Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Terminated Early Phase 1 Interventional Results available

FPA150 in Patients With Advanced Solid Tumors

ClinicalTrials.gov ID: NCT03514121

Public ClinicalTrials.gov record NCT03514121. 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 Oct 6, 2026, 5:32 AM 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 1a/1b Study of FPA150, an Anti-B7-H4 Antibody, in Patients With Advanced Solid Tumors

Brief summary

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

This is a multi-center study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) and preliminary efficacy of FPA150, an anti-B7H4 antibody alone or in combination with pembrolizumab an anti-PD1 antibody in patients with advanced solid tumors. The Phase 1a, open-label, cohort will identify a recommended dose of FPA150 to use for Phase 1a Combination (FPA150 and Pembrolizumab) Safety Lead-in and for Phase 1b monotherapy cohorts.

Study identification

NCT ID
NCT03514121
Recruitment status
Terminated
Study type
Interventional
Phase
Early Phase 1
Lead sponsor
Five Prime Therapeutics, Inc.
Industry
Enrollment
95 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 99 Years
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
Mar 27, 2018 (Actual)
Primary completion
Apr 21, 2021 (Actual)
Completion
Apr 21, 2021 (Actual)
Last update posted
Nov 22, 2024

2018 – 2021

United States locations

U.S. sites
13
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Honor Health Scottsdale Arizona 85258 —
Cedars-Sinai Medical Center Los Angeles California 90048 —
UCLA Los Angeles California 90095 —
Sarcoma Oncology Research Center Santa Monica California 90403 —
Yale Cancer Center New Haven Connecticut 06520 —
Orchard Healthcare Research Inc. Skokie Illinois 60077 —
Karmanos Cancer Institute Detroit Michigan 48201 —
Stephenson Cancer Center Oklahoma City Oklahoma 73104 —
Sarah Cannon Research Institute Nashville Tennessee 37203 —
The University of Texas MD Anderson Cancer Center Houston Texas 77030 —
South Texas Accelerated Research Therapeutics San Antonio Texas 78229 —
Utah Cancer Specialists Salt Lake City Utah 84106 —
Medical Oncology Associates, PS Spokane Washington 99208 —

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03514121, 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 Nov 22, 2024 · Synced Oct 6, 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 public registry record, listed eligibility criteria, and available contact information for NCT03514121 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →