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                    New Jersey Paid Clinical Trials
A listing of 1696  clinical trials  in New Jersey  actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
            697 - 708 of 1696
        
                New Jersey is currently home to 1696 active clinical trials, seeking participants for engagement in research studies. These trials take place at a variety of cities in the state, including New Brunswick, Hackensack, Newark and Morristown. 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.
As a valued user, you’re eligible for $50 off your first program with code policy-lab-50.
    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 Study of Additional Chemotherapy After Surgery for People With Malignant Peritoneal Mesothelioma
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to find out whether intraperitoneal or intravenous chemotherapy given after cytoreductive surgery and HIPEC are effective treatments for people with malignant peritoneal mesothelioma. Outcomes will be compared by observing intraperitoneal versus intravenous treatments to analyze if one is better than the other.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/17/2025
            
            Locations: Memorial Sloan Kettering Basking Ridge (Limited Protocol Activities), Basking Ridge, New Jersey         
        
        
            Conditions: Malignant Peritoneal Mesothelioma, Peritoneal Mesothelioma, Mesothelioma, Mesothelioma, Malignant, Malignant Mesothelioma
        
            
        
    
                
                                    A Study to Evaluate the Safety and Efficacy of NEXAGON® (Lufepirsen Ophthalmic Gel) in Subjects With PCED
                                
            
            
        Recruiting
                            
            
                This study is to evaluate the safety and efficacy of NEXAGON® (lufepirsen ophthalmic gel) (NEXAGON) in subjects with persistent corneal epithelial defects (PCED). The objectives of the study are to evaluate the safety and efficacy of NEXAGON in this population.             
        
        
    Gender:
                ALL
            Ages:
                2 years and above
            Trial Updated:
                07/17/2025
            
            Locations: Glaukos Investigative Site, Palisades Park, New Jersey         
        
        
            Conditions: Persistent Corneal Epithelial Defect
        
            
        
    
                
                                    Clinical Trial for Integrated Care to Help At Risk Teen (iCHART) Intervention
                                
            
            
        Recruiting
                            
            
                This protocol will test the effectiveness of an intervention, iCHART (integrated Care to Help At-Risk Teens) and facilitate recruitment for other studies in the larger ETUDES Center grant, which are focused on treatment development for target risk factors for suicidal behavior, specifically, sleep, anhedonia, and stress related to cybervictimization. This study will recruit 900 adolescents which will be enrolled in a randomized controlled trial to test iCHART and will be randomized to iCHART or...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 12 years and 18 years
            Trial Updated:
                07/17/2025
            
            Locations: Gibbsboro, Gibbsboro, New Jersey         
        
        
            Conditions: Suicide and Depression, Adolescent Behavior
        
            
        
    
                
                                    A Study of Amivantamab in Participants With Advanced or Metastatic Solid Tumors Including Epidermal Growth Factor Receptor (EGFR)-Mutated Non-Small Cell Lung Cancer
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to assess the anti-tumor activity and safety of amivantamab which will be administered as a co-formulation with recombinant human hyaluronidase PH20 (rHuPH20) (subcutaneous co-formulation \[SC-CF\]) in combination treatment (all cohorts except Cohort 4) and to characterize the safety of amivantamab SC-CF (Cohort 4).             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/17/2025
            
            Locations: Hackensack University Medical Center, Hackensack, New Jersey         
        
        
            Conditions: Carcinoma, Non-small-Cell Lung
        
            
        
    
                
                                    A Long-term Study for Participants Previously Treated With Ciltacabtagene Autoleucel
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to collect long-term follow-up data on delayed adverse events after administration of ciltacabtagene autoleucel (cilta-cel), and to characterize and understand the long-term safety profile of cilta-cel.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/17/2025
            
            Locations: Hackensack University Medical Center, Hackensack, New Jersey         
        
        
            Conditions: Multiple Myeloma
        
            
        
    
                
                                    Intracavitary Carrier-embedded Cs131 Brachytherapy for Recurrent Brain Metastases: a Randomized Phase II Study
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to see if Cs-131 brachytherapy is effective in people with recurrent brain cancer who are scheduled to have brain surgery for removal of their tumor(s). The researchers would like to see whether Cs-131 prevents brain tumors from growing back after surgery.The researchers will compare Cs-131 brachytherapy (which occurs during brain surgery) with the usual approach of brain surgery without brachytherapy. The researchers will compare both the effectiveness and safety of...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/17/2025
            
            Locations: Memorial Sloan Kettering at Basking Ridge (Consent Only), Basking Ridge, New Jersey         
        
        
            Conditions: Recurrent Brain Metastases
        
            
        
    
                
                                    ATTUNE® Revision- Complex Primary in Total Knee Arthroplasty Population
                                
            
            
        Recruiting
                            
            
                Five-year, Prospective, multi-center, non-randomized, non-controlled study of the ATTUNE® Revision total knee prostheses, utilizing the fixed bearing (FB) and rotating platform (RP) tibial component with the posterior stabilizing (PS) femoral component in complex primary total knee arthroplasty.             
        
        
    Gender:
                ALL
            Ages:
                Between 22 years and 80 years
            Trial Updated:
                07/17/2025
            
            Locations: Rothman Institute, Egg Harbor Township, New Jersey         
        
        
            Conditions: Primary Knee Arthroplasty
        
            
        
    
                
                                    Post-Operative Analgesic Selection in Patients Planned for Third Molar Extraction After Undergoing Shared Decision Making Using 2- Versus 3-Option Decision-Aids
                                
            
            
        Recruiting
                            
            
                This research protocol is exploring a behavioral intervention: shared decision making with the use of a decision aid to select a post-operative analgesic. Specifically, the investigators will examine the impact of shared decision making on analgesic selection for acute pain management when 2 options are presented to the patient as compared to 3 options which includes an opioid prescription for "just-in-case" pain management. The investigators hypothesize that significantly more patients will cho...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 90 years
            Trial Updated:
                07/16/2025
            
            Locations: Rutgers School of Dental Medicine, Newark, New Jersey         
        
        
            Conditions: Pain Management, Shared Decision Making
        
            
        
    
                
                                    Study With Phage for CF Subjects With Pseudomonas Lung Infection
                                
            
            
        Recruiting
                            
            
                The goal of this Phase 2b clinical trial is to see if nebulized phage (BX004) can treat chronic Pseudomonas aeruginosa (PsA) lung infection in CF subjects. The primary goal is to see if 8 weeks of twice daily BX004 can reduce the amount of PsA in the sputum compared to placebo (on top of background CF therapy).             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/16/2025
            
            Locations: Rutgers, Robert Wood Johnson Medical School, New Brunswick, New Jersey         
        
        
            Conditions: Chronic Pseudomonas Aeruginosa Infection, Cystic Fibrosis (CF)
        
            
        
    
                
                                    A Study to Evaluate INCB177054 in Participants With Select Advanced or Metastatic Solid Tumors
                                
            
            
        Recruiting
                            
            
                This study will be conducted to evaluate INCB177054 given as monotherapy or in combination with retifanlimab in participants with select advanced or metastatic solid Tumors.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/16/2025
            
            Locations: Hackensack University Medical Center, Hackensack, New Jersey         
        
        
            Conditions: Solid Tumors, Advanced Solid Tumors, Metastatic Solid Tumors
        
            
        
    
                
                                    Study to Evaluate Efficacy and Safety of Ropanicant in MDD Patients
                                
            
            
        Recruiting
                            
            
                The primary objective is to evaluate the efficacy of Ropanicant at two different dosage levels compared to placebo in patients with Major Depressive Disorder (MDD).             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 65 years
            Trial Updated:
                07/16/2025
            
            Locations: Hassman Research Institue, Marlton, New Jersey         
        
        
            Conditions: Major Depressive Disorder (MDD)
        
            
        
    
                
                                    Light Therapy Device for Neonatal Intraventricular Hemorrhage Grade 3 and 4
                                
            
            
        Recruiting
                            
            
                The primary purpose of this study is to serve as a pilot study of the EFIL device treatment feasibility of IVH grades 3,4 to guide development of a larger trial. Primary outcomes will assess the following: safety of intervention, recruitment and consent process, acceptability of intervention by parents, retention rates, selection of most appropriate outcome measures, provide sample size estimates for a larger trial, increase the researchers\' experience with the study intervention. A complet...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 0 days and 1 month
            Trial Updated:
                07/16/2025
            
            Locations: Rutgers - New Jersey Medical School / University Hospital, Newark, New Jersey         
        
        
            Conditions: Intraventricular Hemorrhage of Prematurity, Hydrocephalus
        
            
        
    