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

Overview

Información sobre este estudio

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.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

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.

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

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

Abierto para la inscripción

Contact information:

Charles Madsen CCRP

(507) 266-9391

Madsen.Charles@mayo.edu

Jacksonville, Fla.

Investigador principal de Mayo Clinic

Fouad Chebib, M.D.

Abierto para la inscripción

Contact information:

Clinical Studies Unit

(904) 953-2255

More information

Publicaciones

Publications are currently not available
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CLS-20543555

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