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Clinical Trials/EUCTR2004-001101-10-ES
EUCTR2004-001101-10-ES
Active, not recruiting
Not Applicable

A prospective, multicenter, randomized phase III study to evaluate the efficacy of Zometa (zoledronic acid) in preventing or delaying of bone metastasis in patients with stage III non-small cell lung cancer

ovartis Farmacéutica, S.A0 sites446 target enrollmentDecember 1, 2005

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Patients with unresectable stage IIIA and IIIB Non small cell lung cancer (NSCLC) without bone metastases
Sponsor
ovartis Farmacéutica, S.A
Enrollment
446
Status
Active, not recruiting
Last Updated
11 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 1, 2005
End Date
TBD
Last Updated
11 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
ovartis Farmacéutica, S.A

Eligibility Criteria

Inclusion Criteria

  • Age \= 18 years
  • Histologically confirmed NSCLC (squamous cell carcinoma, adenocarcinoma, large cell
  • carcinoma) NOTE: Mixed tumors with small cell carcinoma and aplastic carcinoma are not eligible
  • Newly diagnosed, Stage IIIA and Stage IIIB excluding patients with pleural effusion
  • Life expectancy of at least 6 months
  • ECOG performance status of 0 or 1 (Post\-text suppl. 1\)
  • Weight loss \= 5% in past 6 months
  • Women of childbearing potential must use a medically acceptable form of contraception
  • during the study and must have a negative urine or serum pregnancy test within 7 days of
  • randomization.

Exclusion Criteria

  • Patients with NSCLC with pleural effusion.
  • Patients who received any prior bisphosphonates in past 12 months
  • Presence of metastasis
  • Patients with current malignancy within past 5 years other than NSCLC (exceptions
  • include treated melanoma, ductal carcinoma in situ of the cervix or other cancer cured by reception alone)
  • Patients who have received radiotherapy \= 3 weeks before randomization must have recovered from any adverse events occurring during radiotherapy
  • Previous thoracotomy must have been performed \= 3 weeks prior to randomization and patient must have recovered.
  • Any previous radiotherapy completed \< 3 weeks before randomization
  • Patients with abnormal renal function (Creatinine \> 3mg/dL)
  • Corrected serum calcium \< 8\.0 mg/dL

Outcomes

Primary Outcomes

Not specified

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