Last updated: 11/07/2018 00:46:38
An Open-Label, Non-Comparative, Phase II Study of Topotecan as Single Agent, First-Line Therapy Administered as a Continuous 21-Day Infusion Every 28 Days to Patients with Stage IIIB and IV Non-Small Cell Lung Cancer.
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: An Open-Label, Non-Comparative, Phase II Study of Topotecan as Single Agent, First-Line Therapy Administered as a Continuous 21-Day Infusion Every 28 Days to Patients with Stage IIIB and IV Non-Small Cell Lung Cancer.
Trial description: An Open-Label, Non-Comparative, Phase II Study of Topotecan as Single Agent, First-Line Therapy Administered as a Continuous 21-Day Infusion Every 28 Days to Patients with Stage IIIB and IV Non-Small Cell Lung Cancer.
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Continuous infusion topotecan as first-line therapy in patients with non-small cell lung cancer: a phase ii study. Kindler, H L MD, Kris, M G MD, Smith, I E MD, Slevin, M L MD, and Krebs, J B MD American Society of Clinical Oncology Annual Meeting American Society of Clinical Oncology (ASCO) 33rd Annual Meeting 5/17/1997 Denver, CO; USA
Kindler, H et.al. Phase II trial of topotecan administerd as a 21 day continuous infusion in previously untreated patients with stage IIIB and IV non small cell lung cancer. American Journal of Clinical Oncology 21 438-441, 1998
Medical condition
Lung Cancer, Non-Small Cell
Product
topotecan
Collaborators
Not applicable
Study date(s)
April 1994 to February 1996
Type
Not applicable
Phase
2
Participation criteria
Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
1996-12-02
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Not applicable
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