OXLUMO (lumasiran sodium)

The pharmacokinetic (PK) properties of OXLUMO were evaluated following administration of single and multiple dosages in patients with PH1 as summarized in Table 3. Table 3. Pharmacokinetic Parameters of Lumasiran Lumasiran General Information Steady-State Exposure C max [Median (Range)] 462 (38.5 to 1500) ng/mL AUC 0-last [Median (Range)] 6810 (2890 to 10700) ng∙h/mL Dose Proportionality Lumasiran exhibited an approximately dose proportional increase in plasma exposure following single subcutane...

14.1 ILLUMINATE-A ILLUMINATE-A was a randomized, double-blind trial comparing lumasiran and placebo in 39 patients 6 years of age and older with PH1 and an eGFR ≥30 mL/min/1.73 m 2 (ILLUMINATE-A; NCT03681184). Patients received 3 loading doses of 3 mg/kg OXLUMO (N=26) or placebo (N=13) administered once monthly, followed by quarterly maintenance doses of 3 mg/kg OXLUMO or placebo [see Dosage and Administration (2.1) ] . After six months, all patients received OXLUMO. The median age of patients at first dose was 15 years (range 6 to 61 years), 67% were male, and 77% were White. At baseline, the...

The most common adverse reaction (reported in ≥20% of patients) is injection site reactions. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Alnylam Pharmaceuticals at 1-877-256-9526 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not refle...

None. None. ( 4 )