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A Study of LY3322207 in Healthy Participants and in Participants With Hypertension (High Blood Pressure)

22 februari 2019 uppdaterad av: Eli Lilly and Company

A Safety, Tolerability, and Pharmacokinetic Study of Single and Multiple Ascending Doses of LY3322207 in Healthy Subjects and Subjects With Hypertension on ACE I/ARB Therapy

The purpose of this study is to investigate the safety of the study drug known as LY3322207. Participants must be healthy or must have hypertension (high blood pressure). Participants with hypertension may already be taking a common drug to reduce blood pressure called an angiotensin-converting enzyme inhibitor (ACE-I) or an angiotensin II receptor blocker (ARB).

Studieöversikt

Status

Avslutad

Betingelser

Studietyp

Interventionell

Inskrivning (Faktisk)

62

Fas

  • Fas 1

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

      • Groningen, Nederländerna, 9728 NZ
        • PRA Health Sciences

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 65 år (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  • Healthy males, as determined by medical history and physical examination, must agree to use a medically appropriate method of birth control and agree not to donate sperm from start of dosing until 90 days beyond last dose
  • Healthy females, as determined by medical history and physical examination, of non-child bearing potential due to:

    • Menopause: spontaneous amenorrhea for at least 12 months, not induced by a medical condition such as anorexia nervosa and not taking medications that induced the amenorrhea (for example: oral contraceptives, hormones, gonadotropin releasing hormone, anti-estrogens, selective estrogen receptor modulators, or chemotherapy)
    • Surgical sterilization
  • Are reliable and willing to make themselves available for the duration of the study and are willing to follow site specific study procedures
  • Have a Body Mass Index (BMI) 18 to 30 kilogram per square meter (kg/m²) at entry
  • Have clinical laboratory test results within normal reference range for the population or site, or results with acceptable deviations that are judged not clinically significant
  • Be 18 to 55 years old for either Part A or Part B of the study, or 18 to 65 years old for Part C only
  • For Part C: must have been treated with a stable dose of ACE-I or ARB for at least 1 month

Exclusion Criteria:

  • 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
  • Have previously completed or withdrawn from this study or any other study investigating this study drug
  • Have a history or presence of medical illness including, but not limited to, any cardiovascular, hepatic, respiratory, hematological, endocrine, psychiatric or neurological disease, significant atopy, or any clinically significant laboratory abnormality that would preclude study participation
  • Have abnormality in the 12-lead electrocardiogram (ECG) which increases study risk
  • Have confirmed QT interval corrected by Bazett's method (QTcB) or Fridericia's (QTcF) method >450 millisecond (msec) for men and >470 msec for women
  • Have prior Q-wave myocardial infarction or other, specific heart abnormalities, arrhythmias or fibrillations
  • Have an abnormal blood pressure (supine) defined as diastolic blood pressure greater than (>)95 or less than (<)50 millimeters of mercury (mmHg) and/or systolic blood pressure >160 or <90 mmHg
  • Show evidence of human immunodeficiency virus (HIV), hepatitis C, or hepatitis B
  • Have donated blood of more than 100 mL (milliliters) within the last month
  • Are unwilling to stop alcohol consumption while resident in the Clinical Research Unit
  • Have an average weekly alcohol intake that exceeds 21 units per week (1 unit equal to (=) 12 ounces (oz) or 360 mL of beer; 5 oz or 150 mL of wine; 1.5 oz or 45 mL of distilled spirits)
  • Have an abnormal blood pressure (supine) defined as diastolic blood pressure >95 or <50 mmHg and/or systolic blood pressure >160 or <90 mmHg
  • Have serum potassium outside normal range
  • Have had lymphoma, leukemia, or any malignancy within the past 5 years
  • Have clinically significant multiple or severe drug allergies or intolerance
  • Are lactating women
  • Positive findings for known drugs of abuse
  • Have received treatment with biologic agents within 3 months or 5 half-lives prior to dosing
  • Participation in any other clinical trial involving a study drug or off-label use of a drug or device, or any other type of medical research judged not to be compatible with this study
  • Have estimated glomerular filtration rate (eGFR) < 60 milliliters per minute per 1.73 square meter (mL/min/1.73 m²) for Parts A and B of this study, or eGFR < 50 mL/min/1.73 m² in Part C only
  • For Part C: have a history of severe hypertension (defined as SBP greater than or equal to (≥)180 mmHg and/or DBP ≥120 mmHg), secondary hypertension, symptomatic postural hypotension, or hospitalization due to hypertension
  • For Part C: have a history of supraventricular tachycardia (for example, atrial fibrillation), ventricular tachycardia, or other cardiac arrhythmia
  • For Part C: have resting tachycardia (heart rate ≥100 beats per minute)
  • For Part C: have New York Heart Association (NYHA) Class II, III, or IV heart failure, or had any of the following in the previous 3 months: coronary angioplasty, coronary stent placement, coronary bypass surgery or any significant cardiac surgery, myocardial infarction, unstable angina pectoris, cerebrovascular accident, or transient ischemic attack
  • For Part C: have an automatic internal cardioverter-defibrillator
  • For Part C: have diabetes

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Grundläggande vetenskap
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Dubbel

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: LY3322207 (Part A)
LY3322207 administered subcutaneously (SC)
Administered by SC injection
Placebo-jämförare: Placebo (Part A)
Placebo matching LY3322207 administered SC
Administreras genom SC-injektion
Experimentell: LY3322207 (Part B)
LY3322207 administered SC once weekly
Administered by SC injection
Placebo-jämförare: Placebo (Part B)
Placebo matching LY3322207 administered SC once weekly
Administreras genom SC-injektion
Experimentell: LY3322207 (Part C)
LY3322207 administered SC in participants with hypertension
Administered by SC injection

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Number of Participants with One or More Serious Adverse Events (Part A)
Tidsram: Baseline up to approximately 31 days
Serious and other non-serious adverse events will be reported in the Adverse Events Module
Baseline up to approximately 31 days
Number of Participants with One or More Serious Adverse Events (Part B)
Tidsram: Baseline up to approximately 9 weeks
Serious and other non-serious adverse events will be reported in the Adverse Events Module
Baseline up to approximately 9 weeks
Number of Participants with One or More Serious Adverse Events (Part C)
Tidsram: Baseline up to approximately 9 weeks
Serious and other non-serious adverse events will be reported in the Adverse Events Module
Baseline up to approximately 9 weeks

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Area Under the Concentration Versus Time Curve (AUC) of LY3322207 (Part A)
Tidsram: Predose up approximately 31 days
Pharmacokinetics (PK): AUC of LY3322207
Predose up approximately 31 days
Area Under the Concentration Versus Time Curve (AUC) of LY3322207 (Part B)
Tidsram: Predose up to approximately 9 weeks
PK: AUC of LY3322207
Predose up to approximately 9 weeks
Area Under the Concentration Versus Time Curve (AUC) of LY3322207 (Part C)
Tidsram: Predose up to approximately 9 weeks
PK: AUC of LY3322207
Predose up to approximately 9 weeks
Maximum Concentration (Cmax) of LY3322207 (Part A)
Tidsram: Predose up approximately 31 days
PK: Cmax of LY3322207
Predose up approximately 31 days
Maximum Concentration (Cmax) of LY3322207 (Part B)
Tidsram: Predose up to approximately 9 weeks
PK: Cmax of LY3322207
Predose up to approximately 9 weeks
Maximum Concentration (Cmax) of LY3322207 (Part C)
Tidsram: Predose up to approximately 9 weeks
PK: Cmax of LY3322207
Predose up to approximately 9 weeks
Time to reach Cmax (Tmax) of LY3322207 (Part A)
Tidsram: Predose up to approximately Day 31
PK: Tmax of LY3322207
Predose up to approximately Day 31
Time to reach Cmax (Tmax) of LY3322207 (Part B)
Tidsram: Predose up to approximately 9 weeks
PK: Tmax of LY3322207
Predose up to approximately 9 weeks
Time to reach Cmax (Tmax) of LY3322207 (Part C)
Tidsram: Predose up to approximately 9 weeks
PK: Tmax of LY3322207
Predose up to approximately 9 weeks
Change from Baseline in Systolic Blood Pressure (SBP) (Part A)
Tidsram: Baseline up approximately 31 days
Supine position
Baseline up approximately 31 days
Change from Baseline in Systolic Blood Pressure (SBP) (Part B)
Tidsram: Baseline up to approximately 9 weeks
Supine position
Baseline up to approximately 9 weeks
Change from Baseline in Systolic Blood Pressure (SBP) (Part C)
Tidsram: Baseline up to approximately 9 weeks
Supine position
Baseline up to approximately 9 weeks
Change from Baseline in Diastolic Blood Pressure (DBP) (Part A)
Tidsram: Baseline up approximately 31 days
Supine position
Baseline up approximately 31 days
Change from Baseline in Diastolic Blood Pressure (DBP) (Part B)
Tidsram: Baseline up to approximately 9 weeks
Supine position
Baseline up to approximately 9 weeks
Change from Baseline in Diastolic Blood Pressure (DBP) (Part C)
Tidsram: Baseline up to approximately 9 weeks
Supine position
Baseline up to approximately 9 weeks
Change from Baseline in Heart Rate (Part A)
Tidsram: Baseline up approximately 31 days
Supine position
Baseline up approximately 31 days
Change from Baseline in Heart Rate (Part B)
Tidsram: Baseline up to approximately 9 weeks
Supine position
Baseline up to approximately 9 weeks
Change from Baseline in Heart Rate (Part C)
Tidsram: Baseline up to approximately 9 weeks
Supine position
Baseline up to approximately 9 weeks

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

13 juli 2018

Primärt slutförande (Faktisk)

17 januari 2019

Avslutad studie (Faktisk)

17 januari 2019

Studieregistreringsdatum

Först inskickad

6 juli 2018

Först inskickad som uppfyllde QC-kriterierna

6 juli 2018

Första postat (Faktisk)

18 juli 2018

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

25 februari 2019

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

22 februari 2019

Senast verifierad

1 februari 2019

Mer information

Termer relaterade till denna studie

Ytterligare relevanta MeSH-villkor

Andra studie-ID-nummer

  • 16771
  • I9K-MC-UCAA (Annan identifierare: Eli Lilly and Company)
  • 2018-002337-38 (EudraCT-nummer)

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Ja

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

produkt tillverkad i och exporterad från U.S.A.

Ja

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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