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Monrovia, California Clinical Trials

A listing of Monrovia, California clinical trials actively recruiting patient volunteers.

RESULTS

Found (577) clinical trials

Safety and Efficacy of Selonsertib GS-0976 GS-9674 and Combinations in Participants With Bridging Fibrosis or Compensated Cirrhosis Due to Nonalcoholic Steatohepatitis (NASH)

The primary objectives of this study are: To assess the safety and tolerability of selonsertib (SEL), GS-0976, and GS-9674, administered alone or in combination, in participants with bridging fibrosis or compensated cirrhosis due to Nonalcoholic Steatohepatitis (NASH) To evaluate changes in liver fibrosis, without worsening of NASH

Phase

9.26 miles

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A Study to Evaluate the Efficacy and Safety of RO6867461 in Participants With Diabetic Macular Edema

This study will evaluate the efficacy, safety, and pharmacokinetics of RO6867461 administered at 8-week intervals or as specified in the protocol following treatment initiation, compared with aflibercept once every 8 weeks (Q8W), in participants with diabetic macular edema (DME).

Phase

9.26 miles

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Non Exudative AMD Imaged With SS-OCT

This is a longitudinal observational study where the investigators will look at 450 subjects, 200 with intermediate AMD in at least one eye, or with AMD in one eye, either early or intermediate, and with late AMD (exudative) in the other eye, and 250 subjects with nGA or GA in ...

Phase N/A

9.26 miles

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Phase 2 Herniorrhaphy Study for Opioid Elimination

This is a Phase 2, open-label study in subjects undergoing unilateral open inguinal herniorrhaphy.

Phase

9.26 miles

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Efficacy and Safety Trial of Conbercept Intravitreal Injection for Neovascular Age-related Macular Degeneration (PANDA-1)

A multicenter, multinational, double-masked, parallel-group, dose-ranging, active-controlled, randomized trial, which will randomize approximately 1140 subjects in a ratio of 1:1:1 to receive IVT injections of 0.5 mg conbercept, 1.0 mg conbercept, or 2.0 mg aflibercept. The trial includes a screening period of less than or equal to 14 days, followed ...

Phase

9.26 miles

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Translational Obesity Research

The proposed project takes an innovative approach to childhood obesity prevention, for which there currently no evidence-based programs, and for which results of current trials have produced mainly short-term or disappointing effects. The aim of this project is to adapt and revise parts of two nationally recognized programs for drug ...

Phase N/A

9.42 miles

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Lotus Clinical Research is conducting a research study to evaluate the safety and tolerability of an investigational medication in patients following hernia repair surgery.

Phase

9.49 miles

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Lotus Clinical Research is conducting a research study to evaluate the efficacy, safety, and tolerability of an investigational medication in patients following tummy tuck surgery.

Phase

9.49 miles

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Lotus Clinical Research is conducting a research study to evaluate the efficacy of an investigational pain medication in patients who require hernia repair surgery.

Phase

9.49 miles

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You could qualify to have your bunion removed at no cost to you. Lotus Clinical Research is conducting a research study to evaluate the safety and tolerability of an investigational pain medication administered for postoperative pain following bunion removal surgery.

Phase

9.49 miles

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