Search
                    Minnesota Paid Clinical Trials
A listing of 2107  clinical trials  in Minnesota  actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
            613 - 624 of 2107
        
                Minnesota is currently home to 2107 active clinical trials, seeking participants for engagement in research studies. These trials take place at a variety of cities in the state, including Minneapolis, Rochester, Saint Paul and Duluth. 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 to Evaluate the Safety and Efficacy of OPB-101 in Platinum-resistant Ovarian Cancer
                                
            
            
        Recruiting
                            
            
                The goal of this clinical trial is to learn if OPB-101 is safe in platinum resistant ovarian cancer participants and also to find the optimal dose of OPB-101.
Participants will have their own T cells modified in a laboratory and given back to them as OPB-101 in this one-time treatment. Participants will be in the hospital when they receive OPB-101 and then be checked at the clinical site frequently for the first few months.             
        
        
    Gender:
                FEMALE
            Ages:
                18 years and above
            Trial Updated:
                07/28/2025
            
            Locations: University of Minnesota, Minneapolis, Minnesota         
        
        
            
        
    
                
                                    A Study of Paramedic HF Management
                                
            
            
        Recruiting
                            
            
                The purpose of this research is to see if having community paramedic (CP) visit patients at home to manage their heart failure help them stay out of the hospital and improve their overall health compared to standard care. The investigators want to find out if their approach is better for patients in terms of their quality of life, hospital stays, emergency visits, and cost. The investigators are also looking to see how happy patients and doctors are with this method and if it's a practical and s...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/28/2025
            
            Locations: Mayo Clinic, Rochester, Minnesota         
        
        
            Conditions: Heart Failure
        
            
        
    
                
                                    A Study to Evaluate Efficacy of Remibrutinib Compared to Dupilumab at Early Timepoints in Adults With Chronic Spontaneous Urticaria Inadequately Controlled by Second Generation H1-antihistamines
                                
            
            
        Recruiting
                            
            
                This is a US, multi-center, randomized, double-blind, double-dummy, Phase 3b study to evaluate efficacy of remibrutinib (25 mg twice daily \[b.i.d.\] by mouth \[p.o.\]) compared to dupilumab (600 mg loading dose administered subcutaneously (s.c.) followed by 300 mg every 2 weeks s.c.) at early timepoints (4 weeks and earlier), when administered as an add-on treatment to second generation H1-antihistamines (sgH1-AH) (standard label dose as background therapy) in adult US participants with moderat...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/28/2025
            
            Locations: Clinical Research Institute, Minneapolis, Minnesota         
        
        
            Conditions: Chronic Spontaneous Urticaria (CSU)
        
            
        
    
                
                                    Phase 1 BIO 300 Oral Suspension
                                
            
            
        Recruiting
                            
            
                This is a two-part study of BIO 300 Oral Suspension in healthy male and female volunteers. The first part is a multiple ascending dose (MAD) study to test the safety, pharmacokinetics (PK) and pharmacodynamics (PD) of the drug when given as daily doses over 14 days. The study will enroll three cohorts each receiving a different daily dose: 2000 mg, 3000 mg, or 4000 mg. A fourth group may be added depending on results on the first three cohorts. Each cohort will include 10 participants (5 men, 5...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 64 years
            Trial Updated:
                07/28/2025
            
            Locations: Nucleus Network, LLC, Saint Paul, Minnesota         
        
        
            Conditions: Healthy Volunteer Study
        
            
        
    
                
                                    PUL-042 Treatment in Patients With Parainfluenza Virus (PIV), Human Metapneumovirus (hMPV) or Respiratory Syncytial Virus (RSV)
                                
            
            
        Recruiting
                            
            
                The purpose of this research study is to try to see whether an experimental drug, PUL 042 Inhalation Solution (PUL 042), is effective in reducing the severity of lung infections in patients with hematologic malignancies and recipients of hematopoietic stem cell transplantation with documented viral infections due to PIV, hMPV, or RSV. PUL-042 or a placebo will be administered 3 times over a 6-day period. The total duration of the study will be approximately 30 days.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/28/2025
            
            Locations: University of Minnesota, Minneapolis, Minnesota         
        
        
            Conditions: Hematologic Malignancies, Hematopoietic Stem Cell Transplant (HSCT)
        
            
        
    
                
                                    A Study to Evaluate the Efficacy and Safety of GDC-8264 in Preventing Cardiac Surgery-Associated Acute Kidney Injury (AKI) and Major Adverse Kidney Events (MAKE)
                                
            
            
        Recruiting
                            
            
                The aim of this study is to evaluate the efficacy and safety of GDC-8264 compared with placebo in participants undergoing cardiac surgery who are determined to be at moderate to high risk of developing AKI and subsequent MAKE at 90 days after surgery (MAKE90). The study will be performed in two parts- Part 1 and Part 2.             
        
        
    Gender:
                ALL
            Ages:
                40 years and above
            Trial Updated:
                07/28/2025
            
            Locations: Mayo Clinic - PPDS, Rochester, Minnesota         
        
        
            Conditions: Acute Kidney Injury
        
            
        
    
                
                                    A Study Evaluating Efruxifermin in Subjects With Compensated Cirrhosis Due to NASH/MASH
                                
            
            
        Recruiting
                            
            
                This is a multi-center evaluation of efruxifermin (EFX) in a randomized, double-blind, placebo-controlled study in subjects with compensated cirrhosis due to NASH/MASH.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 80 years
            Trial Updated:
                07/28/2025
            
            Locations: Akero Clinical Study Site, Rochester, Minnesota         
        
        
            Conditions: NASH - Nonalcoholic Steatohepatitis, MASH - Metabolic Dysfunction-Associated Steatohepatitis
        
            
        
    
                
                                    Clinical Trial of Upfront Haploidentical or Unrelated Donor BMT to Restore Normal Hematopoiesis in Aplastic Anemia
                                
            
            
        Recruiting
                            
            
                BMT CTN 2207 will investigate the use of marrow transplantation for treatment of severe aplastic anemia that has not previously been treated.             
        
        
    Gender:
                ALL
            Ages:
                Between 3 years and 75 years
            Trial Updated:
                07/28/2025
            
            Locations: Mayo Clinic, Rochester, Minnesota         
        
        
            Conditions: Severe Aplastic Anemia
        
            
        
    
                
                                    A Phase 3 Study to Evaluate Petosemtamab Compared With Investigator's Choice Monotherapy in Previously Treated Head and Neck Squamous Cell Carcinoma Patients
                                
            
            
        Recruiting
                            
            
                This is a phase 3 open-label, randomized, controlled, multicenter study to compare petosemtamab vs investigator's choice monotherapy in HNSCC patients for the second- and third-line treatment of incurable metastatic/recurrent disease.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/28/2025
            
            Locations: Site 49, Maple Grove, Minnesota         
        
        
            Conditions: Head and Neck Squamous Cell Carcinoma
        
            
        
    
                
                                    MAGNITUDE: A Phase 3 Study of NTLA-2001 in Participants With Transthyretin Amyloidosis With Cardiomyopathy (ATTR-CM)
                                
            
            
        Recruiting
                            
            
                To evaluate the efficacy and safety of a single dose of NTLA-2001 compared to placebo in participants with ATTR-CM.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 90 years
            Trial Updated:
                07/28/2025
            
            Locations: Mayo Clinic, Rochester, Minnesota         
        
        
            Conditions: Transthyretin Amyloidosis (ATTR) With Cardiomyopathy
        
            
        
    
                
                                    A Study of Adjuvant Cretostimogene Grenadenorepvec for Treatment of Intermediate Risk NMIBC Following TURBT
                                
            
            
        Recruiting
                            
            
                This is a Phase 3, open-label, randomized trial designed to evaluate the RFS of TURBT followed by cretostimogene grenadenorepvec versus TURBT followed by surveillance for the treatment of participants with IR-NMIBC.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/28/2025
            
            Locations: Mayo Clinic, Rochester, Minnesota         
        
        
            Conditions: Non Muscle Invasive Bladder Cancer, Urologic Cancer, Bladder Cancer, Urothelial Carcinoma
        
            
        
    
                
                                    Mitigating PTSD-CUD After Sexual Assault
                                
            
            
        Recruiting
                            
            
                683,000 women are sexually assaulted annually in the United States, half of whom develop chronic posttraumatic stress disorder (PTSD) and thus have markedly increased risk for cannabis use disorder (CUD). The current proposal will test the acceptability, initial efficacy, and mechanisms underlying a novel digital therapeutic targeting risk for PTSD-CUD, which could address the critical need for PTSD-CUD prevention for the 100,000 women who annually present for emergency care after sexual assault...  Read More             
        
        
    Gender:
                FEMALE
            Ages:
                18 years and above
            Trial Updated:
                07/28/2025
            
            Locations: Hennepin Assault Response Team, Minneapolis, Minnesota         
        
        
            Conditions: Posttraumatic Stress Disorder, Cannabis Use Disorder
        
            
        
    