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DOI 10.1016/j.ebiom.2022.104069

Медицинская библиотека · EBioMedicine · 2022

Safety, tolerability, and anti-fibrotic efficacy of the CBP/β-catenin inhibitor PRI-724 in patients with hepatitis C and B virus-induced liver cirrhosis: An investigator-initiated, open-label, non-randomised, multicentre, phase 1/2a study.

Kimura Kiminori, Kanto Tatsuya, Shimoda Shinji, Harada Kenichi, Kimura Masamichi, Nishikawa Koji, Imamura Jun, Ogawa Eiichi, Saio Masanao, Ikura Yoshihiro, Okusaka Takuji, Inoue Kazuaki, Ishikawa Tetsuya, Ieiri Ichiro, Kishimoto Junji, Todaka Koji, Kamisawa Terumi

Клиническое исследование I фазыКонтролируемое клиническое исследованиеСтатьяМногоцентровое исследованиеПеревод пока не подготовлен

Аннотация

BACKGROUND

We conducted an exploratory study to assess the safety tolerability, and anti-fibrotic effects of PRI-724, a CBP/β-catenin inhibitor, in patients with hepatitis C virus (HCV)- and hepatitis B virus (HBV)-induced cirrhosis.

METHODS

This multicentre, open-label, non-randomised, non-placebo-controlled phase 1/2a trial was conducted at three hospitals in Japan. Between July 27, 2018, and July 13, 2021, we enrolled patients with HCV- and HBV-induced cirrhosis classified as Child-Pugh (CP) class A or B. In phase 1, 15 patients received intravenous infusions of PRI-724 at escalating doses of 140, 280, and 380 mg/m2/4 h twice weekly for 12 weeks. In phase 2a, 12 patients received the recommended PRI-724 dose. The primary endpoints of phases 1 and 2a were the frequency and severity of adverse events and efficacy in treating cirrhosis based on liver biopsy. This study was registered at ClinicalTrials.gov (no. NCT03620474).

FINDINGS: Three patients from phase 1 who received the recommended PRI-724 dose were evaluated to obtain efficacy and safety data in phase 2a. Serious adverse events occurred in three patients, one of which was possibly related to PRI-724. The most common adverse events were diarrhoea and nausea. PRI-724 did not decrease hepatic fibrosis with any statistical significance, either by ordinal scoring or measurement of collagen proportionate area at 12 weeks; however, we observed statistically significant improvements in liver stiffness, Model for End-stage Liver Disease score, and serum albumin level.

INTERPRETATION: Intravenous administration of 280 mg/m2/4 h PRI-724 over 12 weeks was preliminarily assessed to be well tolerated; however, further evaluation of anti-fibrotic effects in patients with cirrhosis is warranted.

FUNDING: AMED, Ohara Pharmaceutical.

Для цитирования: Kimura Kiminori, Kanto Tatsuya, Shimoda Shinji, Harada Kenichi, Kimura Masamichi, Nishikawa Koji, Imamura Jun, Ogawa Eiichi, Saio Masanao, Ikura Yoshihiro, Okusaka Takuji, Inoue Kazuaki, Ishikawa Tetsuya, Ieiri Ichiro, Kishimoto Junji, Todaka Koji, Kamisawa Terumi. Safety, tolerability, and anti-fibrotic efficacy of the CBP/β-catenin inhibitor PRI-724 in patients with hepatitis C and B virus-induced liver cirrhosis: An investigator-initiated, open-label, non-randomised, multicentre, phase 1/2a study.. EBioMedicine. 2022. DOI: 10.1016/j.ebiom.2022.104069.

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