WebOct 14, 2024 · Ofev is an approved anti-fibrotic therapy (a medication that reduces lung tissue scarring), marketed by Boehringer Ingelheim , for the treatment of idiopathic pulmonary fibrosis (IPF) and scleroderma. The medication works by interfering with the PDGF and FGF signaling pathways, known to be overly active in patients with lung fibrosis … WebOFEV is proven to reduce lung function decline1 OFEV (nintedanib) SIGNIFICANTLY REDUCED THE ANNUAL RATE OF DECLINE IN FVC BY 57% IN PATIENTS WITH CHRONIC FIBROSING ILDs WITH A PROGRESSIVE PHENOTYPE VS PLACEBO1* INBUILD®1,2 Zoom * The annual rate of decline in FVC (mL/year) was analyzed using a random coefficient …
InPedILD_trial_enrollment Boehringer Ingelheim
WebAug 12, 2024 · This new study builds on the Phase III INBUILD® trial and approval of Ofev® in adult patients with fibrosing ILDs with a progressive phenotype1,2,3 Global Phase III multicentre clinical trial is planned to be conducted in approximately 70 sites in 24 countries WebReferences. 1. Clinical Study Report: c26471552-02. INBUILD®: A double-blind, randomized, placebo-controlled trial evaluating the efficacy and safety of nintedanib over 52 weeks in patients with Progressive Fibrosing … my glamm india
OFEV® Safety Profile & Side Effects OFEV® (nintedanib) Global
WebOFEV is a prescription medication used to treat adults with IPF and a chronic ILD with worsening fibrosis. It is also used to slow the rate of decline in lung function in adults with SSc-ILD. Take a closer look at how OFEV performed in clinical trials. Idiopathic Pulmonary Fibrosis (IPF) Chronic ILD with Worsening Fibrosis WebMar 4, 2024 · The INBUILD trial, which was published in the New England Journal of Medicine, was a randomized, double-blind, placebo-controlled, parallel group trial conducted at 153 sites in 15 countries that evaluated the efficacy and safety of OFEV ® (150 mg, twice-daily) over 52 weeks in patients with chronic fibrosing ILDs with a progressive disease ... WebA post hoc subgroup analysis of the INBUILD® trial data was used to evaluate the treatment effect (annual rate of FVC decline) of OFEV in patients with underlying autoimmune disease. Of the 663 patients in the trial, 170 (25.6%) had an underlying autoimmune ILD This is a post hoc subgroup analysis. my g kozhikode contact number