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Study 19 of 25Pasireotide literatureClinical pharmacology in drug development · RCT2026

Phase 1 Study of Paltusotine, a Novel Oral Once‑Daily, Nonpeptide Selective Somatostatin Receptor 2 Agonist, in Healthy Japanese Adults.

Paltusotine shows a dose-dependent pharmacokinetic profile and safety in healthy adults, but the small sample size and short duration of the study limit the conclusions about its clinical utility.

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Where it sits

this study against the rest of the pasireotide corpus
1
Preclinical
16
Observational
0
Open-label
3
Randomised · this one
5
Reviews

Summary and findings

This study evaluated the pharmacokinetics, pharmacodynamics, and safety of paltusotine in healthy Japanese adults at single doses of 20, 40, 60, and 80 mg, and at a repeated dose of 40 mg once daily for 7 days. No deaths or serious adverse events were reported. The study aimed to support the development of paltusotine for conditions like acromegaly and pituitary gigantism.

How much of this paper we could read: full text read (0.80). We had a clear abstract, so the summary below closely tracks the paper. What this means →
Elimination half-life (t<sub>1/2</sub>) was 24-28 h.2026

Abstract

The authors’ words, as Clinical pharmacology in drug development supplied them

Paltusotine is a novel, nonpeptide, once-daily oral, selective somatostatin 2 receptor (SST2) agonist. We evaluated the pharmacokinetics, pharmacodynamics, and safety of oral paltusotine in healthy Japanese adults in single‑dose (20, 40, 60, 80 mg) and repeated‑dose (40 mg once daily for 7 days in a two-sequence, two‑period crossover design) studies. In addition, the effects of food intake and pharmacodynamics were examined in the repeated-dose study. Eight participants were enrolled in each dose of the single-dose study, and 12 participants were enrolled in the repeated-dose study. In both studies, there were no deaths, serious adverse events, or severe adverse events. In the single-dose study, plasma paltusotine exposures increased in a dose-dependent manner for the dose range of 20 to 80 mg (based on C<sub>max</sub> and AUC<sub>0-∞</sub>), and the elimination half-life (t<sub>1/2</sub>) was 24-28 h. In the repeated-dose study, similar reductions from baseline in serum insulin-like growth factor-1 (IGF-I) were observed for 1-h pre-prandial (-60.1 ± 26.0 ng/mL) and 3-h post-prandial administration (-61.6 ± 17.7 ng/mL) on Day 7. Overall, this study establishes the pharmacokinetics, pharmacodynamics, and safety in healthy Japanese adults to support the development of paltusotine as a treatment for acromegaly and pituitary gigantism.

Elsewhere in the Pasireotide corpus

BApproach to the patient: precision medicine-guided evaluation and treatment of acromegaly.The Journal of clinical endocrinology and metabolism · 2026 · 80% of patients achieved hormonal control with biomarker-guided treatment.reviewBTirzepatide for pasireotide-induced hyperglycemia in a GH/TSH-producing pituitary adenoma/PitNET: a case report and literature review.Endocrine journal · 2026 · n=1 · HbA1c decreased from 7.7% to 6.3% after switching to tirzepatide.HumanBTirzepatide for pasireotide-induced hyperglycemia in a GH/TSH-producing pituitary adenoma/PitNET: a case report and literature review.Endocrine journal · 2026 · n=1 · HbA1c decreased from 7.7% to 6.3%.HumanBCase Report: Pasireotide treatment in neonatal congenital hyperinsulinism due to a homozygous ABCC8 mutation.Frontiers in endocrinology · 2023 · n=1 · Not reported in abstract.HumanBFourteen-year bridge to cure in occult ectopic ACTH syndrome: resection of a 3-mm pulmonary carcinoid.JCEM case reports · 2026 · Not reported in abstract.HumanAReduced breakthrough symptom exacerbations in patients with biochemically controlled acromegaly switched from injected depot somatostatin receptor ligands to once-daily oral paltusotine in the PATHFNDR-1 clinical trial.Pituitary · 2026 · 6.2% (1.6%) of days with symptom exacerbations after switching to paltusotine, n=22, p<0.0001.Human