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Completed

NCT Number: NCT00263484

Higher Frequency Zoledronic Acid in the Treatment of Multiple Myeloma

The purpose of this study is to determine whether lower than conventional doses of dexamethasone and thalidomide; and a higher dosing frequency of zoledronic acid are effective in the treatment of newly-diagnosed multiple myeloma.

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Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Tata Memorial Hospital, Mumbai, India

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About this study

Patients with newly-diagnosed multiple myeloma (MM) may be treated using monthly cycles of dexamethasone plus thalidomide (DT). Unfortunately, the use of conventional doses of DT is associated with significant treatment-related morbidity and mortality, which is comparable to that observed with conventional chemotherapy. Hence, for safety reasons, patients frequently receive lower than conventional doses of DT (i.e. dt), and potentially experience a poorer anti-MM effect. The highly-potent aminobisphosphonate, zoledronic acid (Z), has been shown in pre-clinical mouse models to exhibit an impressive anti-MM effect. It is therefore possible to combined dt with Z (i.e. dtZ) to enhance the efficacy of (lower dose) dt. In addition, the anti-tumor effect of dtZ may potentially be augmented by using Z at a higher (three-weekly) dosing frequency.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age at or above 21 years
  • Clinical diagnosis of MM
  • Active MM with measurable disease
  • Signed written informed consent
  • Signed consent for drug safety program for thalidomide

Exclusion criteria

  • Patients with Monoclonal Gammopathy of Undetermined Significance (MGUS)
  • Patients with Indolent MM (IMM), or Smouldering MM (SMM)
  • Known hypersensitivity (including severe cutaneous reactions) to d, t or Z
  • Fulminant sepsis
  • Females in the reproductive age group who refuse contraception
  • Pregnancy
  • 24 hr urinary creatinine clearance time (CCT) <30 ml/min
  • Previous renal transplantation
  • Severe peripheral neuropathy
  • Recurrent DVT or PE
  • Severe arrhythmias and cardiac conduction disorders
  • Liver dysfunction of active viral hepatitis
  • Osteonecrosis of the jaws (ONJ)

Treatment and study plan

Dexamethasone

Drug

20 mg, PO (orally) on days 1-4, 8-11 and 15-18 of each 21 day cycle. 6 Cycles: until progression or unacceptable toxicity develops.

Other names: DEXAMETHASONE BEACONS

thalidomide

Drug

100 mg, PO (orally) on days 1-21 of each 21 day cycle. 6 Cycles: until progression or unacceptable toxicity develops.

Other names: THALOMID (PHARMION), THADO (TTY)

Zoledronic acid

Drug

4 mg, IV (in the vein) on day 1 of each 21 day cycle. 6 Cycles: until progression or unacceptable toxicity develops.

Other names: ZOMETA

Primary outcomes

  1. 1. To determine response rates (RR) and disease progression rates in all MM patients treated with dtZ regimen.

    Time frame: 4 months

Secondary outcomes

  1. To assess overall survival (OS) in all patients treated with dtZ regimen.

    Time frame: 4 months

  2. Assessment of incidence of skeletal related events (SREs).

    Time frame: 4 months

  3. Assessment of percent change in renal function in all patients.

    Time frame: 4 months

Sponsors and collaborators

Lead sponsor

Gleneagles Hospital

Other

Collaborators

  • Asan Medical Center
  • Chonnam National University Hospital
  • Christian Medical College, Vellore, India
  • National Cancer Centre, Singapore
  • Samsung Medical Center
  • Seoul National University Hospital
  • Singapore General Hospital
  • Tan Tock Seng Hospital
  • Tata Memorial Hospital

Registry information

Official study title

An International, Multicenter, Non-Randomized, Open-Labeled Study to Evaluate the Efficacy of Lower Dose Dexamethasone/Thalidomide and Higher Frequency ZOMETA(TM) in the Treatment of Previously Untreated Patients With Multiple Myeloma

Acronym: dtZ

Important dates

Study start
2005
Primary completion
2008
Study completion
2010
First posted
Dec 8, 2005
Registry last updated
Jul 21, 2011

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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