Cardiology and CTVS Medicine

REMAIN-2 Trial Reveals Long-Term Safety And Efficacy Of Recaticimab In Patients With Non-FH And Mixed Hyperlipidemia

• byDoctor News Daily Team
• 18 February, 2025
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China: A recent study has shown the long-term efficacy and safety of add-on recaticimab as a treatment option in patients with non-familial hypercholesterolemia (non-FH) and mixed hyperlipidemia not adequately controlled on stable statin therapy. The findings from the REMAIN-2 study were presented at the American Heart Association (AHA) 2023.
Recaticimab is a new PCSK9 inhibitor that can be injected every one to three months. It represents a novel and innovative approach in cardiovascular therapeutics as a long-acting monoclonal antibody (mAb) targeting proprotein convertase subtilisin/kexin type 9 (PCSK9). It belongs to the immunoglobulin G1 (IgG1) class that modulates PCSK9 activity and contributes to the expanding landscape of therapeutic interventions for hyperlipidemia and cardiovascular health.

The REMAIN-2 trial is a multicenter, phase 3, double-blind, randomized, placebo-controlled study conducted in China that aimed to evaluate the long-term safety and efficacy of recaticimab (SHR-1209), as an add-on therapy for patients with non-FH and mixed hyperlipidemia.
The study included 689 participants (mean age 56 years; 64% men) with non-familial hypercholesterolemia and mixed hyperlipidemia not controlled by ongoing moderate or high-intensity statin therapy.
Participants were categorized into three groups: one which received 150 mg of recaticimab or a placebo injection every four weeks, the second group received 300 mg of recaticimab or a placebo injection every eight weeks, and the third group received 450 mg of recaticimab or placebo injection every 12 weeks. The primary efficacy endpoint was determined as the percentage change from baseline to week 24 in calculated LDL-C levels.
The researchers reported the following findings:
Participants who received recaticimab, regardless of dosing level, had lower bad cholesterol levels at 24 weeks than those receiving a placebo. These levels were maintained at 48 weeks.
Bad cholesterol was reduced by 62% among those taking recaticimab in the four-week injection group vs. 0% among those in the placebo group, and reduced by 59% vs. +0.4%, respectively in the 8-week group.
In the 12-week injection group, bad cholesterol was reduced by 51% vs. +2%, respectively.
Recaticimab demonstrated a comparable safety profile to placebo, with a similar amount of injection site reactions, including soreness and redness, common across both groups during the 48 weeks.
Other types of lipids like lipoprotein(a) and apolipoprotein B were also reduced significantly in the recaticimab groups compared with the placebo groups.
"Our findings provide encouraging evidence for the safety and effectiveness of recaticimab as an add-on therapy for non-familial hypercholesterolaemia and mixed hyperlipidemia," the researchers wrote.
"Recaticimab achieved a comparable reduction in essential lipid parameters as other PCSK9 inhibitors, offering additional confirmation of significant treatment benefits, even with a less frequent dosing schedule," they concluded.