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NCT05521191CompletedPhase 1

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

A Phase 1b, Double-Blind, Placebo-Controlled, Multiple Ascending Dose and an Open-Label Fixed-Dose Study in Patients With Autosomal Dominant Polycystic Kidney Disease to Evaluate the Safety, Tolerability, Pharmacodynamics, and Pharmacokinetics of RGLS8429

Source: ClinicalTrials.gov · Last updated 3 Jun 2025

Brief summary (registry, in English)

Primary Objectives * To assess the safety and tolerability of RGLS8429 * To assess the impact of RGLS8429 on ADPKD biomarkers Secondary Objectives * To assess the impact of RGLS8429 on height-adjusted total kidney volume (htTKV) * To characterize the pharmacokinetic (PK) properties of RGLS8429 * To assess the impact of RGLS8429 on renal function

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
68 (actual)
First submitted
24 Aug 2022
Start date
6 Oct 2022
Primary completion date
27 Jan 2025
Lead sponsor
Regulus Therapeutics Inc.
NCT number
NCT05521191

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 68
  • From 6 Oct 2022 to the primary completion date, 27 Jan 2025
  • 21 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Administration of tolvaptan in the 28 days before randomization
  • History or presence of alcoholism or drug abuse within the past 2 years prior to screening
  • Only one kidney or kidney transplant recipient
  • 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.

Other illness

  • 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

Other

  • Subject is mentally incapacitated or has significant emotional problems

Who the study is looking for

  • Male or female ADPKD patients, 18 to 70 years old
  • 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)
  • eGFR between 30 to 90 mL/min/1.73 m2
  • Body mass index (BMI) 18 to 35 kg/m2
  • Must understand and consent to the study procedures explained in the ICF and be willing and able to comply with the protocol

Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (21)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Southeastern Clinical Research Institute, LLC
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AugustaUnited StatesUnknown status
University of Maryland School of Medicine, Nephrology
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BaltimoreUnited StatesUnknown status
Northeast Clinical Research Center
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BethlehemUnited StatesUnknown status
CARE Institute
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BoiseUnited StatesUnknown status
Tufts Medical Center
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BostonUnited StatesUnknown status
University of Chicago
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ChicagoUnited StatesUnknown status
Research by Design, LLC
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ChicagoUnited StatesUnknown status
Care Institute
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ChubbuckUnited StatesUnknown status
University of Texas Southwestern Medical Center
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DallasUnited StatesUnknown status
The Idaho Kidney Institute
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Idaho FallsUnited StatesUnknown status
University of Iowa
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Iowa CityUnited StatesUnknown status
Mayo Clinic Florida
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JacksonvilleUnited StatesUnknown status
University of Kansas Medical Center Jared Grantham Kidney Institute
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Kansas CityUnited StatesUnknown status
Academic Medical Research Institute
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Los AngelesUnited StatesUnknown status
Centricity Research Phoenix Multispecialty
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MesaUnited StatesUnknown status
Yale Nephrology Outpatient Clinic
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New HavenUnited StatesUnknown status
Elixia
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OrlandoUnited StatesUnknown status
Mayo Clinic - Rochester
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RochesterUnited StatesUnknown status
St. Clair Nephrology Research
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RosevilleUnited StatesUnknown status
Swedish Center for Comprehensive Care
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SeattleUnited StatesUnknown status
Witchita Nephrology Group, PA
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WichitaUnited StatesUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.