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RecruitingNCT04571658ClinicalTrials.gov record

NEPTUNE Match Study

Nephrotic Syndrome in Children · Focal Segmental Glomerulosclerosis · Minimal Change Disease · Minimal Change Nephrotic Syndrome · Membranous Nephropathy · FSGS · MCD · MCD - Minimal Change Disease · Alport Syndrome

THE QUICK READ

What this study involves

The registry says this study is recruiting. Individual locations may have different availability.

Study type
Interventional
Phase
Not applicable
Age range
1 years - 80 years
Sex eligible
All sexes
Healthy volunteers
Not accepted
Participants
375 Estimated

These are starting points, not an eligibility decision. The research team must review the full requirements.

About the research

NEPTUNE Match is an additional opportunity offered to NEPTUNE study participants to prospectively recruit and communicate patient-specific clinical trial matching with kidney patients and their physician investigators.

Read the full description

This is a prospective, open-label study testing the ability to effectively communicate patient-specific clinical trial matching with kidney patients and clinician investigators. The study consists of four components:

1. Recruitment of participants from the NEPTUNE observational cohort study
2. Generation of participant profile-trial match assessment using data from the NEPTUNE observational study and profiling units by the NEPTUNE Molecular Nephrology Board
3. Establishing and testing a framework to communicate disease-trial drug mechanism matching with investigators and patients
4. Retrospective comparison of kidney health outcomes in subjects enrolled in trials that aligned with their match vs. trial subjects with mis-aligned or unknown match alignment.

Who may be able to participate?

The list below is the sponsor’s full registry wording. It can include conditions, prior treatment, test results and other requirements. A match in search does not mean you qualify.

Inclusion Criteria:

1. Consented and eligible participants in the biopsied or non-biopsied cohorts of the NEPTUNE observational study
2. Must be potentially eligible for the NEPTUNE Match partnering trials (e.g. if no trial is enrolling a participant under age 6, those under 6 are not eligible).

Note: NEPTUNE Match partnering trials and associated eligibility criteria are expected to be dynamic and change as trial protocols are developed, activated, and amended.
3. Regular nephrology healthcare provided at a NEPTUNE study site.
4. Willing and able to consent, and as appropriate assent, to participate in NEPTUNE Match

Exclusion Criteria:

Currently non-NEPTUNE observational study participants are not eligible to be matched to a clinical trial using these biomarker assessments.

Exclusion Criteria:

1\. Non-English or non-Spanish speaking

Understand screening

Treatment, groups and participation

The registry may describe treatments and study duration without a complete visit calendar. Ask the study team for the exact schedule, procedures, risks, costs and alternatives. Keep your usual care plan unless your treating clinician tells you otherwise.

Assignment
Not applicable
Masking
No masking
NEPTUNE Match Participants

Approximately 375 participants will be consented from the NEPTUNE observational study with age and demographic groups representing the patient population in the NEPTUNE study site geographical areas.

NEPTUNE observational cohort eligibility includes: participants in NEPTUNE observational cohort A are of any age and have a biopsy-confirmed diagnosis of Focal Segmental Glomerulosclerosis (FSGS), Minimal Change Disease (MCD), or Membranous Nephropathy (MN). Participants in NEPTUNE observational cohort B have documented NS based on proteinuria, serum albumin, and/or edema with age of onset less than 19 years.

Other: Communication

Communication OTHER

The NEPTUNE Match study includes an interdisciplinary Communication Team that will translate findings from the Molecular Nephrology Board (MNB) to inform patients of the matching assessment with ongoing clinical trials. This team has considerable experience with conveying complex biomedical research information to patients and families and includes experts in precision nephrology, nephrology patient \[adult and pediatric\] communication, and health education.

Prepare your questions

What researchers are measuring

Outcome measures describe what is being studied. They are not proof that a treatment works.

Primary measures

Matched participants with at least one clinical trial receive a MNB assessment

Time frame: 0-4 weeks

Proportion of NEPTUNE Match participants with at least one matching clinical trial, defined as receiving a Molecular Nephrology Board (MNB) assessment that provides a match to at least one targeted therapy in an ongoing clinical trial

Efficacy of communication methods at time of communication visit, measured by Teach Back 1 summary score

Time frame: 12 weeks

Key findings from MNB trial matching analyses and deliberations will be conveyed to study participants using a NEPTUNE Match Report that summarizes the findings. The report indicates the strength of matching to ongoing clinical trials and the uncertainty and research origins of the information. A sample Match Report can be found in Appendix C. The report will not contain individual data elements reviewed by the MNB. The creation of NEPTUNE Match Reports will follow health education principles including matching of content to patients' informational needs and health literacy levels, use of visual aids to clarify meaning of information, and avoidance of information overload of the participant.

Kidney health endpoints that are specific to each individual trial

Time frame: 0-60 months

The analytic integration supporting the Molecular Nephrology Board (MNB) case review will be initiated and will occur. The MNB will conduct the discussion and generate the integrated data summary and case report inclusive of clinical trial matching by webinar. Input from the MNB will be used to generate a final version of the participant NEPTUNE Match Report. This is a longitudinal outcome that will be assessed at the end of the study relative to endpoints specific to matched clinical trials, assessing the superiority of stratification (matching or alignment of patient molecular profiles to targeted therapies in clinical trials) to non-stratification.

Secondary measures

Efficacy of communication methods at follow up, measured by Teach Back of key concepts

Time frame: 14-18 weeks

3 defined teachback concepts will be scored to indicate the participant's understanding of strength of matching.

Psychological distress measured by the STAI assessment

Time frame: 14-18 weeks

State Trait Anxiety Inventory (mini-STAI) scale will be used to assess a participant's psychological distress around their participation in NEPTUNE Match at the consent visit and the follow up visit.

Psychological distress measured by the FACToR-NEPTUNE assessment

Time frame: 14-18 weeks

FACToR-NEPTUNE is a measure that has been modified from the Feelings About genomiC Testing Results (FACToR). FACToR-12 is used to assess the psychosocial impact of returning genomic findings to patients in research and clinical practice. In the FACToR-NEPTUNE assessment the measure will assess the psychosocial impact after receiving the NEPTUNE Match Report.

No results are flagged as posted.

Review the complete result tables and limitations in the official record.

Open official results ↗

Research locations (16)

The overall study status and a local site’s status can differ. Confirm that location’s availability before traveling.

16 locations

Emory University Hospital - Children's Hospital of AtlantaAtlanta, Georgia, United StatesRecruiting
Emily YunCONTACTemily.yun@emory.edu
Laurence Greenbaum, MD, PhDPRINCIPAL_INVESTIGATOR
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John H. Stroger, Jr., Hospital of Cook CountyChicago, Illinois, United StatesRecruiting
University of Kansas Medical CenterKansas City, Kansas, United StatesRecruiting
Catherine CreedCONTACTccreed@kumc.edu
Ellen McCarthy, MDPRINCIPAL_INVESTIGATOR
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Johns Hopkins MedicineBaltimore, Maryland, United StatesRecruiting
MIahje WilliamsCONTACTmwil296@jhmi.edu
Meredith Adkinson, MDPRINCIPAL_INVESTIGATOR
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University of MichiganAnn Arbor, Michigan, United StatesBy invitation
Children's Mercy HospitalKansas City, Missouri, United StatesRecruiting
Kelsey MarkusCONTACTkemarkus@cmh.edu
Tarak Srivastava, MDPRINCIPAL_INVESTIGATOR
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Northwell/Cohen's Children's HospitalNew Hyde Park, New York, United StatesRecruiting
Suzanne Vento, BSNCONTACTsvento@northwell.edu
Christine Sethna, MD, MSPRINCIPAL_INVESTIGATOR
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Columbia University Medical CenterNew York, New York, United StatesRecruiting
Anup PradhanCONTACT
Pietro Canetta, MDPRINCIPAL_INVESTIGATOR
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University of North Carolina Chapel HillChapel Hill, North Carolina, United StatesRecruiting
Anne FromentCONTACTanne_froment@med.unc.edu
Maria Fernanda Ochoa ToroCONTACTferochoc@email.unc.edu
Vimal Derebail, MD, MSPRINCIPAL_INVESTIGATOR
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Cleveland Clinic FoundationCleveland, Ohio, United StatesRecruiting
Stefanie LarsonCONTACTlarsons2@ccf.org
Katherine Dell, MDPRINCIPAL_INVESTIGATOR
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Hospital of the University of PennsylvaniaPhiladelphia, Pennsylvania, United StatesRecruiting
Krishna Kallem, MSCONTACTKrishna.Kallem@pennmedicine.upenn.edu
Larry Holzman, MDPRINCIPAL_INVESTIGATOR
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Temple UniversityPhiladelphia, Pennsylvania, United StatesRecruiting
Zoe PfefferCONTACTzoe.pfeffer@tuhs.temple.edu
Iris Lee, MDPRINCIPAL_INVESTIGATOR
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Medical University of South CarolinaCharlotte, South Carolina, United StatesRecruiting
David Selewski, MD, MSPRINCIPAL_INVESTIGATOR
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Seattle Children's HospitalSeattle, Washington, United StatesRecruiting
Sangeeta Hingorani, MDPRINCIPAL_INVESTIGATOR
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University of Washington Medical CenterSeattle, Washington, United StatesRecruiting
Linda Manahan, BSNCONTACTlmanahan@nephrology.washington.edu
Ashley Jefferson, MDPRINCIPAL_INVESTIGATOR
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Providence Sacred Heart Medical CenterSpokane, Washington, United StatesRecruiting
Kelli KuykendallCONTACTkelli.kuykendall@providence.org
Katherine Tuttle, MDPRINCIPAL_INVESTIGATOR
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Study team and timeline

Lead sponsor
University of Michigan
Study start
May 2, 2022 Actual
Primary completion
Dec 30, 2029 Estimated
Study completion
Dec 30, 2029 Estimated
First posted
Oct 1, 2020 Actual
Last updated
Nov 10, 2026 Actual

Official study contacts

Hailey E Desmond, MSCONTACTheturner@med.umich.edu734-232-4851
Chrysta C Lienczewski, BSCONTACTboridley@med.umich.edu734-615-5021
Official study title

Implementing Precision Medicine for Glomerular Diseases in the Nephrotic Syndrome Study Network (NEPTUNE)

A HUMAN NEXT STEP

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Source: ClinicalTrials.gov API v2. Information is submitted by sponsors and investigators. NLM does not approve the safety or science of all listed studies. Registry disclaimer.

Retrieved: Nov 11, 2026 · Last registry update: Nov 10, 2026