- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07732387
A Study to Assess the Safety, Tolerability and Pharmacokinetics of Viaca (Sildenafil + Cabergoline) Compared With Sildenafil and Cabergoline
23. Juli 2026 aktualisiert von: Yanping Kong
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
This is a Phase 1, open-label, single-ascending-dose study evaluating the safety, tolerability, and pharmacokinetics (PK) of Viaca - a fixed-dose oral combination of sildenafil (a PDE5 inhibitor) and cabergoline (a dopamine D2 agonist) - versus sildenafil monotherapy and cabergoline monotherapy in healthy adult male volunteers.
Approximately 30 participants are enrolled across 5 sequential cohorts (6 each).
Each participant receives a single oral dose.
The combination targets erectile dysfunction through both vascular and neuroendocrine pathways, aiming for efficacy at lower component doses.
Studienübersicht
Status
Noch keine Rekrutierung
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
Five cohorts of 6 healthy male participants each (n≈30).
Viaca dose cohorts: Cohort 1 (25/0.25 mg), Cohort 2 (50/0.5 mg), Cohort 3 (75/0.75
mg).
Active-comparator cohorts: Cohort 4 (sildenafil 50 mg) and Cohort 5 (cabergoline 0.5 mg).
Cohort 1 runs first; after Safety Review Committee (SRC) review of safety/tolerability/PK through Day 3, Cohorts 2, 4 and 5 may proceed in parallel; Cohort 3 proceeds after SRC review of Cohort 2. Participants fast ≥8 h overnight before dosing and 2 h after.
They are confined to a Phase 1 unit and discharged on Day 5 (Cohorts 1-3 and 5) or Day 2 (Cohort 4), with a follow-up visit on Day 8 (±1).
Total participation ~33 days including screening.
(V2.0 amendment removed the former optional high-dose Viaca cohort.)
Studientyp
Interventionell
Einschreibung (Geschätzt)
30
Phase
- Phase 1
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienkontakt
- Name: Clinical Research Coordinator at Nucleus Network Brisbane
- Telefonnummer: 1800 243 733
- E-Mail: brisbane@nucleusnetwork.com
Studienorte
-
-
Queensland
-
Herston, Queensland, Australien, 4006
- Nucleus Network Brisbane
-
-
Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Ja
Beschreibung
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.
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Grundlegende Wissenschaft
- Zuteilung: Nicht randomisiert
- Interventionsmodell: Sequenzielle Zuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
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.
|
fixed-dose oral tablet of sildenafil + cabergoline (low-dose 25/0.25 mg; high-dose 50/0.5 mg).
Single oral dose.
|
|
Experimental: Cohort 2: Viaca 50/0.5 mg
Single oral dose of Viaca (sildenafil 50 mg / cabergoline 0.5 mg; one high-dose tablet
|
fixed-dose oral tablet of sildenafil + cabergoline (low-dose 25/0.25 mg; high-dose 50/0.5 mg).
Single oral dose.
|
|
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
|
fixed-dose oral tablet of sildenafil + cabergoline (low-dose 25/0.25 mg; high-dose 50/0.5 mg).
Single oral dose.
|
|
Aktiver Komparator: Cohort 4: Sildenafil 50 mg
Single oral dose of sildenafil 50 mg (two 25 mg tablets).
|
single oral dose
|
|
Aktiver Komparator: Cohort 5: Cabergoline 0.5 mg
Single oral dose of cabergoline 0.5 mg (one 0.5 mg tablet).
|
single oral dose
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Participants with AEs/SAEs
Zeitfenster: Day 1 (dosing) through Day 8
|
Number of participants with treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs).
Unit: participants (summarised by severity and relatedness).
|
Day 1 (dosing) through Day 8
|
|
Blood pressure
Zeitfenster: Baseline through Day 8.
|
Change from Baseline in systolic and diastolic blood pressure.
Unit: mmHg.
|
Baseline through Day 8.
|
|
Pulse rate
Zeitfenster: Baseline through Day 8.
|
Change from Baseline in pulse rate.
Unit: beats/min.
|
Baseline through Day 8.
|
|
Respiratory rate
Zeitfenster: Baseline through Day 8.
|
Change from Baseline in respiratory rate.
Unit: breaths/min.
|
Baseline through Day 8.
|
|
Body temperature
Zeitfenster: Baseline through Day 8.
|
Change from Baseline in body temperature.
Unit: °C.
|
Baseline through Day 8.
|
|
ECG heart rate
Zeitfenster: Baseline through Day 8.
|
Change from Baseline in 12-lead ECG heart rate.
Unit: beats/min.
|
Baseline through Day 8.
|
|
ECG intervals
Zeitfenster: Baseline through Day 8.
|
Change from Baseline in 12-lead ECG intervals (QTcF, PR, QRS).
Unit: milliseconds.
|
Baseline through Day 8.
|
|
Laboratory tests
Zeitfenster: Baseline through Day 8.
|
Number of participants with clinically significant safety laboratory abnormalities.
Unit: participants.
|
Baseline through Day 8.
|
|
Physical examination
Zeitfenster: Baseline through Day 8.
|
Number of participants with clinically significant physical examination findings.
Unit: participants.
|
Baseline through Day 8.
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Cmax
Zeitfenster: Predose (Day 1) through 168 hours post-dose (Day 8).
|
Maximum observed plasma concentration (Cmax).
Unit: e.g.
ng/mL.
|
Predose (Day 1) through 168 hours post-dose (Day 8).
|
|
Tmax
Zeitfenster: Predose (Day 1) through 168 hours post-dose (Day 8).
|
Time to maximum plasma concentration (Tmax).
Unit: hours.
|
Predose (Day 1) through 168 hours post-dose (Day 8).
|
|
AUC0-t
Zeitfenster: Predose (Day 1) through 168 hours post-dose (Day 8)
|
Area under the plasma concentration-time curve from time 0 to the last measurable concentration (AUC0-t).
Unit: e.g.
ng·h/mL.
|
Predose (Day 1) through 168 hours post-dose (Day 8)
|
|
AUC0-24
Zeitfenster: Predose (Day 1) through 168 hours post-dose (Day 8).
|
AUC from time 0 to 24 hours (AUC0-24).
Unit: e.g.
ng·h/mL.
|
Predose (Day 1) through 168 hours post-dose (Day 8).
|
|
AUC0-inf
Zeitfenster: Predose (Day 1) through 168 hours post-dose (Day 8).
|
AUC from time 0 extrapolated to infinity (AUC0-inf).
Unit: e.g.
ng·h/mL.
|
Predose (Day 1) through 168 hours post-dose (Day 8).
|
|
%AUCextrap
Zeitfenster: Predose (Day 1) through 168 hours post-dose (Day 8).
|
Percentage of AUC0-inf obtained by extrapolation (%AUCextrap).
Unit: percentage.
|
Predose (Day 1) through 168 hours post-dose (Day 8).
|
|
t½
Zeitfenster: Predose (Day 1) through 168 hours post-dose (Day 8).
|
Apparent terminal elimination half-life (t½).
Unit: hours.
|
Predose (Day 1) through 168 hours post-dose (Day 8).
|
|
kel
Zeitfenster: Predose (Day 1) through 168 hours post-dose (Day 8).
|
Terminal elimination rate constant (kel).
Unit: 1/hour.
|
Predose (Day 1) through 168 hours post-dose (Day 8).
|
|
CL/F
Zeitfenster: Predose (Day 1) through 168 hours post-dose (Day 8).
|
Apparent total clearance after oral dosing (CL/F).
Unit: e.g.
L/h.
|
Predose (Day 1) through 168 hours post-dose (Day 8).
|
|
Vz/F
Zeitfenster: Predose (Day 1) through 168 hours post-dose (Day 8).
|
Apparent volume of distribution during the terminal phase after oral dosing (Vz/F).
Unit: e.g.
L.
|
Predose (Day 1) through 168 hours post-dose (Day 8).
|
|
Cmax/D
Zeitfenster: Predose (Day 1) through 168 hours post-dose (Day 8).
|
Dose-normalised maximum plasma concentration (Cmax/D).
Unit: e.g.
ng/mL per mg.
|
Predose (Day 1) through 168 hours post-dose (Day 8).
|
|
AUC0-inf/D
Zeitfenster: Predose (Day 1) through 168 hours post-dose (Day 8).
|
Dose-normalised AUC0-inf (AUC0-inf/D).
Unit: e.g.
ng·h/mL per mg.
|
Predose (Day 1) through 168 hours post-dose (Day 8).
|
|
AUC0-t/D
Zeitfenster: Predose (Day 1) through 168 hours post-dose (Day 8).
|
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).
|
|
Dose proportionality
Zeitfenster: Predose (Day 1) through 168 hours post-dose (Day 8).
|
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).
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Mitarbeiter
Ermittler
- Hauptermittler: Emma Trowbridge, MD, Nucleus Network Brisbane
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Geschätzt)
1. August 2026
Primärer Abschluss (Geschätzt)
19. September 2026
Studienabschluss (Geschätzt)
19. September 2026
Studienanmeldedaten
Zuerst eingereicht
13. Juli 2026
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
23. Juli 2026
Zuerst gepostet (Tatsächlich)
28. Juli 2026
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
28. Juli 2026
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
23. Juli 2026
Zuletzt verifiziert
1. Juli 2026
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Urogenitale Erkrankungen
- Genitalerkrankungen
- Psychische Störungen
- Genitalerkrankungen, männlich
- Männliche Urogenitalerkrankungen
- Sexuelle Dysfunktion, Physiologisch
- Sexuelle Dysfunktionen, Psychisch
- Erektile Dysfunktion
- Schwefelverbindungen
- Organische Chemikalien
- Heterocyclische Verbindungen, 1-Ring
- Heterocyclische Verbindungen
- Heterocyclische Verbindungen, 2-Ring
- Heterocyclische Verbindungen, Fusionsring
- Alkaloide
- Amides
- Purines
- Heterocyclische Verbindungen, 4 oder mehr Ringe
- Sulfonamide
- Sulfone
- Piperazines
- Ergot -Alkaloide
- Ergoline
- Sildenafil Citrat
- Cabergolin
Andere Studien-ID-Nummern
- CR-067-001
- EC00372 (Andere Kennung: Bellberry HREC code)
- 462/26 (Andere Kennung: Alfred governance)
Plan für individuelle Teilnehmerdaten (IPD)
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Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Nein
Produkt, das in den USA hergestellt und aus den USA exportiert wird
Nein
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