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Recruiting Phase 1 Interventional

Evaluation of RBS2418 in Subjects With Advanced, Metastatic Solid Tumors

ClinicalTrials.gov ID: NCT05270213

Public ClinicalTrials.gov record NCT05270213. 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 2, 2026, 8:06 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 First-In-Human, Phase 1 a/b Dose Escalation and Expansion Study to Evaluate RBS2418 as Monotherapy and in Combination With Pembrolizumab in Subjects With Advanced Unresectable, Recurrent or Metastatic Tumors

Brief summary

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

RBS2418 (investigational product) is a specific immune modulator, working through ectonucleotide pyrophosphatase/phosphodiesterase I (ENPP1), designed to lead to anti-tumor immunity by increasing endogenous 2'-3'-cyclic guanosine monophosphate-adenosine monophosphate (cGAMP) and adenosine triphosphate (ATP levels) and reducing adenosine production in the tumors. RBS2418 has the potential to be an important therapeutic option for subjects both as monotherapy and in combination with other cancer treatments including monotherapy and in combination with other cancer treatments including immunotherapy or chemotherapy. This study is an open-label, multi-site Phase 1a/1b study of RBS2418, a selective ENPP1 inhibitor, in combination with pembrolizumab or other approved anticancer therapies or as a monotherapy in subjects with advanced unresectable, recurrent or metastatic tumors. The phase 1a (dose escalation phase) has been completed. The Phase 1b expansion phase of the study has been increased in size and scope.

Study identification

NCT ID
NCT05270213
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 1
Lead sponsor
Riboscience, LLC.
Industry
Enrollment
164 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
Jul 10, 2022
Primary completion
Mar 31, 2027
Completion
Nov 30, 2027
Last update posted
Dec 18, 2025

2022 – 2027

United States locations

U.S. sites
14
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Honor Health Research Institute Scottsdale Arizona 85258 Recruiting
University of Arizona Tucson Arizona 85724 Recruiting
Stanford Cancer Institute Palo Alto California 94305 Recruiting
UCLA Hematology/Oncology - Santa Monica Santa Monica California 90404 Recruiting
Christiana Care Health Services Newark Delaware 19713 Recruiting
Norton Cancer Institute Louisville Kentucky 40202 Recruiting
Ochsner Clinic Foundation New Orleans Louisiana 70121 Recruiting
Johns Hopkins Sidney Kimmel Comprehensive Cancer Center Baltimore Maryland 21224 Recruiting
American Oncology Partners of Maryland Bethesda Maryland 20817 Recruiting
Ichan School of Medicine at Mount Sinai New York New York 10029 Recruiting
Carolina BioOncology Institute Huntersville North Carolina 28078 Completed
Vanderbilt-Ingram Cancer Center Nashville Tennessee 37235 Recruiting
Tranquil Research Webster Texas 77598 Withdrawn
NEXT Virigina 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 NCT05270213, 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 Dec 18, 2025 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05270213 live on ClinicalTrials.gov.

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