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Recruiting Phase 1 Interventional

A Phase 1 Study of NRM-823 in Participants With Locally Advanced or Metastatic Refractory Solid Tumors

ClinicalTrials.gov ID: NCT07182149

Public ClinicalTrials.gov record NCT07182149. 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 7, 2026, 5:30 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 NRM-823 as Monotherapy and in Combination With Immune Checkpoint Inhibition in Participants With Locally Advanced or Metastatic Refractory Solid Tumors

Brief summary

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

This study is being done to find out of NRM-823 is safe and can treat participants with locally advanced or metastatic solid tumors.

Study identification

NCT ID
NCT07182149
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 1
Lead sponsor
Normunity AccelCo, Inc.
Industry
Enrollment
150 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 29, 2025
Primary completion
May 29, 2027
Completion
Oct 30, 2028
Last update posted
Aug 17, 2026

2025 – 2028

United States locations

U.S. sites
18
U.S. states
14
U.S. cities
16
Facility City State ZIP Site status
Normunity Investigational Site Denver Colorado 80220 Recruiting
Normunity Investigational Site New Haven Connecticut 06519 Recruiting
Normunity Investigational Site Washington D.C. District of Columbia 20007 Recruiting
Normunity Investigational Site Boston Massachusetts 02114 Recruiting
Normunity Investigational Site Boston Massachusetts 02215 Recruiting
Normunity Investigational Site Minneapolis Minnesota 55425 Recruiting
Normunity Investigational Site St Louis Missouri 63108 Recruiting
Normunity Investigational Site Hackensack New Jersey 07601 Recruiting
Normunity Investigational Site Maumee Ohio 43537 Recruiting
Normunity Investigational Site Oklahoma City Oklahoma 73104 Recruiting
Normunity Investigational Site Philadelphia Pennsylvania 19107 Recruiting
Normunity Investigational Site Philadelphia Pennsylvania 19111 Recruiting
Normunity Investigational Site Charleston South Carolina 29425 Recruiting
Normunity Investigational Site Nashville Tennessee 37203 Recruiting
Normunity Investigational Site Dallas Texas 75230 Recruiting
Normunity Investigational Site Houston Texas 77030 Recruiting
Normunity Investigational Site San Antonio Texas 78229 Recruiting
Normunity Investigational Site Fairfax Virginia 22031 Recruiting

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 NCT07182149, 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 17, 2026 · Synced Sep 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07182149 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →