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P2X3 receptor antagonists reduce objective cough frequency by 29.3% in refractory chronic coughP2X3 Receptor Antagonists Show Promise for Chronic Cough Relief

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Key Takeaway
Note that P2X3 receptor antagonists reduce cough frequency but increase risk of taste-related adverse events.

This meta-analysis evaluated the efficacy and safety of oral P2X3 receptor antagonists in 3568 adults with refractory or unexplained chronic cough. The primary outcome of objective cough frequency showed a 29.3% relative reduction compared to placebo (0.71 ratio; 95% CI 0.63 to 0.79). Secondary outcomes included improvements in the Leicester Cough Questionnaire total score (MD 1.44; 95% CI 0.78 to 2.09) and the cough severity visual analogue scale (MD -12.73 mm; 95% CI -17.10 to -8.36).

Safety data indicated that P2X3 receptor antagonists were associated with an increased risk of taste-related adverse events (RR 7.36; 95% CI 4.84 to 11.21) and a higher rate of discontinuation due to adverse events (RR 3.62; 95% CI 2.65 to 4.93). Overall adverse events also increased (RR 1.21; 95% CI 1.07 to 1.38). The authors noted small-study effects for the objective cough frequency outcome.

Clinicians should consider the clinical utility of P2X3 receptor antagonists for refractory cough while weighing the objective reduction in cough frequency against the significant risk of taste disturbances and potential for treatment discontinuation. The evidence for these findings is of moderate certainty.

How this fits prior evidence

This meta-analysis addresses a gap in treatment options for refractory chronic cough, a condition that may be influenced by hormonal changes in menopausal patients. While mepolizumab failed to improve refractory chronic cough in patients with eosinophilic airways disease, these findings suggest that P2X3 receptor antagonists may provide a different mechanism for reducing cough frequency and improving patient-reported outcomes, despite associated risks of taste-related adverse events.

A meta-analysis of data from 3,568 adults with chronic coughs looked at the effects of oral P2X3 receptor antagonists. The study compared these medications against a placebo to see if they could reduce cough frequency and improve how patients felt about their condition.

The results showed that patients taking the P2X3 receptor antagonists had a 29.3% relative reduction in objective cough frequency compared to those taking a placebo. Patients also reported improvements in their quality of life scores and a decrease in how severe they felt their cough was on a visual scale.

While the results are promising, there are important safety considerations. Patients taking these medications reported more side effects than those on a placebo, particularly regarding taste. There was also a higher rate of people stopping the medication due to these side effects. Because the evidence is based on a meta-analysis with some limitations, these findings should be discussed with a doctor to weigh the benefits against the risks.

What this means for you:
P2X3 receptor antagonists may reduce cough frequency but are linked to higher rates of taste-related side effects.

Common questions

How effective are P2X3 receptor antagonists for chronic cough?

The study found that these medications led to a 29.3% relative reduction in objective cough frequency compared to a placebo. Patients also reported better scores on cough quality of life and lower ratings for how severe their cough felt.

Are there any side effects to these medications?

Yes, there were more side effects reported in the group taking P2X3 receptor antagonists. Specifically, there was a significant increase in taste-related issues. Some patients also chose to stop taking the medication because of these side effects.

Who is this treatment intended for?

The study specifically looked at adults who suffer from a chronic cough that is either not explained by other causes or is difficult to treat with standard methods.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedSep 2026
View Original Abstract ↓
BackgroundRefractory chronic cough and unexplained chronic cough are increasingly understood as clinical expressions of cough hypersensitivity. P2X3 receptor antagonists have been developed to reduce ATP-mediated airway sensory nerve activation, but their benefit must be balanced against taste-related adverse events.MethodsRandomized placebo-controlled trials evaluating oral P2X3 receptor antagonists in adults with refractory or unexplained chronic cough were included. Objective cough frequency and taste-related adverse events were selected as primary efficacy and safety/tolerability outcomes. Secondary outcomes included Leicester Cough Questionnaire (LCQ) total score, cough severity visual analogue scale (VAS), overall adverse events, and discontinuation due to adverse events. Effects were pooled using random-effects inverse-variance models. Sensitivity analyses, publication-bias assessment, and GRADE certainty ratings were performed.ResultsEleven trial reports involving 3568 participants were included, yielding 13 independent comparisons for objective cough frequency. P2×3 receptor antagonists reduced objective cough frequency compared with placebo (ratio 0.71, 95% CI 0.63–0.79), corresponding to a 29.3% relative reduction. They also improved LCQ total score (MD 1.44, 95% CI 0.78–2.09) and cough severity VAS (MD -12.73 mm, 95% CI -17.10 to −8.36). Taste-related adverse events were increased (RR 7.36, 95% CI 4.84–11.21), as were overall adverse events (RR 1.21, 95% CI 1.07–1.38) and discontinuation due to adverse events (RR 3.62, 95% CI 2.65–4.93). Leave-one-out analyses did not alter the direction of any pooled estimate. Egger and Begg tests suggested small-study effects for objective cough frequency, but not for safety outcomes with sufficient comparisons. The certainty of evidence was rated as moderate for all prespecified outcomes.ConclusionP2×3 receptor antagonists were associated with reductions in objective cough frequency and improvements in patient-reported outcomes in refractory or unexplained chronic cough. These benefits should be balanced against increased safety and tolerability concerns, especially taste disturbance, although receptor selectivity appears to attenuate this risk.Systematic Review Registrationhttps://www.crd.york.ac.uk/prospero/, identifier CRD420261422476.
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