Study of LY3016859 in Participants With Diabetic Nephropathy

NCT ID: NCT01774981

Last Updated: 2019-09-19

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-03-31
• Study Completion Date: 2015-08-31

Brief Summary

The purpose of this two-part study is to investigate the safety, tolerability and efficacy of LY3016859 after multiple intravenous (IV) dosing's in participants with diabetic nephropathy (DN). Part A will be dose escalation for safety and tolerability and Part B will evaluate Proteinuria.

Conditions

Diabetic Nephropathy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

Placebo (Part A)

Part A: Placebo administered by 60 minute Intravenous (IV) infusion at Week 1 and Week 4.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Administered IV

10 mg LY3016859 (Part A)

Part A: 10 milligram (mg) LY3016859 administered by 60 minute IV infusion at Week 1 and Week 4.

Group Type: EXPERIMENTAL

LY3016859

Intervention Type: DRUG

Administered IV

100 mg LY3016859 (Part A)

Part A: 100 mg LY3016859 administered by 60 minute IV infusion at Week 1 and Week 4.

Group Type: EXPERIMENTAL

LY3016859

Intervention Type: DRUG

Administered IV

750 mg LY3016859 (Part A)

Part A: 750 mg LY3016859 administered by 60 minute IV infusion at Week 1 and Week 4.

Group Type: EXPERIMENTAL

LY3016859

Intervention Type: DRUG

Administered IV

Placebo (Part B)

Part B: Placebo administered by 60 minute IV infusion at Weeks 1, 4, 7, 10 and 13.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Administered IV

50 mg LY3016859 (Part B)

Part B: 50 mg LY3016859 administered by 60 minute IV infusion at Weeks 1, 4, 7, 10 and 13.

Group Type: EXPERIMENTAL

LY3016859

Intervention Type: DRUG

Administered IV

250 mg LY3016859 (Part B)

Part B: 250 mg LY3016859 administered by 60 minute IV infusion at Weeks 1, 4, 7, 10 and 13.

Group Type: EXPERIMENTAL

LY3016859

Intervention Type: DRUG

Administered IV

750 mg LY3016859 (Part B)

Part B: 750 mg LY3016859 administered by 60 minute IV infusion at Weeks 1, 4, 7, 10 and 13.

Group Type: EXPERIMENTAL

LY3016859

Intervention Type: DRUG

Administered IV

Interventions

Placebo

Administered IV

Intervention Type: DRUG

LY3016859

Administered IV

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Stable diabetic kidney disease (DKD) while taking Standard of Care medication (SOC), as defined by:

• Estimated glomerular filtration rate (eGFR) less than (<) 90 milliliter per minute per 1.73 square meter (ml/min/1.73m²) as determine utilizing the Modification of Diet in Renal Disease (MDRD) equation
• Taking an angiotensin convertible enzyme (ACE) inhibitor or angiotensin II receptor blocker (ARB) at a stable dose for greater than or equal to (≥) 2 months prior to randomization and agree to continue to take such throughout the duration of the study
• Type 1 or Type 2 diabetes on a stable treatment regimen and adequately controlled in the opinion of the investigator
• First morning protein-creatine ratio (PCR) at screening ≥400 milligrams per gram (mg/g) (Part B only)
• Clinical chemistry labs within acceptable range for the participant population, as per investigator judgment
• Men and women of non-childbearing potential as determined by medical history and physical examination

• Non-vasectomized male participants must agree to use a medically accepted method of contraception with all sexual partners during the study and for 90 days following the final dosing. Medically accepted effective forms of contraception may include condoms with contraceptive foam or having partners use diaphragms with contraceptive jelly or cervical caps with contraceptive jelly
• Female participants must be postmenopausal or surgically sterile to participate in this study. This is defined as females between age 45 to 75 years, inclusive, and either 12 months without a menstrual period [no follicle stimulating hormone (FSH) test required] or 6-12 months without a menstrual period and follicle stimulating hormone (FSH) greater than (>) 40 international units per liter (IU/L)
• Must weigh ≥50 kilograms (kg) at time of screening and dosing
• Acceptable sitting blood pressure (BP) per the following American Heart Association (AHA) guidelines:

• Normal: systolic blood pressure (SBP) <120 millimeters of mercury (mmHg) and diastolic blood pressure (DBP) <80 mmHg
• Prehypertension: SBP 120-139 or DBP 80-89
• High Blood Pressure (Hypertension) Stage 1: SBP 140-159 mmHg or DBP 90-99
• Have given written informed consent prior to any study-specific procedures
• Are reliable and willing to make themselves available for the duration of the study and are willing to follow site specific study procedures
• Have venous access sufficient to allow blood sampling
• Have laboratory values and other safety parameters that are, in the opinion of the investigator, acceptable fo participation for the study

Exclusion Criteria

• Have a diagnosis of chronic kidney disease (CKD) other than DKD, (hypertensive nephrosclerosis superimposed on DKD is acceptable)
• Have SBP >160 mmHg or DBP >100 mmHg

o Individuals with Stage 1 BP elevation (SBP 140-159 mmHg or DBP 90-99 mmHg) on some occasions during study, may be acceptable, as long as only non-protein-lowering antihypertensives are adjusted to achieve target BP goals (<140/90 mmHg)

• Current use of (or within 2 weeks of enrollment), or projected need for a renin inhibitor or aldosterone antagonist, or a combination of Angiotensin-converting enzyme inhibitors/angiotensin II receptor blockers (ACEi/ARB)
• Individuals in whom dialysis or transplantation is anticipated within 6 months of screening
• Have a history of acute kidney injury within 3 months of screening
• Are currently enrolled in, or discontinued within the last 60 days from, a clinical trial involving an investigational drug that has not received regulatory approval for any indication and/or have received treatment with biologic agents (such as monoclonal antibodies) within 3 months or 5 half-lives of the administered drug (whichever is longer) prior to dosing
• Have previously completed or withdrawn from this study or any other study investigating LY3016859
• Have a diagnosis of Class III or IV congestive heart failure (as defined by the New York Heart Association)
• Have an abnormality in the 12-lead Electrocardiogram (ECG) that, in the opinion of the investigator increases the risks associated with participating in the study. In addition, individuals with the following findings will be excluded:

• Confirmed corrected QT (QTcF) interval >450 milliseconds (msec) for men and >470 msec for women
• Irregular rhythms other than sinus arrhythmia or occasional, rare supraventricular ectopic beats
• History of unexplained syncope
• Family history of unexplained sudden death or sudden death due to long QT syndrome
• T-wave configurations are not of sufficient quality for assessing QT interval, as determined by the investigator
• Have evidence of human immunodeficiency virus (HIV) and/or positive human HIV antibodies; have a history of cirrhosis or hepatitis C or are positive for hepatitis C antibody at the screening visit; are known to be hepatitis B surface antigen-positive or are positive for hepatitis B surface antigen at the screening visit
• Are unwilling to discontinue use of Chinese herbs for at least 2 weeks prior to randomization and for the duration of their study participation
• Are unwilling or unable to comply with the use of a data collection device to directly record data from the participant
• Have donated blood of more than 500 milliliters (mL) within the last 60 days prior to screening
• Have an average weekly alcohol intake that exceeds 21 units per week or are unwilling to stop alcohol intake within 48 hours of entry into study and for the duration of the study (1 unit = 12 ounces (oz) or 360 mL of beer; 5 oz or 150 mL of wine; 1.5 oz or 45 mL of distilled spirits)
• Individuals who, in the opinion of the investigator, show evidence of regular use of drugs of abuse

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Eli Lilly and Company

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Call 1-877-CTLilly (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST_

Role: STUDY_DIRECTOR

Eli Lilly and Company

Locations

Innovative Research of West Florida

Clearwater, Florida, United States

Creighton University Medical Center

Omaha, Nebraska, United States

Northeast Clinical Research Center

Bethlehem, Pennsylvania, United States

Southeast Renal Research Institute

Chattanooga, Tennessee, United States

TAD Clinical Research

Lufkin, Texas, United States

Renal Associates, PA

San Antonio, Texas, United States

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Sofia, , Bulgaria

Countries

United States; Bulgaria

Other Identifiers

I5V-MC-TGAB

Identifier Type: OTHER

Identifier Source: secondary_id

2012-004496-40

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

14353

Identifier Type: -

Identifier Source: org_study_id