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

22 febbraio 2019 aggiornato da: 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).

Panoramica dello studio

Stato

Terminato

Condizioni

Intervento / Trattamento

Tipo di studio

Interventistico

Iscrizione (Effettivo)

62

Fase

  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

      • Groningen, Olanda, 9728 NZ
        • PRA Health Sciences

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 18 anni a 65 anni (Adulto, Adulto più anziano)

Accetta volontari sani

Sessi ammissibili allo studio

Tutto

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Scienza basilare
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Doppio

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: LY3322207 (Part A)
LY3322207 administered subcutaneously (SC)
Administered by SC injection
Comparatore placebo: Placebo (Part A)
Placebo matching LY3322207 administered SC
Somministrato mediante iniezione SC
Sperimentale: LY3322207 (Part B)
LY3322207 administered SC once weekly
Administered by SC injection
Comparatore placebo: Placebo (Part B)
Placebo matching LY3322207 administered SC once weekly
Somministrato mediante iniezione SC
Sperimentale: LY3322207 (Part C)
LY3322207 administered SC in participants with hypertension
Administered by SC injection

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Number of Participants with One or More Serious Adverse Events (Part A)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Area Under the Concentration Versus Time Curve (AUC) of LY3322207 (Part A)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: Predose up to approximately 9 weeks
PK: AUC of LY3322207
Predose up to approximately 9 weeks
Maximum Concentration (Cmax) of LY3322207 (Part A)
Lasso di tempo: Predose up approximately 31 days
PK: Cmax of LY3322207
Predose up approximately 31 days
Maximum Concentration (Cmax) of LY3322207 (Part B)
Lasso di tempo: Predose up to approximately 9 weeks
PK: Cmax of LY3322207
Predose up to approximately 9 weeks
Maximum Concentration (Cmax) of LY3322207 (Part C)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: Baseline up approximately 31 days
Supine position
Baseline up approximately 31 days
Change from Baseline in Systolic Blood Pressure (SBP) (Part B)
Lasso di tempo: Baseline up to approximately 9 weeks
Supine position
Baseline up to approximately 9 weeks
Change from Baseline in Systolic Blood Pressure (SBP) (Part C)
Lasso di tempo: Baseline up to approximately 9 weeks
Supine position
Baseline up to approximately 9 weeks
Change from Baseline in Diastolic Blood Pressure (DBP) (Part A)
Lasso di tempo: Baseline up approximately 31 days
Supine position
Baseline up approximately 31 days
Change from Baseline in Diastolic Blood Pressure (DBP) (Part B)
Lasso di tempo: Baseline up to approximately 9 weeks
Supine position
Baseline up to approximately 9 weeks
Change from Baseline in Diastolic Blood Pressure (DBP) (Part C)
Lasso di tempo: Baseline up to approximately 9 weeks
Supine position
Baseline up to approximately 9 weeks
Change from Baseline in Heart Rate (Part A)
Lasso di tempo: Baseline up approximately 31 days
Supine position
Baseline up approximately 31 days
Change from Baseline in Heart Rate (Part B)
Lasso di tempo: Baseline up to approximately 9 weeks
Supine position
Baseline up to approximately 9 weeks
Change from Baseline in Heart Rate (Part C)
Lasso di tempo: Baseline up to approximately 9 weeks
Supine position
Baseline up to approximately 9 weeks

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

13 luglio 2018

Completamento primario (Effettivo)

17 gennaio 2019

Completamento dello studio (Effettivo)

17 gennaio 2019

Date di iscrizione allo studio

Primo inviato

6 luglio 2018

Primo inviato che soddisfa i criteri di controllo qualità

6 luglio 2018

Primo Inserito (Effettivo)

18 luglio 2018

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

25 febbraio 2019

Ultimo aggiornamento inviato che soddisfa i criteri QC

22 febbraio 2019

Ultimo verificato

1 febbraio 2019

Maggiori informazioni

Termini relativi a questo studio

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • 16771
  • I9K-MC-UCAA (Altro identificatore: Eli Lilly and Company)
  • 2018-002337-38 (Numero EudraCT)

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

prodotto fabbricato ed esportato dagli Stati Uniti

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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