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Completed Phase 1Phase 2 Interventional Results available

Trial of X4P-001 in Participants With Advanced Renal Cell Carcinoma

ClinicalTrials.gov ID: NCT02667886

Public ClinicalTrials.gov record NCT02667886. 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 Sep 3, 2026, 10:08 PM EDT

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 Trial of X4P-001 as Single Agent and in Combination With Axitinib in Patients With Advanced Renal Cell Carcinoma

Brief summary

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

The purpose of the study is to test different doses of X4P-001 given alone and in combination with axitinib in participants diagnosed with advanced renal cell carcinoma. The goals of the study are to determine the safety and tolerability of X4P-001, as well as the potential effect it may have on the body and the cancer tumor.

Study identification

NCT ID
NCT02667886
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
X4 Pharmaceuticals
Industry
Enrollment
74 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
Apr 26, 2016
Primary completion
Apr 13, 2022
Completion
Apr 13, 2022
Last update posted
Oct 2, 2024

2016 – 2022

United States locations

U.S. sites
18
U.S. states
17
U.S. cities
18
Facility City State ZIP Site status
Not listed Scottsdale Arizona 85259
Not listed Washington D.C. District of Columbia 20057
Not listed Jacksonville Florida 32224
Not listed Chicago Illinois 60637
Not listed Indianapolis Indiana 46237
Not listed Iowa City Iowa 52242
Not listed New Orleans Louisiana 70121
Not listed Boston Massachusetts 02215
Not listed Detroit Michigan 48201
Not listed Saint Paul Minnesota 55101
Not listed St Louis Missouri 63110
Not listed Hackensack New Jersey 07601
Not listed New York New York 10029
Not listed The Bronx New York 10461
Not listed Toledo Ohio 43623
Not listed Philadelphia Pennsylvania 19104
Not listed Greenville South Carolina 29605
Not listed Houston Texas 77030

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02667886, 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 Oct 2, 2024 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02667886 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →