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10 Studies Recruiting

Clinical Trials Near Orlando, FL

Find research studies actively recruiting participants near Orlando. Studies are run at established research institutions including AdventHealth and Orlando Health.

Top Research Institutions in Orlando

1

AdventHealth

2

Orlando Health

3

UCF College of Medicine

Recruiting Studies Near Orlando

#1

PyloPlus Urea Breath Test System Pediatric Safety and Efficacy Study

RECRUITINGPHASE3ARJ Medical, Inc.

This is a multi-center, non-randomized, open label study. Subjects will be enrolled on a walk-in basis. Screening data will be reviewed to determine subject eligibility. Subjects who meet all inclusion criteria and none of the exclusion criteria will be entered into the study. All children will be exposed to non-radioactive 13C-Urea with citric acid, and shall submit a stool sample. Centers will house a PyloPlus UBT Analyzer to document results. PyloPlus Analyzer results shall remain blinded to the investigator and treating physician. No patient management decisions should be made based on the investigational PyloPlus® UBT System. Treating physician will prescribe a H. Pylori Stool Antigen Test to Stool test at either LabCorp or Quest Diagnostic, for the patient, which will be used for diagnostic purposes by the ordering physician. Total duration of study is anticipated to be approximately 6 months.

📍 Doral, Florida📍 Orlando, Florida📍 El Paso, Texas
#2

Tipifarnib and Naxitamab for Relapsed/Refractory Neuroblastoma

RECRUITINGPHASE2Giselle Sholler

The purpose of this study is to evaluate the investigational drug, tipifarnib (a pill taken by mouth), in combination with the Food and Drug Administration (FDA) approved drug, naxitimab, administered intravenously (IV; a liquid that continuously goes into your body through a tube that has been placed during a surgery into one of your veins). Naxitamab is FDA approved for pediatric patients 1 year of age and older and adult patients with relapsed or refractory high-risk neuroblastoma in the bone or bone marrow who have demonstrated a partial response, minor response, or stable disease to prior therapy, it may not be approved in the type of disease used in this study. The goals of this part of the study are: * Test the safety and tolerability of tipifarnib in combination with naxitimab in participants with cancer * To determine the activity of study treatments chosen based on: * How each participant responds to the study treatment * How long a participant lives without their disease returning/progressing

📍 Little Rock, Arkansas📍 Hartford, Connecticut📍 Miami, Florida
#3

Natural History Evaluation of Charcot Marie Tooth Disease (CMT) Types CMT1B, CMT2A, CMT4A, CMT4C, and Others

RECRUITINGNot SpecifiedMichael Shy

This is an observational longitudinal study to determine the natural history and genotype-phenotype correlations of disease causing mutations in Charcot Marie Tooth disease (CMT) type 1B (CMT1B), 2A (CMT2A), 4A (CMT4A), and 4C (CMT4C). The investigators will also be determine the capability of the newly developed CMT Pediatric Scale (CMT Peds scale) and the Minimal Dataset to measure impairment and perform longitudinal measurements in patients with multiple forms of CMT over a five year window

📍 Los Angeles, California📍 Palo Alto, California📍 Aurora, Colorado
#4

A Study Evaluating the Real World Experience of Participants Treated With BRIUMVI® (Ublituximab-xiiy) for Relapsing Multiple Sclerosis (RMS)

RECRUITINGNot SpecifiedTG Therapeutics, Inc.

The purpose of this study is to evaluate safety, effiectiveness, and to gain insight into the treatment experience of participants prescribed BRIUMVI® (ublituximab-xiiy) in the real-world setting

📍 Birmingham, Alabama📍 Cullman, Alabama📍 Huntsville, Alabama
#5

A Study to Assess the Efficacy, Safety, and Tolerability of IMVT-1402 as Treatment for Adult Participants With Graves' Disease

RECRUITINGPHASE2Immunovant Sciences GmbH

This is a study to assess the efficacy, safety, and tolerability of IMVT-1402 in adult participants with Graves' disease (GD) who are hyperthyroid despite antithyroid drug (ATD) treatment. The primary objective of this study is to evaluate the efficacy of IMVT-1402 versus placebo as assessed by T3 (total triiodothyronine \[T3\] or free triiodothyronine \[FT3\]), free thyroxine (FT4), thyroid-stimulating hormone (TSH), and ATD dose at Week 26.

📍 Phoenix, Arizona📍 Huntington Beach, California📍 Los Angeles, California
#6

Diabetes RElated to Acute Pancreatitis and Its Mechanisms: Metabolic Outcomes Using Novel CGM Metrics

RECRUITINGNot SpecifiedMilton S. Hershey Medical Center

The DREAM-ON study will investigate whether continuous glucose monitoring (CGM) is useful to predict risk for developing diabetes mellitus (DM) and pre-diabetes mellitus (PDM), the need for insulin therapy among those who develop DM, and to determine whether CGM can provide insight into the pathophysiology and DM subtype among participants who have experienced an episode of acute pancreatitis (AP). Thus, the results of the DREAM-ON study could inform future clinical practice guidelines for the management AP as well as potentially extending the licensing authorization for CGM to include use in patients with pancreatogenic (Type 3c) DM.

📍 Los Angeles, California📍 Los Angeles, California📍 Stanford, California
#7

Post-sleeve Gastrectomy Gastroesophageal Reflux Disease Prediction

RECRUITINGNAMayo Clinic

Researchers are trying to identify predictors for gastroesophageal reflux disease after sleeve gastrectomy.

📍 Rochester, Minnesota
#8

Safety and Tolerability Trial of Lumateperone in Pediatric Patients With Schizophrenia, Bipolar Disorder or Autism Spectrum Disorder

RECRUITINGPHASE3Intra-Cellular Therapies, Inc.

This is a multicenter, global, 26-week, open-label study to assess the safety and tolerability of lumateperone in pediatric patients with schizophrenia, bipolar disorder or autism spectrum disorder.

📍 Phoenix, Arizona📍 Little Rock, Arkansas📍 Anaheim, California
#9

A Study of Bleximenib, Venetoclax and Azacitidine For Treatment of Participants With Newly Diagnosed Acute Myeloid Leukemia (AML)

RECRUITINGPHASE3Janssen Research & Development, LLC

The purpose of this study is to assess how bleximenib and Venetoclax (VEN)+ Azacitidine (AZA) works as compared to placebo and VEN+AZA alone for the treatment of participants with newly diagnosed Acute Myeloid Leukemia (AML) with a mutation in the NPM1 or KMT2A gene.

📍 Birmingham, Alabama📍 Goodyear, Arizona📍 Tucson, Arizona
#10

Investigation of the BrioVAD System for the Treatment of Left Ventricular Heart Failure

RECRUITINGNABrioHealth Solutions, Inc.

The goal of this study is to evaluate the safety and efficacy of the BrioVAD System by demonstrating non-inferiority to the HeartMate 3 Left Ventricular Assist System when used for the treatment of advanced, refractory, left ventricular heart failure.

📍 Birmingham, Alabama📍 Little Rock, Arkansas📍 Los Angeles, California

Clinical Trials in Orlando: FAQ

How do I find clinical trials near Orlando?

Corterve aggregates all actively recruiting clinical trials near Orlando, FL from the ClinicalTrials.gov database. Simply browse the listings on this page or take our assessment to find trials that may be relevant.

Does it cost anything to take part in a study?

Costs, travel support, and any payment for taking part vary by study. Ask the study team what is covered before you decide to join.

What research institutions are located in Orlando?

Orlando is home to several leading research institutions, including AdventHealth, Orlando Health, UCF College of Medicine. These facilities run clinical trials across Oncology, Neurology, Cardiology, and other therapeutic areas.

Ready to see studies near you?

Take our assessment to see research studies recruiting near Orlando that may be relevant. Study teams decide who joins. No insurance required.

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