Phase 2
Completed N=57
Ketoconazole, Hydrocortisone and Dutasteride in Asymptomatic Hormone Refractory Prostate Cancer
Source: ClinicalTrials.gov NCT00673127 ↗Enrolled (actual)
57
Serious AEs
1.8%
Results posted
Apr 2015
Primary outcomePrimary: PSA Response — 56 percentage of participants
Summary
The combination of ketaconazole and hydrocortisone is commonly used for the treatment of prostate cancer. The purpose of this study is to determine if the addition of a drug called dutasteride to this approved combination will make the combination more effective in treating prostate cancer.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY PSA Response |
56 | — |
| SECONDARY Time to Progression |
14.5 | — |
Eligibility Criteria
Inclusion Criteria
- Histologically documented evidence of prostate cancer (needle biopsy or prostatectomy). In the abscence of histologically documented evidence of prostate cancer, the diagnosis must be based on elevated serum PSA and metastatic lesions on bone scan.
- Progressive HRPC defined as a PSA increase over baseline of >25% or 5ng/ml or new lesions on bone/CT scan after conventional androgen deprivation and antiandrogen withdrawal. Evidence of metastatic disease based on positive CT or bone scan is not required.
- PSA of greater than or equal to 2ng/ml and serum total testosterone less than or equal to 50ng/ml
- Prior chemotherapy is permitted if discontinued > 4 weeks prior to starting therapy
- Prior therapy with estrogens is permitted but must have been discontinued > 4 weeks prior to registration
- ECOG Performance Status 0-2
- Adequate renal function, hepatic function, and bone marrow function as outlined in protocol
- ECG showing a normal QT interval
Exclusion Criteria
- Prior therapy with ketoconazole or corticosteroids for HRPC
- Major surgery or radiation therapy within 4 weeks
- Strontium-89 or samarium-153 therapy within 4 weeks
- Thromboembolism in past 6 months
- Patients who are taking drugs that may further prolong QT intervals and present a known risk for Torsades de Pointes.
- Concomitant use of drugs known to be narrow therapeutic index CTP3A4
- Drugs that are sensitive CYP3A4 substrates
- Alcohol or drug dependence currently or in the last 6 months
Data sourced from ClinicalTrials.gov (NCT00673127). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.