Hycamtin
DrugObserving patients on HYCAMTIN and other drugs for SCLC.
NCT Number: NCT00997061
The registry is an international, multicenter, observational registry of newly diagnosed patients with SCLC.
Data will be entered into an electronic CRF (eCRF) via Internet access. Treatment plan remains the responsibility of the patient's physician and data collected in this registry will reflect a "real world" approach of the diagnosis and treatment of patients with SCLC.
Approximately 60 centres in 13 countries will take part in this registry. It is expected that about 500 patients will be recruited during a period of 6 to 9 months according to the feasibility.
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
GSK Investigational Site, Graz, Austria
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Observing patients on HYCAMTIN and other drugs for SCLC.
Time frame: 6-9mth recruitment period, 18mth study duration.
Time frame: 18 month period
GlaxoSmithKline
Industry
Acronym: SCOT
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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