Evolocumab Comparison in Healthy Subjects

Not currently recruiting at 4 trial locations
AC
Overseen ByAmgen Call Center
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests two versions of a drug called evolocumab to observe how the body processes them. Evolocumab helps manage cholesterol levels. Researchers aim to understand how each version works in healthy individuals. The trial seeks adults with a BMI between 18 and 32 and a specific range of LDL cholesterol levels. As a Phase 1 trial, the research focuses on understanding the treatment's effects in people, offering participants an opportunity to contribute to groundbreaking medical research.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research has shown that evolocumab is generally safe for people. Studies have found that common side effects, such as a sore throat or a cold, occur in about 6.5% of patients and are mild. Serious issues are rare. The FDA has approved evolocumab to help lower bad cholesterol (LDL) for those needing more assistance than standard treatments provide. Long-term studies in animals did not find any cancer-related problems with evolocumab. Overall, evolocumab appears safe for people when used as directed by healthcare providers.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about evolocumab because it offers a novel approach to managing high cholesterol levels. Unlike traditional statins, which reduce cholesterol by blocking its production in the liver, evolocumab is a monoclonal antibody that targets and inhibits a protein called PCSK9. This results in more LDL receptors being available to clear LDL cholesterol from the bloodstream, potentially leading to a more significant reduction in LDL cholesterol levels. Evolocumab is administered as a subcutaneous injection, which may be more convenient for some patients compared to daily oral medications. This unique mechanism and delivery method could provide a powerful option for those who don’t respond well to or cannot tolerate statins.

What evidence suggests that this trial's treatments could be effective?

This trial will compare two formulations of evolocumab: Drug Substance A (Test) and Drug Substance B (Reference). Studies have shown that evolocumab effectively lowers LDL cholesterol, often called "bad" cholesterol, reducing LDL levels by about 60% in people with high cholesterol. Research also shows that evolocumab can lower the risk of heart problems, such as heart attacks, especially when combined with other cholesterol-lowering treatments. Previous findings have demonstrated the drug's safety and effectiveness over long periods, consistently reducing heart-related risks. These results suggest evolocumab could be a strong option for managing cholesterol-related health issues.678910

Who Is on the Research Team?

M

MD

Principal Investigator

Amgen

Are You a Good Fit for This Trial?

This trial is for healthy men and women aged 18 to 60 with a BMI between 18.0 and 32.0, and LDL cholesterol levels between 70 and 190 mg/dL. Women cannot be pregnant or breastfeeding.

Inclusion Criteria

Body mass index (BMI) between 18.0 and 32.0 kg/m^2 inclusive
LDL-C level ≥ 70 mg/dL (1.8 mmol/L) and ≤ 190 mg/dL (4.9 mmol/L) at screening
I am not pregnant or breastfeeding.
See 1 more

Exclusion Criteria

Participation in another investigational device or drug trial within the past 30 days or 5 half-lives prior to check-in
History or evidence of any clinically significant disorder, condition, or disease that would pose a risk to participant safety or interfere with the trial evaluation, procedures, or completion
I have had heart disease or currently have heart-related symptoms.
See 5 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

1-2 weeks

Treatment

Participants receive a single subcutaneous dose of either evolocumab drug substance A or B

1 day

Follow-up

Participants are monitored for pharmacokinetics and safety after receiving the dose

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Evolocumab Drug Substance A (Test)
  • Evolocumab Drug Substance B (Reference)

Trial Overview

The study compares how two different versions of the drug evolocumab are absorbed in the body after a single injection under the skin in healthy volunteers.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Group I: Evolocumab Drug Substance B (Reference)Experimental Treatment1 Intervention
Group II: Evolocumab Drug Substance A (Test)Experimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Amgen

Lead Sponsor

Trials
1,508
Recruited
1,433,000+
Founded
1980
Headquarters
Thousand Oaks, USA
Known For
Human Therapeutics
Top Products
Enbrel, Prolia, Neulasta, Otezla
Robert A. Bradway profile image

Robert A. Bradway

Amgen

Chief Executive Officer since 2012

MBA from Harvard Business School

Paul Burton profile image

Paul Burton

Amgen

Chief Medical Officer since 2023

MD from University of London, PhD in Molecular and Cellular Biology from Imperial College London

Citations

Review of Evolocumab for the Reduction of LDL Cholesterol ...

Both have demonstrated remarkable LDL-C reductions of ~60% in adult patients with hyperlipidemia on background statin therapy ( other LLT) in the clinical trial ...

Office of Clinical Pharmacology Review

a 20 30% lower mean Cmax and 40 50% lower mean AUC were observed as compared to healthy patients.

Clinical Review - Evolocumab (Repatha) - NCBI Bookshelf - NIH

Of the patients who experienced an MI in the previous year, the end point of cardiovascular death was met by 1.77% (n = 50) of patients taking evolocumab versus ...

Press Releases

Amgen presents results highlighting the long-term safety and efficacy of Repatha (Evolocumab) in the longest duration study of a PCSK9 inhibitor to date.

Amgen Presents Results Highlighting The Long-Term ...

Patients treated with Repatha achieved a 59 percent reduction in mean LDL-C from baseline during the first year of treatment (n=785).

Adverse Reactions to Evolocumab: Analysis of Real-World ...

The purpose of this study is to update knowledge of the safety of evolocumab through an analysis of post-marketing real-world data on suspected adverse ...

SAFETY DATA SHEET

EVOLOCUMAB (Repatha®) not classified as hazardous Classification … is intended for laboratory use by professional uses only. Toxic if swallowed H311 Toxic in ...

125522Orig1s000 - accessdata.fda.gov

Evolocumab did not cause any drug-related tumors when administered to hamsters for up to 2 years in a lifetime carcinogenicity assay at doses.

Efficacy and Safety of Evolocumab in Reducing Lipids and ...

Evolocumab reduced the level of LDL cholesterol by 61%, from a median of 120 mg per deciliter to 48 mg per deciliter.

Repatha®

Avoid inhalation, skin contact, eye contact, and accidental ingestions. Does not meet GHS classification criteria and therefore is not classified.