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Completed Phase 1 Interventional

A Phase 1 in Patients With HLA-A*0201+ and WT1+ Recurrent/Metastatic Cancers

ClinicalTrials.gov ID: NCT05360680

Public ClinicalTrials.gov record NCT05360680. 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, 5:37 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 1, Open-Label, Dose Escalation and Expansion Study of CUE-102 Monotherapy in HLA-A*0201 Positive Patients With WT1 Positive Recurrent/Metastatic Cancers

Brief summary

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

This is a Phase 1, open-label, 2-part, multi-center study evaluating the safety, tolerability, PK, pharmacodynamics (PD), immunogenicity, and antitumor activity of CUE-102 intravenous (IV) monotherapy in HLA-A\*0201 positive patients with WT1 positive recurrent/metastatic solid tumors who have failed conventional therapies.

Study identification

NCT ID
NCT05360680
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Cue Biopharma
Industry
Enrollment
42 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
Jun 14, 2022 (Actual)
Primary completion
Mar 12, 2025 (Actual)
Completion
Mar 12, 2025 (Actual)
Last update posted
Jan 22, 2026

2022 – 2025

United States locations

U.S. sites
15
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
Mayo Clinic Phoenix Arizona 85054 —
Cedars-Sinai Medical Center Los Angeles California 90048 —
Stanford Advanced Medicine Cancer Center Palo Alto California 94304 —
Moffitt Cancer Center Tampa Florida 33612 —
Winship Cancer Institute Atlanta Georgia 30322 —
Johns Hopkins University Baltimore Maryland 21231 —
Mayo Clinic - Rochester Rochester Minnesota 55905 —
Carol G. Simon Cancer Center - Morristown Medical Center Morristown New Jersey 07960 —
Montefiore Medical Center The Bronx New York 10461 —
Carolina BioOncology Institute Huntersville North Carolina 28078 —
Gabrail Cancer Center Canton Ohio 44718 —
Cleveland Medical Center (University Hospitals) Cleveland Ohio 44106 —
MD Anderson Cancer Center Houston Texas 77030 —
Northwest Medical Specialties, PLLC Tacoma Washington 98405 —
Carbone Cancer Center Madison Wisconsin 53792 —

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 NCT05360680, 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 Jan 22, 2026 · 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 NCT05360680 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →