- Sepiapterin is rapidly converted to BH4 and normalises blood phenylalanine to less than 130 µmol/L by Day 2 at all tested doses.
- Blood BH4 concentrations increased with dose, peaking approximately 3 to 4 hours, about 2 to 3 hours after the sepiapterin peak.
- Well tolerated; seven of eight participants had non-severe treatment-emergent adverse events; none were serious, dose-limiting, or led to discontinuation.
Mol Ther. 2026 Sep 10:S1525-0016(26)00775-6. doi: 10.1016/j.ymthe.2026.09.005. Online ahead of print.
ABSTRACT
Oral sepiapterin (PTC923), a precursor of tetrahydrobiopterin (BH4), was evaluated in patients with 6-pyruvoyl-tetrahydropterin synthase (PTPS) deficiency in a phase 1/2, multicenter, open-label, randomized, intra-individual dose-escalation study. Patients stopped sapropterin (used to control hyperphenylalaninemia) for 2-4-days before being randomized 1:1 into 2 cohorts receiving sepiapterin at 2 doses (Cohort 1: 2.5 and 10 mg/kg/day; Cohort 2: 5 and 20 mg/kg/day) each for 7 days, separated by a 2-4-day washout period. Eight participants (5 male, 3 female, aged 2.2-20.0 years) completed the study (4 in each cohort). Overall, 7/8 participants (87.5%) experienced a total of 35 treatment-emergent adverse events; none were severe, serious, or led to discontinuation. Mean phenylalanine levels increased (up to 800-1200 μmol/L) after discontinuation of sepiapterin or sapropterin, and normalized (<130 μmol/L) with sepiapterin at all tested doses by Day 2. Blood BH4 concentrations increased with increasing single doses of sepiapterin, reaching a peak at approximately 3-4 hours, which was 2-3 hours after the sepiapterin peak. These results show that in patients with PTPS deficiency, sepiapterin is rapidly converted to BH4 and normalizes blood phenylalanine concentrations, with no dose-limiting toxicity or dose-related adverse events.
PMID:42723281 | DOI:10.1016/j.ymthe.2026.09.005
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