Drug-Drug Interaction Study of HBI-3000 and Paroxetine in Healthy Adult Male and Female Subjects
Study Details
Study Description
Brief Summary
Drug-Drug Interaction Study of HBI-3000 and Paroxetine in Healthy Adult Male and Female Subjects
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 1 |
Detailed Description
This is a Phase 1 study in healthy volunteers to evaluate the potential effect of multiple doses of paroxetine on the pharmacokinetics and safety of HBI-3000. Each subject serves as his/her own control: Period 1 vs. Period 2.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: HBI-3000 alone (Period 1) followed by HBI-3000 with Paroxetine (Period 2) HBI-3000: 350 mg, 50 mL intravenous infusion (IV) over 30 minutes on Day 1 of Period 1 and approximately 15 days later on Day 1 of Period 2 Paroxetine: 20 mg dose twice a day on Days 1 and 2 of Period 2, and once a day on Days 3 through 7 inclusive of Period 2 |
Drug: HBI-3000
small molecule, multi-ion channel blocker
Other Names:
Drug: Paroxetine
serotonin uptake inhibitor, CYP2D6 inhibitor
|
Outcome Measures
Primary Outcome Measures
- Plasma pharmacokinetics (PK): Maximum observed plasma concentration (Cmax) [72 hours]
To determine the plasma Cmax of a single dose of HBI 3000 administered intravenously (IV), in the absence and the presence of CYP2D6 inhibition, achieved with multiple oral doses of paroxetine, a strong CYP2D6 inhibitor, in healthy male and female subjects. Blood samples will be taken from 0 through 72 hours after the start of HBI-3000 infusion.
- Plasma pharmacokinetics (PK): Area Under the Curve (AUC) from time 0 to last measurable concentration (AUC0 - tau) [72 hours]
To determine the plasma AUC of a single dose of HBI 3000 administered intravenously (IV), in the absence and the presence of CYP2D6 inhibition, achieved with multiple oral doses of paroxetine, a strong CYP2D6 inhibitor, in healthy male and female subjects. Blood samples will be taken from 0 through 72 hours after the start of HBI-3000 infusion.
- Plasma pharmacokinetics (PK): Area Under the Curve (AUC) from time 0 to infinity (AUC0 - infinity), if data permits [72 hours]
To determine the plasma AUC of a single dose of HBI 3000 administered intravenously (IV), in the absence and the presence of CYP2D6 inhibition, achieved with multiple oral doses of paroxetine, a strong CYP2D6 inhibitor, in healthy male and female subjects. Blood samples will be taken from 0 through 72 hours after the start of HBI-3000 infusion.
Secondary Outcome Measures
- Treatment-Emergent Adverse Events (TEAEs), including serious TEAEs [25 days]
To evaluate the safety and tolerability of HBI-3000 in the absence and the presence of paroxetine, as measured by Treatment-Emergent Adverse Events (TEAEs), including serious TEAEs. TEAE is defined as follows: An AE that emerges during treatment, having been absent at pretreatment (Baseline), an AE that re emerges during treatment, having been present at pretreatment (Baseline) but stopped before treatment, or an AE that worsens in severity during treatment relative to the pretreatment state, when the AE is ongoing. TEAEs will be recorded for approximately 25 days commencing with the start of HBI-3000 infusion.
- Routine hematology and coagulation [25 days]
To evaluate the safety and tolerability of HBI-3000 in the absence and the presence of paroxetine, as measured by routine hematology and coagulation tests, at Screening and periodically during the study, including: Hematocrit (Packed cell volume); Hemoglobin; Lymphocytes; Mean cell hemoglobin Mean cell hemoglobin concentration; Mean cell volume; Basophils; Eosinophils; Monocytes; Neutrophils; Platelet count; Red blood cell count; White blood cell count; Coagulation Tests; Prothrombin time; International normalised ratio; Partial thromboplastin time
- Routine serum chemistry [25 days]
To evaluate the safety and tolerability of HBI-3000 in the absence and the presence of paroxetine, as measured by routine serum clinical chemistry tests, at Screening and periodically during the study, including: Alanine aminotransferase; Albumin; Alkaline phosphatase; Aspartate aminotransferase; Bicarbonate; Bilirubin (total); Bilirubin (direct); Calcium; Chloride; Cholesterol; Creatine kinase; Creatinine, estimated clearance; Gamma glutamyl transferase; Triglycerides; Globulin; A/G ratio; Glucose; Magnesium; Potassium; Phosphate (inorganic); Protein (total); Sodium; Urea; Uric acid
- Vitals signs [25 days]
To evaluate the safety and tolerability of HBI-3000 in the absence and the presence of paroxetine, as measured by vitals signs including heart rate and blood pressure using an automated blood pressure device, at Screening and periodically during the study.
- 12-lead ECG [25 days]
To evaluate the safety and tolerability of HBI-3000 in the absence and the presence of paroxetine, as measured by 12-lead ECG. Twelve-lead ECGs will be measured at Screening and periodically during the study using standardized equipment provided by the core ECG laboratory and reviewed locally by the Investigator. QTc interval will be calculated from Fridericia's formula.
- Continuous telemetry [8 hours beginning at the start of infusion]
To evaluate the safety and tolerability of HBI-3000 in the absence and the presence of paroxetine, as measured by monitoring via a continuous cardiac telemetry monitoring system for 8 hours commencing with the start of HBI-3000 infusion
- Infusion site (local) reactions [25 days]
To evaluate the safety and tolerability of HBI-3000 in the absence and the presence of paroxetine, as measured by observing infusion site (local) reactions for the duration of the study (approximately 25 days) commencing with the start of HBI-3000 infusion
- Physical examination findings [25 days]
To evaluate the safety and tolerability of HBI-3000 in the absence and the presence of paroxetine, as measured by examination of body systems and symptom directed examination as indicated, at Screening and during the study (approximately 25 days)
- Left ventricular ejection fraction (LVEF), Exploratory [At baseline and 2 hours beginning at the start of infusion]
To evaluate the safety and tolerability of HBI-3000 in the absence of paroxetine, as measured by 2D transthoracic echocardiogram to measure changes in cardiac contractility, determined at baseline and at 30 minutes and 2 hours after the start of infusion
Eligibility Criteria
Criteria
Inclusion Criteria:
Healthy adult males and females
-
18 - 50 years of age
-
BMI 18 - 32 kg/m2
-
Subject has no clinically significant abnormality on electrocardiogram (ECG)
-
Subject has been a nonsmoker and/or has not used nicotine or nicotine-containing products for at least 4 months
-
Subject is willing to comply with the study restrictions, including contraception requirements
Exclusion Criteria:
-
Evidence of a clinically significant disease or abnormalities, including an active, current infection or clinically significant infection within 8 weeks prior to the first dose
-
Severe allergic reaction, angioedema, or anaphylaxis to drugs, or food or latex allergies
-
Subject has an estimated creatinine clearance of ≤ 70 mL
-
Subject has evidence of a clinically significant deviation from normal in the physical examination, vital signs, or clinical laboratory determinations
-
Subject has significant ECG abnormality, history or presence of cardiac arrhythmia or conduction abnormalities, or bradycardia (< 45 bpm)
-
Subject has a history of vasovagal syncope, or symptomatic orthostatic hypotension
-
Subject has as a history of or current alcohol abuse and/or other drug addiction
-
Subject has received an investigational drug (including investigational vaccines) within 5 half-lives of such drug prior to Study Day 1
-
Subject has received CYP2D inhibitors (e.g., fluoxetine, sertraline, duloxetine, bupropion, chloroquine, cimetidine, diphenhydramine) less than 3 weeks prior to administration of the initial dose of study drug
-
Subject has suicidal thinking and behavior (suicidality) or other significant psychiatric disorders based on self-disclosure during interview (Screening visit)
-
Subject has a history of acute narrow-angle glaucoma
-
Subject has as any condition that would make him or her, in the opinion of the Investigator or Sponsor, unsuitable for the study
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Spaulding Clinical | West Bend | Wisconsin | United States | 53095 |
| 2 | Nucleus Network Pty Ltd. | Melbourne | Victoria | Australia |
Sponsors and Collaborators
- HUYABIO International, LLC.
Investigators
- Principal Investigator: Jason Lickliter, MD, Nucleus Network
- Principal Investigator: Jennifer Deering, MSN, ARNP, Spaulding Clinical
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- HBI-3000-401