Prolonged Emend in a Study (NYU 03-67) of Oxaliplatin and Topotecan in Previously Treated Ovarian Cancer
Withdrawn before enrolling · Not applicable
Conditions studied: Ovarian Cancer
In brief
The investigators propose to totally abolish the emesis (vomiting) associated with the regimen of oxaliplatin + topotecan by adding a daily administration of aprepitant (Emend) for 17 days to the HT3 blocker routinely given on days 1 and 15.
Key facts
- Study ID
- NCT01017809
- Run by
- NYU Langone Health
- People needed
- 0
- Starts
- 2010-12-01
- Expected to finish
- 2013-12-01
- Last updated by the study team
- 2015-03-18
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- All patients fulfilling the requirement for entering the study NYU 03-67 will be eligible to enter the supplementary protocol with Emend. Please see NCT0031361 for eligibility.
You may not qualify if…
- Patients not enrolled on NYU 03-67(NCT0031361).
Where it is running
- NYU Clinical Cancer Center — New York, New York, United States
Full record on ClinicalTrials.gov
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