Study on SKB264 and Pembrolizumab for Treating Certain Solid Tumors
Sponsor: Klus Pharma Inc.
Sponsor score: 0
Inactive
ClinicalTrials ID:NCT05642780
This clinical trial is testing a new combination of drugs, SKB264 and Pembrolizumab, to see if they are safe and effective in treating certain types of solid tumors, including cervical, urothelial, ovarian, and prostate cancers.
Patient Parameters
| Parameter | Options |
|---|
Program Overview
The aim of this study is to find out if a combination of two drugs, SKB264 and Pembrolizumab, can help treat patients with specific types of solid tumors, such as cervical, urothelial, ovarian, and prostate cancers. Researchers are looking at how well the treatment works and how safe it is for patients.
Eligibility Criteria
Inclusion Criteria
- Must be in good general health, able to perform daily activities with minimal restrictions.
- Expected to live for at least 3 more months.
- Have one of the following conditions:
- Recurrent or metastatic cervical cancer
- Locally advanced or metastatic urothelial carcinoma
- Recurrent ovarian cancer
- Metastatic prostate cancer
- Have at least one tumor that can be measured by standard criteria.
- Able to provide a sample of the tumor for testing.
- Have good organ and bone marrow function.
- Must have recovered from any side effects of previous treatments, except those not considered risky.
- Must agree to use effective birth control during the study, following local guidelines.
- Must be able to understand and sign a consent form to participate.
Exclusion Criteria
- Have untreated or active cancer spread to the brain or spinal cord.
- Have significant heart disease.
- Have serious or uncontrolled other medical conditions.
- Have active hepatitis B or C infections.
- Have HIV that is not well controlled.
- Have active tuberculosis.
- Are allergic to Pembrolizumab, SKB264, or their ingredients.
- Have had a tissue or organ transplant from another person.
- Have been treated with TROP2 targeted therapy before.
- Have received a live vaccine within 30 days before starting the study or plan to receive one during the study.
- Are participating in another clinical trial, unless it is non-interventional or in the follow-up phase.
- Any other conditions that the study doctor believes could interfere with the study or pose a risk to the participant.
Get This Program In Your Inbox
Receive detailed information about this treatment opportunity to review with your healthcare provider.
