Emerging treatments

Tezepelumab

Tezepelumab is a monoclonal antibody directed against thymic stromal lymphopoietin (TSLP).[165]​ TSLP activates a broad range of immune cells to support a Th2 cell inflammatory response.[166] Tezepelumab has been granted orphan drug designation by the FDA.

RPC4046

In one phase 2 trial of patients with EoO, RPC4046, a monoclonal antibody directed against interleukin (IL)-13, reduced histological and endoscopic features compared with placebo.[167]

Immunomodulators

Mercaptopurine and azathioprine can suppress oesophageal eosinophilia. They may play a role in maintaining long-term remission in limited cases: for example, those with refractory disease or those in whom corticosteroid therapy is contraindicated. At present, however, there is insufficient evidence to recommend immunomodulators and biologicals typically used for inflammatory bowel diseases in the management of EoO.[2][106]​​ 

Etrasimod

Etrasimod is a selective sphingosine-1 phosphate (S1P) receptor modulator. S1P is an extracellular signalling molecule which regulates lymphocyte trafficking and modulates vascular tone and barrier function.[168] In the phase 2 VOYAGE study, 108 patients with EoO were randomised to receive oral etrasimod at different doses (n=41 and n=39) or placebo (n=28). Statistically significant reductions in percentage change from baseline (CFB) in oesophageal peak eosinophil count (PEC) and reductions in absolute CFB in EoO-Histology Scoring System grade and stage scores were observed at week 24 with both doses, with no serious treatment-emergent adverse effects. A 46.1% decrease in PEC (P=0.0103) at week 16 was observed with the higher dose of etrasimod, thus meeting the primary endpoint. Further evaluation is warranted.[169][170]​​

Immune-resetting peptides

An immune-resetting peptide known as ′1104 has been granted orphan drug designation by the FDA. The designation is based on findings of one phase 2A trial comprising patients with EoO in whom a statistically significant improvement in DSQ was observed with ′1104, compared with the placebo, which sustained for four weeks post the last dose.[171] Additionally, a statistically significant reduction in eosinophils, CD4+, and CD8+ cells from baseline is reported.[171] A phase 2B trial is planned.​​

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