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Clinical Trial Summary

Asymptomatic patients with metastatic castrate resistant prostate cancer (mCRPC) without pain due to prostate cancer will be treated on an open label study to evaluate effectiveness of sequential treatment with the combination of difluoromethylornithine (DFMO) and high dose testosterone in sequence with enzalutamide to improve primary and secondary outcomes.


Clinical Trial Description

Eligible patients are those with mCRPC who have progressive disease after treatment with Abiraterone (Abi) used as treatment for castration-sensitive or castration-resistant disease. Patients will continue on androgen deprivation therapy (ADT) with luteinizing hormone-releasing hormone (LHRH) agonist (i.e. Zoladex, Trelstar, Eligard, or Lupron) or LHRH antagonist (Degarelix or Relugolix) if not surgically castrated throughout the duration of the study to inhibit endogenous testosterone production. One cycle of treatment will be 119 days and will involve: 1. 7 days of DFMO at a dose of 1000 mg PO BID (D1-D7), followed by 2. 56 days of combined testosterone and DFMO (testosterone cypionate 400 mg IM on D8 and D36 with continued DFMO 1000 mg PO BID) (D8-D63), followed by 3. 56 days of enzalutamide (enzalutamide 160 mg PO daily) (D64-D119) Patients will receive repeat cycles of treatment until clinical or radiographic progression or toxicity requiring drug cessation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06059118
Study type Interventional
Source Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Contact Laura Sena, MD, PhD
Phone 410-502-3825
Email laura.sena@jhmi.edu
Status Recruiting
Phase Phase 2
Start date October 4, 2023
Completion date November 30, 2029

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