Trials / Completed
CompletedNCT00881569
Extended Use Protocol for Participants With Cancer to Receive Continued Treatment With CS-7017
Extended Use of CS 7017 Upon Completion of Participation in a Clinical Study of CS-7017 in Subjects With Cancer
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 2 (actual)
- Sponsor
- Daiichi Sankyo · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
This is a study of CS-7017 designed to allow participants who completed participation in a clinical study of CS-7017 without experiencing disease progression or unacceptable toxicity to continue treatment with study drug. Participants who have not progressed while receiving CS-7017 will continue to benefit from longer administration of the agent.
Detailed description
This is an open-label non-randomized study of CS-7017 designed to allow participants who completed participation in a clinical study of CS-7017 without experiencing disease progression or unacceptable toxicity to continue treatment with study drug.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | CS-7017 | CS-7017 administered orally, twice daily continuously for 6 weeks |
Timeline
- Start date
- 2009-03-01
- Primary completion
- 2011-03-01
- Completion
- 2011-09-01
- First posted
- 2009-04-15
- Last updated
- 2020-09-28
- Results posted
- 2020-08-14
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00881569. Inclusion in this directory is not an endorsement.