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                    Georgia Paid Clinical Trials
A listing of 1949  clinical trials  in Georgia  actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
            1813 - 1824 of 1949
        
                Georgia is currently home to 1949 active clinical trials, seeking participants for engagement in research studies. These trials take place at a variety of cities in the state, including Atlanta, Augusta, Decatur and Savannah. 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 Randomized, Double-blind, Parallel-group, Two-arm, Multiple Dose, Multicenter, Bioequivalence Study With Clinical Endpoint in the Treatment of Subjects With Chronic Open-angle Glaucoma or Ocular Hypertension in Both Eyes
                                
            
            
        Recruiting
                            
            
                A randomized, double-blind, parallel-group, two-arm, multiple dose, multicenter, clinical endpoint bioequivalence study             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                08/05/2024
            
            Locations: Clayton Eye Research, Morrow, Georgia         
        
        
            Conditions: Open-angle Glaucoma, Ocular Hypertension
        
            
        
    
                
                                    Type 1 Diabetes Education and Support Study
                                
            
            
        Recruiting
                            
            
                Diabetes distress has been identified as one of the largest contributors to the racial disparity in glycemic control that disproportionately burdens Black patients ages 18-30 years with type 1 diabetes (T1D). In order to combat this issue, this study assesses the feasibility of the culturally tailored intervention T1DES and evaluates the effect of the T1DES intervention on diabetes outcomes in a pilot randomized clinical trial among Black young adults with T1D.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 30 years
            Trial Updated:
                08/02/2024
            
            Locations: Kaiser Permanente Georgia, Atlanta, Georgia         
        
        
            Conditions: Type1diabetes
        
            
        
    
                
                                    A Study to Evaluate the Safety, PK/PD of (OriCAR-017) in Subjects With RR/MM - RIGEL Study
                                
            
            
        Recruiting
                            
            
                The is a first clinical study for Oricell Therapeutics Inc. in the United States to evaluate the safety, PK, PD and preliminary efficacy of our anti-GPRC5D cell product (OriCAR-017) in subjects with relapsed/refractory multiple myeloma.
RIGEL Study             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 75 years
            Trial Updated:
                08/01/2024
            
            Locations: Northside Hospital, Atlanta, Georgia         
        
        
            Conditions: Neoplasms, Plasma Cell, Neoplasms by Histologic Type, Neoplasms, Hemostatic Disorders, Vascular Diseases, Cardiovascular Diseases, Paraproteinemias, Blood Protein Disorders, Hematologic Diseases, Hemorrhagic Disorders, Lymphoproliferative Disorders, Immunoproliferative Disorders, Immune System Diseases, Multiple Myeloma
        
            
        
    
                
                                    Perturbation Training Reduces Falls in People With AD
                                
            
            
        Recruiting
                            
            
                This study will examine the overall capacity of people with Alzheimer's disease learning fall-resistant skills from perturbation training.             
        
        
    Gender:
                ALL
            Ages:
                Between 65 years and 90 years
            Trial Updated:
                08/01/2024
            
            Locations: Reminiscent, Valdosta, Georgia         
        
        
            Conditions: Alzheimer Disease
        
            
        
    
                
                                    Smoke Free SafeCare: Establishing a Smoke Free Home in CPS-involved Families
                                
            
            
        Recruiting
                            
            
                Smoke Free SafeCare (SFSC) is a proposed braided intervention consisting of two evidence-based interventions: Some Things are Better Outside (STBO), aimed at promoting smoke free home rules, and SafeCare, aimed at reducing child maltreatment and improving mother and child outcomes. STBO is effective in creating smoke free homes and reducing second-hand smoke in low-SES (socioeconomic status) households. SafeCare is an effective parent training program that is broadly disseminated in child protec...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 89 years
            Trial Updated:
                08/01/2024
            
            Locations: Georgia State University, Atlanta, Georgia         
        
        
            Conditions: Child Maltreatment, Smoking Behaviors
        
            
        
    
                
                                    Cabozantinib in Combination With 13-cis-Retinoic Acid in Children With Relapsed or Refractory Solid Tumors
                                
            
            
        Recruiting
                            
            
                This study is being conducted in order to determine the safety, dose-limiting toxicities, and maximum tolerated dose of cabozantinib in combination with 13-cis-retinoic acid in patients with relapsed or refractory solid tumors including tumors of the central nervous system (CNS)             
        
        
    Gender:
                ALL
            Ages:
                Between 2 years and 26 years
            Trial Updated:
                08/01/2024
            
            Locations: Children's Healthcare of Atlanta, Atlanta, Georgia         
        
        
            Conditions: Solid Tumor
        
            
        
    
                
                                    Glycemic Excursion Minimization (GEM) to Outshine Health Disparities
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to see if the GEM intervention is acceptable and helpful to Black adults with type 2 diabetes. The GEM intervention (coaching to reduce carbohydrate intake and increase physical activity after meals, with feedback from a continuous glucose monitor, CGM) might improve blood glucose levels, reduce diabetes distress, and increase empowerment and confidence in managing diabetes.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/29/2024
            
            Locations: Georgia Prevention Institute, Augusta, Georgia         
        
        
            Conditions: Type 2 Diabetes
        
            
        
    
                
                                    Study to Assess Safety of HDP-101 in Patients With Relapsed Refractory Multiple Myeloma
                                
            
            
        Recruiting
                            
            
                This study will assess the safety, tolerability, pharmacokinetics (PK) and the therapeutic potential of HDP-101 in patients with plasma cell disorders including multiple myeloma.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/22/2024
            
            Locations: Winship Cancer Institute of Emory University, Atlanta, Georgia         
        
        
            Conditions: Multiple Myeloma, Plasma Cell Disorder
        
            
        
    
                
                                    Study to Determine the Pharmacokinetics and Pharmacodynamic Effects of Phenylephrine on BP Via IV
                                
            
            
        Recruiting
                            
            
                The primary objective of this study is to evaluate the dose effect of Phenylephrine Hydrochloride Injection on the treatment of clinically relevant decreased blood pressure in the pediatric population, ≥12 to 16 year old patients undergoing general and neuraxial anesthesia.
The secondary objectives are to describe changes in blood pressure and heart rate, time to onset and to maximal response, and the duration of response; to assess the safety of the product in this population; and to character...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 12 years and 16 years
            Trial Updated:
                07/22/2024
            
            Locations: Children's Healthcare of Atlanta at Egleston, Atlanta, Georgia         
        
        
            Conditions: Hypotension
        
            
        
    
                
                                    Study of INBRX-106 and INBRX-106 in Combination With Pembrolizumab (Keytruda®) in Subjects With Locally Advanced or Metastatic Solid Tumors (Hexavalent OX40 Agonist)
                                
            
            
        Recruiting
                            
            
                This is a Phase 1/2, open-label, non-randomized, 4-part trial to determine the safety profile and identify the maximum tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D) of INBRX 106 administered as a single agent or in combination with the anti-PD-1 checkpoint inhibitor (CPI) pembrolizumab (Keytruda®). KEYTRUDA is a registered trademark of Merck Sharp \& Dohme LLC, a subsidiary of Merck \& Co., Inc., Rahway, NJ, USA.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/17/2024
            
            Locations: Winship Cancer Institute - Emory University, Atlanta, Georgia         
        
        
            Conditions: Solid Tumor, Non-Small Cell Lung Cancer, Melanoma, Head and Neck Cancer, Gastric Cancer, Renal Cell Carcinoma, Urothelial Carcinoma
        
            
        
    
                
                                    Allogeneic Expanded Gamma Delta T Cells With GD2 Chemoimmunotherapy in Relapsed /Refractory Neuroblastoma or Refractory/ Relapsed Osteosarcoma
                                
            
            
        Recruiting
                            
            
                The goal of this clinical trial is to determine the maximum tolerated dose (MTD) and recommended Phase II dose (RP2D) of allogeneic expanded γδ T cells when delivered with Dinutuximab, temozolomide, irinotecan, and zoledronate in children with refractory or recurrent neuroblastoma or refractory/ relapsed osteosarcoma as well as to define the toxicities of allogeneic expanded γδ T cells when delivered with Dinutuximab, temozolomide, irinotecan, and zoledronate             
        
        
    Gender:
                ALL
            Ages:
                12 months and above
            Trial Updated:
                07/15/2024
            
            Locations: Children's Healthcare of Atlanta, Atlanta, Georgia         
        
        
            Conditions: Neuroblastoma, Refractory Neuroblastoma, Relapsed Neuroblastoma, Relapsed Osteosarcoma, Refractory Osteosarcoma
        
            
        
    
                
                                    Chiauranib for Advanced Solid Malignant Tumors and Relapsed/Refractory SCLC.
                                
            
            
        Recruiting
                            
            
                This is a Phase 1b/2, single-arm, open-label, dose-escalation study including 2 stages:
Phase 1b: Dose-Escalation Stage (Single-Dose and Consecutive-Dose Periods)
Phase 2: recommended Phase 2 dose (RP2D) of chiauranib will be given to all patients enrolled in this phase once daily for 28-day cycles continuously with no interruption between cycles.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/15/2024
            
            Locations: Winship Cancer Institute of Emory University, Atlanta, Georgia         
        
        
            Conditions: Advanced Solid Malignant Tumor, Small Cell Lung Cancer
        
            
        
    