A Study of RGLS8429 in Patients With Autosomal Dominant Polycystic Kidney Disease

Overview

About this study

The purpose of ths study is to assess the safety and tolerability of RGLS8429. Addiitionally, to assess the impact of RGLS8429 on ADPKD biomarkers

Other objectives are o assess the impact of RGLS8429 on height-adjusted total kidney volume (htTKV) and to characterize the pharmacokinetic (PK) properties of RGLS8429 -To assess the impact of RGLS8429 on renal function.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Key Inclusion Criteria:

1. Male or female ADPKD patients, 18 to 70 years old.

2. Class 1C, 1D, or 1E Mayo Imaging Classification of ADPKD (based upon either the MRI
obtained during screening, or a prior MRI obtained within 5 years of screening with
documented Mayo classification).

3. eGFR between 30 to 90 mL/min/1.73 m^2.

4. Body mass index (BMI) 18 to 35 kg/m^2.

5. Must understand and consent to the study procedures explained in the ICF and be
willing and able to comply with the protocol.

Key Exclusion Criteria:

1. Administration of tolvaptan in the 28 days before randomization.

2. Subject is mentally incapacitated or has significant emotional problems.

3. Any medical condition or social circumstance that, in the opinion of the Investigator,
may make the subject unlikely to complete the study or comply with study procedures
and requirements; or may pose a risk to the subject's safety.

4. History or presence of alcoholism or drug abuse within the past 2 years prior to
screening.

5. Only one kidney or kidney transplant recipient.

6. Participation in another clinical trial and/or exposure to any investigational drug or
approved therapy for investigational use within 28 days or 5 half-lives of the
investigational drug's dosing, whichever is longer, prior to dosing. The 28-day or
5-half-life windows will be calculated from the date of the last dosing in the
previous study to Day 1 of the current study.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 10/7/22. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Marie Hogan, M.D., Ph.D.

Open for enrollment

Contact information:

Charles Madsen CCRP

(507) 266-9391

Madsen.Charles@mayo.edu

Jacksonville, Fla.

Mayo Clinic principal investigator

Fouad Chebib, M.D.

Open for enrollment

Contact information:

Clinical Studies Unit

(904) 953-2255

More information

Publications

Publications are currently not available