At a glance
ClinicalIndex Comparison Record- ✓Histologically confirmed locally advanced or metastatic pure adenocarcinoma of the urinary tract, pure squamous cell carcinoma of the urinary tract, or treatment-refractory testicular germ cell tumors
- ✓Measurable disease per RECIST 1.1
- ✓Locally advanced or metastatic disease with new or progressive lesions on cross sectional imaging
- ✓Age ≥18 years
- ✕Prior investigational drug, chemotherapy, immunotherapy, or radiotherapy (except palliative bone directed) within 2 weeks prior to first study drug
- ✕Prior treatment with EV or other MMAE-based ADCs
- ✕Preexisting sensory or motor neuropathy Grade ≥2
- ✕History of severe allergic reactions to compounds similar to EV and/or pembrolizumab
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Phase II Multicenter Study of Enfortumab Vedotin With or Without Pembrolizumab in Rare Genitourinary Tumors (E-VIRTUE)
In Brief
A Phase 2 clinical trial evaluating Pembrolizumab and Enfortumab vedotin for Adenocarcinoma of the Bladder and 2 related conditions. Currently recruiting, targeting 68 participants across 1 site.
Detailed Summary
Background: Many cancers of the testicles and urinary tract are rare diseases; these are diseases that affect less than 200,000 people in the United States. It can be hard to study treatments for these diseases. One combination of drugs-enfortumab vedotin (EV) and pembrolizumab-has already been approved to treat some urinary cancers. Researchers want to see if they can help people with other types of testicle and urinary cancers. Objective: To test EV, with or without pembrolizumab, in patients with rarer cancers of the testicles or urinary tract. Eligibility: People aged 18 and older with rarer cancers of the testicles or urinary tract. Design: Participants will be screened. They will have a physical exam with blood and urine tests. Their ability to perform normal daily activities will be tested. They will have exams of their skin and eyes. They will have imaging scans. A biopsy may be needed: A sample of tissue will be removed from the tumor. The study drugs are both given through a tube attached to a needle inserted into a vein in the arm. Some participants will receive treatments 3 times during 28-week cycles; others will receive treatments 2 times during 21-day cycles. All participants may continue to receive treatments for up to 5 years. Imaging scans and other tests will be repeated. Participants who stop taking the drugs will have follow-up visits every 3 to 4 weeks until the disease gets worse. They will have imaging scans and blood tests. After that, follow-up visits will continue by phone every 3 months for up to 5 years after study therapy is finished.
Study Details
Timeline
Arms & Interventions
Treatment with enfortumab vedotin
Treatment with enfortumab vedotin and pembrolizumab
Interventions
Pembrolizumab is administered IV at 200 mg on day 1 of each 21-day cycle.
EV is administered IV at 1.25 mg/kg on days 1, 8, and 15 of each 28-day cycle (Arm 1) and on days 1 and 8 of each 21-day cycle (Arm 2).