A Study of SNS-101 (Anti VISTA) Monotherapy and in Combination With Cemiplimab in Patients With Advanced Solid Tumors
Part of paid clinical trials in Los Angeles, California.
- Sponsor
- Sensei Biotherapeutics, Inc.
- Study ID
- NCT05864144
- Phase
- PHASE1/PHASE2
- Status
- Active Not Recruiting
Conditions
- Advanced Cancer
- Advanced Solid Tumor
- Bladder Cancer
- Breast Cancer
- Cervix Cancer
- Colon Cancer
- Esophageal Cancer
- Gastric Cancer
- Head and Neck Cancer
- Kidney Cancer
- Melanoma
- Merkel Cell Carcinoma
- Metastatic Cancer
- Non Small Cell Lung Cancer
- Ovarian Cancer
- Pancreatic Cancer
- Prostate Cancer
- Refractory Cancer
- Sarcoma
- Solid Tumor, Adult
- Thyroid Cancer
- Uterine Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- SNS-101 (anti-VISTA) — DRUGSNS-101 IV every 21 days.
- Cemiplimab — DRUGCemiplimab IV every 21 days.
Study Details
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.
Key Dates
- Start date
- May 31, 2023
- Status verified
- Aug 2025
- Primary completion
- Jun 30, 2027
- Completion
- Jun 30, 2027
Study Design
- Enrollment
- 98 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Part A - SNS-101 Monotherapy Dose Escalation and Dose ExpansionSNS-101 IV alone every 21 days. Patients will initially enroll in dose escalation cohorts.
- Experimental: Part B - SNS-101 in combination with cemiplimab and Dose ExpansionSNS-101 IV and cemiplimab IV every 21 days. Patients will initially enroll in dose escalation cohorts.
- Experimental: Part C - Cohort Expansion - SNS-101 alone or in combination with cemiplimabSNS-101 IV alone or in combination with cemplimab IV every 21 days at the RP2D.
Primary Outcome Measure
Adverse Events - Part A & B [ Time Frame: Day 1 through 90 days after the last dose ]
Locations (10)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| 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 | - |
Find similar trials in Los Angeles, CA
By condition
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UCLA Hematology/Oncology· Los Angeles, CAUniversity of Colorado Cancer Center - Anschutz Medical· Aurora, CONorton Healthcare· Louisville, KYHenry Ford Cancer· Detroit, MIIcahn School of Medicine at Mt. Sinai· New York, NYUniversity of Pennsylvania, Perelman Center for Advanced Medicine· Philadelphia, PA
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