Trial of ARV-110 in Patients With Metastatic Castration Resistant Prostate Cancer
Public ClinicalTrials.gov record NCT03888612. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Phase 1/2, Open-label, Dose Escalation, and Cohort Expansion Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ARV-110 in Patients With Metastatic Castration Resistant Prostate Cancer
Study identification
- NCT ID
- NCT03888612
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 1, Phase 2
- Lead sponsor
- Arvinas Inc.
- Industry
- Enrollment
- 248 participants
Conditions and interventions
Conditions
Interventions
- ARV-110 Drug
Drug
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- Male
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Feb 28, 2019
- Primary completion
- Apr 28, 2024
- Completion
- Jan 26, 2025
- Last update posted
- Mar 31, 2025
2019 – 2025
United States locations
- U.S. sites
- 54
- U.S. states
- 14
- U.S. cities
- 54
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Clinical Trial Site | Los Angeles | California | 90095 | — |
| Clinical Trial Site | Orange | California | 92868 | — |
| Clinical Trial Site | San Francisco | California | 94158 | — |
| Clinical Trial Site | New Haven | Connecticut | 06510 | — |
| Clinical Trial Site | Altamonte Springs | Florida | 32701 | — |
| Clinical Trial Site | Bonita Springs | Florida | 34135 | — |
| Clinical Trial Site | Bradenton | Florida | 34211 | — |
| Clinical Trial Site | Brandon | Florida | 33511 | — |
| Clinical Trial Site | Cape Coral | Florida | 33939 | — |
| Clinical Trial Site | Clearwater | Florida | 33761 | — |
| Clinical Trial Site | Daytona Beach | Florida | 32117 | — |
| Clinical Trial Site | Fleming Island | Florida | 32003 | — |
| Clinical Trial Site | Fort Myers | Florida | 33908 | — |
| Clinical Trial Site | Gainesville | Florida | 32605 | — |
| Clinical Trial Site | Largo | Florida | 33770 | — |
| Clinical Trial Site | Lecanto | Florida | 34461 | — |
| Clinical Trial Site | Naples | Florida | 34102 | — |
| Clinical Trial Site | New Port Richey | Florida | 34655 | — |
| Clinical Trial Site | Ocala | Florida | 34474 | — |
| Clinical Trial Site | Orange City | Florida | 32763 | — |
| Clinical Trial Site | Orlando | Florida | 32806 | — |
| Clinical Trial Site | Port Charlotte | Florida | 33980 | — |
| Clinical Trial Site | Sarasota | Florida | 34236 | — |
| Clinical Trial Site | Spring Hill | Florida | 34608 | — |
| Clinical Trial Site | St. Petersburg | Florida | 33705 | — |
| Clinical Trial Site | Stuart | Florida | 34994 | — |
| Clinical Trial Site | Tampa | Florida | 33607 | — |
| Clinical Trial Site | Tavares | Florida | 32778 | — |
| Clinical Trial Site | The Villages | Florida | 32159 | — |
| Clinical Trial Site | Venice | Florida | 34292 | — |
| Clinical Trial Site | Vero Beach | Florida | 32960 | — |
| Clinical Trial Site | Wellington | Florida | 33414 | — |
| Clinical Trial Site | West Palm Beach | Florida | 33401 | — |
| Clinical Trial Site | Winter Park | Florida | 32792 | — |
| Clinical Trial Site | Chicago | Illinois | 60611 | — |
| Clinical Trial Site | New Orleans | Louisiana | 70112 | — |
| Clinical Trial Site | Boston | Massachusetts | 02114 | — |
| Clinical Trial Site | Detroit | Michigan | 48201 | — |
| Clinical Trial Site | Omaha | Nebraska | 68130 | — |
| Clinical Trial Site | Las Vegas | Nevada | 89169 | — |
| Clinical Trial Site | New York | New York | 10065 | — |
| Clinical Trial Site | Portland | Oregon | 97239 | — |
| Clinical Trial Site | Dickson | Tennessee | 37055 | — |
| Clinical Trial Site | Franklin | Tennessee | 37067 | — |
| Clinical Trial Site | Gallatin | Tennessee | 37066 | — |
| Clinical Trial Site | Hendersonville | Tennessee | 37075 | — |
| Clinical Trial Site | Hermitage | Tennessee | 37076 | — |
| Clinical Trial Site | Lebanon | Tennessee | 37090 | — |
| Clinical Trial Site | Murfreesboro | Tennessee | 37129 | — |
| Clinical Trial Site | Nashville | Tennessee | 37211 | — |
| Clinical Trial Site | Shelbyville | Tennessee | 37160 | — |
| Clinical Trial Site | Smyrna | Tennessee | 37167 | — |
| Clinical Trial Site | Salt Lake City | Utah | 84112 | — |
| Clinical Trial Site | Charlottesville | Virginia | 22903 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT03888612, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Mar 31, 2025 · Synced Jul 23, 2026
Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.
Open the official record
The complete protocol, eligibility criteria, and contact information for NCT03888612 live on ClinicalTrials.gov.