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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00043927
Other study ID # 104864-A/389
Secondary ID
Status Completed
Phase Phase 3
First received August 14, 2002
Last updated August 20, 2013
Start date April 2001

Study information

Verified date August 2013
Source GlaxoSmithKline
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug AdministrationUnited Kingdom: Medicines and Healthcare Products Regulatory Agency
Study type Interventional

Clinical Trial Summary

This study will gather and compare data about the effectiveness and safety of two different treatments for extensive Small Cell Lung Cancer (SCLC) in patients who have not received previous chemotherapy. One treatment will use an investigational drug in combination with an FDA approved chemotherapy. The other treatment will use a combination of two FDA approved chemotherapy drugs.


Recruitment information / eligibility

Status Completed
Enrollment 760
Est. completion date
Est. primary completion date January 2004
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Written informed consent (patient's written understanding of and agreement to participate in this study).

- Patients with confirmed extensive small cell lung cancer (SCLC).

- No prior chemotherapy within 5 years of the diagnosis of SCLC.

- Presence of either measurable or non-measurable SCLC by X-ray or physical examination.

- At least 3 weeks since last major surgery (a lesser period is acceptable if decided to be in the best interest of the patient).

- At least 24 hours since prior radiotherapy. Patients who have received radiotherapy must have recovered from any reversible side effects, such as nausea and vomiting.

- Laboratory criteria: Patients must have adequate bone marrow reserve and adequate kidney and liver function.

Exclusion Criteria:

- Symptoms of spreading of the disease to the brain that requires treatment with drugs called steroids.

- Any active infection.

- Severe medical problems other than the diagnosis of SCLC, that would limit the ability of the patient to follow study guidelines or that would expose the patient to extreme risk.

- Ongoing or planned chemotherapy, immunotherapy, radiotherapy, or investigational therapy for the treatment of SCLC.

- Use of an investigational drug within 30 days before the first dose of study medication.

- Women who are pregnant or lactating.

- Patients of child-bearing potential who refuse to practice an adequate form of birth control.

- Patients with clinical evidence of any stomach or intestinal (GI) condition.

- Patients requiring treatment with the drug cyclosporin A.

Study Design

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


Intervention

Drug:
topotecan/cisplatin

etoposide/cisplatin


Locations

Country Name City State
Austria GSK Clinical Trials Call Center Vienna
Austria GSK Clinical Trials Call Center Vienna
Austria GSK Clinical Trials Call Center Vienna
Belgium GSK Clinical Trials Call Center Charleroi
Belgium GSK Clinical Trials Call Center Edegem
Belgium GSK Clinical Trials Call Center Haine-Saint- Paul
Belgium GSK Clinical Trials Call Center Leuven
Belgium GSK Clinical Trials Call Center Liege
Belgium GSK Clinical Trials Call Center Luxembourg
Brazil GSK Clinical Trials Call Center Belo Horizonte
Brazil GSK Clinical Trials Call Center Caxias do Sul
Brazil GSK Clinical Trials Call Center Fortaleza
Brazil GSK Clinical Trials Call Center Porto Alegre
Brazil GSK Clinical Trials Call Center Porto Alegre
Brazil GSK Clinical Trials Call Center Rio de Janeiro
Brazil GSK Clinical Trials Call Center Salvador
Brazil GSK Clinical Trials Call Center Sao Paulo
Brazil GSK Clinical Trials Call Center Sao Paulo
Bulgaria GSK Clinical Trials Call Center Bourgas
Bulgaria GSK Clinical Trials Call Center Plovdiv
Bulgaria GSK Clinical Trials Call Center Sofia
Bulgaria GSK Clinical Trials Call Center Sofia
Bulgaria GSK Clinical Trials Call Center Varna
Canada GSK Clinical Trials Call Center Calgary Alberta
Canada GSK Clinical Trials Call Center Edmonton Alberta
Canada GSK Clinical Trials Call Center Greenfield Park Quebec
Canada GSK Clinical Trials Call Center Montreal Quebec
Canada GSK Clinical Trials Call Center Montreal Quebec
Canada GSK Clinical Trials Call Center Montreal Quebec
Canada GSK Clinical Trials Call Center Newmarket Ontario
Canada GSK Clinical Trials Call Center Oshawa Ontario
Canada GSK Clinical Trials Call Center Ottawa Ontario
Canada GSK Clinical Trials Call Center Peterborough Ontario
Canada GSK Clinical Trials Call Center Sainte-Foy Quebec
Canada GSK Clinical Trials Call Center Sault Sainte Marie Ontario
Canada GSK Clinical Trials Call Center Sydney Nova Scotia
Canada GSK Clinical Trials Call Center Thunder Bay Ontario
Canada GSK Clinical Trials Call Center Toronto Ontario
Canada GSK Clinical Trials Call Center Weston Ontario
Canada GSK Clinical Trials Call Center Winnipeg Manitoba
Chile GSK Clinical Trials Call Center Santiago
China GSK Clinical Trials Call Center Beijing
China GSK Clinical Trials Call Center Shanghai
China GSK Clinical Trials Call Center Wangfujing
China GSK Clinical Trials Call Center Xian
Costa Rica GSK Clinical Trials Call Center San Jose
Czech Republic GSK Clinical Trials Call Center Hradec Kralove
Czech Republic GSK Clinical Trials Call Center Olomouc
Czech Republic GSK Clinical Trials Call Center Plzen
Czech Republic GSK Clinical Trials Call Center Praha
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Estonia GSK Clinical Trials Call Center Tallinn
Finland GSK Clinical Trials Call Center Helsinki
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Honduras GSK Clinical Trials Call Center Tegucigalpa
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Italy GSK Clinical Trials Call Center Genova Liguria
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Jamaica GSK Clinical Trials Call Center Kingston
Korea, Republic of GSK Clinical Trials Call Center Seoul
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Lithuania GSK Clinical Trials Call Center Kaunas
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Slovakia GSK Clinical Trials Call Center Banska Bystrica
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Slovakia GSK Clinical Trials Call Center Kosice
Slovakia GSK Clinical Trials Call Center Nitra
South Africa GSK Clinical Trials Call Center Johannesburg Gauteng
Spain GSK Clinical Trials Call Center Lerida
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Taiwan GSK Clinical Trials Call Center Taipei
Taiwan GSK Clinical Trials Call Center Taipei
United Kingdom GSK Clinical Trials Call Center Aberdeen Aberdeenshire
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United States GSK Clinical Trials Call Center Abingdon Virginia
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United States GSK Clinical Trials Call Center Atlanta Georgia
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United States GSK Clinical Trials Call Center Aurora Illinois
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United States GSK Clinical Trials Call Center Chicago Illinois
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United States GSK Clinical Trials Call Center Cummings Georgia
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United States GSK Clinical Trials Call Center Fountain Valley California
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United States GSK Clinical Trials Call Center Lemoyne Pennsylvania
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United States GSK Clinical Trials Call Center Memphis Tennessee
United States GSK Clinical Trials Call Center Miami Shores Florida
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United States GSK Clinical Trials Call Center Norfolk Virginia
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United States GSK Clinical Trials Call Center Rochester New York
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United States GSK Clinical Trials Call Center Yakima Washington

Sponsors (1)

Lead Sponsor Collaborator
GlaxoSmithKline

Countries where clinical trial is conducted

United States,  Austria,  Belgium,  Brazil,  Bulgaria,  Canada,  Chile,  China,  Costa Rica,  Czech Republic,  Estonia,  Finland,  France,  Germany,  Honduras,  Hungary,  Italy,  Jamaica,  Korea, Republic of,  Lithuania,  Mexico,  Netherlands,  New Zealand,  Norway,  Panama,  Poland,  Puerto Rico,  Russian Federation,  Singapore,  Slovakia,  South Africa,  Spain,  Taiwan,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall Survival
Secondary response rates, response duration, time to progression, tolerability and patient-perceived disease status and well being for patients
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