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Not recruiting
Phase 1

RGLS8429

Sponsor:

Regulus Therapeutics Inc.

Code:

NCT05521191

Conditions

Autosomal Dominant Polycystic Kidney Disease

ADPKD

Polycystic Kidney, Autosomal Dominant

Eligibility Criteria

Sex: All

Age: 18 - 70

Healthy Volunteers: Not accepted

Interventions

RGLS8429

Placebo

Study Details

Brief summary:

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

Conditions

Autosomal Dominant Polycystic Kidney Disease

ADPKD

Polycystic Kidney, Autosomal Dominant

Study ID

NCT05521191

Start date

Oct 6, 2022

Status verified date

Apr, 2024

Completion date

Jun, 2025

Anticipated

Primary completion date

Apr, 2025

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70

Healthy Volunteers: Not accepted

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 m2
4. Body mass index (BMI) 18 to 35 kg/m2
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.

Study Design

Enrollment

70 participants

Anticipated

Allocation

Randomized

Intervention Model

Sequential

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: RGLS8429

The randomized,double blind part of the study (Part A) will consist of three sequential cohorts of approximately 12 subjects each randomized centrally to receive RGLS8429 or placebo by subcutaneous injection every other week (Q2W) x 7 doses (36 subjects total).

  • Cohort 1: first dose level of RGLS8429 or placebo
  • Cohort 2: second dose level of RGLS8429 or placebo
  • Cohort 3: third dose level of RGLS8429 or placebo

experimental: Placebo

The randomized double blind part of the study (Part A) will consist of three sequential cohorts of approximately 12 subjects each randomized centrally to receive RGLS8429 or placebo by subcutaneous injection every other week (Q2W) x 7 doses (36 subjects total).

  • Cohort 1: first dose level of RGLS8429 or placebo
  • Cohort 2: second dose level of RGLS8429 or placebo
  • Cohort 3: third dose level of RGLS8429 or placebo

experimental: Open Label Fixed Dose RGLS8429

The open-label fixed dose part of the study (Part B and Cohort 4) will consist of a single cohort of up to 30 subjects each receiving 300 mg RGLS8429.

Interventions

RGLS8429

Solution for subcutaneous injection

Placebo

Solution for subcutaneous injection

Primary outcome measure

  • Safety and tolerability of RGLS4829: Incidence of AEs [ Time Frame: Baseline to Day 113 ]
  • Impact of RGLS8429 on ADPKD biomarkers [ Time Frame: Baseline to Day 113 ]

Central Contacts and Locations

Central contacts

Locations

Academic Medical Research Institute

Recruiting

Los Angeles, California, United States, 90022

Contacts

Yale Nephrology Outpatient Clinic

Recruiting

New Haven, Connecticut, United States, 06510

Contacts

Mayo Clinic - Florida

Recruiting

Jacksonville, Florida, United States, 32224

Contacts

Southeastern Clinical Research Institute, LLC

Recruiting

Augusta, Georgia, United States, 30904

Contacts

CARE Institute

Recruiting

Boise, Idaho, United States, 83706

Contacts

CARE Institute

Recruiting

Chubbuck, Idaho, United States, 83202

Contacts

The Idaho Kidney Institute

Recruiting

Idaho Falls, Idaho, United States, 83404

Contacts

University of Chicago

Recruiting

Chicago, Illinois, United States, 60617

Contacts

Research by Design, LLC

Recruiting

Chicago, Illinois, United States, 60643

Contacts

University of Iowa

Recruiting

Iowa City, Iowa, United States, 52242

Contacts

University of Kansas Medical Center Jared Grantham Kidney Institute

Recruiting

Kansas City, Kansas, United States, 66160

Contacts

Witchita Nephrology Group, PA

Recruiting

Wichita, Kansas, United States, 67214

Contacts

University of Maryland School of Medicine, Nephrology

Recruiting

Baltimore, Maryland, United States, 21201

Contacts

Tufts Medical Center

Recruiting

Boston, Massachusetts, United States, 02111

Contacts

St. Clair Nephrology Research

Recruiting

Roseville, Michigan, United States, 48066

Contacts

Rosemarie Henschel, RN

313-432-6273rhenschel@scsp.net

Mayo Clinic - Rochester

Recruiting

Rochester, Minnesota, United States, 55905

Contacts

Northeast Clinical Research Center

Recruiting

Bethlehem, Pennsylvania, United States, 18017

Contacts

Nelson Kopyt, MD

610-433-4100

University of Texas Southwestern Medical Center

Recruiting

Dallas, Texas, United States, 75390

Contacts

Swedish Center for Comprehensive Care

Recruiting

Seattle, Washington, United States, 98104

Contacts

More Information

Sponsor

Regulus Therapeutics Inc.

Last update posted

Apr 30, 2024

Last verified

Apr, 2024

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-13. This information was provided to ClinicalTrials.gov by Regulus Therapeutics Inc. on 2024-04-30.