13 Paid Clinical Research Studies in Scottsdale, Arizona

Filtered for protocols that accept healthy volunteers or mention compensation. Always confirm stipend details and screening with the study coordinator.

Observational / Diagnostic

Safety and Effectiveness of ELLANSร‰ยฎ-S Dermal Filler in the Treatment of Nasolabial Folds

The study will be a prospective, randomized, multi-center, split-face, controlled, double-blind clinical trial to evaluate the safety and effectiveness of ELLANSร‰ยฎ-S for the treatm

๐Ÿ“ Investigate MD โ€” Scottsdale, Arizona

๐Ÿ’ต Subjects may receive a retreatment touch up at 4 weeks after retreatment, and if touched up, will have safety visits at

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Phase1

A Study of HFB200301 as a Single Agent and in Combination With Tislelizumab in Adult Patients With Advanced Solid Tumors

The purpose of this study is to test the safety and tolerability of HFB200301 as a single agent and in combination with tislelizumab in patients with advanced cancers. There are tw

๐Ÿ“ Mayo Clinic โ€” Scottsdale, Arizona

๐Ÿ’ต During the escalation part, groups of participants will receive increasing doses of HFB200301 as a monotherapy or in com

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Observational / Diagnostic

HIFEM and Radiofrequency for Muscular System Function Improvement

The goal of this clinical trial is to investigate the effect of the BTL-899M device on muscular system function in adult subjects seeking treatment for improving their muscular sys

๐Ÿ“ Royal Spine Surgery โ€” Scottsdale, Arizona

๐Ÿ’ต At the last therapy visit, the patients will receive the Subject Satisfaction Questionnaire and Therapy Comfort Question

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Phase1

A Phase 1 Dose-escalation Study of FF-10832 for Treatment of Solid Tumors Including Biliary Tract Cancer

To determine the safety profile, maximum tolerated dose (MTD), dose-limiting toxicities (DLT) and recommended Phase 2 dose (RP2D) in patients who receive FF-10832 (Gemcitabine Lipo

๐Ÿ“ Honor Health Research Institute โ€” Scottsdale, Arizona

๐Ÿ’ต To determine the safety profile, maximum tolerated dose (MTD), dose-limiting toxicities (DLT) and recommended Phase 2 do

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Phase2

ADP-A2M4CD8 Monotherapy and in Combination With Nivolumab in HLA-A2+ Subjects With MAGE-A4 Positive Ovarian Cancer (SURPASS-3)

This is a phase 2, open-label, randomized, non-comparative clinical trial to evaluate the clinical outcome of ADP A2M4CD8 as monotherapy and in combination treatment with nivolumab

๐Ÿ“ Honor Health โ€” Scottsdale, Arizona

๐Ÿ’ต Subjects may receive up to 4 prior regimens of combination or single agent systemic treatment for their disease, which m

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Observational / Diagnostic

Safety and Efficacy of the BTL-043 and BTL-899 Devices in Alleviating Back Pain

The study will evaluate the clinical efficacy and performance of the BTL-043 and BTL-899 devices for alleviating back pain. It is a prospective, multi-center, open-label, single-ar

๐Ÿ“ Royal Spine Surgery โ€” Scottsdale, Arizona

๐Ÿ’ต During each treatment visit, subjects will receive treatments with both study devices, BTL-043 and BTL-899, consecutivel

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Phase3

A Study to Assess Efficacy and Safety of Efgartigimod PH20 SC in Adults With Ocular Myasthenia Gravis

The purpose of this study is to evaluate the efficacy and safety of efgartigimod PH20 SC given by a pre-filled syringe in adult patients with ocular myasthenia gravis. The study co

๐Ÿ“ HonorHealth Neurology - Bob Bovรฉ Neuroscience Institute โ€” Scottsdale, Arizona

๐Ÿ’ต In part A, half of the participants will receive efgartigimod PH20 SC and the other half will receive placebo.

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