- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03590860
A Study of LY3322207 in Healthy Participants and in Participants With Hypertension (High Blood Pressure)
22. februar 2019 opdateret af: 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).
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
62
Fase
- Fase 1
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
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Groningen, Holland, 9728 NZ
- PRA Health Sciences
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år til 65 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
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
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Grundvidenskab
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: LY3322207 (Part A)
LY3322207 administered subcutaneously (SC)
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Administered by SC injection
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Placebo komparator: Placebo (Part A)
Placebo matching LY3322207 administered SC
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Administreret ved SC-injektion
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Eksperimentel: LY3322207 (Part B)
LY3322207 administered SC once weekly
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Administered by SC injection
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Placebo komparator: Placebo (Part B)
Placebo matching LY3322207 administered SC once weekly
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Administreret ved SC-injektion
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Eksperimentel: LY3322207 (Part C)
LY3322207 administered SC in participants with hypertension
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Administered by SC injection
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Number of Participants with One or More Serious Adverse Events (Part A)
Tidsramme: Baseline up to approximately 31 days
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Serious and other non-serious adverse events will be reported in the Adverse Events Module
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Baseline up to approximately 31 days
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Number of Participants with One or More Serious Adverse Events (Part B)
Tidsramme: Baseline up to approximately 9 weeks
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Serious and other non-serious adverse events will be reported in the Adverse Events Module
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Baseline up to approximately 9 weeks
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Number of Participants with One or More Serious Adverse Events (Part C)
Tidsramme: Baseline up to approximately 9 weeks
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Serious and other non-serious adverse events will be reported in the Adverse Events Module
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Baseline up to approximately 9 weeks
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Area Under the Concentration Versus Time Curve (AUC) of LY3322207 (Part A)
Tidsramme: Predose up approximately 31 days
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Pharmacokinetics (PK): AUC of LY3322207
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Predose up approximately 31 days
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Area Under the Concentration Versus Time Curve (AUC) of LY3322207 (Part B)
Tidsramme: Predose up to approximately 9 weeks
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PK: AUC of LY3322207
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Predose up to approximately 9 weeks
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Area Under the Concentration Versus Time Curve (AUC) of LY3322207 (Part C)
Tidsramme: Predose up to approximately 9 weeks
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PK: AUC of LY3322207
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Predose up to approximately 9 weeks
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Maximum Concentration (Cmax) of LY3322207 (Part A)
Tidsramme: Predose up approximately 31 days
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PK: Cmax of LY3322207
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Predose up approximately 31 days
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Maximum Concentration (Cmax) of LY3322207 (Part B)
Tidsramme: Predose up to approximately 9 weeks
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PK: Cmax of LY3322207
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Predose up to approximately 9 weeks
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Maximum Concentration (Cmax) of LY3322207 (Part C)
Tidsramme: Predose up to approximately 9 weeks
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PK: Cmax of LY3322207
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Predose up to approximately 9 weeks
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Time to reach Cmax (Tmax) of LY3322207 (Part A)
Tidsramme: Predose up to approximately Day 31
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PK: Tmax of LY3322207
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Predose up to approximately Day 31
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Time to reach Cmax (Tmax) of LY3322207 (Part B)
Tidsramme: Predose up to approximately 9 weeks
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PK: Tmax of LY3322207
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Predose up to approximately 9 weeks
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Time to reach Cmax (Tmax) of LY3322207 (Part C)
Tidsramme: Predose up to approximately 9 weeks
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PK: Tmax of LY3322207
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Predose up to approximately 9 weeks
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Change from Baseline in Systolic Blood Pressure (SBP) (Part A)
Tidsramme: Baseline up approximately 31 days
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Supine position
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Baseline up approximately 31 days
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Change from Baseline in Systolic Blood Pressure (SBP) (Part B)
Tidsramme: Baseline up to approximately 9 weeks
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Supine position
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Baseline up to approximately 9 weeks
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Change from Baseline in Systolic Blood Pressure (SBP) (Part C)
Tidsramme: Baseline up to approximately 9 weeks
|
Supine position
|
Baseline up to approximately 9 weeks
|
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Change from Baseline in Diastolic Blood Pressure (DBP) (Part A)
Tidsramme: Baseline up approximately 31 days
|
Supine position
|
Baseline up approximately 31 days
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Change from Baseline in Diastolic Blood Pressure (DBP) (Part B)
Tidsramme: Baseline up to approximately 9 weeks
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Supine position
|
Baseline up to approximately 9 weeks
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Change from Baseline in Diastolic Blood Pressure (DBP) (Part C)
Tidsramme: Baseline up to approximately 9 weeks
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Supine position
|
Baseline up to approximately 9 weeks
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Change from Baseline in Heart Rate (Part A)
Tidsramme: Baseline up approximately 31 days
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Supine position
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Baseline up approximately 31 days
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Change from Baseline in Heart Rate (Part B)
Tidsramme: Baseline up to approximately 9 weeks
|
Supine position
|
Baseline up to approximately 9 weeks
|
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Change from Baseline in Heart Rate (Part C)
Tidsramme: Baseline up to approximately 9 weeks
|
Supine position
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Baseline up to approximately 9 weeks
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
13. juli 2018
Primær færdiggørelse (Faktiske)
17. januar 2019
Studieafslutning (Faktiske)
17. januar 2019
Datoer for studieregistrering
Først indsendt
6. juli 2018
Først indsendt, der opfyldte QC-kriterier
6. juli 2018
Først opslået (Faktiske)
18. juli 2018
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
25. februar 2019
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
22. februar 2019
Sidst verificeret
1. februar 2019
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 16771
- I9K-MC-UCAA (Anden identifikator: Eli Lilly and Company)
- 2018-002337-38 (EudraCT nummer)
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ja
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
produkt fremstillet i og eksporteret fra U.S.A.
Ja
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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