Roles
- Professor
- Co-Leader, Translational and Clinical Oncology Research Program
- Director, Phase 1 Clinical Trials Program
-
Biography
Dr. Merchan is a tenured Professor of Medicine in the division of Medical Oncology. He is the Co-leader of the Translational and Clinical Oncology Research Program, the Director of the Phase 1 Clinical Trials Program, and the Associate Director of the NIH funded Calabresi Clinical Oncology Research Career Development Award. As a physician scientist, his contributions to science include redefining the role of the plasminogen activator system in cancer progression, the development of novel preclinical and clinical strategies to overcome resistance in RCC and angiogenesis dependent cancers, and the preclinical and clinical development of tumor and stromal targeted oncolytic viruses and virus-drug combinations. He leads the only academic phase I program in South Florida, bringing novel treatment strategies to many patients with advanced cancer. Dr. Merchan has an established track record in translational cancer research, bringing lab discoveries to the clinic, and has been involved in the development of novel, effective treatment strategies in genitourinary cancers, which resulted in practice changing publications and introduced new treatment options for cancer patients. -
Education & Training
Education
Post Graduate Training
Licensures and Certifications
-
Honors & Awards
-
Teaching Interests
Dr Merchan is the Associate Director of the Calabresi Clinical Oncology Research (K12) Career Development Award. He also serves as mentor for postdoctoral fellows, clinical oncology fellows, and junior faculty in the division of Medical Oncology. In this role, he plays an active role in the training of the next generation of cancer researchers, by teaching them the skills necessary to efficiently transform lab discoveries into clinical trials, giving career advice and serving as advocate for their career development. -
Research Interests
Dr Merchan's research efforts are focused on the preclinical and clinical development of novel strategies to overcome treatment resistance to targeted and immunotherapy agents in renal cell and other cancers. The goals of his funded laboratory research are to characterize the tumor and stromal mechanisms of tumor escape to oncolytic viruses, and the development of novel oncolytic virus - drug combinatorial strategies to enhance viral oncolysis and immunomodulation using xenograft and syngeneic cancer models, respectively. His collaborative research is focused on characterization and validation of understudied kinases as novel targets for kidney cancer drug development. As the director of the Phase 1 Clinical Trials Program, Dr. Merchan oversees a dynamic team of investigators and clinical research staff, to bring promising, innovative treatments, and hope, to patients with advanced cancers. -
Publications
Disclaimer: Information presented in this section has been consolidated using AI and machine learning technologies. While every effort has been made to ensure accuracy, errors may occur. If you identify any inaccuracies, use this link to inform our data team. Your feedback is appreciated and helps us improve the quality of our content.Professional Activities
Articles & News
Sylvester’s Course on Cancer Clinical Trials Goes National, International
Jaime Merchán, M.D., Named Sylvester’s Translational and Clinical Oncology Research Program Co-Leader
Sylvester Part of International Study on Promising New Renal Cell Carcinoma Treatment
Disclaimer:
Information presented in this section has been consolidated using AI and machine learning technologies. While every effort has been made to ensure accuracy, errors may occur. If you identify any inaccuracies, use this link to inform our data team. Your feedback is appreciated and helps us improve the quality of our content.
Clinical Trials
Viewing 0 of 25 clinical trials.
-
The purpose of this study is to learn about the effects of the research medicine, FX-909, to find the best dose for treating metastatic urothelial carcinoma and to see how safe FX-909 is for patients with this type of cancer. FX-909 is a drug that binds to certain areas on cells that may be related to disease progression. When FX-909 binds to those areas, it has the potential to slow down or stop the tumor growth, and in some cases it may decrease the tumor size.
- Principal Investigator: Jaime Merchan
- Study Phase: Phase I
- Enrollment Status: Not Accepting
-
To determine the safety profile, maximum tolerable dose (MTD), minimally reproducible active dose (MRAD), and recommended dose range (RDR) of BHV-1530 administered by intravenous infusion dosed once every 3 weeks
- Principal Investigator: Jaime Merchan
- Study Phase: Phase I
- Enrollment Status: Open
-
The purpose of this clinical research study is to test the safety of the investigational study drug NEO-811 at different dose. The study will also help to understand the way your body processes and responds to NEO-811. Also to find out what effects NEO-811 may have on you and your kidney cancer.
- Principal Investigator: Jaime Merchan
- Study Phase: Phase I
- Enrollment Status: Open
-
The purpose of this trial is to test safety and anti-cancer activity of MK-3120 (SKB410) in people.
- Principal Investigator: Jaime Merchan
- Study Phase: Phase I/II
- Enrollment Status: Not Accepting
-
The goals of this study are:•To see how safe and tolerable MDX2001 is at different dose levels in people with tumors and cancers.•To assess any anti tumor activity (preventing or inhibiting the formation or growth of tumors) of MDX2001 in participants with selected advanced solid tumor metastatic cancer.•To determine the best (optimal) dose of MDX2001 for further development of MDX2001 in Phase 2a.•To see how much MDX2001 is in your blood and for how long it stays in your blood, also known as pharmacokinetics (PK).•To explore the immunogenicity activity of MDX2001 in participants with advanced solid tumor metastatic cancer. Immunogenicity is the ability of a foreign substance, such as an antigen, to produce an immune response in the human body.
- Principal Investigator: Jaime Merchan
- Study Phase: Phase I/II
- Enrollment Status: Open
-
A Dose-Escalation and Expansion Study of the Safety and Pharmacokinetics of XL092 as Single-Agent and Combination Therapy in Subjects With Inoperable Locally Advanced or Metastatic Solid Tumors
- Principal Investigator: Jaime Merchan
- Study Phase: Phase 1
- Enrollment Status: Not Accepting
-
To determine the recommended phase 2 dose of the combination of CA-4948 plus pembrolizumab in patients with immune checkpoint blockade (ICB)-resistant metastatic urothelial cancer (Dose Escalation Cohort).
- Principal Investigator: Jaime Merchan
- Study Phase: Phase I
- Enrollment Status: Open
-
This study aims to test a new investigational drug (TUB-030) in three phases for participants with various types of cancer known as solid tumors. TUB-030 is a new type of potential cancer treatment that aims to destroy cancer cells in patients with various cancer types called solid tumors.
- Principal Investigator: Jaime Merchan
- Study Phase: Phase I/II
- Enrollment Status: Open
-
A Multicenter, Double-blind, Randomized Phase 3 Study to Compare the Efficacy and Safety of Belzutifan (MK-6482) Plus Pembrolizumab (MK-3475) Versus Placebo Plus Pembrolizumab, in the Adjuvant Treatment of Clear Cell Renal Cell Carcinoma (ccRCC) Post Nephrectomy (MK-6482-022)
- Principal Investigator: Jaime Merchan
- Study Phase: Phase 3
- Enrollment Status: Not Accepting
-
This is an open-label, dose-escalation, multi-center phase I study evaluating the safety of CF33-hNIS (hNIS - human sodium iodide symporter) administered via two routes of administration, intratumoral (IT) or intravenous (IV), either as a monotherapy or in combination with pembrolizumab in patients with metastatic or advanced solid tumors.
- Principal Investigator: Jaime Merchan
- Study Phase: Phase I
- Enrollment Status: Closed
-
To determine the safety and tolerability and to establish a preliminary maximum tolerated dose/recommended Phase 2 dose of MK-1088 administered as monotherapy and in combination with pembrolizumab infusion
- Principal Investigator: Jaime Merchan
- Study Phase: Phase I/II
- Enrollment Status: Closed
-
To compare PFS of casdatifan + cabozantinib versus placebo + cabozantinib in all randomized patients. To compare OS of casdatifan + cabozantinib versus placebo + cabozantinib in all randomized patients. To assess additional measures of clinical activity in all randomized patients.
- Principal Investigator: Jaime Merchan
- Study Phase: Phase III
- Enrollment Status: Open
-
The main purpose of the Escalation Phase of this study is to help determine if the study drug is safe and to find the best DCSZ11 dose that can be given without unacceptable side effects, how the study drug makes people feel, and how the body absorbs and processes the study drug. The study drug (DCSZ11) will be administered as an intravenous (IV) infusion.
- Principal Investigator: Jaime Merchan
- Study Phase: Phase I
- Enrollment Status: Closed
-
The purpose of this study is to evaluate the safety and tolerability of casdatifan (AB521) when taken alone in participants with advanced solid tumor malignancies and clear cell renal cell carcinoma (ccRCC).
- Principal Investigator: Jaime Merchan
- Study Phase: Phase I
- Enrollment Status: Open
-
Phase 1/2 Study of RTX-240 Monotherapy and in Combination With Pembrolizumab
- Principal Investigator: Jaime Merchan
- Study Phase: Phase 1/Phase 2
- Enrollment Status: Closed
-
Phase 1/1b Study to Evaluate the Safety and Activity of TTX-030 (Anti-CD39) in Combination With Pembrolizumab or Budigalimab and/or Chemotherapy in Subjects With Advanced Solid Tumors
- Principal Investigator: Jaime Merchan
- Study Phase: Phase 1
- Enrollment Status: Closed
-
Phase 2 Study of MK-6482 in Participants With Advanced Renal Cell Carcinoma
- Principal Investigator: Jaime Merchan
- Study Phase: Phase 2
- Enrollment Status: Closed
-
A Phase 2 Trial of PT2977 in Combination With Cabozantinib in Patients With Advanced Clear Cell Renal Cell Carcinoma
- Principal Investigator: Jaime Merchan
- Study Phase: Phase 2
- Enrollment Status: Not Accepting
-
A Multicenter, Open-label, Randomized, Phase 3 Trial to Compare the Efficacy and Safety of Lenvatinib in Combination With Everolimus or Pembrolizumab Versus Sunitinib Alone in First-Line Treatment of Subjects With Advanced Renal Cell Carcinoma (CLEAR)
- Principal Investigator: Jaime Merchan
- Study Phase: Phase 3
- Enrollment Status: Closed
-
A Phase 1b/2a Dose-escalation and Safety/Efficacy Evaluation Study of Pexa-Vec (Thymidine Kinase-Deactivated Vaccinia Virus Plus GM-CSF) in Combination With Cemiplimab (REGN2810; Anti-PD-1) in Patients With Metastatic or Unresectable Renal Cell Carcinoma (RCC)
- Principal Investigator: Jaime Merchan
- Study Phase: Phase 1/Phase 2
- Enrollment Status: Closed
-
A PHASE 1/1b MULTICENTER STUDY TO EVALUATE THE HUMANIZED ANTI-CD73 ANTIBODY, CPI-006, AS A SINGLE AGENT OR IN COMBINATION WITH CIFORADENANT, WITH PEMBROLIZUMAB, AND WITH CIFORADENANT PLUS PEMBROLIZUMAB IN ADULT SUBJECTS WITH ADVANCED CANCERS
- Principal Investigator: Jaime Merchan
- Study Phase: Phase 1
- Enrollment Status: Closed
-
- Evaluate the safety and tolerability of VET3-TGI alone and in combination with pembrolizumab when administered via ITu injection or IV infusion.- Establish the recommended Phase 2 dose and define the MTD or MFD of VET3-TGI alone and in combination with atezolizumab when administered via ITu injection or IV infusion.
- Principal Investigator: Jaime Merchan
- Study Phase: Phase I
- Enrollment Status: Open
-
- To determine the safety and tolerability of IK- 595- To determine the recommended phase II dose (RP2D) and/or maximum tolerated dose (MTD) of IK-595
- Principal Investigator: Jaime Merchan
- Study Phase: Phase I
- Enrollment Status: Closed
-
A Phase III, Multicenter, Randomized, Placebo-Controlled, Double-Blind Study of Atezolizumab (Anti-PD-L1 Antibody) as Adjuvant Therapy in Patients With Renal Cell Carcinoma at High Risk of Developing Metastasis Following Nephrectomy
- Principal Investigator: Jaime Merchan
- Study Phase: Phase 3
- Enrollment Status: Closed
-
A Study of Enfortumab Vedotin (ASG-22CE) as Monotherapy or in Combination With Other Anticancer Therapies for the Treatment of Urothelial Cancer
- Principal Investigator: Jaime Merchan
- Study Phase: Phase 1/Phase 2
- Enrollment Status: Closed
