Healthy Volunteers
Conditions
Brief summary
Verasone™ is an aqueous suspension of the combination of two marketed drugs to be dosed by sinonasal irrigation in the treatment of Chronic Rhinosinusitis (CRS). This Phase 1 first-in-human study will assess the safety, tolerability, and pharmacokinetics (PK) of single and multiple ascending doses of Verasone versus placebo in healthy normal participants and will evaluate the PK profiles of the Verasone active components administered individually vs in combination.
Interventions
DRUGVerasone
Administered by sinonasal irrigation.
Sponsors
Diceros Therapeutics Australia Pty Ltd
Diceros Therapeutics
Study design
Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Masking description
Double-Blind, Placebo-Controlled
Intervention model description
Single Ascending Dose (SAD), Single Dose Active Components PK Crossover, Multiple Ascending Dose (MAD)
Eligibility
Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes
Inclusion criteria
Main Inclusion Criteria: 1. In good general health based on medical history, physical examination, vital signs, ECG, laboratory parameters, and other relevant tests 2. Able to perform study procedures, including self-administration of sinonasal irrigation of 60 mL in each nostril 3. Able and willing to attend the necessary visits to the study site. Additional inclusion criteria for Part B: 4. Participant met all eligibility criteria for Part A, completed Part A with no major protocol deviations, and all Part A safety and PK assessments were completed, in the opinion of the PI. 5. Participant did not experience local toxicity AEs or anterior rhinoscopy findings during Part A. Main
Exclusion criteria
1. History of allergy, hypersensitivity, or contraindication to corticosteroids or calcium channel blockers. 2. History of severe allergic or anaphylactic reactions or sensitivity to the IP or its constituents. 3. Any clinical obstruction of the nasal cavities that would reduce access for topical irrigations 4. Nasal candidiasis, nasal mucosal ulceration, thinning or eroded nasal septum, or nasal septum perforation. 5. History or clinical evidence of CRS, fungal rhinosinusitis, or rhinitis medicamentosa at any time, or any active allergic rhinitis, acute sinusitis, or upper respiratory infection within 4 weeks prior to Screening. 6. Ongoing nasal congestion at Screening or Day -1 (Nasal Congestion Score \> 0). 7. Inability to have anterior rhinoscopy nasal examination (Parts A and B only) or endoscopic nasal cavity examination (Part C only). 8. More than 1 episode of epistaxis. 9. History of or planned sinus or intranasal surgery. 10. Use of immunomodulating drugs, except glucocorticoids, within 90 days prior to Screening or intent to use these drugs during the study. 11. Exposure to any glucocorticoid treatment via any route (nasal, topical, inhaled, oral, intravenous, etc.) within 1 month prior to Screening. 12. Received biologic therapy/systemic immunosuppressant to treat inflammatory or autoimmune disease. 13. Oral steroid-dependent or monoclonal antibody-dependent (eg, omalizumab, mepolizumab, dupilumab) condition. 14. Use of potent cytochrome P450 3A4 (CYP3A4) inhibitor(s) or inducer(s) within 14 days prior to Screening. 15. Known history of HPA axial dysfunction, or previous pituitary or adrenal surgery. 16. History or diagnosis of eustachian tube dysfunction, recurrent otitis media. 17. Any history or ongoing clinically significant cardiac disease. 18. Abnormal vital signs or ECG findings. 19. History or current diagnosis of any form of glaucoma or ocular hypertension. 20. A history of cancer, HIV, or other immunodeficiency, or immune system-mediated disorder. 21. History of insulin-dependent diabetes mellitus. 22. History of any clinically significant hepatic or renal disease. 23. Clinically significant abnormal laboratory parameters at Screening. 24. Any underlying physical or psychological medical condition. 25. A recent clinically significant history of drug or alcohol use, abuse, or dependence. 26. Positive screen for drugs of abuse or alcohol at Screening or Day -1.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Part A: Single Ascending Dose (SAD) | 1 week | The proportion of subjects with Adverse Events at each dose level |
| Part B: Single Dose Component Crossover | 3 weeks | Plasma drug levels of Verasone's components |
| Part C: Multiple Ascending Dose (MAD) | 2 weeks | The proportion of subjects with Adverse Events at each dose level |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| To assess the volume of retained fluid and amount of mucosal absorption in the sinonasal system immediately following single dose Verasone vs placebo administered by sinonasal irrigation in healthy participants. | 30 min | To assess the volume of fluid retained in the sinonasal system following dosing. |
Countries
Australia
Outcome results
None listed