A Study of SBT6050 Alone and in Combination With PD-1 Inhibitors in Subjects With Advanced HER2 Expressing Solid Tumors
NCT04460456 · Status: UNKNOWN · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 58
Last updated 2022-06-30
Summary
A first-in-human (FIH) study using SBT6050 and SBT6050 in combination with PD-1 inhibitors in HER2 expressing or amplified advanced malignancies
Conditions
- HER2 Positive Solid Tumors
Interventions
- DRUG
-
SBT6050
Escalating doses of SBT6050 in Part 1 and recommended dose in Part 2
- DRUG
-
400 mg IV
- DRUG
-
350 mg IV
Sponsors & Collaborators
-
Silverback Therapeutics
lead INDUSTRY
Principal Investigators
-
Naomi Hunder, MD · Silverback Therapeutics
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-07-27
- Primary Completion
- 2022-12-31
- Completion
- 2022-12-31
- FDA Drug
- Yes
Countries
- United States
- Australia
- South Korea
Study Locations
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