13 Paid Clinical Research Studies in Phoenix, Arizona
Filtered for protocols that accept healthy volunteers or mention compensation. Always confirm stipend details and screening with the study coordinator.
Intensity Modulated Proton or X-Ray Therapy After Surgery for Treatment of Head and Neck Cancer, the HEADLIGHT Study
This clinical trial studies how well intensity modulated proton therapy (IMPT) or intensity modulated X-ray (radiation) therapy (IMRT) works after surgery in treating patients with
๐ Mayo Clinic Hospital in Arizona โ Phoenix, Arizona
๐ต Patients may receive cisplatin intravenously (IV) over 1-2 hours per standard of care.
View Study & Checklist โTrial of Niraparib in Participants With Newly-diagnosed Glioblastoma and Recurrent Glioma
This is an open-label, multi-center Phase 0 study with an expansion phase that will enroll up to 24 participants with newly-diagnosed glioblastoma and up to 18 recurrent glioma par
๐ St. Joseph's Hospital and Medical Center โ Phoenix, Arizona
๐ต Participants may receive erythrocyte transfusions to achieve this hemoglobin level at the discretion of the investigator
View Study & Checklist โFlavored, Oral Irinotecan VAL-413 (Orotecanยฎ) Given With Temozolomide for Treatment of Recurrent Pediatric Solid Tumors
A pilot pharmacokinetic trial to determine the safety and efficacy of a flavored, orally administered irinotecan VAL-413 (Orotecanยฎ) given with temozolomide for treatment of recurr
๐ Phoenix Children's Hospital โ Phoenix, Arizona
๐ต During the first cycle of treatment, each patient will receive 4 daily doses of VAL-413 (Orotecanยฎ) and one daily dose o
View Study & Checklist โDeveloping an Internet-Delivered Sexual Health Program for Breast Cancer Survivors, SHINE Trial
The goal of this clinical trial is to develop an effective internet-delivered program to help breast cancer survivors manage cancer-related sexual concerns. This study is being do
๐ Cancer Center at Saint Joseph's โ Phoenix, Arizona
๐ต Participants will receive a certain combination of these four different Cores to make up their SHINE program.
View Study & Checklist โRelacorilant in Combination With Nab-Paclitaxel in Advanced, Platinum-Resistant, High-Grade Epithelial Ovarian, Primary Peritoneal, or Fallopian-Tube Cancer
The primary objectives of this study are to evaluate progression-free survival (PFS) by blinded independent central review (BICR) and overall survival (OS) (evaluated independently
๐ Site 318 โ Phoenix, Arizona
๐ต Patients will receive study treatment until confirmed progressive disease (PD) or unacceptable toxicity.
View Study & Checklist โA Study to Assess Disease Activity and Safety of Subcutaneous Lutikizumab (ABT-981) in Adult Participants With Moderate to Severe Hidradenitis Suppurativa Who Have Failed Anti-Tumor Necrosis Factor (TNF) Therapy and Who Are Naรฏve to Biologic Therapy
Hidradenitis suppurativa (HS) is a chronic and often painful inflammatory skin disease which includes the forming of lumps, abscesses and scars in areas of the skin such as under t
๐ Medical Dermatology Specialists /ID# 240641 โ Phoenix, Arizona
๐ต In the Main Study, participants will receive subcutaneous injections of lutikizumab (ABT-981) or placebo every week for
View Study & Checklist โEffects of Brain Stimulation on Food Intake and Behavioral Weight Loss Treatment
This study will determine whether electrical stimulation of an area of the brain called the dorsolateral prefrontal cortex, which is important in determining the feeling of fullnes
๐ NIDDK, Phoenix โ Phoenix, Arizona
View Study & Checklist โTibulizumab Skin Healing and Inflammation Evaluation for Lasting Defense
The study is a Phase 2, multi-center, randomized, double-blind, placebo-controlled study to evaluate the effects of tibulizumab over 16 weeks (Period 1) in adults with hidradenitis
๐ Medical Dermatology Specialists (Phoenix) โ Phoenix, Arizona
๐ต The study is a Phase 2, multi-center, randomized, double-blind, placebo-controlled study to evaluate the effects of tibu
View Study & Checklist โOpen-label Study of Cenobamate Monotherapy in Adult Subjects With Newly Diagnosed or Recurrent Partial-Onset Epilepsy
Cenobamate (YKP3089) is a small molecule approved in the United States (US), Europe and several other countries around the world for the treatment of Partial-Onset (focal) seizures
๐ Arizona Neuroscience Research โ Phoenix, Arizona
๐ต During the 2-week Titration Phase, subjects will receive cenobamate 150 mg/day before entering the 26-week 200 mg/day Ma
View Study & Checklist โAutologous Adult Adipose-Derived Regenerative Cell Injection Into Chronic Partial-Thickness Rotator Cuff Tears
The purpose of this investigation is to evaluate the safety and superior effectiveness in functional improvement in patients with partial-thickness rotator cuff tears (PTRCTs) afte
๐ Arizona Research Center โ Phoenix, Arizona
View Study & Checklist โMicrofragmented Adipose Tissue Compared to Saline Injection for the Treatment of Knee Osteoarthritis
The goal of this clinical trial is to examine the effect of a single autologous, intra-articular injection of MFat versus saline injection for the treatment of pain and function as
๐ Arizona Bone, Joint and Sports Medicine Center LLC โ Phoenix, Arizona
๐ต Participants will receive an injection of MFat or saline.
View Study & Checklist โSetrusumab vs Bisphosphonates in Pediatric Subjects With Osteogenesis Imperfecta
The primary objective of the study is to evaluate the effect of setrusumab vs intravenous bisphosphonates (IV-BP) on reduction in fracture rate, including morphometric vertebral fr
๐ Phoenix Children's Hospital โ Phoenix, Arizona
๐ต Following randomization, participants will receive setrusumab or IV-BP for up to 24 months during the Active-controlled
View Study & Checklist โEvaluation of the Safety and Efficacy of Revitaยฎ DMR on Body Weight Maintenance in Subjects With Obesity Who Have Achieved at Least 15% Weight Loss on Tirzepatide
Fractyl is evaluating Revita Duodenal Mucosal Resurfacing (DMR) in the REMAIN-1 pivotal study, which is designed to include two cohorts - an open label cohort referred to as REVEAL
๐ Helios Clinical Research โ Phoenix, Arizona
๐ต Eligible participants will receive an open-label, tirzepatide run-in, dose-escalation period of approximately 16-26 week
View Study & Checklist โ