Abstract

Chronic respiratory diseases are the third leading cause of death, behind cardiovascular diseases and cancer, affecting approximately 550 million of people all over the world. Most of the chronic respiratory diseases are attributable to asthma and chronic obstructive pulmonary disease (COPD) with this latter being the major cause of deaths. Despite differences in etiology and symptoms, a common feature of asthma and COPD is an underlying degree of airways inflammation. The nature and severity of this inflammation might differ between and within different respiratory conditions and pharmacological anti-inflammatory treatments are unlikely to be effective in all patients. A precision medicine approach is needed to selectively target patients to increase the chance of therapeutic success. Inhibitors of the phosphodiesterase 4 (PDE4) enzyme like the oral PDE4 inhibitor roflumilast have shown a potential to reduce inflammatory-mediated processes and the frequency of exacerbations in certain groups of COPD patients with a chronic bronchitis phenotype. However, roflumilast use is dampened by class related side effects as nausea, diarrhea, weight loss and abdominal pain, resulting in both substantial treatment discontinuation in clinical practice and withdrawal from clinical trials. This has prompted the search for PDE4 inhibitors to be given by inhalation to reduce the systemic exposure (and thus optimize the systemic safety) and maximize the therapeutic effect in the lung. Tanimilast (international non-proprietary name of CHF6001) is a novel highly potent and selective inhaled PDE4 inhibitor with proven anti-inflammatory properties in various inflammatory cells, including leukocytes derived from asthma and COPD patients, as well as in experimental rodent models of pulmonary inflammation. Inhaled tanimilast has reached phase III clinical development by showing promising pharmacodynamic results associated with a good tolerability and safety profile, with no evidence of PDE4 inhibitors class-related side effects. In this review we will discuss the main outcomes of preclinical and clinical studies conducted during tanimilast development, with particular emphasis on the characterization of the pharmacodynamic profile that led to the identification of target populations with increased therapeutic potential in inflammatory respiratory diseases.

Highlights

  • Phosphodiesterase-4 (PDE4) is a cyclic adenosine 3 monophosphate-specific phosphodiesterase located predominantly in cells involved in inflammation

  • Tanimilast was selected among a series of novel benzoic ester derivatives for its potent and selective inhibitory activity versus phosphodiesterase 4 (PDE4) combined with ADME and pharmacokinetics properties rendering it suitable for inhaled administration

  • Preclinical studies conducted with tanimilast in different rodent models of acute and sub-chronic pulmonary inflammation triggered by different stimuli, ranging from bacterial endotoxins, to allergens and cigarette smoke, showed robust anti-inflammatory effects

Read more

Summary

Introduction

Phosphodiesterase-4 (PDE4) is a cyclic adenosine 3 monophosphate (cAMP)-specific phosphodiesterase located predominantly in cells involved in inflammation. Approximately 30–40% of patients are reported to continue to have moderate or severe exacerbations despite being treated with triple inhaled therapy (ICS plus LABA plus LAMA) (Vestbo et al, 2017; Langham et al, 2019) These patients have limited additional add-on treatment options: GOLD suggests azithromycin treatment for former smokers or the oral PDE4 inhibitor roflumilast in patients with a chronic bronchitis phenotype and with forced expiratory volume in 1 s (FEV1) lower than 50% of their predicted value (GOLD, 2021). Tanimilast (international nonproprietary name (INN) of CHF6001) is a novel PDE4 inhibitor that has been designed and formulated to be delivered via inhalation and to have a robust pulmonary anti-inflammatory profile coupled with low systemic exposure and low emetic effects (Moretto et al, 2015) (Villetti et al, 2015).

Objectives
Methods
Findings
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call