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Novel PDE4B inhibitor offers breakthrough for IPF

Presented by
Prof. Luca Richeldi, UniversitĆ  Cattolica del Sacro Cuore, Italy
Conference
ATS 2022
Trial
Phase 2
Doi
https://doi.org/10.55788/ec3f9465
Findings from a phase 2, randomised, placebo-controlled trial in patients with idiopathic pulmonary fibrosis (IPF) showed that the investigational drug BI 1015550, either alone or with background use of an antifibrotic agent, significantly prevented a decrease in lung function.

The anti-inflammatory and immunomodulatory abilities of oral, selective phosphodiesterase 4B (PDE4B) inhibition had not yet been explored clinically for IPF. Prof. Luca Richeldi (UniversitĆ  Cattolica del Sacro Cuore, Italy) presented the first clinical results of the novel, investigational, preferential, oral PDE4B inhibitor BI 1015550 with or without background antifibrotics in a phase 2 study (NCT04419506) [1]. The findings were simultaneously published in the New England Journal of Medicine [2].

IPF is a progressive, irreversible lung disease with high mortality. Currently, 2 antifibrotic drugs (i.e. nintedanib and pirfenidone) have been approved that slow but do not stop fibrotic progression [3,4]. There remains an unmet need for additional treatments that can be used alone or with existing antifibrotic therapies. In preclinical studies, the preferential PDE4B inhibitor BI 1015550 demonstrated anti-inflammatory and antifibrotic effects [5].

The participants were randomised to receive either 18 mg of the investigational drug oral twice daily (n=97) or placebo (n=50) for 12 weeks, with an additional 1 week of follow-up. Randomisation was based on stratification of use of antifibrotics. The primary endpoint was change in baseline in forced vital capacity (FVC) at 12 weeks. The secondary endpoint was the percentage of participants with treatment-emergent adverse events.

The primary endpoint was evaluated separately in participants with and without background antifibrotic therapy at baseline in a 2-step procedure. Firstly, data from the current trial were analysed with a restricted maximum likelihood-based approach using a mixed model with repeated measurements (MMRM). Secondly, the pre-specified primary analysis of FVC change was based on a Bayesian approach combining MMRM estimates and historical data for the placebo arm.

The primary endpoint was met; the change in FVC at week 12 and over time in all participants showed a remarkable improvement in the participants taking the investigational drug with an adjusted mean of +4.6 mL versus -83.8 mL for the placebo arm (D88.4 mL; 95% CI 40.7ā€“136.0). When stratifying the groups based on background antifibrotic therapy, the effect was maintained; using Bayesian modelling, patients without background antifibrotics showed a +5.7 mL mean improvement in FVC vs -81.4 mL (D87.1 mL) and those with background antifibrotics had a +2.9 mL FVC improvement on the drug as opposed to a -59.2 mL decrease in the placebo (D62.1 mL). Both calculations predicted a >98% probability that BI 1015550 is superior to placebo. The trial also met the secondary endpoint, as BI 1015550 demonstrated acceptable safety and tolerability in trial participants over 12 weeks.

In conclusion, compared with placebo, treatment with the investigational PDE4B inhibitor BI 1015550, either alone or concomitant with background antifibrotic agents, prevented a decline in lung function in patients with IPF. The observed safety and tolerability of BI 1015550 were acceptable and, in combination with the beneficial effects on FVC, warrant further clinical development as a treatment for IPF and possibly other forms of progressive pulmonary fibrosis.

  1. Richeldi L, et al. Phosphodiesterase Inhibition as a Novel Strategy to Stop Fibrosis in the Lung. Session B12, ATS International Conference 2022, San Francisco, CA, USA, 13ā€“18 May.
  2. Richeldi L, et al. N Engl J Med 2022. Doi: 10.1056/NEJMoa2201737.
  3. Richeldi L, et al. N Engl J Med 2014;370(22):2071ā€“2082.
  4. Noble PW, et al. Eur Respir J. 2016;47(1):243ā€“253.
  5. Herrmann FE, et al. Front Pharmacol. 2022;13:838449.

 

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