A Study to Assess the Safety, Tolerability and Pharmacokinetics of Viaca (Sildenafil + Cabergoline) Compared With Sildenafil and Cabergoline
An Open-Label Single-Ascending Dose Study to Investigate the Safety, Tolerability and Pharmacokinetics of Viaca (Sildenafil + Cabergoline) Compared With Sildenafil and Cabergoline in Healthy Volunteers
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
Intervención / Tratamiento
Intervención / Tratamiento
Descripción detallada
Tipo de estudio
Tipo de estudio
Inscripción (Estimado)
Inscripción
Fase
Fase
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
Estudio Contacto
- Nombre: Clinical Research Coordinator at Nucleus Network Brisbane
- Número de teléfono: 1800 243 733
- Correo electrónico: brisbane@nucleusnetwork.com
Ubicaciones de estudio
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Queensland
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Herston, Queensland, Australia, 4006
- Nucleus Network Brisbane
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Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Male participants, aged 18 to 65 years (inclusive) at the time of informed consent.
- In good general health (Investigator judgement) with no significant medical history and no clinically significant abnormalities on physical examination, vital signs, or 12-lead ECG - including systolic blood pressure 110-140 mmHg (inclusive) at Screening and Day -1 - at Screening and/or before first IP administration.
- BMI ≥ 18.0 and ≤ 32.0 kg/m² and weight ≥ 50 kg.
- Nonsmoker or casual smoker (< 5 cigarettes/week equivalent) with no tobacco use within 2 months prior to Screening (Investigator discretion).
- Clinical laboratory values within normal range (or not clinically significant per Investigator).
- Fertile men agree to acceptable contraception from Screening until 90 days after last IP dose, and no sperm donation from first dose until ≥ 90 days after last dose.
- Able and willing to attend required study visits.
- Able and willing to provide written informed consent before any study procedures.
Exclusion Criteria:
- Physical or psychological condition that would impair protocol compliance or study completion (Investigator judgement).
- History of, or condition that would contraindicate study medication or interfere with study evaluations (Investigator judgement).
- Previous history of any of: myocardial infarction; cerebrovascular accident; arrhythmia; congestive heart failure; unstable angina; recent (<6 months) need for calcium-channel/beta-blocker/nitrate/anti-epileptic therapy; uncontrolled hypertension (SBP >140 or DBP >100 mmHg); hypotension (SBP <90 or DBP <60 mmHg) incl. syncope/orthostatic/vasovagal; pulmonary/pericardial/retroperitoneal fibrotic disorders; sickle-cell disease or trait; cardiac valve disease; severe psychiatric disorders; Raynaud's/vasospastic disorders; bariatric surgery (cholecystectomy acceptable).
- Blood/plasma donation or significant blood loss (450 mL) within 30 days prior to first IP dose.
- Fever (>38°C) or symptomatic viral/bacterial infection within 2 weeks prior to Screening.
- Infections requiring parenteral antibiotics within 1 month prior to Screening.
- Concomitant use of an indwelling urethral catheter.
- Concomitant nitrates/nitric-oxide donors, potent CYP3A4 inhibitors (e.g. ritonavir, indinavir, ketoconazole) or moderate inhibitors (e.g. erythromycin); unwilling to avoid St. John's wort and CYP3A4-active herbals (e.g. grapefruit) within 14 days prior and throughout the study.
- Medications that significantly affect BP: nitrates (any form), alpha-blockers (e.g. doxazosin, terazosin, tamsulosin), guanylate cyclase stimulators (e.g. riociguat).
- Positive HCV antibody, HBsAg, or HIV antibody.
- Live vaccine within 4 weeks prior to first IP dose.
- Poor pill-swallowing ability or poor venous access.
- History of severe allergic/anaphylactic reactions or sensitivity to IP or constituents.
- History of malignancy (except non-melanoma skin cancer excised >5 years prior to Screening).
- Clinically significant abnormal Screening ECG (e.g. QRS ≥ 120 msec and/or QTcF > 450 msec, per Investigator).
- History/evidence of renal disease or eGFR < 60 mL/min/1.73 m² at Screening (2021 CKD-EPI creatinine equation).
- Immunosuppressive drug exposure (incl. experimental therapies) within 4 months or 5 half-lives (whichever longer) prior to Screening.
- Positive urine toxicology panel (barbiturates, THC, amphetamines/methamphetamines, methadone, MDMA, phencyclidine, tricyclic antidepressants, benzodiazepines, opiates, cocaine) or positive alcohol breath test.
- Unwilling to abstain from alcohol, caffeine and nicotine from 48 h prior to admission, during confinement, and 48 h prior to follow-up visits.
- History of substance abuse/dependency or recreational IV drug use in the last 12 months (self-declared).
- Unwilling to refrain from strenuous exercise (incl. weightlifting) 48 h prior to admission and follow-up visits.
- Anything the Investigator considers would jeopardize participant safety, prevent full participation, or compromise data interpretation.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Ciencia básica
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación Secuencial
- Enmascaramiento: Ninguno (etiqueta abierta)
Número de brazos
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
|---|---|
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Experimental: Cohort 1: Viaca 25/0.25 mg
Single oral dose of Viaca (sildenafil 25 mg / cabergoline 0.25 mg; one low-dose tablet) in 6 healthy male participants.
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fixed-dose oral tablet of sildenafil + cabergoline (low-dose 25/0.25 mg; high-dose 50/0.5 mg).
Single oral dose.
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Experimental: Cohort 2: Viaca 50/0.5 mg
Single oral dose of Viaca (sildenafil 50 mg / cabergoline 0.5 mg; one high-dose tablet
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fixed-dose oral tablet of sildenafil + cabergoline (low-dose 25/0.25 mg; high-dose 50/0.5 mg).
Single oral dose.
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Experimental: Cohort 3: Viaca 75/0.75 mg
Single oral dose of Viaca (sildenafil 75 mg / cabergoline 0.75 mg; one low + one high tablet
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fixed-dose oral tablet of sildenafil + cabergoline (low-dose 25/0.25 mg; high-dose 50/0.5 mg).
Single oral dose.
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Comparador activo: Cohort 4: Sildenafil 50 mg
Single oral dose of sildenafil 50 mg (two 25 mg tablets).
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single oral dose
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Comparador activo: Cohort 5: Cabergoline 0.5 mg
Single oral dose of cabergoline 0.5 mg (one 0.5 mg tablet).
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single oral dose
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¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Participants with AEs/SAEs
Periodo de tiempo: Day 1 (dosing) through Day 8
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Number of participants with treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs).
Unit: participants (summarised by severity and relatedness).
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Day 1 (dosing) through Day 8
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Blood pressure
Periodo de tiempo: Baseline through Day 8.
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Change from Baseline in systolic and diastolic blood pressure.
Unit: mmHg.
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Baseline through Day 8.
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Pulse rate
Periodo de tiempo: Baseline through Day 8.
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Change from Baseline in pulse rate.
Unit: beats/min.
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Baseline through Day 8.
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Respiratory rate
Periodo de tiempo: Baseline through Day 8.
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Change from Baseline in respiratory rate.
Unit: breaths/min.
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Baseline through Day 8.
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Body temperature
Periodo de tiempo: Baseline through Day 8.
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Change from Baseline in body temperature.
Unit: °C.
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Baseline through Day 8.
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ECG heart rate
Periodo de tiempo: Baseline through Day 8.
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Change from Baseline in 12-lead ECG heart rate.
Unit: beats/min.
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Baseline through Day 8.
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ECG intervals
Periodo de tiempo: Baseline through Day 8.
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Change from Baseline in 12-lead ECG intervals (QTcF, PR, QRS).
Unit: milliseconds.
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Baseline through Day 8.
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Laboratory tests
Periodo de tiempo: Baseline through Day 8.
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Number of participants with clinically significant safety laboratory abnormalities.
Unit: participants.
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Baseline through Day 8.
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Physical examination
Periodo de tiempo: Baseline through Day 8.
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Number of participants with clinically significant physical examination findings.
Unit: participants.
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Baseline through Day 8.
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Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Cmax
Periodo de tiempo: Predose (Day 1) through 168 hours post-dose (Day 8).
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Maximum observed plasma concentration (Cmax).
Unit: e.g.
ng/mL.
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Predose (Day 1) through 168 hours post-dose (Day 8).
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Tmax
Periodo de tiempo: Predose (Day 1) through 168 hours post-dose (Day 8).
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Time to maximum plasma concentration (Tmax).
Unit: hours.
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Predose (Day 1) through 168 hours post-dose (Day 8).
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AUC0-t
Periodo de tiempo: Predose (Day 1) through 168 hours post-dose (Day 8)
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Area under the plasma concentration-time curve from time 0 to the last measurable concentration (AUC0-t).
Unit: e.g.
ng·h/mL.
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Predose (Day 1) through 168 hours post-dose (Day 8)
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AUC0-24
Periodo de tiempo: Predose (Day 1) through 168 hours post-dose (Day 8).
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AUC from time 0 to 24 hours (AUC0-24).
Unit: e.g.
ng·h/mL.
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Predose (Day 1) through 168 hours post-dose (Day 8).
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AUC0-inf
Periodo de tiempo: Predose (Day 1) through 168 hours post-dose (Day 8).
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AUC from time 0 extrapolated to infinity (AUC0-inf).
Unit: e.g.
ng·h/mL.
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Predose (Day 1) through 168 hours post-dose (Day 8).
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%AUCextrap
Periodo de tiempo: Predose (Day 1) through 168 hours post-dose (Day 8).
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Percentage of AUC0-inf obtained by extrapolation (%AUCextrap).
Unit: percentage.
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Predose (Day 1) through 168 hours post-dose (Day 8).
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t½
Periodo de tiempo: Predose (Day 1) through 168 hours post-dose (Day 8).
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Apparent terminal elimination half-life (t½).
Unit: hours.
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Predose (Day 1) through 168 hours post-dose (Day 8).
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kel
Periodo de tiempo: Predose (Day 1) through 168 hours post-dose (Day 8).
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Terminal elimination rate constant (kel).
Unit: 1/hour.
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Predose (Day 1) through 168 hours post-dose (Day 8).
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CL/F
Periodo de tiempo: Predose (Day 1) through 168 hours post-dose (Day 8).
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Apparent total clearance after oral dosing (CL/F).
Unit: e.g.
L/h.
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Predose (Day 1) through 168 hours post-dose (Day 8).
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Vz/F
Periodo de tiempo: Predose (Day 1) through 168 hours post-dose (Day 8).
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Apparent volume of distribution during the terminal phase after oral dosing (Vz/F).
Unit: e.g.
L.
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Predose (Day 1) through 168 hours post-dose (Day 8).
|
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Cmax/D
Periodo de tiempo: Predose (Day 1) through 168 hours post-dose (Day 8).
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Dose-normalised maximum plasma concentration (Cmax/D).
Unit: e.g.
ng/mL per mg.
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Predose (Day 1) through 168 hours post-dose (Day 8).
|
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AUC0-inf/D
Periodo de tiempo: Predose (Day 1) through 168 hours post-dose (Day 8).
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Dose-normalised AUC0-inf (AUC0-inf/D).
Unit: e.g.
ng·h/mL per mg.
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Predose (Day 1) through 168 hours post-dose (Day 8).
|
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AUC0-t/D
Periodo de tiempo: Predose (Day 1) through 168 hours post-dose (Day 8).
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Dose-normalised AUC0-t (AUC0-t/D).
Unit: e.g.
ng·h/mL per mg.
|
Predose (Day 1) through 168 hours post-dose (Day 8).
|
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Dose proportionality
Periodo de tiempo: Predose (Day 1) through 168 hours post-dose (Day 8).
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Dose proportionality of Cmax and AUC across Viaca dose levels.
Unit: e.g.
slope (power-model estimate).
|
Predose (Day 1) through 168 hours post-dose (Day 8).
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Colaboradores e Investigadores
Patrocinador
Patrocinador
Colaboradores
Colaboradores
Investigadores
Investigadores
- Investigador principal: Emma Trowbridge, MD, Nucleus Network Brisbane
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Inicio del estudio
Finalización primaria (Estimado)
Finalización primaria
Finalización del estudio (Estimado)
Finalización del estudio
Fechas de registro del estudio
Enviado por primera vez
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Publicado por primera vez
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización publicada
Última actualización enviada que cumplió con los criterios de control de calidad
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Enfermedades urogenitales
- Enfermedades Genitales
- Desordenes mentales
- Enfermedades Genitales Masculinas
- Enfermedades urogenitales masculinas
- Disfunción Sexual Fisiológica
- Disfunciones Sexuales Psicológicas
- Disfuncion erectil
- Compuestos de azufre
- Químicos orgánicos
- Compuestos heterocíclicos, 1 anillo
- Compuestos heterocíclicos
- Compuestos heterocíclicos, 2 anillos
- Compuestos heterocíclicos, anillo fusionado
- Alcaloides
- Amidas
- Purinas
- Compuestos heterocíclicos, 4 o más anillos
- Sulfonamidas
- Sulfonas
- Piperazines
- Alcaloides de Ergot
- Ergolinas
- Citrato de sildenafilo
- Cabergolina
Otros números de identificación del estudio
Otros números de identificación del estudio
- CR-067-001
- EC00372 (Otro identificador: Bellberry HREC code)
- 462/26 (Otro identificador: Alfred governance)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
producto fabricado y exportado desde los EE. UU.
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