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Search / Trial NCT06952530

A Master Protocol Study of Orforglipron (LY3502970) in Participants With Hypertension and Obesity or Overweight (ATTAIN-Hypertension) GZL2

Launched by ELI LILLY AND COMPANY · Apr 28, 2025

Trial Information

Current as of June 08, 2025

Not yet recruiting

Keywords

ClinConnect Summary

The ATTAIN-Hypertension study is a clinical trial looking at a new medication called orforglipron (LY3502970) to see how well it works in lowering high blood pressure, also known as hypertension, in people who are overweight or obese. This is a Phase 3 trial, which means it’s one of the final steps in testing this medication before it can potentially be approved for general use. The study is not yet recruiting participants, but when it does, it will include men and women aged 65 to 74.

To be eligible for this trial, participants will need to meet certain criteria outlined in a larger study called the GZPL master protocol. While specifics are not detailed here, generally, potential participants will need to have a confirmed diagnosis of hypertension and be classified as overweight or obese. Those who join the study can expect to receive the medication orforglipron and will be monitored for its effects on their blood pressure and overall health. This trial could help determine if orforglipron is a safe and effective treatment option for managing high blood pressure in individuals who are overweight.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • refer to the GZPL master protocol study for screening eligibility.
  • Exclusion Criteria:
  • refer to the GZPL master protocol study for screening eligibility.

About Eli Lilly And Company

Eli Lilly and Company is a global healthcare leader dedicated to creating innovative medicines that improve patient outcomes across a range of therapeutic areas, including diabetes, oncology, immunology, and neurodegenerative diseases. With a rich history of scientific research and a commitment to advancing healthcare, Lilly invests significantly in clinical trials to develop new treatments and enhance existing therapies. The company prioritizes patient safety and ethical standards in its clinical research, fostering collaboration with healthcare professionals and stakeholders to ensure the delivery of high-quality, evidence-based solutions that address unmet medical needs worldwide.

Locations

Baltimore, Maryland, United States

Ogden, Utah, United States

Richmond, Virginia, United States

Honolulu, Hawaii, United States

Newport News, Virginia, United States

Berlin, , Germany

Waterbury, Connecticut, United States

Phoenix, Arizona, United States

Wuxi, Jiangsu, China

Chengdu, Sichuan, China

Northridge, California, United States

Sevilla, Andalucía, Spain

Bydgoszcz, Kujawsko Pomorskie, Poland

Chuo Ku, Tokyo, Japan

Siping, Jilin, China

Saint Peters, Missouri, United States

Columbus, Ohio, United States

Lishui, Zhejiang, China

Jinan, Shandong, China

Boca Raton, Florida, United States

Mckinney, Texas, United States

Covina, California, United States

Chuo Ku, Tokyo, Japan

Saratoga Springs, New York, United States

Bhubaneswar, Odisha, India

Oldenburg, Schleswig Holstein, Germany

New Delhi, Delhi, India

Sevilla, , Spain

Las Vegas, Nevada, United States

Troy, Michigan, United States

Essen, Nordrhein Westfalen, Germany

Leipzig, Sachsen, Germany

Athens, Attikí, Greece

Wroclaw, Dolnośląskie, Poland

Buenos Aires, , Argentina

Luoyang Shi, Henan, China

Bangalore, Karnataka, India

Yamato Shi, Kanagawa, Japan

Las Vegas, Nevada, United States

North Richland Hills, Texas, United States

Redmond, Washington, United States

Port Charlotte, Florida, United States

Kamakura Shi, Kanagawa, Japan

Changchun, Jilin, China

Mauldin, South Carolina, United States

Dorado, , Puerto Rico

Ponce, , Puerto Rico

Białystok, Podlaskie, Poland

Beijing, Beijing, China

Dresden, Sachsen, Germany

Praha 5, , Czechia

Córdoba, , Argentina

Pardubice V, Pardubice, Czechia

Granadero Baigorria, Santa Fe, Argentina

Rosario, Santa Fe, Argentina

Rosario, Santa Fe, Argentina

Xian, Shaanxi, China

Bad Homburg, Hessen, Germany

Ioannina, Ioánnina, Greece

León, Castilla Y León, Spain

Jacksonville, Florida, United States

Piotrkow Trybunalski, łódzkie, Poland

Changde, Hunan, China

Dayton, Ohio, United States

Thessaloniki, Thessaloníki, Greece

Przemysl, Podkarpackie, Poland

Buenos Aires, , Argentina

Rochester, New York, United States

Wenatchee, Washington, United States

Thessaloniki, Thessaloníki, Greece

New Bedford, Massachusetts, United States

Köln, Nordrhein Westfalen, Germany

Dresden, Sachsen, Germany

Baltimore, Maryland, United States

Warsaw, Mazowieckie, Poland

Tarnów, Małopolskie, Poland

Buenos Aires, Ciudad Autónoma De Buenos Aires, Argentina

Lishui City, Zhejiang, China

Prague, Praha 12, Czechia

A Coruña, A Coruña [La Coruña], Spain

Athens, Attikí (Region), Greece

Shanghai, Shanghai, China

Brandon, Florida, United States

Hodonin, Hodonín, Czechia

Sun City Center, Florida, United States

La Coruña, A Coruña [La Coruña], Spain

Centelles, Barcelona [Barcelona], Spain

Tigard, Oregon, United States

Manassas, Virginia, United States

San Isidro, Buenos Aires, Argentina

Chongqing, Chongqing, China

Brno, Brno Město, Czechia

Brno, Brno Město, Czechia

Ostrava, Moravskoslezský Kraj, Czechia

Ledec Nad Sazavou, Vysočina, Czechia

Praha 4, , Czechia

Leipzig, Sachsen, Germany

Thessaloniki, Thessaloníki, Greece

Ulhasnagar, Maharashtra, India

Matsuyama, Ehime, Japan

Bydgoszcz, Kujawsko Pomorskie, Poland

Barcelona, Barcelona [Barcelona], Spain

Patients applied

0 patients applied

Trial Officials

Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)

Study Director

Eli Lilly and Company

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported