A Study of Clazakizumab (LY5724886) in Adults With Elevated hsCRP and at Increased Risk for Cardiovascular Event
Recruiting
Phase 2Interventional Study
AtherosclerosisCardiovascular DiseaseObesityHypertensionDiabetes Mellitus, Type 2Renal Insufficiency, Chronic
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
120 (estimated)
Sponsor
Eli Lilly and Company · Industry
Who this trial is looking for
This trial is looking for adults with high levels of inflammation and increased risk for heart issues. Participants will take clazakizumab or a placebo for about 9 months to see how it affects inflammation levels in the body.
Are You a Good Fit for This Trial?
Rules you outType 1 diabetesNew York Heart Association Class III or IV heart failure
You may be able to join if
I have high-sensitivity C-reactive protein levels between 2 and 15 mg/L.
I have been diagnosed with type 2 diabetes.
I have high blood pressure.
I am classified as obese.
I have chronic kidney disease.
I have established heart disease.
You may not be able to join if
I have had a heart attack in the past 60 days.
I have been hospitalized for heart failure in the past 60 days.
I have uncontrolled high blood pressure.
I have type 1 diabetes.
My blood sugar level is too high for type 2 diabetes.
I have active tuberculosis or untreated hepatitis.
I have a serious autoimmune disease.
I have had a recent serious infection.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
The purpose of this study is to measure the change in high-sensitivity C-reactive protein (hsCRP), a marker of inflammation in the body, with clazakizumab compared with placebo in adults who have elevated hsCRP and at increased risk for cardiovascular event.
Participation in the study will last about 9 months.
Trial Locations
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Status
Eligibility Criteria
Inclusion Criteria:
* hsCRP ≥2 mg/L and ≤15 mg/L at screening
* At least one of the following chronic conditions:
* Established atherosclerotic cardiovascular disease (ASCVD)
* Obesity (body mass index (BMI) ≥30 kg/m2)
* Type 2 diabetes
* Hypertension
* Chronic kidney disease Grade 3 or …
Inclusion Criteria:
* hsCRP ≥2 mg/L and ≤15 mg/L at screening
* At least one of the following chronic conditions:
* Established atherosclerotic cardiovascular disease (ASCVD)
* Obesity (body mass index (BMI) ≥30 kg/m2)
* Type 2 diabetes
* Hypertension
* Chronic kidney disease Grade 3 or 4
Exclusion Criteria:
* Acute cardiovascular event within 60 days prior to screening
* Acute decompensated heart failure hospitalization within 60 days prior to screening
* Planned coronary revascularization (percutaneous coronary intervention or coronary artery bypass grafting) or major surgery at the time of randomization
* New York Heart Association Class III or IV heart failure
* Uncontrolled hypertension at screening (systolic blood pressure (BP) ≥160 mmHg or diastolic BP ≥100 mmHg)
* Type 1 diabetes
* Type 2 diabetes with Hemoglobin A1c ≥9.0% (86 mmol/mol) at screening
* Nephrotic syndrome, estimated glomerular filtration rate (eGFR) \<15 mL/min/1.73 m², or history of kidney transplant
* Dialysis or acute kidney injury within 60 days prior to screening
* Congenital/hereditary kidney disease, polycystic kidney disease, lupus nephritis, or antineutrophil cytoplasmic antibody-associated vasculitis
* Active tuberculosis, untreated latent tuberculosis, or known hepatitis B or hepatitis C infection
* Serious, opportunistic, chronic, or recurrent infection requiring treatment within 12 weeks prior to screening
* Significant active autoimmune disease
* Suspected or confirmed immunocompromised state (e.g., HIV infection)
* History of peptic ulcer disease or gastrointestinal ulceration within 12 months prior to screening
* History of diverticular disease, gastrointestinal perforation, or major gastrointestinal surgery
* Mechanical heart valve prosthesis requiring chronic vitamin K antagonist anticoagulation
* Use of colchicine within 14 days prior to screening or anticipated need during the study
* Use of immunosuppressive or immunomodulatory agents, including other biologic anti-IL-6 therapies, within specified windows prior to screening
* Use of systemic corticosteroids within 14 days prior to screening
* Chronic use of nonsteroidal anti-inflammatory drugs (NSAIDs)
Contacts
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or
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