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RecruitingNCT07286175

A Study of Brenipatide in Adult Participants With Bipolarity (RENEW-Bipolar-1)

This study evaluates the safety and effectiveness of Brenipatide for people with bipolarity.

Medication studyAges 18–75Multiple countries
The study in practice

Understand this study

What is this study about?

This study evaluates the safety and effectiveness of Brenipatide for people with bipolarity.

Who could participate?

This study is for people with bipolarity. Listed age limits: 18 years to 75 years. Other eligibility criteria apply.

Listed locations
Orange, United States · New Haven, United States and 74 more locationsSee all locations and recruitment
Activities
Medication described in the protocol · Placebo comparator
Compensation
Payment and expense reimbursement have not been verified.

Registry last updated: · Record retrieved: . These dates do not confirm site availability.

What to know before participating

A point to clarify

This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Things to check before joining

Study start dateStarted: November 24, 2025
Recruitment status
Recruiting
Enrollment listed in the registry
400
Sponsor
Eli Lilly and Company
Sponsor type
Other organization
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
United States, Argentina, Brazil, ...
Age range
From 18 Years to 75 Years
Official registry ID
NCT07286175
Official title
A Phase 2, Multicenter, Randomized, Double-Blind, Parallel-Arm Study to Investigate the Efficacy and Safety of Adjunctive Treatment With Brenipatide in Delaying Time to Relapse Compared With Placebo in Adult Participants With Bipolar Disorder (RENEW-Bipolar-1)

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Recruitment & locations

Recruiting

Orange, United States · New Haven, United States · Hialeah, United States

73 more locations
  • Maitland, United States
  • Miami Lakes, United States
  • Naples, United States
  • Orlando, United States
  • Weston, United States
  • Atlanta, United States
  • Waterloo, United States
  • Gaithersburg, United States
  • Springfield, United States
  • Watertown, United States
  • Philadelphia, United States
  • McKinney, United States
  • Richardson, United States
  • Clinton, United States
  • Fairfax, United States
  • Bellevue, United States
  • ABB, Argentina
  • Buenos Aires, Argentina
  • Córdoba, Argentina
  • La Plata, Argentina
  • Mendoza, Argentina
  • Rosario, Argentina
  • Santiago del Estero, Argentina
  • Brasília, Brazil
  • Campinas, Brazil
  • Marília, Brazil
  • Rio de Janeiro, Brazil
  • São Bernardo do Campo, Brazil
  • São Paulo, Brazil
  • Valinhos, Brazil
  • Changsha, China
  • Hangzhou, China
  • Huzhou, China
  • Jinan, China
  • Shanghai, China
  • Shijiazhuang, China
  • Tianjin, China
  • Xiamen, China
  • Zhumadian, China
  • Aurangabad, India
  • Belgavi, India
  • Bhopal, India
  • Chhatrapati Sambhajinagar, India
  • Dehradun, India
  • Dharwad, India
  • Lucknow, India
  • Mysore, India
  • Nashik, India
  • Pune, India
  • Tiruchirappalli, India
  • Varanasi, India
  • Chikugo, Japan
  • Chiyoda City, Japan
  • Fukushima, Japan
  • Iruma, Japan
  • Karatsu, Japan
  • Kōtō City, Japan
  • Kumamoto, Japan
  • Kure, Japan
  • Kurume, Japan
  • Sagamihara, Japan
  • Shibuya-ku, Japan
  • Tokyo, Japan
  • Toshima City, Japan
  • Yamagata, Japan
  • Yokohama, Japan
  • Chihuahua City, Mexico
  • Guadalajara, Mexico
  • Mazatlán, Mexico
  • Mexico City, Mexico
  • Mérida, Mexico
  • Morelia, Mexico
  • Bayamón, Puerto Rico

A listed location does not confirm current availability.

FAQ

Questions about this study

What is this study about?

This study evaluates the safety and effectiveness of Brenipatide for people with bipolarity.

Who is behind this study?

The study sponsor is Eli Lilly and Company.

Does this study involve medication?

Yes. The study involves medication, including Brenipatide and Placebo.

Who can participate?

This study is for people with bipolarity. Listed age limits: 18 years to 75 years. Other eligibility criteria apply.

Is this study still recruiting?

The registry lists this study as recruiting.

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