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Profil bibliographique

Y Liu

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

3Publications signalées
12Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Interstitial Lung Diseases and Idiopathic Pulmonary FibrosisPulmonary Hypertension Research and TreatmentsSystemic Sclerosis and Related DiseasesInflammatory Myopathies and DermatomyositisPhosphodiesterase function and regulation

Les publications récentes

2025 conference-paper OpenAlex

Baseline characteristics of patients enrolled in FIBRONEER(TM)-IPF, a Phase III randomised placebo-controlled trial of the preferential PDE4B inhibitor BI 1015550 in patients with idiopathic pulmonary fibrosis

D. Koschel, Luca Richeldi, S Assassi, Arata Azuma et autres

Rationale Current antifibrotic (AF) treatments for idiopathic pulmonary fibrosis (nintedanib and pirfenidone) slow, but do not stop decline in pulmonary function. BI 1015550 is an oral preferential phosphodiesterase 4B (PDE4B) inhibitor that is under investigation for treatment of IPF. In a randomized …

it, jp, fr, no, de, us, tw, gb, ca, es, nl (code pays fourni par la source)

0 citations Pneumologie
Accès ouvert 2023 article OpenAlex

Effects of nintedanib in patients with limited cutaneous systemic sclerosis and interstitial lung disease

Yannick Allanore, Dinesh Khanna, Vanessa M. Smith, Martin Aringer et autres

OBJECTIVES: To investigate the course of interstitial lung disease (ILD) and the effects of nintedanib in patients with limited cutaneous systemic sclerosis (lcSSc). METHODS: In the SENSCIS trial, patients with SSc-ILD were randomized to receive nintedanib or placebo. Patients who completed the …

fr, us, be, de, no, jp, cn, il, gb (code pays fourni par la source)

12 citations Lara D. Veeken
2023 article OpenAlex

Design of Phase III, Randomized, Placebo-Controlled Trials of BI 1015550 in Patients with Progressive Fibrosing Interstitial Lung Disease and Idiopathic Pulmonary Fibrosis (FIBRONEER-ILD / -IPF)

Michael Kreuter, Toby M. Maher, Arata Azuma, Vincent Cottin et autres

Background/Purpose There is a need for better treatments that modify the disease course and improve symptoms of idiopathic pulmonary fibrosis (IPF) and other progressive fibrosing interstitial lung diseases (PF-ILD). BI 1015550, a preferential phosphodiesterase 4B inhibitor, prevented lung function decline in a …

de, us, jp, fr, no, es, nl, it (code pays fourni par la source)

0 citations Pneumologie

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