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Recruiting Phase 1 Interventional

A Study of NPX887 for Participants With Solid Tumors Known to Express B7-H7/HHLA2

ClinicalTrials.gov ID: NCT06240728

Public ClinicalTrials.gov record NCT06240728. 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 4, 2026, 9:23 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 1a/1b Dose Escalation and Dose Expansion Study of NPX887 in Participants With Solid Tumor Malignancies Known to Express B7-H7/HHLA2

Brief summary

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

NPX887 is a human, antagonistic immunoglobulin G1 (IgG1) monoclonal antibody targeting B7-H7 (HHLA2) that may potentiate an anti-tumor immune response. The goal of this first-in-human study is to learn whether NPX887 is safe and tolerable and shows a preliminary efficacy in participants with B7-H7 (HHLA2) expressing tumors at selected dose(s). The main questions it aims to answer are: * what is an appropriate dose to be given to participants? * are the side effects of treatment manageable? * what is the preliminary anti-tumor activities? Participants who are treated will receive an intravenous (IV) infusion of NPX887 if their disease has not progressed, and be closely monitored by the treating physicians.

Study identification

NCT ID
NCT06240728
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 1
Lead sponsor
NextPoint Therapeutics, Inc.
Industry
Enrollment
144 participants

Conditions and interventions

Interventions

Drug

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
Jan 22, 2024 (Actual)
Primary completion
Aug 2027 (Estimated)
Completion
Aug 2027 (Estimated)
Last update posted
Jun 27, 2025

2024 – 2027

United States locations

U.S. sites
6
U.S. states
5
U.S. cities
6
Facility City State ZIP Site status
Johns Hopkins University Sidney Kimmel Comprehensive Cancer Center Baltimore Maryland 21287 Active, not recruiting
Beth Israel Deaconess Medical Center (BIDMC) Boston Massachusetts 02215 Active, not recruiting
Albert Einstein Medical College Montefiore Medical Center The Bronx New York 10461 Active, not recruiting
MD Anderson Cancer Center Houston Texas 77030 Active, not recruiting
Next Oncology San Antonio Texas 78229 Active, not recruiting
NEXT Oncology-Fairfax Fairfax Virginia 22031 Active, not recruiting

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06240728, 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 Jun 27, 2025 · Synced Oct 4, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06240728 live on ClinicalTrials.gov.

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