A (Thalidomide + Dexamethasone)
DrugThalidomide 50mg/day + Dexamethasone 40mg
Other names: Thalidomide
NCT Number: NCT00057564
To compare the efficacy of combination oral thalidomide plus oral dexamethasone treatment to that of oral dexamethasone-alone treatments as induction (first-line) therapy for subjects with active multiple myeloma
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Royal Brisbane Hospital, Herston, Queensland, Australia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Thalidomide 50mg/day + Dexamethasone 40mg
Other names: Thalidomide
Placebo + Dexamethasone 40mg
Other names: Dexamethasone, placebo
Time frame: Up to 3 years
Time to tumor progression (TTP)
Time frame: Up to 3 years
Number of patients who survived
Time frame: Up to 3 years
Time to first symptomatic skeletal-related event (SRE)(clinical need for radiation therapy or surgery to bone)
Time frame: Up to 3 years
Myeloma response determination criteria developed by Bladé et al 1998
Time frame: Up to 3 years
Number of participants with adverse events
Celgene Corporation
Industry
A Multicenter, Randomized, Parallel-group , Double Blind, Placebo-controlled Study of Combination Thalidomide Plus Dexamethasone Therapy vs. Dexamethasone Therapy Alone as Induction Therapy for Previously Untreated Subjects With Multiple Myeloma
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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