Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06021626

A Study of CRD3874-SI in People With Solid Tumors

A Phase I Trial of CRD3874-SI, a STING Agonist, in Patients With Advanced/Metastatic Malignant Solid Tumors

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
72 (estimated)
Sponsor
Memorial Sloan Kettering Cancer Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study will test the safety of a study drug called CRD3874-SI. The researchers will test different doses of CRD3874-SI to find the highest dose that causes few or mild side effects in participants. After the researchers find the highest safe dose of CRD3874-SI, they will test that dose in new groups of participants to help them learn more about the side effects of the study drug and find out whether CRD3874-SI is an effective treatment for for patients with advanced or metastatic malignant solid tumors including sarcoma and Merkel Cell Carcinoma.

Conditions

Interventions

TypeNameDescription
DRUGCRD3874Starting dose is 0.1 mg/kg for weekly IV infusion of CRD3874-SI. Cohort CRD3874-SI Dose level (mg/kg) 1. 0.1 2. 0.3 3. 0.9 4. 1.8 5. 2.7 6. 4.05

Timeline

Start date
2023-08-25
Primary completion
2029-08-01
Completion
2029-08-01
First posted
2023-09-01
Last updated
2025-12-19

Locations

7 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06021626. Inclusion in this directory is not an endorsement.

A Study of CRD3874-SI in People With Solid Tumors (NCT06021626) · Clinical Trials Directory