Glycan Mediated Immune Regulation With a Bi-Sialidase Fusion Protein (GLIMMER-01)
Part of paid clinical trials in La Jolla, California.
- Sponsor
- Palleon Pharmaceuticals, Inc.
- Study ID
- NCT05259696
- Phase
- PHASE1/PHASE2
- Status
- Completed
Conditions
- Bladder Cancer
- Breast Cancer
- CRC
- Cancer
- Colon Cancer
- Colorectal Cancer
- EGJ
- Esophagogastric Junction Cancer
- Gastric Cancer
- Head and Neck Cancer
- Melanoma
- NSCLC
- Non Small Cell Lung Cancer
- Oncology
- Ovarian Cancer
- Pancreatic Cancer
- Urothelial Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- E-602 — BIOLOGICALSubjects will receive E-602 (administered weekly, via IV infusion).
- Cemiplimab — BIOLOGICALSubjects will receive cemiplimab (administered once every 3 weeks, via IV infusion).
Study Details
This is a Phase 1/2, first-in-human, open-label, dose escalation and dose-expansion study of E-602, administered alone and in combination with cemiplimab.
Key Dates
- First listed
- Feb 28, 2022
- Start date
- Feb 11, 2022
- Status verified
- Aug 2025
- Primary completion
- Oct 24, 2024
- Completion
- Oct 24, 2024
Study Design
- Enrollment
- 69 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Dose Escalation - MonotherapySubjects will receive E-602 as monotherapy. Planned monotherapy dose levels: 1 mg/kg, 3 mg/kg, 10 mg/kg, 20 mg/kg, and 30 mg/kg.
- Experimental: Dose Escalation - CombinationSubjects will receive E-602 in combination with cemiplimab. E-602 dose(s): Will be initiated at dose level(s) that have previously completed dosing and DLT assessments as monotherapy. Cemiplimab dose: 350 mg.
- Experimental: Expansion - MonotherapySubjects will receive E-602 as monotherapy at the recommended Phase 2 dose determined in Phase 1.
- Experimental: Expansion - CombinationSubjects will receive E-602 in combination with cemiplimab. E-602 dose: Subjects will receive E-602 at the recommended Phase 2 dose determined in Phase 1 in combination with cemiplimab. Cemiplimab dose: 350 mg.
Primary Outcome Measure
Number of Participants Who Experienced AEs or SAEs [ Time Frame: 15 Months ]
Locations (13)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| UC San Diego Moores Cancer Center | La Jolla | California | 92093 | - |
| University of Southern California | Los Angeles | California | 90033 | - |
| Stanford Health Care | Stanford | California | 94305 | - |
| Yale University Cancer Center | New Haven | Connecticut | 06520 | - |
| Massachusetts General Hospital | Boston | Massachusetts | 02114 | - |
| START Midwest | Grand Rapids | Michigan | 49546 | - |
| Roswell Park Comprehensive Cancer Center | Buffalo | New York | 14263 | - |
| Columbia University | New York | New York | 10032 | - |
| Providence Cancer Institute | Portland | Oregon | 97213 | - |
| University of Pittsburgh Medical Center | Pittsburgh | Pennsylvania | 15232 | - |
| Sarah Cannon Research Institute | Nashville | Tennessee | 37203 | - |
| NEXT Oncology | San Antonio | Texas | 78229 | - |
| Virginia Cancer Specialists | Fairfax | Virginia | 22031 | - |
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