Trials / Withdrawn
WithdrawnNCT01000896
Study to Assess Safety and Tolerability of AZD0530 in Combination With Carboplatin and Paclitaxel
A Phase I, Open-Label, Study to Assess the Safety, Tolerability, and Pharmacokinetics of Ascending Doses of AZD0530 in Combination With Carboplatin and Paclitaxel Chemotherapy in Japanese Patients With Advanced Solid Malignancies
- Status
- Withdrawn
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 27 (estimated)
- Sponsor
- AstraZeneca · Industry
- Sex
- All
- Age
- 20 Years
- Healthy volunteers
- Not accepted
Summary
The primary purpose of this study is to explore the safety and tolerability of AZD0530 in combination with carboplatin and paclitaxel in Japanese patients with non small cell lung cancer and epithelial ovarian cancer.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | AZD0530 | film coated tablet, PO, daily |
| DRUG | Carboplatin | intravenous, 3 weeks |
| DRUG | paclitaxel | intravenous, 3 weeks |
Timeline
- Start date
- 2010-01-01
- Primary completion
- 2010-09-01
- Completion
- 2011-03-01
- First posted
- 2009-10-23
- Last updated
- 2010-02-04
Locations
2 sites across 1 country: Japan
Source: ClinicalTrials.gov record NCT01000896. Inclusion in this directory is not an endorsement.