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.

Phase2

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

๐Ÿ“ Mayo Clinic Hospital in Arizona โ€” Phoenix, Arizona

๐Ÿ’ต Patients may receive cisplatin intravenously (IV) over 1-2 hours per standard of care.

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Early Phase1

Trial 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

๐Ÿ“ St. Joseph's Hospital and Medical Center โ€” Phoenix, Arizona

๐Ÿ’ต Participants may receive erythrocyte transfusions to achieve this hemoglobin level at the discretion of the investigator

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Phase1

Flavored, 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

๐Ÿ“ Phoenix Children's Hospital โ€” Phoenix, Arizona

๐Ÿ’ต During the first cycle of treatment, each patient will receive 4 daily doses of VAL-413 (Orotecanยฎ) and one daily dose o

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Observational / Diagnostic

Developing 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

๐Ÿ“ Cancer Center at Saint Joseph's โ€” Phoenix, Arizona

๐Ÿ’ต Participants will receive a certain combination of these four different Cores to make up their SHINE program.

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Phase3

Relacorilant 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

๐Ÿ“ Site 318 โ€” Phoenix, Arizona

๐Ÿ’ต Patients will receive study treatment until confirmed progressive disease (PD) or unacceptable toxicity.

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Phase2

A 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

๐Ÿ“ Medical Dermatology Specialists /ID# 240641 โ€” Phoenix, Arizona

๐Ÿ’ต In the Main Study, participants will receive subcutaneous injections of lutikizumab (ABT-981) or placebo every week for

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Phase2

Tibulizumab 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

๐Ÿ“ Medical Dermatology Specialists (Phoenix) โ€” Phoenix, Arizona

๐Ÿ’ต The study is a Phase 2, multi-center, randomized, double-blind, placebo-controlled study to evaluate the effects of tibu

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Phase4

Open-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

๐Ÿ“ Arizona Neuroscience Research โ€” Phoenix, Arizona

๐Ÿ’ต During the 2-week Titration Phase, subjects will receive cenobamate 150 mg/day before entering the 26-week 200 mg/day Ma

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Observational / Diagnostic

Evaluation 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

๐Ÿ“ Helios Clinical Research โ€” Phoenix, Arizona

๐Ÿ’ต Eligible participants will receive an open-label, tirzepatide run-in, dose-escalation period of approximately 16-26 week

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