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Completed Phase 2 Interventional Results available

A Single-Arm Study of Bempegaldesleukin (NKTR-214) Plus Nivolumab in Cisplatin Ineligible Patients Who Have Locally Advanced or Metastatic Urothelial Cancer

ClinicalTrials.gov ID: NCT03785925

Public ClinicalTrials.gov record NCT03785925. 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 19, 2026, 3:37 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 2, Single-Arm Study of Bempegaldesleukin (NKTR-214) in Combination With Nivolumab in Cisplatin Ineligible, Locally Advanced or Metastatic Urothelial Cancer Patients

Brief summary

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

The main purpose of this study is to evaluate the anti-tumor activity of bempegaldesleukin (NKTR-214) in combination with nivolumab by assessing the objective response rate (ORR) in cisplatin ineligible, locally advanced or metastatic urothelial cancer patients.

Study identification

NCT ID
NCT03785925
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Nektar Therapeutics
Industry
Enrollment
192 participants

Conditions and interventions

Interventions

Biological

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 29, 2019 (Actual)
Primary completion
Feb 9, 2022 (Actual)
Completion
Jun 30, 2022 (Actual)
Last update posted
Mar 28, 2023

2019 – 2022

United States locations

U.S. sites
8
U.S. states
6
U.S. cities
8
Facility City State ZIP Site status
San Francisco VA Medical Center - NAVREF - PPDS San Francisco California 94143 —
Innovative Clinical Research Institute, LLC Whittier California 90603 —
Rocky Mountain Cancer Centers Aurora Colorado 80012 —
Winship Cancer Institute, Emory University Atlanta Georgia 30322 —
Southeastern Regional Medical Center - CTCA - PPDS Newnan Georgia 30265 —
Investigator Site - Peoria Peoria Illinois 61615 —
Laura And Isaac Perlmutter Cancer Center New York New York 10016 —
MD Anderson Cancer Center 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 62 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03785925, 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 28, 2023 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03785925 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →