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Terminated Phase 1Phase 2 Interventional Results available

A Study of NM21-1480 in Adult Patients With Advanced Solid Tumors

ClinicalTrials.gov ID: NCT04442126

Public ClinicalTrials.gov record NCT04442126. 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 24, 2026, 11:38 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 Study of NM21-1480 (Anti-PDL-1/Anti-4-1BB/Anti-HSA Tri-Specific Antibody) in Adult Patients With Advanced Solid Tumors

Brief summary

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

This is a first-in-human, open-label, multi-center, Phase 1/2, dose-escalation study with expansion cohorts to evaluate NM21-1480 for safety and immunogenicity, to determine the maximal tolerated dose and recommended Phase 2 dose, define the pharmacokinetics, to explore the pharmacodynamics, and to obtain preliminary evidence of the clinical activity in adult patients with selected advanced solid tumors.

Study identification

NCT ID
NCT04442126
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Numab Therapeutics AG
Industry
Enrollment
52 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
Aug 19, 2020 (Actual)
Primary completion
Feb 6, 2024 (Actual)
Completion
Feb 6, 2024 (Actual)
Last update posted
May 23, 2025

2020 – 2024

United States locations

U.S. sites
14
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
UCHealth Poudre Valley Hospital Fort Collins Colorado 80524 —
Augusta University Medical Center Augusta Georgia 30912 —
Tulane University Medical Center New Orleans Louisiana 70112 —
Henry Ford Health System Detroit Michigan 48202 —
St. Joseph Mercy Hospital Ypsilanti Michigan 48197 —
Dartmouth Cancer Center Lebanon New Hampshire 03766 —
NYU Langone Medical Center - Perlmutter Cancer Center (NYU Cancer Institute) New York New York 10016 —
Montefiore Medical Center The Bronx New York 10461-2374 —
Thomas Jefferson University Philadelphia Pennsylvania 19107 —
UPMC Hillman Cancer Center Pittsburgh Pennsylvania 15232 —
Medical University of South Carolina (MUSC) Charleston South Carolina 29425 —
Sarah Cannon Cancer Center Nashville Tennessee 37203 —
The University Of Texas MD Anderson Cancer Center Houston Texas 77030 —
Virginia Cancer Specialists Fairfax Virginia 22031 —

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 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04442126, 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 May 23, 2025 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04442126 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →