Trials / Withdrawn
WithdrawnNCT02232646
A Study of BBI503 in Adult Patients With Advanced Urologic Malignancies
A Phase II Clinical Study of BBI503 in Adult Patients With Advanced Urologic Malignancies
- Status
- Withdrawn
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Sumitomo Pharma America, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is an open label, multi-center, Phase II study of BBI503 administered to adult patients with selected advanced urologic malignancies. The primary objective of this study is to evaluate the disease control rate of patients with renal cell cancer and urothelial carcinoma treated with BBI503.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | BBI503 | BBI503 will be administered orally, daily, in continuous 28-day cycles at a dose of 300 mg once daily. |
Timeline
- Start date
- 2017-01-01
- Primary completion
- 2018-08-01
- Completion
- 2018-08-01
- First posted
- 2014-09-05
- Last updated
- 2023-11-14
Source: ClinicalTrials.gov record NCT02232646. Inclusion in this directory is not an endorsement.