Key result
Subcutaneous APF530 causes no clinically significant QTcF prolongation compared to placebo.
Why the study?
Regulatory concern about potential QT-interval prolongation by serotonin-receptor antagonist antiemetics prompted evaluation of APF530 effects on electrocardiographic intervals.
Does APF530 1 g SC prolong the QTcF interval compared to placebo in healthy adults?
RCT (n=56)
Double-blind
1:1:1:1 to one of four treatment sequences
No
Does APF530 1 g SC prolong the QTcF interval compared to placebo in healthy adults?
APF530 1 g SC, a sustained-release formulation of granisetron, does not cause clinically significant QT prolongation in healthy adults, suggesting it may be a safer antiemetic option for patients at risk for arrhythmias.
APF530 1 g SC can be used without QTcF monitoring concerns in arrhythmia-prone patients; confirms cardiac safety of sustained-release granisetron in a definitive QT study.
BACKGROUND: Regulatory concern about potential QT-interval prolongation by serotonin-receptor antagonist antiemetics prompted product-label changes. The first-generation serotonin-receptor antagonist granisetron is available in oral (PO), intravenous (IV), and transdermal formulations. APF530 is a formulation that provides sustained release of granisetron when administered as a single subcutaneous (SC) injection. The Phase I study reported here evaluated effects of APF530 on electrocardiographic intervals. METHODS: This single-site, double-blind, placebo-controlled, four-period crossover trial randomized healthy men and women to receive varying sequences of APF530 1 g SC, granisetron 50 μg/kg IV, moxifloxacin 400 mg PO, and placebo. Subjects were assessed for 49 hours after each treatment. The primary objective was to evaluate differences between baseline-adjusted, heart rate-corrected QT-interval change using the Fridericia rate correction (dQTcF) for APF530 1 g SC and placebo. Electrocardiograms were performed at various times throughout the assessment period. Pharmacokinetics and safety were evaluated. RESULTS: The upper one-sided 95% confidence interval (CI) for mean baseline-adjusted dQTcF at each post-dose time point between APF530 and placebo excluded 10 ms, indicating that APF530 1 g SC had no clinically significant effect on QTcF. Maximum observed QTcF change was 4.15 ms (90% CI, 0.94 to 7.36) at Hour 3. No clinically significant changes in other electrocardiogram intervals were observed. APF530 SC pharmacokinetics were as expected, with slow absorption (maximum plasma concentration 35.8 ng/mL, median time to maximum plasma concentration 11.1 hours) and slow elimination (mean half-life 18.6 hours; systemic clearance 20.2 L/hour) of granisetron versus the expected early peak concentration and elimination of granisetron IV. APF530 SC was well tolerated. Adverse events, most commonly constipation and SC injection-site reactions, were generally mild and quickly resolved. CONCLUSION: APF530 1 g SC did not induce clinically significant QTcF interval prolongation or changes in the other electrocardiogram intervals, and was well tolerated at twice the recommended dose.
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Mason et al. (2014) conducted an RCT in Healthy volunteers (n=56). APF530 vs. Placebo was evaluated on Baseline- and placebo-adjusted change in QTcF (ddQTcF) (MD 4.15 ms, 95% CI 0.94 to 7.36). APF530 1 g SC did not induce clinically significant QTcF interval prolongation compared to placebo, with a maximum observed placebo-adjusted change of 4.15 ms that excluded the 10 ms threshold.
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