A Phase II Safety and Efficacy Study of Ipilimumab Monotherapy Following Completion of Chemotherapy in Recurrent Platinum Sensitive Ovarian Cancer Subjects with Residual Measurable Disease
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- STATUS
- Not Recruiting
Updated on 19 February 2024
Summary
The purpose of this study is to assess the incidence of drug-related adverse events of Grade 3 or higher during the induction period of Ipilimumab.
Description
The purpose of this study is to assess the incidence of drug-related adverse events of Grade 3 or higher during the induction period of Ipilimumab.
Details
| Condition | Ovarian Cancer |
|---|---|
| Age | 18years - 100years |
| Clinical Study Identifier | TX3763 |
| Last Modified on | 19 February 2024 |
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