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Completed

NCT Number: NCT00057564

A Study of Combination Thalidomide Plus Dexamethasone Therapy vs. Dexamethasone Therapy Alone in Previously Untreated Subjects With Multiple Myeloma

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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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Royal Brisbane Hospital, Herston, Queensland, Australia

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Active Multiple Myeloma Stage II or III Durie Salmon
  • Measurable levels of myeloma paraprotein in serum (≥1.0g/dL) or urine (≥ 0.2g excreted in a 24-hour collection sample)
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, 2
  • Women of child bearing potential must agree to abstain for heterosexual intercourse or use 2 methods of contraception, one effective (for example hormonal or tubal ligation) and one barrier (for example latex condom, diaphragm)
  • Males must agree to use barrier contraception (latex condoms) when engaging in reproductive activity

Exclusion criteria

  • Pregnant or lactating females
  • Peripheral neuropathy ≥ to grade 2 of the NCI CTC.
  • Prior history of malignancy unless subject has been free of disease for ≥ 3 years
  • Lab abnormality: Absolute neutrophil count (ANC) <1,000 cells/mm^3 (1.0 x 10^9/L)
  • Lab abnormality: Platelet count <50,000/mm^3 (50.0 x 10^9/L)
  • Lab abnormality: Serum creatinine >3.0 mg/dL (265 µmol/L)
  • Lab abnormality: Serum glutamic oxaloacetic transaminase (SGOT) /Aspartate aminotransferase (AST) or Serum glutamic pyruvic transaminase (SGPT)/Alanine transaminase (ALT) >3.0 x upper limit of normal (ULN)
  • Lab abnormality: Serum total bilirubin > 2.0 mg/dL (34 µmol/L)

Treatment and study plan

A (Thalidomide + Dexamethasone)

Drug

Thalidomide 50mg/day + Dexamethasone 40mg

Other names: Thalidomide

B (Placebo + Dexamethasone)

Drug

Placebo + Dexamethasone 40mg

Other names: Dexamethasone, placebo

Primary outcomes

  1. Time to tumor progression (TTP)

    Time frame: Up to 3 years

    Time to tumor progression (TTP)

Secondary outcomes

  1. Number of patients who survived

    Time frame: Up to 3 years

    Number of patients who survived

  2. Time to first symptomatic skeletal-related event (SRE)(clinical need for radiation therapy or surgery to bone)

    Time frame: Up to 3 years

    Time to first symptomatic skeletal-related event (SRE)(clinical need for radiation therapy or surgery to bone)

  3. Myeloma response rate

    Time frame: Up to 3 years

    Myeloma response determination criteria developed by Bladé et al 1998

  4. Number of participants with adverse events

    Time frame: Up to 3 years

    Number of participants with adverse events

Sponsors and collaborators

Lead sponsor

Celgene Corporation

Industry

Registry information

Official study title

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

Important dates

Study start
2003
Primary completion
2006
Study completion
2013
First posted
Apr 7, 2003
Registry last updated
Sep 11, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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