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Completed Phase 1Phase 2 Interventional

A Study of SNS-101 (Anti VISTA) Monotherapy and in Combination With Cemiplimab in Patients With Advanced Solid Tumors

ClinicalTrials.gov ID: NCT05864144

Public ClinicalTrials.gov record NCT05864144. 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 16, 2026, 4:45 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 1/2, Open-label Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of SNS-101 (Anti VISTA) as Monotherapy and in Combination With Cemiplimab in Patients With Advanced Solid Tumors

Brief summary

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

Phase 1/2 study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy of SNS-101, a novel anti VISTA IgG1 monoclonal antibody as monotherapy or in combination with cemiplimab in patients with advanced solid tumors.

Study identification

NCT ID
NCT05864144
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Sensei Biotherapeutics, Inc.
Industry
Enrollment
98 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
May 31, 2023 (Actual)
Primary completion
Jun 2, 2026 (Actual)
Completion
Jun 2, 2026 (Actual)
Last update posted
Sep 2, 2026

2023 – 2026

United States locations

U.S. sites
10
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
UCLA Hematology/Oncology Los Angeles California 90095 —
University of Colorado Cancer Center - Anschutz Medical Aurora Colorado 80045 —
Norton Healthcare Louisville Kentucky 40202 —
Henry Ford Cancer Detroit Michigan 48202 —
Icahn School of Medicine at Mt. Sinai New York New York 10029 —
University of Pennsylvania, Perelman Center for Advanced Medicine Philadelphia Pennsylvania 19104 —
Sanford Cancer Center Sioux Falls South Dakota 57104 —
NEXT Oncology Dallas Irving Texas 75039 —
South Texas Accelerated Research Therapeutics (START) San Antonio San Antonio Texas 78229 —
START Mountain Region West Valley City Utah 84119 —

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 NCT05864144, 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 Sep 2, 2026 · Synced Oct 16, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05864144 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →