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Terminated Phase 1Phase 2 Interventional Results available

A Safety, Tolerability and Efficacy Study of NC410 Plus Pembrolizumab in Participants With Advanced Unresectable or Metastatic Solid Tumors

ClinicalTrials.gov ID: NCT05572684

Public ClinicalTrials.gov record NCT05572684. 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 21, 2026, 7:42 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 1b/2, Open-Label, Safety, Tolerability and Efficacy Study of NC410 Plus Pembrolizumab for Participants With Advanced Unresectable and/or Metastatic Immune Checkpoint Inhibitor (ICI) Refractory Solid Tumors or ICI Naïve MSS/MSI-Low Solid Tumors

Brief summary

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

This is an open-label, non-randomized, Phase 1b/2 study to determine the safety and tolerability of NC410 when combined with a standard dose of pembrolizumab. This study will also assess the clinical benefit of combination therapy in participants with advanced unresectable and/or metastatic ICI refractory solid tumors OR ICI naïve MSS/MSI-low solid tumors

Study identification

NCT ID
NCT05572684
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
NextCure, Inc.
Industry
Enrollment
97 participants

Conditions and interventions

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
Oct 6, 2022 (Actual)
Primary completion
Apr 30, 2025 (Actual)
Completion
Apr 30, 2025 (Actual)
Last update posted
Aug 13, 2026

2022 – 2025

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Arizona Oncology Associates Tucson Arizona 85711 —
Rocky Mountain Cancer Centers Aurora Colorado 80012 —
St. Elizabeth Edgewood Hospital Edgewood Kentucky 41017 —
Ochsner Cancer Institute New Orleans Louisiana 70121 —
Johns Hopkins Sidney Kimmel Comprehensive Cancer Center Baltimore Maryland 21231 —
Hackensack Meridian Health University Medical Center- John Theurer Cancer Center Hackensack New Jersey 07601 —
Roswell Park Comprehensive Cancer Center Buffalo New York 14203 —
NYU Langone Health New York New York 10016 —
University of Cincinnati Cancer Center Cincinnati Ohio 45267 —
UT Southwestern Medical Center Dallas Texas 75235 —
Texas Oncology - Baylor Charles A. Sammons Cancer Center Dallas Texas 75246 —
MD Anderson Cancer Center Houston Texas 77030 —
UT Health San Antonio San Antonio Texas 78229 —
Texas Oncology - San Antonio San Antonio Texas 78240 —
Inova Schar Cancer Institute Fairfax Virginia 22031 —
Virginia Cancer Specialist Fairfax Virginia 22031 —
Northwest Cancer Specialist Vancouver Washington 98684 —

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 NCT05572684, 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 Aug 13, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05572684 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →