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NCT06839235 · ClinicalTrials.gov registry record · Phase 1

Phase 1/2 Study of ABO-101 in Primary Hyperoxaluria Type 1 (redePHine)

A Phase 1 study of Primary Hyperoxaluria Type 1 (PH1), sponsored by Arbor Biotechnologies.

Recruiting
Registry status
Phase 1
Development phase
23
Enrollment target
7
Study locations

NCT06839235 is a Phase 1 study of Primary Hyperoxaluria Type 1 (PH1) that is actively recruiting participants, run by Arbor Biotechnologies. The registered enrollment target is 23 participants. The trial reports 7 study locations across 2 states.

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The verdict

NCT06839235, a Phase 1 study of Primary Hyperoxaluria Type 1 (PH1), is actively recruiting participants, sponsored by Arbor Biotechnologies.

RECRUITING
Registry status
Phase 1
Development phase
23 participants
Enrollment target
7
Study locations

Study Summary

The goal of the redePHine study is to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of ABO-101 in participants with primary hyperoxaluria type 1 (PH1). The trial will consist of 2 Study Periods. During the first Study Period, there will be 2 parts. In Part A, adult participants will be treated with a single ascending dose to identify a recommended dose. In Part B, pediatric participants will be treated with the recommended dose. Following the first Study Period, participants will start Study Period 2, a long-term monitoring program to comply with local and national requirements.

Interventions

  • DRUG ABO-101

Study Locations (7)

Other

  • Hospices Civils de Lyon- Hôpital Femmes Mères Enfants - Lyon
  • Kindernierenzentrum Bonn - Bonn
  • Heidi Chaker - Sfax
  • Queen Elizabeth Hospital Birmingham - Birmingham
  • Royal Free Hospital - London

Minnesota

  • Mayo Clinic - Rochester
  • Nucleus Network - Saint Paul

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2025-06-16
Est. Completion 2043-02
Phase Phase 1

Sponsor

Arbor Biotechnologies

1 total trials

What the Registry Record Tells You About NCT06839235

The ClinicalTrials.gov registry entry for NCT06839235 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 23 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Arbor Biotechnologies, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Primary Hyperoxaluria Type 1 (PH1) appearing as the primary indexed condition, and to 1 intervention - of which ABO-101 is the first listed.

NCT06839235 reports 7 study locations spanning 2 distinct geographic areas - top geographies include Other, Minnesota.

Frequently Asked Questions

What is clinical trial NCT06839235 about?

NCT06839235 is a clinical study titled "Phase 1/2 Study of ABO-101 in Primary Hyperoxaluria Type 1 (redePHine)". The goal of the redePHine study is to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of ABO-101 in participants with primary hyperoxaluria type 1 (PH1). The trial will consist of 2 Study Periods. During the first Study Period, there will be 2 parts. In Part A, adult partic...

What is the current status of trial NCT06839235?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 23 participants. The study started on 2025-06-16. Estimated completion is 2043-02.

What conditions does trial NCT06839235 study?

This clinical trial studies the following conditions: Primary Hyperoxaluria Type 1 (PH1).

What interventions are being tested in trial NCT06839235?

The interventions under investigation include: ABO-101 (DRUG).

Who is sponsoring clinical trial NCT06839235?

This trial is sponsored by Arbor Biotechnologies, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06839235 being conducted?

This trial has 7 study locations across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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