Trials / Completed
CompletedNCT01104675
Study of Oral ENMD-2076 Administered to Patients With Ovarian Cancer
A Phase 2 Study of Oral ENMD-2076 Administered to Patients With Platinum Resistant Ovarian Cancer
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 64 (actual)
- Sponsor
- CASI Pharmaceuticals, Inc. · Industry
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine whether oral ENMD-2076 is effective in treatment of patients with platinum resistant ovarian, fallopian, or peritoneal cancer. Additional sites to be added.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | ENMD-2076 | 275 mg (or 250 mg for BSA \< 1.65) per day in oral capsules in 28 day continuous cycles |
Timeline
- Start date
- 2010-04-01
- Primary completion
- 2011-08-01
- Completion
- 2012-12-01
- First posted
- 2010-04-15
- Last updated
- 2014-08-06
Locations
6 sites across 2 countries: United States, Canada
Source: ClinicalTrials.gov record NCT01104675. Inclusion in this directory is not an endorsement.