A Study of AZD8233 in Participants With Dyslipidemia

Dyslipidaemia Clinical Trial

Official title:

A Randomized, Parallel, Double-blind, Placebo-controlled, Dose-ranging, Phase 2b Study to Evaluate the Efficacy, Safety and Tolerability of AZD8233 Treatment in Participants With Dyslipidemia

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04641299
• Other study ID #: D7990C00003
• Status: Completed
• Phase: Phase 2
• Start date: October 28, 2020
• Est. completion date: July 20, 2021

Study information

• Verified date: October 2022
• Source: AstraZeneca
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

AZD8233 is a PCSK9-targeted ASO for the reduction of circulating levels of LDL-C. This study aims to evaluate the dose-dependent reduction in LDL-C after SC administration of multiple doses of AZD8233 as well as the associated adverse effects profile. The data generated will be used to guide choice of doses, dosing regimens, and sample sizes, as well as safety and PD monitoring in the further clinical development program.

Description:

This is a randomized parallel, double-blind, placebo-controlled, dose-ranging Phase 2b study in approximately 108 participants with dyslipidemia. The primary objective of the study is to investigate the effect of AZD8233 on LDL-C across different dose levels. The study will be conducted at up to 25 sites in up to 4 countries.

The screening period starts up to 42 days before the randomization visit and ends on Day -1. Eligible participants will attend 7 visits during the treatment period and 7 additional visits during the safety follow up period. Eligible participants are randomized across four different treatment arms in a 1:1:1:1 ratio for a 12-week treatment period. The planned treatment arms are AZD8233 low dose, AZD8233 medium dose, AZD8233 high dose, and Placebo. Participants will be dosed SC on Days 1, 8, 29, and 57.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 119
• Est. completion date: July 20, 2021
• Est. primary completion date: July 20, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Key Inclusion Criteria:

• Male or female.

• Participant must be 18 to 75 years of age.

• Body mass index between 19 and 40 kg/m2.

• Participants who have a fasting LDL-C = 70 mg/dL but < 190 mg/dL.

• Have fasting triglycerides < 400 mg/dL.

• Should be receiving moderate- or high-intensity statin therapy.

• Should be on stable medication for = 3 months prior to screening with no planned medication or dose change during study participation. The exception to this restriction is for fenofibrate; if the participant is receiving fenofibrate, the therapy must be stable for at least 6 weeks prior to randomization at a dose that is appropriate for the duration of the study in the judgement of the Investigator. Other fibrate therapy (and derivatives) are prohibited.

Key Exclusion Criteria:

• Estimated glomerular filtration rate < 40 mL/min/1.73m2 CKD-EPI.

• Any uncontrolled or serious disease, or any medical 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.

• Poorly controlled type 2 diabetes mellitus, defined as HbA1c > 10% at Visit 1.

• Acute ischaemic cardiovascular event in the last 12 months prior to randomization.

• Heart failure with New York Heart Association (NYHA) Class III-IV.

• High-risk of bleeding as judged by the Investigator.

• Malignancy (except non-melanoma skin cancers, cervical in-situ carcinoma, breast ductal

• Carcinoma in-situ, or Stage 1 prostate carcinoma) within the last 10 years.

• LDL or plasma apheresis within 12 months prior to randomization.

• Uncontrolled hypertension defined as average supine SBP > 160 mmHg or DBP > 90 mmHg at Visit 1 or Visit 3.

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

• Any laboratory values with the following deviations at Screening:

• Positive result on screening for hepatitis B, hepatitis C or HIV.

• ALT > 1.5 × ULN.

• AST > 1.5 × ULN.

• TBL > ULN.

• ALP > 1.5 × ULN.

• WBC < LLN.

• Haemoglobin < 12 g/dL in men or < 11 g/dL in women.

• Platelet count = LLN.

• aPTT > ULN and PT > ULN.

• UACR > 11.3 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 as judged by the Investigator.

• Mipomersen, or lomitapide within 12 months prior to randomization.

• Previous administration of AZD8233/AZD6615.

• Previous administration of PCSK9 inhibition treatment.

• Participation in another clinical study with a study intervention administered in the last 3 months prior to randomization or 5 half-lives from last dose to first administration of study intervention, whichever is the longest.

Related Conditions & MeSH terms

• Dyslipidaemia
• Dyslipidemias

Intervention

Drug:
• AZD8233
PCSK9-targeted ASO for the reduction of circulating levels of LDL-C.
• Placebo
Placebo solution

Locations

Country	Name	City	State
Denmark	Research Site	Aarhus N
Denmark	Research Site	Frederiksberg
Denmark	Research Site	Herlev
Denmark	Research Site	Roskilde
Denmark	Research Site	Viborg
Slovakia	Research Site	Bratislava
Slovakia	Research Site	Bratislava
Slovakia	Research Site	Rožnava
Slovakia	Research Site	Trebišov
United States	Research Site	Cincinnati	Ohio
United States	Research Site	Fargo	North Dakota
United States	Research Site	Greensboro	North Carolina
United States	Research Site	Indianapolis	Indiana
United States	Research Site	Inverness	Florida
United States	Research Site	Jacksonville	Florida
United States	Research Site	Meridian	Idaho
United States	Research Site	New Windsor	New York
United States	Research Site	Pembroke Pines	Florida
United States	Research Site	Roseville	California

Sponsors (1)

Lead Sponsor	Collaborator
AstraZeneca

Countries where clinical trial is conducted

United States,  Denmark,  Slovakia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Number of Subjects With an ECG Determined to be Abnormal and Clinically Significant	Number of subjects with an ECG determined to be abnormal and clinically significant at baseline and end of treatment.	Baseline to Week 24
Primary	Change in Low-density Lipoprotein Cholesterol (LDL-C) at Week 12.	Change from baseline in low-density lipoprotein cholesterol (LDL-C) at week 12. Results are based on Mixed Model Repeated Measures (MMRM) analysis on the log-transformed change from baseline. Log-transformed change from baseline is calculated as the visit value in log minus the baseline value in log. The results from the model are then back transformed.	Baseline to week 12
Secondary	Relative Change From Baseline in PCSK9 Concentration in Plasma at Week 12.	Relative change from baseline in PCSK9 concentration in plasma at week 12.	Baseline to week 12
Secondary	Percentage Change From Baseline in Concentration of TC, HDL-C, Non-HDL-C, VLDL-C, ApoA1, ApoB, Lp(a), Triglycerides, Remnants Cholesterol	Percentage change from baseline in concentration of TC, HDL-C, Non-HDL-C, VLDL-C, ApoA1, ApoB, Lp(a), Triglycerides, Remnants cholesterol at week 12	Baseline to week 12
Secondary	Plasma Concentration of AZD8233	Plasma concentration of AZD8233 after first dose administration	Measurement at week 1, week 4, week 6, week 8, week 10, week 12, week 16, week 20, week 24 after first dose administration.
Secondary	Anti-drug Antibodies (ADAs) During the Treatment Period and Follow-up Period	ADA titre results for subjects with positive ADA during the treatment period and follow-up period.	Measurement at week 0, week 1, week 4, week 8, week 12, week 16, week 20, week 24
Secondary	Percentage Change From Baseline in Levels of LDL-C in Plasma	Percentage change from baseline in levels of LDL-C in plasma from baseline to week 12.	Baseline to week 12

External Links

•   Redacted Clinical Study Report Synopsis
•   Redacted Protocol
•   redacted Statistical Analysis Plan