STRO-006 for Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This study is a first-in-human (FIH) Phase 1 open-label, multicenter study including three parts:
* Part 1A is a dose escalation of STRO-006 monotherapy in selected tumor types reported to commonly express ITGB6. Part 1A will determine the safety, tolerability, pharmacokinetics (PK), and preliminary anti-tumor activity of STRO-006.
* Part 1B is a dose expansion in one or more indications, as determined by the Sponsor, to further evaluate a STRO-006 monotherapy dose, examine anti-tumor activity, and determine the recommended Phase 2 dose (RP2D) of STRO-006 monotherapy.
* Part 1C is a combination dose escalation to determine safety, tolerability, PK, and preliminary anti-tumor activity of STRO-006 combined with pembrolizumab.
Who Is on the Research Team?
Jennifer Oliver
Principal Investigator
Sutro Biopharma
Are You a Good Fit for This Trial?
This trial is for adults with advanced or recurring solid tumors (like lung, esophageal, colorectal, endometrial, bladder, breast, stomach, or throat cancer) that have not responded to standard treatments. Participants must be in generally stable health aside from their cancer.Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Interventions
- Pembrolizumab
- STRO-006
Trial Overview
Researchers are testing a new drug called STRO-006 alone and in combination with pembrolizumab to find the safest dose and see how well it works against certain cancers. The study has several parts focusing on safety and early signs of effectiveness.
How Is the Trial Designed?
3
Treatment groups
Experimental Treatment
Find a Clinic Near You
Who Is Running the Clinical Trial?
Sutro Biopharma, Inc.
Lead Sponsor
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