Trials / Completed
CompletedNCT01460979
Efficacy,Tolerability,Safety of Temsirolimus in Women With Platinum-refractory Ovarian Carcinoma or Advanced Endometrial Carcinoma
Activity, Tolerability, Safety of Temsirolimus in Women With Ovarian Cancer Who Progressed During Previous Platinum Chemotherapy or Within 6 Months After Therapy or Advanced Endometrial Carcinoma
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 47 (actual)
- Sponsor
- AGO Study Group · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine the activity, tolerability and safety of Temsirolimus in women with ovarian cancer who progressed during the previous platinum chemotherapy alternatively within 6 months from completion of therapy or advanced endometrial carcinoma.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Temsirolimus | 25mg weekly intravenous until progression |
Timeline
- Start date
- 2011-10-01
- Primary completion
- 2015-06-01
- Completion
- 2015-11-01
- First posted
- 2011-10-27
- Last updated
- 2016-02-29
Locations
18 sites across 1 country: Germany
Source: ClinicalTrials.gov record NCT01460979. Inclusion in this directory is not an endorsement.