About the Study
Breast cancer represents a significant challenge, and advancing treatment options is crucial for patients facing this disease. VIKTORIA-1 is a clinical trial aimed at evaluating a new investigational drug for patients with breast cancer.
By participating in VIKTORIA-1, patients have the opportunity to contribute to groundbreaking research that seeks to offer more effective treatments. Join researchers in advancing breast cancer treatment.
Why Participate?
- Participants will be part of advanced breast cancer research.
- Participants will have access to a new investigational treatment.
- Participants will contribute to the development of potential future therapies.
Your Rights
- If you decide to participate in the study and later feel that you no longer wish to be part of it, you can withdraw at any time.
- Any information that you provide will be kept strictly confidential, except as required by law.
- Qualified health professionals will monitor your health as it relates to the study.
Who Can Participate?
- Adults aged 18 years and above who are diagnosed with metastatic or locally advanced breast cancer
- Must be able to swallow oral medication tablets/capsules
- Must not have any known hypersensitivity to the study drugs or their components
- Must be able to attend study visits at the research site
About the Research Centers
This research study is taking place in several locations. To see if there is a research site near you, please see below.
Research Site: American Oncology Partners, PA
Location: 6410 Rockledge Drive #660, Bethesda MD 20817
Lead Researcher: Mark Goldstein, MD
Research Site: Redlands Hematology Oncology (Redlands, CA)
Location: 245 Terracina Blvd. Suite 208 Redlands, CA 92373
Lead Researcher: Dr. Emad Ibrahim
Research Site: South Broward Hospital District d/b/a Memorial Healthcare System
Location: Breast Cancer Center, Medical Office Centre, 1150 N. 35th Ave., Suite 170, 1st Floor, Hollywood, FL 33021
Lead Researcher: Delia Guaqueta, MD
This study has been reviewed and approved by the Advarra Institutional Review Board.