A Study of SBT6050 in Patients With Advanced HER2 Expressing Solid Tumors
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- STATUS
- Recruiting
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- participants needed
- 210
-
- sponsor
- Silverback Therapeutics
Summary
A first-in-human (FIH) study using SBT6050 in HER2 expressing advanced malignancies
Description
This study has 2 parts. Part 1 will evaluate the safety, tolerability and activity of escalating doses of SBT6050 to estimate the maximum tolerated dose (MTD) and determine the dose recommended for Part 2. Part 2 of the study will further evaluate SBT6050 in select HER2 expressing advanced malignancies.
Details
| Condition | HER2 Positive Solid Tumors |
|---|---|
| Age | 18-100 years |
| Treatment | SBT6050 |
| Clinical Study Identifier | NCT04460456 |
| Sponsor | Silverback Therapeutics |
| Last Modified on | 19 February 2024 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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