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ClinicalTrials.gov record
Completed Phase 1Phase 2 Interventional

Trial of ARV-110 in Patients With Metastatic Castration Resistant Prostate Cancer

ClinicalTrials.gov ID: NCT03888612

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.

ClinicalTrials.gov public records Last synced Nov 4, 2026, 10:54 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. 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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Phase 1/2 dose escalation study to assess the safety and tolerability of ARV-110 in men with mCRPC who have progressed on prior approved systemic therapies for their castrate resistant disease (one of which must be enzalutamide or abiraterone).

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

Interventions

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
Mar 1, 2019 (Actual)
Primary completion
Apr 29, 2024 (Actual)
Completion
Jan 27, 2025 (Actual)
Last update posted
Apr 1, 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 Apr 1, 2025 · Synced Nov 4, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03888612 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →