A Phase 1/2 Dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of ABO-101 in Participants With Primary Hyperoxaluria Type 1 (PH1)
Latest Information Update: 01 Jul 2026
At a glance
- Drugs ABO 101 Arbor Biotechnologies (Primary)
- Indications Hyperoxaluria
- Focus Adverse reactions; First in man
- Acronyms RedePHine
- Sponsors Arbor Biotechnologies
Most Recent Events
- 25 Jun 2026 According to an Arbor Biotechnologies media release, Phase 1/2 redePHine clinical study to be highlighted at the upcoming 15th International Hyperoxaluria Workshop on June 26th, 2026 and John Lieske, M.D., Principal Investigator of the redePHine study.
- 06 Oct 2025 According to a Chiesi media release, Arbor and Chiesi will collaborate on the ongoing Phase 1/2 redePHine (NCT06839235) clinical study of ABO-101 in PH1.
- 30 Jul 2025 According to an Arbor Biotechnologies media release, dose escalation ongoing with enrollment at Mayo Clinic in the US and plans to open additional sites in the UK and EU in Q3 of this year.