20 Paid Clinical Research Studies in Louisville, Kentucky

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

Phase4

A Single Center, Open-Label Study to Evaluate the Ability of the TearScienceโ„ข LipiViewโ„ข II Ocular Surface Interferometer and the Keratographยฎ 5M to Detect Tear Film Stability Utilizing Mieboยฎ

A study to investigate the ability of the TearScienceโ„ข LipiViewโ„ข II Ocular Surface Interferometer and the Keratographยฎ 5M to detect tear film stability utilizing Mieboยฎ

๐Ÿ“ Butchertown Clinical Trials โ€” Louisville, Kentucky

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Phase3

Study of Eftilagimod Alfa (Efti) in Combination With Pembrolizumab and Chemotherapy Versus Placebo in Combination With Pembrolizumab and Chemotherapy in Participants With Metastatic Non-Small Cell Lung Cancer (NSCLC) (TACTI-004)

The purpose of this study is to compare eftilagimod alfa (efti) in combination with pembrolizumab and chemotherapy versus placebo in combination with pembrolizumab and chemotherapy

๐Ÿ“ Norton Cancer Institute - Audubon โ€” Louisville, Kentucky

๐Ÿ’ต Participants will receive either efti plus standard treatment (pembrolizumab and platinum doublet chemotherapy) or place

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Phase2 / Phase3

Effects of 5HTP on the Injured Human Spinal Cord

This study will assess how the serotonin precursor, 5-HTP, alter nervous system excitability and motor function in individuals with spinal cord injuries of differing chronicity and

๐Ÿ“ University of Louisville โ€” Louisville, Kentucky

๐Ÿ’ต In a placebo-controlled, randomized crossover design, participants will receive i) 50 mg 5HTP combined with 50 mg carbid

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Observational / Diagnostic

Intermediate Visual Space Perception

The ability to judge the locations of various objects from oneself during self-motion in the intermediate distance range (\~2-25m) is crucial for successful performance of activiti

๐Ÿ“ University of Louisville โ€” Louisville, Kentucky

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Phase1

Safety and Preliminary Effectiveness of BNT317, an Investigational Therapy for Advanced Solid Tumors

This is a first-in-human (FIH), open-label, multiple-site, dose escalation study which will evaluate the safety, tolerability, pharmacokinetics (PK), and immunogenicity of increasi

๐Ÿ“ Norton Cancer Institute PARENT โ€” Louisville, Kentucky

๐Ÿ’ต Participants may receive investigational medicinal product (IMP) for up to 2 years or until they experience disease prog

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Phase1 / Phase2

Combination Therapy for Recurrent Ovarian Cancer

The proposed study "combination therapy with liposomal doxorubicin and withaferin A (Ashwagandha, ASWD) in recurrent ovarian cancer" is focused to determine the feasibility and max

๐Ÿ“ UofL Health Brown Cancer Center โ€” Louisville, Kentucky

๐Ÿ’ต Adequate organ function within 14 days prior to first WFA/ASWD dose or liposomal doxorubicin whichever occurs first, inc

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