Effectiveness of Iptacopan Versus C5 Inhibitors in Complement Inhibitor-Naive Patients With Paroxysmal Nocturnal Haemoglobinuria

Abstract

Background

Paroxysmal nocturnal haemoglobinuria (PNH) is characterised by haemolytic anaemia, bone marrow failure and thrombosis. The single-arm phase 3 APPOINT-PNH trial (NCT04820530) investigating iptacopan monotherapy in complement inhibitor-naive patients demonstrated significant haemoglobin concentration improvements.

Methods

We used target trial emulation to retrospectively predict outcomes if APPOINT-PNH trial patients had received C5 inhibitors instead of iptacopan. Estimates were derived from the real-world APPEX cohort treated with routine C5 inhibitors. The study used benchmarking and comparative effectiveness to evaluate the haematological response in APPOINT-PNH if patients had received C5 inhibitors. Treatment effect was estimated using propensity scores to model the probability of trial inclusion based on baseline covariates, followed by fitting an outcome model to the APPEX cohort.

Results

The analysis of 125 patients showed all estimated treatment effects (95% confidence interval) favoured iptacopan over C5 inhibitors: differences in the proportion of patients achieving haemoglobin increase from baseline of ≥ 2 g/dL, 68.2% (40.9–95.6); haemoglobin levels of ≥ 12 g/dL, 53.4% (31.4–75.3); transfusion independence, 38.8% (15.1–62.5); ratio of percent change from baseline in lactate dehydrogenase levels, 0.51 (0.40–0.67); change from baseline in reticulocytes, −75.5 × 10⁹/L (−106.9, −44.2).

Conclusions

Results indicate C5 inhibitor-naive patients with PNH may experience greater haematological response with iptacopan than with C5 inhibitors.

Trial Registration

ClinicalTrials.gov identifier: NCT05842486