# RNA interference targeting ANGPTL3 for triglyceride and cholesterol lowering: phase 1 basket trial cohorts

**Authors:** Gerald F. Watts, Christian Schwabe, Russell Scott, Patrick A. Gladding, David Sullivan, John Baker, Peter Clifton, James Hamilton, Bruce Given, Stacey Melquist, Rong Zhou, Ting Chang, Javier San Martin, Daniel Gaudet, Ira J. Goldberg, Joshua W. Knowles, Robert A. Hegele, Christie M. Ballantyne

PMC · DOI: 10.1038/s41591-023-02494-2 · Nature Medicine · 2023-08-25

## TL;DR

This study shows that an RNA interference treatment targeting ANGPTL3 is safe and lowers triglycerides and cholesterol in healthy people and those with fatty liver.

## Contribution

First-in-human evidence that RNA interference targeting ANGPTL3 is safe and effectively lowers lipids.

## Key findings

- ARO-ANG3 was well tolerated with similar adverse event rates to placebo.
- ARO-ANG3 reduced ANGPTL3 by up to 78% and triglycerides by up to 54% in healthy participants.
- Non-HDL cholesterol decreased by up to 29% with the highest ARO-ANG3 doses.

## Abstract

Elevated triglycerides and non-high-density lipoprotein cholesterol (HDL-C) are risk factors for atherosclerotic cardiovascular disease (ASCVD). ARO-ANG3 is an RNA interference therapy that targets angiopoietin-like protein 3 (ANGPTL3), a regulator of lipoprotein metabolism. This first-in-human, phase 1, randomized, placebo-controlled, open-label trial investigated single and repeat ARO-ANG3 doses in four cohorts of fifty-two healthy participants and one cohort of nine participants with hepatic steatosis, part of a basket trial. Safety (primary objective) and pharmacokinetics (in healthy participants) and pharmacodynamics (secondary objectives) of ARO-ANG3 were evaluated. ARO-ANG3 was generally well tolerated, with similar frequencies of treatment-emergent adverse events in active and placebo groups. Systemic absorption of ARO-ANG3 in healthy participants was rapid and sustained, with a mean Tmax of 6.0–10.5 h and clearance from plasma within 24–48 h after dosing with a mean t½ of 3.9–6.6 h. In healthy participants, ARO-ANG3 treatment reduced ANGPTL3 (mean −45% to −78%) 85 days after dose. Reductions in triglyceride (median −34% to −54%) and non-HDL-C (mean −18% to −29%) (exploratory endpoints) concentrations occurred with the three highest doses. These early-phase data support ANGPTL3 as a potential therapeutic target for ASCVD treatment. ClinicalTrials.gov identifier: NCT03747224

First-in-human results from five cohorts of healthy volunteers and individuals with hepatic steatosis show that RNA interference treatment targeting ANGPTL3 was well tolerated and led to reduction in triglycerides and non-HDL cholesterol.

## Linked entities

- **Genes:** ANGPTL3 (angiopoietin like 3) [NCBI Gene 27329]
- **Proteins:** ANGPTL3 (angiopoietin like 3)
- **Diseases:** atherosclerotic cardiovascular disease (MONDO:1060134)

## Full-text entities

- **Genes:** CETP (cholesteryl ester transfer protein) [NCBI Gene 1071] {aka BPIFF, HDLCQ10}, CYP19A1 (cytochrome P450 family 19 subfamily A member 1) [NCBI Gene 1588] {aka ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX}, LIPG (lipase G, endothelial type) [NCBI Gene 9388] {aka EDL, EL, PRO719}, APOA1 (apolipoprotein A1) [NCBI Gene 335] {aka AMYLD3, HPALP2, apo(a)}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, LIPC (lipase C, hepatic type) [NCBI Gene 3990] {aka HDLCQ12, HL, HTGL}, ANGPT4 (angiopoietin 4) [NCBI Gene 51378] {aka ANG3, ANG4}, APOC3 (apolipoprotein C3) [NCBI Gene 345] {aka APOCIII, Apo-C3, ApoC-3}, APOB (apolipoprotein B) [NCBI Gene 338] {aka FCHL2, FLDB, LDLCQ4, apoB-100, apoB-48}, AOPEP (aminopeptidase O (putative)) [NCBI Gene 84909] {aka AP-O, APO, C90RF3, C9orf3, DYT31, ONPEP}, ANGPTL3 (angiopoietin like 3) [NCBI Gene 27329] {aka ANG-5, ANGPT5, ANL3, FHBL2}, APOC2 (apolipoprotein C2) [NCBI Gene 344] {aka APO-CII, APOC-II}, APOA5 (apolipoprotein A5) [NCBI Gene 116519] {aka APOAV, RAP3}, LPL (lipoprotein lipase) [NCBI Gene 4023] {aka HDLCQ11, LIPD}, PCSK9 (proprotein convertase subtilisin/kexin type 9) [NCBI Gene 255738] {aka FH3, FHCL3, HCHOLA3, LDLCQ1, NARC-1, NARC1}, LDLR (low density lipoprotein receptor) [NCBI Gene 3949] {aka LDLCQ2}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** heart block (MESH:D006327), CVA (MESH:D020521), erythema (MESH:D004890), vomiting (MESH:D014839), depression (MESH:D003866), pancreatitis (MESH:D010195), Brugada syndrome (MESH:D053840), drugs (MESH:D000081015), TIA (MESH:D002546), unstable angina (MESH:D000789), malignancies (MESH:D009369), bleeding diathesis (MESH:D006474), Diabetes (MESH:D003920), metastatic disease (MESH:D000092182), homozygous familial hypercholesterolemia (MESH:D000090542), familial hypercholesterolemia (MESH:D006938), cardiovascular disease (MESH:D002318), SAEs (MESH:D064420), thrombocytopenia (MESH:D013921), deaths (MESH:D003643), hypertensives (MESH:D006973), sudden cardiac death (MESH:D016757), ULN (MESH:D045745), psychiatric (MESH:D001523), HP (MESH:C537262), myocardial infarction (MESH:D009203), respiratory tract infection (MESH:D012141), ventricular tachycardia or fibrillation (MESH:D014693), HIV (MESH:D015658), in situ cervical cancer (MESH:D002583), coagulopathy (MESH:D001778), hepatitis (MESH:D056486), stable diabetes mellitus (MESH:D003924), familial combined hypolipidemia (MESH:C565732), pulmonary embolism (MESH:D011655), Atherosclerotic cardiovascular disease (MESH:D050197), headache (MESH:D006261), abdominal pain (MESH:D015746), atrial arrhythmias (MESH:D001145), basal cell carcinoma (MESH:D002280), jaundice (MESH:D007565), squamous cell skin cancer (MESH:D018307), cardiovascular or coronary artery disease (MESH:D003324), bradycardia (MESH:D001919), coronary disease (MESH:D003327), fever (MESH:D005334), SAD (MESH:D012640), congenital long QT syndrome (MESH:D008133), dyslipidemia (MESH:D050171), MAD (MESH:D000094625), torsades de pointes (MESH:D016171), bruising (MESH:D003288), CL/F (MESH:D002971), pain medication (MESH:D010146), superficial bladder tumors (MESH:D001749), diarrhea (MESH:D003967), liver injury (MESH:D017093), ventricular rhythm disturbances (MESH:D020178), Hepatic steatosis (MESH:D005234), heart failure (MESH:D006333)
- **Chemicals:** fat (MESH:D005223), cocaine (MESH:D003042), carbohydrate (MESH:D002241), HDL-C. (-), Evinacumab (MESH:C000621590), TG (MESH:D014280), phencyclidine (MESH:D010622), Evra (MESH:C511292), oligonucleotide (MESH:D009841), nicotine (MESH:D009538), alcohol (MESH:D000438), omega-3 fatty acids (MESH:D015525), Glucose (MESH:D005947), blood glucose (MESH:D001786), Lp(a) (MESH:D010649), C peptide (MESH:D002096), MADs (MESH:C110804), NAG (MESH:D000117), Lipid (MESH:D008055), vupanorsen (MESH:C000723171), 3,4-methylenedioxy methamphetamine (MESH:D018817), fibrates (MESH:D058607), cannabinoids (MESH:D002186), cholesterol (MESH:D002784), bilirubin (MESH:D001663), Creatinine (MESH:D003404), N-acetylgalactosamine (MESH:D000116)
- **Species:** Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097], HCV [taxon 11103], Hepatitis B virus (no rank) [taxon 10407]
- **Cell lines:** ARO — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0144)

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10504078/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC10504078/full.md

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Source: https://tomesphere.com/paper/PMC10504078