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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00812266
Other study ID # DOLG7
Secondary ID DOLG7
Status Terminated
Phase Phase 3
First received December 19, 2008
Last updated January 23, 2016
Start date January 2006
Est. completion date January 2015

Study information

Verified date January 2016
Source Danish Oncological Lung Cancer Group
Contact n/a
Is FDA regulated No
Health authority Denmark: Danish Medicines Agency
Study type Interventional

Clinical Trial Summary

Randomised trial comparing standard chemotherapy with carboplatin and etoposide with a combination of topotecan and cisplatin in patients with inoperable lung cancer of small cell type.


Description:

Fase III, multicenter randomised trial comparing up to six cycles of carboplatin and etoposide with up to six cycles of topotecan and cisplatin in patients with extensive stage small cell lung cancer and PS 0-3


Recruitment information / eligibility

Status Terminated
Enrollment 281
Est. completion date January 2015
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Histologically confirmed SCLC

- Extensive stage

- No prior chemotherapy

- WHO PS 0-3

- Adequate organ function (liver, kidney)

- Adequate hematology (bone marrow)

- Informed consent

Exclusion Criteria:

- PS 4

- Inadequate organ function

- Uncontrolled infection

- Concomitant major medical contraindications

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Drug:
topotecan + cisplatin
topotecan IV 2 mg/sqm d1-3 + cisplatin IV 50 mg/sqm d3 q3W
Etoposide + carboplatin
Etoposide 120 mg/sqm IV d 1-3 + carboplatin AUC 5 d1 q3W

Locations

Country Name City State
Denmark Dept. Oncology, Rigshospitalet Copenhagen

Sponsors (1)

Lead Sponsor Collaborator
Danish Oncological Lung Cancer Group

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary 2 years survival 2 years Yes
Secondary Response rates 2 years Yes
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