Phase I/IIa Study Evaluating Safety and Efficacy of an Intratympanic Dose of PIPE-505 in Subjects With Hearing Loss

Phase 1

Completed

• Conditions: Sensorineural Hearing Loss
• Interventions: Drug: PIPE-505; Drug: Placebo

• Registration Number: NCT04462198
• Lead Sponsor: Contineum Therapeutics

Brief Summary

This is a randomized, double-blind study of PIPE-505, or placebo, in subjects with hearing loss associated with speech-in-noise impairment.

Detailed Description

This is a randomized-controlled, double-blind study of PIPE-505 or placebo given as an injection one time in subjects with sensorineural hearing loss associated with speech-in-noise difficulty. Visits to the clinic will occur at baseline, dosing, and days 1, 7, 14, 30, 60 and 90 after treatment. Safety will be assessed by periodic measurement of vital signs, ear examination, electrocardiogram (ECG), blood laboratory analyses and occurrence of adverse events (AE). Efficacy will be assessed by periodic audiometry and other audiological tests.

Study Timeline

• Study First Submitted: 2020-06-29
• Study First Submitted QC: 2020-07-04
• Study First Posted: 2020-07-08
• Study Start: 2020-10-15
• Primary Completion: 2021-06-17
• Study Completion: 2021-06-17
• Status Verified: 2022-06
• Disposition First Submitted: 2022-06-07
• Disposition First Submitted QC: 2022-06-07
• Last Update Submitted: 2022-06-07
• Disposition First Posted: 2022-06-10
• Last Update Posted: 2022-06-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 28

Inclusion Criteria

• Subject's primary language is English.
• Male or female between 18 and 75 years of age, inclusive, at randomization.
• Diagnosis of bilateral sensorineural hearing loss (SNHL).
• Normal tympanogram in the ear intended for injection (as defined in protocol) at Screening.
• Male or female subjects with reproductive potential agree to comply with protocol-approved double barrier contraceptive method during and for 3 months after study drug administration.
• The subject is in general good medical health with no clinically significant or relevant abnormalities, including medical history, physical exam, vital signs, ECG, and laboratory evaluations (hematology, chemistry, and urinalysis) as assessed by the Investigator.

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Exclusion Criteria

• History of chronic otitis externa or media, other chronic middle ear disorders, barotrauma, Meniere's disease, endolymphatic hydrops, perilymph fistula, herpes zoster oticus or other infectious etiology of hearing loss.
• Presence of a genetic, syndromal or developmental auditory disorder or of an autoimmune or serious neurological disorder that could contribute to auditory loss.
• Evidence of current conductive hearing loss, mixed hearing loss or otosclerosis.
• History of auditory loss related to exposure to known high-dose ototoxic drugs; any prior exposure to platinum-based medications.
• Otological disorders that would preclude safe tympanic injection.
• Presence of a cochlear implant.
• Evidence of bothersome tinnitus as determined by the Investigator.
• Intratympanic injection within 6 months of randomization.
• Use of an investigational product or intervention other than a non-interventional registry study (including vaccine studies) within the greater of 30 days or 5 half-lives (if known) prior to Screening or expected during the study.
• History of malignancy under current active treatment or considered at substantial risk for progression or recurrence during the study interval, as determined by the Investigator. Note, central nervous system neoplasms or head and neck cancer are excluded from eligibility regardless of treatment status.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
PIPE-505	PIPE-505	-
Placebo	Placebo	-

Primary Outcome Measures

Name	Time	Method
Safety: Treatment-Emergent Adverse Events (TEAE)	From baseline to 3 months follow up	Number of participants with TEAEs

Secondary Outcome Measures

Name	Time	Method
Pharmacokinetics: Area under the curve (AUC)	From baseline to 3 months follow up
Pharmacokinetics: t1/2 (half life)	From baseline to 3 months follow up

Trial Locations

Locations (7)

Breathe Clear Institute; 🇺🇸 Torrance, California, United States

ENT and Allergy Associates of Florida; 🇺🇸 Boca Raton, Florida, United States

Charlotte Eye Ear Nose Throat Associates; 🇺🇸 Charlotte, North Carolina, United States

Piedmont Ear Nose Throat and Associates; 🇺🇸 Winston-Salem, North Carolina, United States

Advanced ENT & Allergy; 🇺🇸 Louisville, Kentucky, United States

Chrysalis Clinical Research; 🇺🇸 Saint George, Utah, United States

University of Kansas; Dept of Otolaryngology Head & Neck Surgery; 🇺🇸 Kansas City, Kansas, United States