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                    South Carolina Paid Clinical Trials
A listing of 1173  clinical trials  in South Carolina  actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
            385 - 396 of 1173
        
                South Carolina is currently home to 1173 active clinical trials, seeking participants for engagement in research studies. These trials take place at a variety of cities in the state, including Charleston, Greenville, Spartanburg and Columbia. Whether you're a healthy volunteer interested in paid medical research or someone seeking trials related to a specific condition, the state offers a diverse array of opportunities in your vicinity.
            
                                                Featured Trial
                
                Healthy Participants Needed (Colonoscopy + Cancer Screening)
            
        Recruiting
            
        Earn $325 - $475 in electronic payment card compensation for your time and effort by participating in a clinical study to develop a blood test that may one day help screen for colon cancer. Take a quick quiz to see if you qualify.
    
    
                            Conditions: 
                                    
        
            
                        Healthy
                    
                                    
                        Healthy Volunteers
                    
                                    
                        Healthy Subjects
                    
                                    
                        Healthy Volunteer
                    
                                    
                        Healthy Participants
                    
                                    Featured Offer
                
                Lose Weight with GLP-1 Medications
            
        Recruiting
            
        Policy Lab has partnered with OnlineSemaglutide.org to offer trusted access to semaglutide and other GLP-1 medications, including generic alternatives to Ozempic® and Wegovy®. 
GLP-1 medications are scientifically backed to help individuals achieve significant weight loss—on average, 15-20% of body weight within a year.
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    GLP-1 medications are scientifically backed to help individuals achieve significant weight loss—on average, 15-20% of body weight within a year.
As a valued user, you’re eligible for $50 off your first program with code policy-lab-50.
                            Conditions: 
                                    
        
            
                        Overweight
                    
                                    
                        Overweight and Obesity
                    
                                    
                        Obesity
                    
                                    
                        Weight Loss
                    
                                    
                        Morbid Obesity
                    
                                    Featured Trial
                
                Stroke Clinical Study
            
        Recruiting
            
        A clinical study for people that suffer with Stroke
    
    
                            Conditions: 
                                    
        
            
                        Stroke
                    
                                    Featured Trial
                
                Chronic Kidney Disease (CKD) Clinical Study
            
        Recruiting
            
        A clinical study for people that suffer with Chronic Kidney Disease (CKD)
    
    
                            Conditions: 
                                    
        
            
                        Chronic Kidney Disease (CKD)
                    
                                    Featured Trial
                
                Ischemic heart disease (IHD) Clinical Study
            
        Recruiting
            
        A clinical study for people that suffer with Ischemic heart disease (IHD)
    
    
                            Conditions: 
                                    
        
            
                        Ischemic heart disease (IHD)
                    
                                    
                
                                    A Surveillance Study of Susceptibility to Baloxavir Marboxil in Pediatric Participants With Influenza and Transmission of Influenza to Household Contacts
                                
            
            
        Recruiting
                            
            
                This study consists of two parts: Part A Surveillance and Part B Transmission.
The main purpose of Part A is to evaluate the prevalence of pre-dose and treatment-emergent amino acid substitutions in pediatric participants' susceptibility \<12 years with influenza treated with baloxavir marboxil.
Part B will include a subset of Part A participants who have household contacts (HHCs) recruited to the study. Part B will evaluate the incidence of onward influenza transmission from pediatric index p...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 3 weeks and 11 years
            Trial Updated:
                08/01/2025
            
            Locations: Coastal Pediatric Research, Charleston, South Carolina         
        
        
            Conditions: Influenza
        
            
        
    
                
                                    A Study to Evaluate Glofitamab as a Single Agent vs. Investigator's Choice in Participants With Relapsed/Refractory Mantle Cell Lymphoma
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to evaluate the efficacy of glofitamab monotherapy compared with an investigator's choice of either rituximab plus bendamustine (BR), or lenalidomide with rituximab (R-Len) in patients with relapsed or refractory (R/R) mantle cell lymphoma (MCL).             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                08/01/2025
            
            Locations: Medical University of S. Carolina, Charleston, South Carolina         
        
        
            Conditions: Lymphoma
        
            
        
    
                
                                    Safety and Efficacy Study of Intravesical Instillation of TARA-002 in Adults With High-grade Non-muscle Invasive Bladder Cancer
                                
            
            
        Recruiting
                            
            
                TARA-002-101-Ph2 is an open-label study to investigate the safety and anti-tumor activity of intravesical instillation of TARA-002 in adults 18 years of age or older with high-grade CIS NMIBC (± Ta/T1).
The purpose of this Phase 2 study (TARA-002-101-Ph2) is to further assess the safety and anti-tumor activity of TARA-002 at the RP2D which has been established in the Phase 1a dose finding study (TARA-002-101-Ph1a).
This Phase 2 study includes participants with CIS NMIBC (± Ta/T1) with active d...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                08/01/2025
            
            Locations: Carolina Urologic Research Center, Myrtle Beach, South Carolina         
        
        
            Conditions: Non-muscle Invasive Bladder Cancer
        
            
        
    
                
                                    Evaluating the Addition of Adjuvant Chemotherapy to Ovarian Function Suppression Plus Endocrine Therapy in Premenopausal Patients With pN0-1, ER-Positive/HER2-Negative Breast Cancer and an Oncotype Recurrence Score Less Than or Equal to 25
                                
            
            
        Recruiting
                            
            
                This Phase III Trial will determine whether adjuvant chemotherapy (ACT) added to ovarian function suppression (OFS) plus endocrine therapy (ET) is superior to OFS plus ET in improving invasive breast cancer-free survival (IBCFS) among premenopausal, early- stage breast cancer (EBC) patients with estrogen receptor (ER)-positive, HER2-negative tumors and 21-gene recurrence score (RS) between 16-25 (for pN0 patients) and 0-25 (for pN1 patients).             
        
        
    Gender:
                FEMALE
            Ages:
                Between 18 years and 60 years
            Trial Updated:
                08/01/2025
            
            Locations: Saint Joseph's/Candler - Bluffton Campus, Bluffton, South Carolina         
        
        
            Conditions: Breast Cancer
        
            
        
    
                
                                    A Study to Evaluate the Long-Term Safety of Astegolimab in Participants With Chronic Obstructive Pulmonary Disease (COPD)
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to assess the long-term safety and to explore the efficacy of astegolimab in participants with chronic obstructive pulmonary disease (COPD) who have completed the 52-week placebo-controlled treatment period in parent studies GB43311 or GB44332.             
        
        
    Gender:
                ALL
            Ages:
                Between 40 years and 90 years
            Trial Updated:
                08/01/2025
            
            Locations: Medtrial, LLC, Columbia, South Carolina         
        
        
            Conditions: Chronic Obstructive Pulmonary Disease
        
            
        
    
                
                                    Testing Radiation and HER2-targeted Therapy Versus HER2-targeted Therapy Alone for Low-risk HER2-positive Breast Cancer
                                
            
            
        Recruiting
                            
            
                This Phase III trial compares the recurrence-free interval (RFI) among patients with early-stage, low risk HER2+ breast cancer who undergo breast conserving surgery and receive HER2-directed therapy, and are randomized to not receive adjuvant breast radiotherapy versus those who are randomized to receive adjuvant radiotherapy per the standard of care.             
        
        
    Gender:
                ALL
            Ages:
                40 years and above
            Trial Updated:
                08/01/2025
            
            Locations: Medical University of South Carolina, Charleston, South Carolina         
        
        
            Conditions: HER2-positive Breast Cancer
        
            
        
    
                
                                    Study to Check the Safety of Fazirsiran and Learn if Fazirsiran Can Help People With Liver Disease and Scarring (Fibrosis) Due to an Abnormal Version of Alpha-1 Antitrypsin Protein
                                
            
            
        Recruiting
                            
            
                The main aim of this study is to learn if fazirsiran reduces liver scarring (fibrosis) compared to placebo. Other aims are to learn if fazirsiran slows down the disease worsening in the liver, to get information on how fazirsiran affects the body (called pharmacodynamics), to learn if fazirsiran reduces other liver injury (inflammation) and the abnormal Z-AAT protein in the liver, to get information on how the body processes fazirsiran (called pharmacokinetics), to test how well fazirsiran works...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 75 years
            Trial Updated:
                08/01/2025
            
            Locations: Medical University of South Carolina, Charleston, South Carolina         
        
        
            Conditions: Alpha1-Antitrypsin Deficiency
        
            
        
    
                
                                    A Study to Evaluate Astegolimab in Participants With Chronic Obstructive Pulmonary Disease
                                
            
            
        Recruiting
                            
            
                This study will evaluate the efficacy and safety of astegolimab compared with placebo in participants with chronic obstructive pulmonary disease (COPD) who are former or current smokers and have a history of frequent exacerbations.             
        
        
    Gender:
                ALL
            Ages:
                Between 40 years and 80 years
            Trial Updated:
                08/01/2025
            
            Locations: Medtrial, LLC, Columbia, South Carolina         
        
        
            Conditions: Chronic Obstructive Pulmonary Disease (COPD)
        
            
        
    
                
                                    Colon Adjuvant Chemotherapy Based on Evaluation of Residual Disease
                                
            
            
        Recruiting
                            
            
                This Phase II/III trial will evaluate the what kind of chemotherapy to recommend to patients based on the presence or absences of circulating tumor DNA (ctDNA) after surgery for colon cancer.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                08/01/2025
            
            Locations: Prisma Health Cancer Institute - Spartanburg, Boiling Springs, South Carolina         
        
        
            Conditions: Stage III Colon Cancer
        
            
        
    
                
                                    Five or Ten Year Colonoscopy for 1-2 Non-Advanced Adenomatous Polyps
                                
            
            
        Recruiting
                            
            
                This trial examines colorectal cancer incidence in participants with 1 to 2 non-advanced adenomas randomized to surveillance colonoscopy at 10 years compared to participants randomized to surveillance colonoscopy at 5 and 10 years.             
        
        
    Gender:
                ALL
            Ages:
                Between 45 years and 70 years
            Trial Updated:
                08/01/2025
            
            Locations: Ralph H Johnson VA Medical Center, Charleston, South Carolina         
        
        
            Conditions: Adenocarcinoma of the Colon, Adenocarcinoma of the Rectum
        
            
        
    
                
                                    De-Escalation of Breast Radiation Trial for Hormone Sensitive, HER-2 Negative, Oncotype Recurrence Score Less Than or Equal to 18 Breast Cancer (DEBRA)
                                
            
            
        Recruiting
                            
            
                This Phase III Trial evaluates whether breast conservation surgery and endocrine therapy results in a non-inferior rate of invasive or non-invasive ipsilateral breast tumor recurrence (IBTR) compared to breast conservation with breast radiation and endocrine therapy.             
        
        
    Gender:
                ALL
            Ages:
                Between 50 years and 70 years
            Trial Updated:
                08/01/2025
            
            Locations: Saint Joseph's/Candler - Bluffton Campus, Bluffton, South Carolina         
        
        
            Conditions: Stage I Breast Cancer
        
            
        
    
                
                                    A Multi-phase Study of ASTX030 (Azacitidine and Cedazuridine) in Myeloid Neoplasm Alone or in Combination With Venetoclax in AML (AZTOUND Study)
                                
            
            
        Recruiting
                            
            
                Study ASTX030-01 is a multi-phase study comprising of Phases 1-3 Monotherapy arms and a Phase 1 Combination Therapy arm Phase 1 Monotherapy consists of an open-label Dose Escalation Stage (Stage A) using multiple cohorts at escalating dose levels of oral cedazuridine and azacitidine (only one study drug will be escalated at a time) followed by a Dose Expansion Stage (Stage B). Phase 2 Monotherapy is a randomized, open-label, crossover study to compare oral ASTX030 to subcutaneous (SC) azacitidin...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                08/01/2025
            
            Locations: Hollings Cancer Center, Charleston, South Carolina         
        
        
            Conditions: Myelodysplastic Syndromes, Acute Myeloid Leukemia, Myelodysplastic Syndrome/Neoplasm, Chronic Myelomonocytic Leukemia
        
            
        
    