Dr. Ronald Tutrone, MD
Claim this profileChesapeake Urology Research Associates
Studies Prostate Cancer
Studies Pancreatic Cancer
6 reported clinical trials
12 drugs studied
Area of expertise
1Prostate Cancer
Stage IV
Stage I
Stage II
2Pancreatic Cancer
Stage IV
Affiliated Hospitals
Clinical Trials Ronald Tutrone, MD is currently running
Registry
for Advanced Prostate Cancer
Our intent is to establish the International Registry to Improve Outcomes in Men with Advanced Prostate Cancer (IRONMAN) as a prospective, international cohort of minimum 5,000 men with advanced cancer, including men with mHSPC and M0/M1 CRPC. The goal is to establish a population-based registry and recruit patients across academic and community practices from Australia, Barbados, Brazil, Canada, Ireland, Jamaica, Kenya, Nigeria, Norway, Spain, South Africa, Sweden, Switzerland, the United Kingdom (UK), and the United States (US). Target accrual number and number of participating sites are subject to change based on accrual, funding, and interest in participation by other international sites. This cohort study will facilitate a better understanding of the variation in care and treatment of advanced prostate cancer across countries and across academia and community based practices. Detailed data will be collected from patients at study enrollment and then during follow-up, for a minimum of five years. Patients will be followed prospectively for overall survival, clinically significant adverse events, comorbidities, changes in cancer treatments, and PROMs. PROMs questionnaires will be collected at enrollment and every three months thereafter. Physician Questionnaires will be collected from all participating sites at patient enrollment, time of first change in treatment and/or one year follow-up, at each subsequent change of treatment, and discontinuation of treatment. As such, this registry will help identify the treatment sequences or combinations that optimize overall survival and PROMs for men with mHSPC and M0/M1 CRPC. By collecting blood at enrollment, time of first change in treatment and/or one year follow-up (plasma, cell free DNA, buffy coat / RNA), this registry will further identify and validate molecular phenotypes of disease that predict response and resistance to specific therapeutics. Additionally, every effort will be made to collect blood specimen at each subsequent change in treatment due to progression of disease. When feasible, existing tumor tissue may be collected for correlation with described blood based studies. All samples will be used for future research. This cohort study will provide the research community with a unique biorepository to identify biomarkers of treatment response and resistance.
Recruiting1 award N/A5 criteria
PRL-02 Injection
for Prostate Cancer
This trial tests a muscle injection called PRL-02 for patients with advanced prostate cancer. It aims to slowly release the medication to help manage the disease.
Recruiting1 award Phase 14 criteria
More about Ronald Tutrone, MD
Clinical Trial Related8 years of experience running clinical trials · Led 6 trials as a Principal Investigator · 2 Active Clinical TrialsTreatments Ronald Tutrone, MD has experience with
- Abemaciclib
- Abiraterone
- Standard Of Care
- ProstAtak® Immunotherapy
- UGN-102
- TURBT
Breakdown of trials Ronald Tutrone, MD has run
Prostate Cancer
Genitourinary Cancers
Steroid Synthesis Inhibitors
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Frequently asked questions
Do I need insurance to participate in a trial?
Almost all clinical trials will cover the cost of the ‘trial drug’ — so no insurance is required for this. For trials where this trial drug is given alongside an already-approved medication, there may be a cost (which your insurance would normally cover).
What does Ronald Tutrone, MD specialize in?
Ronald Tutrone, MD focuses on Prostate Cancer and Pancreatic Cancer. In particular, much of their work with Prostate Cancer has involved Stage IV patients, or patients who are Stage I.
Is Ronald Tutrone, MD currently recruiting for clinical trials?
Yes, Ronald Tutrone, MD is currently recruiting for 2 clinical trials in Baltimore Maryland. If you're interested in participating, you should apply.
Are there any treatments that Ronald Tutrone, MD has studied deeply?
Yes, Ronald Tutrone, MD has studied treatments such as Abemaciclib, Abiraterone, Standard of Care.
What is the best way to schedule an appointment with Ronald Tutrone, MD?
Apply for one of the trials that Ronald Tutrone, MD is conducting.
What is the office address of Ronald Tutrone, MD?
The office of Ronald Tutrone, MD is located at: Chesapeake Urology Research Associates, Baltimore, Maryland 21204 United States. This is the address for their practice at the Chesapeake Urology Research Associates.
Is there any support for travel costs?
The coverage of travel expenses can vary greatly between different clinical trials. Please see more financial detail in the trials you’re interested to apply.
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