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Looking for participantsPhase3

Assessing the Impact of Muvalaplin on Major Cardiovascular Events in Adults With Elevated Lipoprotein(a)

Sponsor: Eli Lilly and Company

NCT ID: NCT07157774

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Muvalaplin (drug), Placebo (drug)
How long the study runs
Study runs about 66 months (dates as stated)
About the drug or intervention
Muvalaplin — drug: Administered orally · Placebo — drug: Administered orally
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years and over
Who
All
Number of participants
10,450
Started
2025-09-02
Last checked
2026-09

Plain English Summary

What is this study?

  • • Testing a new treatment for elevated lp(a)
  • • Phase3 - 10,450 participants
  • • The purpose of this study is to evaluate the efficacy of muvalaplin in reducing cardiovascular risk in participants with high lipoprotein(a) who have cardiovascular disease or are at risk of a heart attack or stroke

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with elevated lp(a)

Where?

  • • Belfast - South Eastern Health and Social Care Trust
  • • Birmingham - FutureMeds - Birmingham
  • • Blackpool - Layton Medical Centre
  • • Bodelwyddan - Glan Clwyd Hospital
  • • +21 more UK sites

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

The purpose of this study is to evaluate the efficacy of muvalaplin in reducing cardiovascular risk in participants with high lipoprotein(a) who have cardiovascular disease or are at risk of a heart attack or stroke.

Elevated Lp(a)Atherosclerotic Cardiovascular Disease (ASCVD)

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Have Lp(a) ≥175 nanomoles per liter (nmol/L)
  • ✓Meet one of the following criteria:
  • ✓Are at risk for a first ASCVD event, defined as one or more of the following:
  • ✓Documented coronary artery disease (CAD), carotid stenosis, or peripheral artery disease (PAD) without a history of...
  • ✓A high coronary artery calcium (CAC) score

Who cannot take part

  • ✗Are planning or expected to undergo a procedure to restore blood flow in the arteries or a major heart surgery...
  • ✗Have uncontrolled high blood pressure
  • ✗Have New York Heart Association (NYHA) class III or IV heart failure
  • ✗Have undergone a procedure to remove cholesterol from the blood within 90 days of screening, or have a planned...
  • ✗Have severe kidney impairment
See the full criteria
Inclusion Criteria: * Have Lp(a) ≥175 nanomoles per liter (nmol/L) * Meet one of the following criteria: * Have had a prior atherosclerotic cardiovascular disease (ASCVD) event (such as heart attack, stroke, or procedure to restore blood flow to the heart or other parts of the body) within 10 years prior to screening * Are at risk for a first ASCVD event, defined as one or more of the following: * Documented coronary artery disease (CAD), carotid stenosis, or peripheral artery disease (PAD) without a history of ASCVD event * A high coronary artery calcium (CAC) score * Reduced kidney function with diabetes * Combination(s) of high risk factors Exclusion Criteria: * Have experienced a major cardiovascular event or surgery, such as heart attack, stroke, or procedure to restore blood flow to the heart or other parts of the body, within 90 days prior to screening or occurring between screening and randomization * Are planning or expected to undergo a procedure to restore blood flow in the arteries or a major heart surgery during the study * Have uncontrolled high blood pressure * Have New York Heart Association (NYHA) class III or IV heart failure * Have undergone a procedure to remove cholesterol from the blood within 90 days of screening, or have a planned procedure during the study * Have severe kidney impairment * Have had cancer within 5 years prior to screening

Where Is This Study? (25 UK sites)

South Eastern Health and Social Care Trust

Belfast BT16 1RH, United Kingdom

Recruiting
Site contact (verified)
Patrick DonnellyPrincipal Investigator

FutureMeds - Birmingham

Birmingham B21 9RY, United Kingdom

NOT_YET_RECRUITING
Site contact (verified)
Imtisal Ul-HaqPrincipal Investigator

Layton Medical Centre

Blackpool FY3 7EN, United Kingdom

Recruiting
Site contact (verified)
Rebecca ClarkPrincipal Investigator

Glan Clwyd Hospital

Bodelwyddan LL18 5UJ, United Kingdom

Recruiting
Site contact (verified)
Satheesh Balakrishnan NairPrincipal Investigator

Bradford on Avon Health Centre

Bradford on Avon BA15 1DQ, United Kingdom

Recruiting
Site contact (verified)
Nell WyattPrincipal Investigator

Bristol Royal Infirmary

Bristol BS2 8HW, United Kingdom

Recruiting
Site contact (verified)
Paul DowniePrincipal Investigator

FutureMeds - Liverpool

Bromborough CH62 6EE, United Kingdom

NOT_YET_RECRUITING
Site contact (verified)
Tamer YousefPrincipal Investigator

Panthera Biopartners - North London

Enfield EN3 4GS, United Kingdom

Recruiting
Site contact (verified)
Delphine NkulizaPrincipal Investigator

FutureMeds Glasgow - CPS Research

Glasgow G20 7BE, United Kingdom

Recruiting
Site contact (verified)
Kristen LaingPrincipal Investigator

Panthera Biopartners - Glasgow

Glasgow G51 4RY, United Kingdom

Recruiting
Site contact (verified)
Charles BoylePrincipal Investigator

Velocity Clinical Research, High Wycombe

High Wycombe HP11 2QW, United Kingdom

Recruiting
Site contact (verified)
Ronnie BebosoPrincipal Investigator

HMC Health Group - Meadows Centre for Health

Hounslow TW4 7NR, United Kingdom

Recruiting
Site contact (verified)
Ivor SinghPrincipal Investigator

Raigmore Hospital

Inverness IV2 3UJ, United Kingdom

Recruiting
Site contact (verified)
Rosemary ClarkePrincipal Investigator

Panthera Biopartners - Keele

Keele ST5 5BG, United Kingdom

Recruiting
Site contact (verified)
Karen FaulknerPrincipal Investigator

Oak Tree Surgery

Liskeard PL14 3XA, United Kingdom

Recruiting
Site contact (verified)
Kate NorthridgePrincipal Investigator

FutureMeds - London

London NW10 2PB, United Kingdom

Recruiting
Site contact (verified)
Pembe OzunluPrincipal Investigator

EMS Healthcare

Macclesfield SK10 4TF, United Kingdom

NOT_YET_RECRUITING
Site contact (verified)
Nicholas ProbertPrincipal Investigator

The Adam Practice

Poole BH16 5PW, United Kingdom

Recruiting
Site contact (verified)
Patrick MoorePrincipal Investigator

Panthera Biopartners - Preston

Preston PR2 9QB, United Kingdom

Recruiting
Site contact (verified)
Samin ChowdhuryPrincipal Investigator

Panthera Biopartners - Manchester

Rochdale OL11 4AU, United Kingdom

Recruiting
Site contact (verified)
Amir AfzulPrincipal Investigator

Panthera Biopartners - Sheffield

Sheffield S2 5FX, United Kingdom

Recruiting
Site contact (verified)
Hannah CollinsPrincipal Investigator

FutureMeds Teesside - Middlefield Centre

Stockton-on-Tees TS19 8PE, United Kingdom

Recruiting
Site contact (verified)
Andreas HajineocliPrincipal Investigator

Rame Group Practice

Torpoint PL11 2TB, United Kingdom

Recruiting
Site contact (verified)
Lawrence BarnesPrincipal Investigator

Sandwell General Hospital

West Bromwich B71 4HJ, United Kingdom

Recruiting
Site contact (verified)
Inessa TraceyPrincipal Investigator

Panthera Clinic - York

York YO24 4LJ, United Kingdom

Recruiting
Site contact (verified)
Henrique FreitasPrincipal Investigator

How to Get in Touch

Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or

Sponsor contact

CONTACT

1-317-615-4559 LillyTrials@Lilly.com

Physicians interested in becoming principal investigators please contact

Sponsor contact

CONTACT

clinical_inquiry_hub@lilly.com
Data sourced from ClinicalTrials.gov · Last verified: 2026-09