AZD8233 is a PCSK9-targeted ASO for the reduction of circulating levels of LDL-C. This study aims to evaluate safety, efficacy and tolerability of AZD8233.

This is a randomized parallel, double-blind, placebo-controlled Phase 2b study in approximately 376 participants with hyperlipidaemia. The primary objective of the study is to assess the safety and tolerability of AZD8233 as compared with placebo, and the effect of AZD8233 versus placebo on relative change in LDL-C. The study will be conducted at up to 100 sites in up to 8 countries.

The screening period starts up to 28 days before the randomization visit and ends on Day -1. Eligible participants will attend 1 enrollment visit and 15 visits during the treatment period and 2 additional visits during the safety follow up period.

Inclusion Criteria:

• Participant must be 18 to 75 years of age, inclusive, at the time of signing the informed consent
• Participants who have a fasting LDL-C ≥ 70 mg/dL (1.8 mmol/L) but < 190 mg/dL (4.9 mmol/L) at screening
• Participants who have fasting triglycerides < 400 mg/dL (< 4.52 mmol/L) at screening
• Participants are receiving a stable dose (≥ 3 months) of maximally tolerated statin and/or ezetimibe therapy
• Male or female of non-childbearing potential
• Signed and dated written informed consent prior to any mandatory study specific procedures, sampling, and analyses

Exclusion Criteria:

• eGFR < 40 mL/min/1.73m2 using the CKD-EPI

• History or presence of gastrointestinal, hepatic or renal disease or any other conditions known to interfere with absorption, distribution, metabolism or excretion of drugs

• Any uncontrolled or serious disease, or any medical (eg,. known major active infection or major haematological, renal, metabolic, gastrointestinal or endocrine dysfunction) or surgical condition that, in the opinion of the investigator, may either interfere with participation in the clinical study and/or put the participant at significant risk (according to the investigator's judgment) if he/she participates in the clinical study

• Poorly controlled T2DM, defined as HbA1c > 10%

• Acute ischaemic cardiovascular events including stroke within 30 days, or heart failure with New York Heart Association (NYHA) Class III to IV

• Blood dyscrasias with increased risk of bleeding including idiopathic thrombocytopenic purpura and thrombotic thrombocytopenic purpura or symptoms of increased risk of bleeding (frequent bleeding gums or nose bleeds)

• High-risk of bleeding diathesis or anti-platelet therapy other than low dose aspirin (≤100mg/day).

• Malignancy within the last 10 years

• Recipient of any major organ transplant

• LDL or plasma apheresis within 12 months prior to randomisation

• Uncontrolled hypertension defined as average supine SBP > 160 mmHg or DBP > 90 mmHg

• Heart rate after 10 minutes supine rest < 50 or > 100 bpm

• Any laboratory values with the following deviations at the Screening Visit; test may be repeated at the discretion of the investigator if abnormal:

  • Any positive result on screening for serum hepatitis B surface antigen, hepatitis C antibody, and human immunodeficiency virus (HIV)
  • ALT > 1.5 × ULN
  • AST > 1.5 × ULN
  • TBL > ULN
  • ALP > 1.5 × ULN
  • WBC < lower limit of normal (LLN).
  • Haemoglobin < 12 g/dL in males or < 11 g/dL in females
  • Platelet count ≤ LLN
  • aPTT > ULN or Prothrombin Time > ULN
  • UACR > 11 mg/mmol (100 mg/g)
  • UPCR > 300 mg/g

• Any clinically important abnormalities in rhythm, conduction or morphology of the resting ECG and any clinically important abnormalities in the 12-lead ECG

• QTcF > 470 ms; high degree atrioventricular (AV)-block grade II-III and sinus node dysfunction with significant sinus pause untreated with pacemaker; and cardiac tachyarrhythmias

• History of drug and/or alcohol abuse or a positive screen for drugs of abuse

• Use of warfarin, direct or indirect thrombin inhibitors or factor Xa inhibitors

• Mipomersen, or lomitapide within 12 months prior to randomisation

• Any fibrate therapy other than fenofibrate; if the participant is on fenofibrate therapy, the dose should be stable for at least 6 weeks prior to randomisation

• Previous administration of AZD8233/AZD6615) or inclisiran (LEQVIO ® Novartis)

• Use of evolocumab (REPATHA® Amgen) and alirocumab (PRALUENT® Regeneron) within 3 months of screening

Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal. All request will be evaluated as per the AZ disclosure commitment: https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.

Yes, indicates that AZ are accepting requests for IPD, but this does not mean all requests will be shared.

AstraZeneca will meet or exceed data availability as per the commitments made to the EFPIA Pharma Data Sharing Principles. For details of our timelines, please rerefer to our disclosure commitment at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.

When a request has been approved AstraZeneca will provide access to the deidentified individual patient-level data in an approved sponsored tool . Signed Data Sharing Agreement (non-negotiable contract for data accessors) must be in place before accessing requested information. Additionally, all users will need to accept the terms and conditions of the SAS MSE to gain access. For additional details, please review the Disclosure Statements at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.