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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05967806
Other study ID # D4325C00007
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 31, 2023
Est. completion date August 21, 2024

Study information

Verified date April 2024
Source AstraZeneca
Contact AstraZeneca Clinical Study Information Center
Phone 1-877-240-9479
Email information.center@astrazeneca.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of the D4325C00007 study is to identify and characterise patients with known or newly diagnosed CKD for possible participation in future renal clinical studies and to obtain an overview on current treatment choices for this patient group in different regions.


Recruitment information / eligibility

Status Recruiting
Enrollment 3000
Est. completion date August 21, 2024
Est. primary completion date August 21, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 130 Years
Eligibility Inclusion criteria: 1. Male or female aged = 18 years at the time of signing the informed consent 2. Express interest to participate in a future CKD clinical study 3. eGFR = 20 to < 90 mL/min/1.73 m2 (eGFRcr[AS], Section 8.2.1) (Delgado et al 2022, Inker et al. 2021) 4. UACR = 700 mg/g or UPCR = 1000 mg/g based on urine sample at time of screening visit 5. Receiving RAS inhibitor therapy (ACEi or ARB) that has been at stable dosing for at least 4 weeks. Exceptions from this requirement will be made for participants who are unable to tolerate RAS inhibitor therapy 6. Provision of signed and dated written informed consent before any study-specific procedures Exclusion criteria: 1. Known NYHA class III or class IV Congestive Heart Failure at the time of enrolment 2. Known T1DM 3. Known history of any life-threatening cardiac dysrhythmia (continuous or paroxysmal) 4. Known history of solid organ transplantation 5. Known history or ongoing allergy/hypersensitivity, as judged by the investigator, to SGLT2i (eg, dapagliflozin, canagliflozin, empagliflozin) or endothelin receptor antagonists (eg, ambrisentan, atrasentan, bosentan) 6. Known blood-borne diseases such as specified in Appendix B (category A and B) 7. Known pregnancy at the time for the visit or have an intention to become pregnant 8. Lupus nephritis, anti-neutrophil cytoplasmic autoantibody vasculitis, minimal change disease, autosomal dominant polycystic kidney disease (polycystic kidney disease), Alport syndrome, patients on renal replacement therapy, or clinical nephrotic syndrome with problematic oedema

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
assessment
2 ml volume of blood withdrawal

Locations

Country Name City State
Argentina Research Site Buenos Aires
Argentina Research Site Caba
Argentina Research Site Ciudad de Buenos Aires
Argentina Research Site Santa Fe
Brazil Research Site Belem
Brazil Research Site Botucatu
Brazil Research Site Curitiba
Brazil Research Site Fortaleza
Brazil Research Site Joinville
Brazil Research Site Porto Alegre
Brazil Research Site Rio de Janeiro
Brazil Research Site Sao Jose Do Rio Preto
Brazil Research Site Sao Paulo
Brazil Research Site Sao Paulo
Canada Research Site Chicoutimi
Canada Research Site Greenfield Park
Canada Research Site London
Canada Research Site Montreal
Canada Research Site Oakville
Canada Research Site Sherbrooke
Canada Research Site Waterloo
China Research Site Baotou
China Research Site Beijing
China Research Site Beijing
China Research Site Chongqing
China Research Site Chuangchun
China Research Site Deyang
China Research Site Foshan
China Research Site Fujian
China Research Site Guangdong
China Research Site Guangdong
China Research Site Guangdong
China Research Site Guiyang
China Research Site Hengyang
China Research Site Hubei
China Research Site Hunan
China Research Site Jiangsu
China Research Site Jiangxi
China Research Site Jilin
China Research Site Nanchang
China Research Site Nanjing
China Research Site Nanning
China Research Site Pingxiang
China Research Site Shanghai
China Research Site Shenzhen
China Research Site Sichuan
China Research Site Sichuan
China Research Site Wenzhou
China Research Site Xi'an
China Research Site Yantai
China Research Site Yinchuan
China Research Site Zhejiang
India Research Site Bangalore
India Research Site Delhi
India Research Site Dhanvantari Nagar
India Research Site Nadiad
India Research Site New Delhi
India Research Site Rajasthan
Mexico Research Site Cuernavaca
Mexico Research Site Mazatlan
Mexico Research Site Mexico
Mexico Research Site Veracruz
Philippines Research Site Angeles City
Philippines Research Site Cainta
Philippines Research Site Davao City
Philippines Research Site Iloilo City
Philippines Research Site Manila
Philippines Research Site Quezon City
Poland Research Site Bielsko-Biala
Poland Research Site Bochnia
Poland Research Site Chrzanow
Poland Research Site Katowice
Poland Research Site Krakow
Poland Research Site Lezajsk
Poland Research Site Lodz
Poland Research Site Lodz
Poland Research Site Lublin
Poland Research Site Piaseczno
Poland Research Site Poznan
Poland Research Site Radom
Poland Research Site Ruda Slaska
Poland Research Site Rzeszów
Poland Research Site Szczecin
Poland Research Site Torun
Poland Research Site Tychy
Poland Research Site Warszawa
Poland Research Site Warszawa
Poland Research Site Wroclaw
Slovakia Research Site Banska Bystrica
Slovakia Research Site Kosice
Slovakia Research Site Lucenec
Slovakia Research Site Presov
Slovakia Research Site Puchov
Slovakia Research Site Roznava
Slovakia Research Site Trebisov
South Africa Research Site Benoni
South Africa Research Site Cape Town
South Africa Research Site Centurion
South Africa Research Site Chatsworth
South Africa Research Site Durban
South Africa Research Site Lenasia
South Africa Research Site Parow
South Africa Research Site Pretoria
South Africa Research Site Soweto
South Africa Research Site Soweto
Sweden Research Site Goteborg
Sweden Research Site Linkoping
Sweden Research Site Lund
Sweden Research Site Rattvik
Sweden Research Site Stockholm
Sweden Research Site Uppsala
Taiwan Research Site Kaohsiung
Taiwan Research Site Kaohsiung city
Taiwan Research Site New Taipei
Taiwan Research Site Taichung
Taiwan Research Site Taipei
Taiwan Research Site Taipei City
Taiwan Research Site Taoyuan
Taiwan Research Site Yongkang
Thailand Research Site Bangkok
Thailand Research Site Bangkok
Thailand Research Site Bangkok
Thailand Research Site Chiang Mai
Thailand Research Site Khon Kaen
Thailand Research Site Songkhla
Turkey Research Site Adapazari
Turkey Research Site Adapazari
Turkey Research Site Afyonkarahisar
Turkey Research Site Ankara
Turkey Research Site Antalya
Turkey Research Site Bursa
Turkey Research Site Kahramanmaras
Turkey Research Site Kayseri
Turkey Research Site Kocaeli
Turkey Research Site Mersin
United States Research Site Arlington Virginia
United States Research Site Bakersfield California
United States Research Site Chatsworth California
United States Research Site Greenville South Carolina
United States Research Site Huntsville Alabama
United States Research Site Jacksonville Florida
United States Research Site Kinston North Carolina
United States Research Site Maumee Ohio
United States Research Site Miami Florida
United States Research Site New Bern North Carolina
United States Research Site Pearland Texas
United States Research Site S. Gate California
United States Research Site San Antonio Texas
United States Research Site San Carlos California
United States Research Site Sun City West Arizona
United States Research Site Tarzana California
United States Research Site Victorville California
United States Research Site Wilmington North Carolina
United States Research Site Winston-Salem North Carolina
Vietnam Research Site Ha Noi
Vietnam Research Site Hai Phong
Vietnam Research Site Ho Chi Minh City

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Countries where clinical trial is conducted

United States,  Vietnam,  Argentina,  Brazil,  Canada,  China,  India,  Mexico,  Philippines,  Poland,  Slovakia,  South Africa,  Sweden,  Taiwan,  Thailand,  Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of patients with UACR>700mg/g or UPCR >1000mg/g and eGFR 20-90 mL/min/1.73 m2 Summary statistics approximately 10 months
Secondary Number and sort of antihypertensive drugs among patients in different geographical regions Use of medications approximately 10 months
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