Obesity Clinical Trials in Cincinnati, Ohio
19 studies are recruiting for obesity in Cincinnati, Ohio right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
Search these by distance from you
Studies now recruiting
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Safety and Efficacy of ABBV-295 in Adults With Obesity or Overweight With Weight-Related Comorbidities
Obesity is a condition where a person has excessive body fat, defined by a body mass index (BMI) of 30 kg/m2 or higher. The goal of this study is to evaluate the effect of various doses of ABBV-295 compared to placebo on reducing body weight at Week 32 in participants with obesity or overweight wit…
- Stage
- Phase 2
- Ages
- 18 to 75
- Site
- CTI Clinical Research Center /ID# 282043, Cincinnati, Ohio
- Locations
- 64 in total
- Run by
- AbbVie
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A Study to Learn About Switching to a Monthly Study Medicine Called Berobenatide (PF-08653944) to Help Keep Weight Off in People With Overweight or Obesity
The purpose of this study is to learn about the safety and effectiveness of berobenatide in adults with overweight or obesity who have already lost weight while taking semaglutide or tirzepatide. The study does not include people with diabetes. Participants will be in the study for about 11 months.
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Velocity Clinical Research, Mt. Auburn, Cincinnati, Ohio
- Locations
- 16 in total
- Run by
- Pfizer
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A Study to Learn About the Study Medicine Called Berobenatide (PF-08653944) in People With Overweight or Obesity
The purpose of this clinical study is to learn about the effects and safety of berobenatide (PF-08653944). This may help people with overweight or obesity lose weight. People in this study may also have type 2 diabetes. About 950 adults will be in this study. Berobenatide will be compared to a plac…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Midwest Eye Center, Cincinnati, Ohio
- Locations
- 72 in total
- Run by
- Pfizer
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Efficacy, Safety, and Pharmacokinetics of Tirzepatide (LY3298176) Once Weekly Versus Placebo in Pediatric Participants 6 to Less Than 12 Years of Age Who Have Obesity (ADVANCE-SURMOUNT-KIDS)
The main purpose of this study, performed under Master Protocol J4M-MC-PWMP (NCT06672549), is to evaluate the efficacy, safety, and pharmacokinetics of tirzepatide as an addition to healthy lifestyle in participants 6 to less than 12 years of age, with obesity. Participation in the study will last …
- Stage
- Phase 3
- Ages
- 6 to 11
- Site
- Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio
- Locations
- 82 in total
- Run by
- Eli Lilly and Company
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A Study of Eloralintide (LY3841136) in Participants With Obstructive Sleep Apnea and Obesity or Overweight
The purpose of the studies is to evaluate the efficacy and safety of eloralintide in participants with moderate-to-severe obstructive sleep apnea and obesity or overweight. YDAO is a master protocol designed to support two independent studies: YSA1 and YSA2. Study YSA1 will include participants who…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- CTI Clinical Research Center, Cincinnati, Ohio
- Locations
- 115 in total
- Run by
- Eli Lilly and Company
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A Study to Investigate Weight Management With Macupatide and Eloralintide, Alone or in Combination, in Adult Participants With Obesity or Overweight
The main purpose of this study, performed under the master protocol W8M-MC-CWMM (NCT06143956), is to examine the body weight-lowering efficacy and safety of macupatide plus eloralintide compared with placebo in participants with obesity or overweight and without type 2 diabetes. Participation will …
- Stage
- Phase 2
- Ages
- 18 to 75
- Site
- CTI Clinical Research Center, Cincinnati, Ohio
- Locations
- 40 in total
- Run by
- Eli Lilly and Company
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A Study of Clazakizumab (LY5724886) in Adults With Elevated hsCRP and at Increased Risk for Cardiovascular Event
The purpose of this study is to measure the change in high-sensitivity C-reactive protein (hsCRP), a marker of inflammation in the body, with clazakizumab compared with placebo in adults who have elevated hsCRP and at increased risk for cardiovascular event. Participation in the study will last abo…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Velocity Clinical Research, Cincinnati, Springdale, Cincinnati, Ohio
- Locations
- 46 in total
- Run by
- Eli Lilly and Company
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A Master Protocol Study (LY900038) of Multiple Intervention-Specific-Appendices (ISAs) in Adult Participants With Obesity or Overweight
The purpose of this Phase-2 chronic weight management master protocol (CWMM) is to create a framework to evaluate the safety and efficacy of various investigational interventions for chronic weight management with intervention-specific appendices (ISAs). The CWMM establishes entry criteria for newl…
- Stage
- Phase 2
- Ages
- 18 to 75
- Site
- CTI Clinical Research Center, Cincinnati, Ohio
- Locations
- 57 in total
- Run by
- Eli Lilly and Company
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AMAZE 4: A Research Study Investigating How Well the Medicine NNC0487-0111 Helps People With Excess Body Weight and Obstructive Sleep Apnoea Treated With Positive Airway Pressure Lose Weight and Improve Sleep Apnoea
This study is being done to look at the efficacy and safety of NNC0487-0111 in participants with overweight or obesity, and obstructive sleep apnoea treated with positive airway pressure. There are 2 study treatments in this study taken as injections under the skin once a week. Participants will ei…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- CTI Clinical Research Center, Cincinnati, Ohio
- Locations
- 92 in total
- Run by
- Novo Nordisk A/S
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Extension Trial to Evaluate the Long-term Efficacy, Safety, and Tolerability of Maridebart Cafraglutide (MARITIME-2-EXTENSION)
The primary objective of this trial is to evaluate the long-term efficacy, safety, and tolerability of maridebart cafraglutide in participants with obesity and type 2 diabetes mellitus. Trial 20210182 is extension of trial 20210184 (NCT06858878).
- Stage
- Phase 3
- Ages
- 18 to 99
- Site
- Velocity Clinical Research - Cincinnati, Cincinnati, Ohio
- Locations
- 45 in total
- Run by
- Amgen
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Extension Trial to Evaluate the Long-term Efficacy, Safety, and Tolerability of Maridebart Cafraglutide (MARITIME-1-EXTENSION)
The primary objective of this trial is to evaluate the long-term efficacy, safety, and tolerability of maridebart cafraglutide in participants with obesity or overweight. Trial 20250197 is an extension of trial 20210181 (NCT06858839).
- Stage
- Phase 3
- Ages
- 18 to 99
- Site
- Clinical Trial Investigator Clinical Research Center, Cincinnati, Ohio
- Locations
- 92 in total
- Run by
- Amgen
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A Study of Eloralintide (LY3841136) in Participants With Persistent Obesity Who Are Treated With a Weekly Incretin
The main purpose of this study is to evaluate the efficacy and safety of eloralintide compared with placebo in participants with persistent obesity or overweight, with or without type 2 diabetes, and on stable incretin background therapy. Participation in the study will last about 80 weeks.
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- CTI Clinical Research Center, Cincinnati, Ohio
- Locations
- 185 in total
- Run by
- Eli Lilly and Company
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A Study of Once-daily Oral ASC30 to Evaluate the Efficacy and Safety in Adult Participants With Obesity or Overweight With Type 2 Diabetes
Study ASC30-302 (AURORA-2) is a Phase III, global, multicenter, randomized, double-blind, placebo-controlled study to investigate the long-term efficacy, safety, and tolerability of three maintenance doses of once-daily oral ASC30 compared with placebo in participants with obesity or overweight and…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- AURORA-2 Clinical Site, Cincinnati, Ohio
- Locations
- 135 in total
- Run by
- Ascletis Pharma (China) Co., Limited
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A Study of Once-daily Oral ASC30 to Evaluate the Efficacy and Safety in Adult Participants With Obesity or Overweight With Weight-Related Comorbidities
Study ASC30-301 (AURORA-1) is a Phase III, global, multicenter, randomized, double-blind, placebo-controlled study to investigate the long-term efficacy, safety, and tolerability of three maintenance doses of once-daily oral ASC30 compared with placebo in participants with obesity or overweight wit…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- AURORA-1 Clinical Site, Cincinnati, Ohio
- Locations
- 122 in total
- Run by
- Ascletis Pharma (China) Co., Limited
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AMAZE 3: A Research Study Investigating How Well the Medicine NNC0487-0111 Helps People With Excess Body Weight and Obstructive Sleep Apnoea Not Treated With Positive Airway Pressure Lose Weight and Improve Sleep Apnoea
This study is being done to look at the efficacy and safety of NNC0487-0111 in participants with excess body weight and obstructive sleep apnoea not treated with positive airway pressure lose weight and improve sleep apnoea. There are 2 study treatments in this study taken as injections under the s…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- CTI Clinical Research Center, Cincinnati, Ohio
- Locations
- 80 in total
- Run by
- Novo Nordisk A/S
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Caloric Restriction and Activity to Reduce Chemoresistance in B-ALL
This study is for older children, adolescents, and young adults with B-cell Acute Lymphoblastic Leukemia (B-ALL). Higher amounts of body fat is associated with resistance to chemotherapy in patients with B-ALL. Chemotherapy during the first month causes large gains in body fat in most people, even …
- Stage
- Phase 2
- Ages
- 7 to 25
- Site
- Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio
- Locations
- 16 in total
- Run by
- Etan Orgel
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A Research Study to Look at How Well NNC0487-0111 Works Compared to Placebo in People With Heart Failure and Obesity
This study is being done to look at the safety and effect of NNC0487-0111 in people with Heart Failure with preserved Ejection Fraction (HFpEF) or Heart Failure with mildly reduced Ejection Fraction (HFmrEF) and excess body weight when compared to placebo. The purpose of this clinical study is to f…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Lindner Center,Christ Hospital, Cincinnati, Ohio
- Locations
- 838 in total
- Run by
- Novo Nordisk A/S
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A Single and Multiple Ascending Dose Study of HM17321 in Healthy and Obese Participants
This is a Phase 1 study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of HM17321 after single and multiple ascending doses in healthy and obese participants.
- Stage
- Phase 1
- Ages
- 18 to 65
- Site
- Medpace Clinical Pharmacology Unit, Cincinnati, Ohio
- Run by
- Hanmi Pharmaceutical Company Limited
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A Novel Obesity Prevention Program for High-Risk Infants in Primary Care
The goal of this clinical trial is to test a responsive parenting obesity prevention program with infants and caregivers of color (e.g., non-White; Hispanic/Latinx) and/or who are economically marginalized (i.e., publicly insured), delivered via Integrated Behavioral Health (IBH) in pediatric prima…
- Stage
- Phase 2
- Ages
- 0 and older
- Site
- Hopple Street Neighborhood Health Center, Cincinnati, Ohio
- Run by
- Children's Hospital Medical Center, Cincinnati
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
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