes

Primary Outcome Measures

overall survival

Secondary Outcome Measures

Quality of life
Time to response
Frequency of response
Time to progression
Time to 2. response
Frequency of 2. response
Time to 2. progression
Toxicity
Time to definitive treatment failure

Full Information

First Posted
September 20, 2005
Last Updated
March 6, 2014
Sponsor
Norwegian University of Science and Technology
Collaborators
The Research Council of Norway, Nordic Myeloma Study Group, Germany
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1. Study Identification

Unique Protocol Identification Number
NCT00218855
Brief Title
Thalidomide to Patients With Previously Untreated Multiple Myeloma
Official Title
A Phase 3 Study With Randomization to Melphalan/Prednisone/Thalidomide Versus Melphalan/Prednisone/Placebo to Patients With Previously Untreated Multiple Myeloma
Study Type
Interventional

2. Study Status

Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
January 2002 (undefined)
Primary Completion Date
April 2007 (Actual)
Study Completion Date
April 2007 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Norwegian University of Science and Technology
Collaborators
The Research Council of Norway, Nordic Myeloma Study Group, Germany

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to test the effect of thalidomide in patients with multiple myeloma. The patients receive either thalidomide or a placebo tablet (neither patient nor doctor know which of these are given) in addition to the ordinary chemotherapeutic drug against multiple myeloma. We will find out for how long time the patients will stay free of the disease and for how long time they will live, and can evaluate whether thalidomide is a beneficial drug against this disease.
Detailed Description
Thalidomide has recently emerged as an effective treatment for patients with myeloma refractory to conventional chemotherapy. So far only limited experience is available on thalidomide for newly diagnosed myeloma. Therefore the Nordic Myeloma Study Group decided to perform a trial comparing traditional melphalan-prednisone therapy with melphalan-prednisone + thalidomide/placebo. The study design is a multicentre double-blind randomised placebo-controlled trial. Mainly patients >65 years of age will be included since patients <65 years will be treated with high dose chemotherapy with autologous stem cell support. The primary end-point is overall survival. Secondary end-points are quality of life, response rate, time to response, response duration and toxicity.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Myeloma
Keywords
Multiple Myeloma, Phase 3, randomised, double blind study, thalidomide

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
363 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Placebo Comparator
Arm Title
B
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
thalidomide
Other Intervention Name(s)
thalidomide, Talix
Intervention Description
tablets thalidomide start 100 mg x 2 escalating to 200 mg x 2 until plateau phase. Maintenance 100 mg x 2 until relapse. The same procedure is repeated by first relapse.
Intervention Type
Drug
Intervention Name(s)
placebo
Other Intervention Name(s)
no other names
Intervention Description
100 mg x 2 mg tablets escalating to 200 mg x 2 until plateau phase. Maintenance 100 mg x 2 until relapse. This procedure is repeated by first relapse.
Primary Outcome Measure Information:
Title
overall survival
Time Frame
october 2007
Secondary Outcome Measure Information:
Title
Quality of life
Time Frame
october 2007
Title
Time to response
Time Frame
october 2007
Title
Frequency of response
Time Frame
october 2007
Title
Time to progression
Time Frame
october 2007
Title
Time to 2. response
Time Frame
october 2007
Title
Frequency of 2. response
Time Frame
october 2007
Title
Time to 2. progression
Time Frame
october 2007
Title
Toxicity
Time Frame
october 2007
Title
Time to definitive treatment failure
Time Frame
october 2007

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with multiple myeloma in need of treatment Exclusion Criteria: Previous treatment against multiple myeloma Need of high dose chemotherapy with autologous stem cell support Women in fertile age Psychiatric disease or mental reduction leading to lack of cooperation Lack of consent Life expectancy below 3 months Active cancer of other etiology
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anders Waage, MD
Organizational Affiliation
Department of Haematology, St. Olavs hospital/NTNU, N-7006 Trondheim
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Haematology, St. Olavs hospital/NTNU
City
Trondheim
ZIP/Postal Code
N-7006
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
20448107
Citation
Waage A, Gimsing P, Fayers P, Abildgaard N, Ahlberg L, Bjorkstrand B, Carlson K, Dahl IM, Forsberg K, Gulbrandsen N, Haukas E, Hjertner O, Hjorth M, Karlsson T, Knudsen LM, Nielsen JL, Linder O, Mellqvist UH, Nesthus I, Rolke J, Strandberg M, Sorbo JH, Wisloff F, Juliusson G, Turesson I; Nordic Myeloma Study Group. Melphalan and prednisone plus thalidomide or placebo in elderly patients with multiple myeloma. Blood. 2010 Sep 2;116(9):1405-12. doi: 10.1182/blood-2009-08-237974. Epub 2010 May 6.
Results Reference
result

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Thalidomide to Patients With Previously Untreated Multiple Myeloma

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