Trials / Completed
CompletedNCT01022671
Study of Camtobell Inj (Belotecan) on Weekly Schedule in Non-small Cell Lung Cancer (NSCLC) Patients Previously Treated With Chemotherapy
Single-Arm, Open-label, Multicenter, Phase 2 Clinical Trial to Assess the Efficacy and Safety of Single-Agent Camtobell Inj.(Belotecan) Administered on A Weekly Schedule in Locally Advanced or Metastatic Non-small Cell Lung Cancer Patients Previously Treated With Chemotherapy
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 52 (actual)
- Sponsor
- Chong Kun Dang Pharmaceutical · Industry
- Sex
- All
- Age
- 19 Years
- Healthy volunteers
- Not accepted
Summary
A phase II study is conducted to determine the efficacy and safety of a single agent Camtobell inj.(belotecan) on a weekly schedule in locally advanced or metastatic non-small cell lung cancer patients previously treated with chemotherapy. The usefulness of the this regimen is evaluated by response rate, median survival time, progression free survival and duration of response.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Belotecan | 3.0 mg/m2, Day 1, 8, 15 every 4 weeks |
Timeline
- Start date
- 2009-09-01
- Primary completion
- 2010-02-01
- Completion
- 2010-03-01
- First posted
- 2009-12-01
- Last updated
- 2016-01-28
Source: ClinicalTrials.gov record NCT01022671. Inclusion in this directory is not an endorsement.