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                    Alabama Paid Clinical Trials
A listing of 1237  clinical trials  in Alabama  actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
            25 - 36 of 1237
        
                Alabama is currently home to 1237 active clinical trials, seeking participants for engagement in research studies. These trials take place at a variety of cities in the state, including Birmingham, Mobile, Huntsville and Anniston. 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)
                    
                                    
                
                                    Testing the Effects of Novel Therapeutics for Newly Diagnosed, Untreated Patients With High-Risk Acute Myeloid Leukemia (A MyeloMATCH Treatment Trial)
                                
            
            
        Recruiting
                            
            
                This phase II MyeloMATCH treatment trial tests whether the standard approach of cytarabine and daunorubicin in comparison to the following experimental regimens works to shrink cancer in patients with high risk acute myeloid leukemia (AML): 1) daunorubicin and cytarabine liposome alone; 2) cytarabine and daunorubicin with venetoclax; 3) azacitidine and venetoclax; 4) daunorubicin and cytarabine liposome and venetoclax. "High-risk" refers to traits that have been known to make the AML harder to t...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 59 years
            Trial Updated:
                08/22/2025
            
            Locations: University of Alabama at Birmingham Cancer Center, Birmingham, Alabama         
        
        
            Conditions: Acute Myeloid Leukemia, Acute Myeloid Leukemia Arising From Previous Myelodysplastic/Myeloproliferative Neoplasm, Acute Myeloid Leukemia Post Cytotoxic Therapy, Acute Myeloid Leukemia, Myelodysplasia-Related
        
            
        
    
                
                                    A Study to Evaluate the Efficacy, Safety, Pharmacokinetics (PK), and Pharmacodynamics (PD) of Satralizumab in Participants With Anti-N-methyl-D-aspartic Acid Receptor (NMDAR) or Anti-leucine-rich Glioma-inactivated 1 (LGI1) Encephalitis
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to assess the efficacy, safety, PK, and PD of satralizumab in participants with NMDAR and LGI1 encephalitis.             
        
        
    Gender:
                ALL
            Ages:
                12 years and above
            Trial Updated:
                08/22/2025
            
            Locations: University of Alabama at Birmingham, Birmingham, Alabama         
        
        
            Conditions: NMDAR Autoimmune Encephalitis, LGI1 Autoimmune Encephalitis
        
            
        
    
                
                                    A Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Satralizumab in Participants With Myelin Oligodendrocyte Glycoprotein Antibody-associated Disease
                                
            
            
        Recruiting
                            
            
                The main objective of this study is to evaluate the efficacy of satralizumab compared with placebo based on time from randomization to the first occurrence of an adjudicated MOGAD relapse in the double-blind (DB) treatment period. Participants who experience an adjudicated relapse or complete the DB period can enter open-label extension (OLE) period. After the primary clinical cutoff date (CCOD), additional adolescent participants may be enrolled directly into the OLE period.             
        
        
    Gender:
                ALL
            Ages:
                12 years and above
            Trial Updated:
                08/22/2025
            
            Locations: University of Alabama at Birmingham, Birmingham, Alabama         
        
        
            Conditions: Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD)
        
            
        
    
                
                                    4D-710 in Adult Patients With Cystic Fibrosis
                                
            
            
        Recruiting
                            
            
                This is a Phase 1/2 multicenter, open-label, single dose trial of 4D-710 investigational gene therapy in adults with cystic fibrosis.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                08/22/2025
            
            Locations: University of Alabama Child Health Research Unit, Birmingham, Alabama         
        
        
            Conditions: Cystic Fibrosis Lung
        
            
        
    
                
                                    A Study of the Drug Selinexor With Radiation Therapy in Patients With Newly-Diagnosed Diffuse Intrinsic Pontine (DIPG) Glioma and High-Grade Glioma (HGG)
                                
            
            
        Recruiting
                            
            
                This phase I/II trial tests the safety, side effects, and best dose of selinexor given in combination with standard radiation therapy in treating children and young adults with newly diagnosed diffuse intrinsic pontine glioma (DIPG) or high-grade glioma (HGG) with a genetic change called H3 K27M mutation. It also tests whether combination of selinexor and standard radiation therapy works to shrink tumors in this patient population. Glioma is a type of cancer that occurs in the brain or spine. Gl...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 12 months and 21 years
            Trial Updated:
                08/22/2025
            
            Locations: Children's Hospital of Alabama, Birmingham, Alabama         
        
        
            Conditions: Malignant Glioma
        
            
        
    
                
                                    Tumor-agnostic Precision Immuno-oncology and Somatic Targeting Rational for You (TAPISTRY) Platform Study
                                
            
            
        Recruiting
                            
            
                TAPISTRY is a Phase II, global, multicenter, open-label, multi-cohort study designed to evaluate the safety and efficacy of targeted therapies or immunotherapy as single agents or in rational, specified combinations in participants with unresectable, locally advanced or metastatic solid tumors determined to harbor specific oncogenic genomic alterations or who are tumor mutational burden (TMB)-high as identified by a validated next-generation sequencing (NGS) assay. Participants with solid tumors...  Read More             
        
        
    Gender:
                ALL
            Ages:
                All
            Trial Updated:
                08/22/2025
            
            Locations: Southern Cancer Center, Daphne, Alabama         
        
        
            Conditions: Solid Tumors
        
            
        
    
                
                                    Testing the Addition of Radiation Therapy to the Usual Immune Therapy Treatment (Atezolizumab) for Extensive Stage Small Cell Lung Cancer, The RAPTOR Trial
                                
            
            
        Recruiting
                            
            
                This phase II/III trial compares the effect of adding radiation therapy to the usual maintenance therapy with atezolizumab versus atezolizumab alone in patients who have already received atezolizumab plus chemotherapy for the treatment of small cell lung cancer that has spread outside of the lung or to other parts of the body (extensive stage). Immunotherapy with monoclonal antibodies, such as atezolizumab, may help the body's immune system attack the cancer, and may interfere with the ability o...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                08/22/2025
            
            Locations: University of Alabama at Birmingham Cancer Center, Birmingham, Alabama         
        
        
            Conditions: Extensive Stage Lung Small Cell Carcinoma
        
            
        
    
                
                                    A 12-Month Study of Lasmiditan (LY573144) Treatment in Children Aged 6 to 17 With Migraine
                                
            
            
        Recruiting
                            
            
                The reason for this 12-month, open-label study is to see if the study drug lasmiditan is safe and effective for the intermittent acute treatment of migraine in children aged 6 to 17. The study will last about 12 months and may include up to 7 visits.             
        
        
    Gender:
                ALL
            Ages:
                Between 6 years and 17 years
            Trial Updated:
                08/22/2025
            
            Locations: Central Research Associates, Birmingham, Alabama         
        
        
            Conditions: Migraine
        
            
        
    
                
                                    A Study of Lasmiditan (LY573144) Treatment in Children Aged 6 to 17 With Migraine
                                
            
            
        Recruiting
                            
            
                The reason for this study is to see if lasmiditan is safe and effective in children aged 6 to 17 with migraine. The study will last up to 20 weeks and may include up to 4 visits.             
        
        
    Gender:
                ALL
            Ages:
                Between 6 years and 17 years
            Trial Updated:
                08/22/2025
            
            Locations: Central Research Associates, Birmingham, Alabama         
        
        
            Conditions: Migraine
        
            
        
    
                
                                    A Study of the Drugs Selumetinib vs. Carboplatin and Vincristine in Patients With Low-Grade Glioma
                                
            
            
        Recruiting
                            
            
                This phase III trial compares the effect of selumetinib versus the standard of care treatment with carboplatin and vincristine (CV) in treating patients with newly diagnosed or previously untreated low-grade glioma (LGG) that does not have a genetic abnormality called BRAFV600E mutation and is not associated with systemic neurofibromatosis type 1. Selumetinib works by blocking some of the enzymes needed for cell growth and may kill tumor cells. Carboplatin and vincristine are chemotherapy drugs...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 2 years and 21 years
            Trial Updated:
                08/22/2025
            
            Locations: Children's Hospital of Alabama, Birmingham, Alabama         
        
        
            Conditions: Low Grade Glioma, Low Grade Astrocytoma, Metastatic Low Grade Astrocytoma, Metastatic Low Grade Glioma
        
            
        
    
                
                                    HPV DNA Vaccine Via Electroporation for HPV16 Positive Cervical Neoplasia
                                
            
            
        Recruiting
                            
            
                The primary goal of this phase I open label study is to determine the safety and tolerability of pNGVL4aCRTE6E7L2 DNA vaccine, as administered by intramuscular (IM) injection with TriGrid™ electroporation to both HIV- or HIV+ adult female subjects (≥ 19 years), with biopsy confirmed cervical intraepithelial (CIN) II or III that is human papillomavirus (HPV) 16+.             
        
        
    Gender:
                FEMALE
            Ages:
                19 years and above
            Trial Updated:
                08/22/2025
            
            Locations: University of Alabama at Birmingham, Birmingham, Alabama         
        
        
            Conditions: Human Papillomavirus Type 16, Cervical Intraepithelial Neoplasia Grade II, Cervical Intraepithelial Neoplasia, Grade III
        
            
        
    
                
                                    A Study to Evaluate the Long-Term Efficacy and Safety of Mirikizumab in Participants With Moderately to Severely Active Ulcerative Colitis (LUCENT 3)
                                
            
            
        Recruiting
                            
            
                This study is designed to evaluate the long-term efficacy and safety of mirikizumab in participants with moderately to severely active ulcerative colitis (UC). The study will last up to 3 years. Participants who complete the 3-year study may continue to receive mirikizumab until it is (outside of this study) in their country or until they meet other discontinuation criteria.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 80 years
            Trial Updated:
                08/22/2025
            
            Locations: Digestive Health Specialists, Dothan, Alabama         
        
        
            Conditions: Ulcerative Colitis
        
            
        
    