SBIR-STTR Award

Drug Delivery Method for Sudden Sensorineural Hearing Loss
Award last edited on: 5/15/2020

Sponsored Program
STTR
Awarding Agency
NIH : NIDCD
Total Award Amount
$1,675,517
Award Phase
2
Solicitation Topic Code
-----

Principal Investigator
Irving N Weinberg

Company Information

Weinberg Medical Physics LLC (AKA: Weinberg Medical Physics Inc~Fast Imaging Company LLC)

5611 Roosevelt Street
Bethesda, MD 20817

Research Institution

University of Maryland

Phase I

Contract Number: 1R41DC013534-01A1
Start Date: 8/1/2014    Completed: 7/31/2015
Phase I year
2014
Phase I Amount
$222,527
The ultimate goal of the proposed project is to evaluate and commercialize a combination of proprietary magnet assemblies and magnetic nanoparticles (initially developed by our University STTR partner), that has been shown in preliminary animal studies to improve delivery of medications to the inner ear. Initial animal studies using the system (which uses magnetic forces to inject steroid-eluting magnetic nano-particles into the inner ear) have successfully reduced the degree of hearing loss and tinnitus in rats due to acoustic trauma. These initial studies suggest that the amount of steroids reaching the inner ear is increased ten-fold (compared to the current standard of trans-tympanic injection into the middle ear), without side effects. Our strategy is to demonstrate the utility of the magnetic injection system as a platform technology addressing the $4 billion hearing market, starting with a compelling clinical problem that currently is without a cure. Sudden Sensorineural Hearing Loss (SSHL) is an orphan disease without either a clear cause or a satisfactory therapy, and is considered to be an otologic emergency. Current therapies, which include oral and trans- tympanic steroid injection into the middle ear, are only partially effective. There is n widely-recognized animal model for SSHL, and as a result, we have been advised by regulatory experts that we would need to proceed directly to an investigational new drug (IND) application for human testing after showing improved drug delivery and safety in animals. We plan to advance in step-wise fashion by performing proof-of-principle and toxicity studies in the Phase I portion of the STTR project, and then conducting comprehensive pharmaco- kinetic studies in the STTR Phase II portion in preparation for the IND. The current standard of care in SSHL is to inject steroids into the middle ear. We expect that with preclinical demonstrations of low toxicityand high delivered more-uniform inner-ear concentrations using the magnetic injection system, the FDA would approve an IND augmenting trans-tympanic needle injections with magnetic injection of drug-eluting particles. Eventually we anticipate that the magnetic injection platform technology will be approved for other ear, nose and throat and CNS conditions. In Phase I, we will demonstrate the superiority of magnetic injection in attaining and maintaining physiologically-effective concentration of active ingredient in the inner ear (with low serum concentration). We will collect toxicity data for expected levels of steroid-loaded nanoparticles, quantifying levels of apoptotic and inflammatory responses in-vitro. With animal studies we will show significantly improved drug delivery and cochlear drug uniformity, and will demonstrate non-significant incidences of morbidity, mortality, and ototoxicity in-vivo. In Phase II, we will attempt to conduct rigorous pharmacokinetic studies and work with a strategic partner in the (fairly profitable) Orphan drug market, in preparation for IND submission.

Thesaurus Terms:
Acoustic Trauma;Address;Adverse Effects;Animal Model;Animals;Apoptotic;Auditory;Brain;Cell Injury;Chitosan;Clinical;Cochlear Structure;Data;Development;Diffusion;Distal;Drug Delivery Systems;Drug Formulations;Drug Kinetics;Drug Market;Drug Transport;Ear Structure;Emergency Situation;Fda Approved;Figs - Dietary;Goals;Hearing;Hearing Impairment;Human;Improved;In Vitro;In Vivo;Incidence;Inflammatory Response;Injection Of Therapeutic Agent;Investigational Drugs;Investigational New Drug Application;Iron;Iron Oxide;Labyrinth;Magnetism;Marketing;Maximum Tolerated Dose;Methods;Middle Ear;Morbidity - Disease Rate;Mortality Vital Statistics;Nanoparticle;Needles;Nose;Oral;Orphan Drugs;Ototoxicity;Particle;Patients;Pharmaceutical Preparations;Pharyngeal Structure;Phase;Pre-Clinical;Prednisolone;Preparation;Public Health Relevance;Publishing;Rare Diseases;Rattus;Relative (Related Person);Response;Safety;Sensorineural Hearing Loss;Serum;Small Business Technology Transfer Research;Standard Of Care;Steroids;Sudden Hearing Loss;System;Technology;Temperature;Testing;Therapeutic;Tinnitus;Toxic Effect;Treatment Outcome;Universities;Weights And Measures;Work;

Phase II

Contract Number: 2R44DC013534-02A1
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
2017
(last award dollars: 2019)
Phase II Amount
$1,452,990

The ultimate goal of the proposed project is to evaluate and commercialize a combination of proprietary magnet assemblies and magnetic nanoparticles that has been shown in small animal and cadaveric large animal and human studies to improve delivery of medications to the inner ear. Studies using the system (which uses magnetic forces to inject drug-eluting magnetic nano-particles into the inner ear) have successfully reduced the degree of hearing loss and tinnitus in rats due to acoustic trauma, and have conferred hearing protection against chemotherapy regimens in mice. The amount of drug reaching the inner ear was increased ten-fold and the drug distribution uniformity was increased three-fold, as compared to the current standard of trans-tympanic injection into the middle ear. Our strategy is to demonstrate the utility of the magnetic injection system as a platform technology addressing the $4 billion hearing market, starting with a compelling orphan indication (sudden sensorineural hearing loss) that is currently without a cure and is considered an otologic emergency. Subsequently, we shall address other cochlear conditions such as tinnitus and protection of hearing during chemotherapy regimens that are also not adequately addressed by the current standards-of-care. The FDA recommends testing in at least two mammalian species, the second of which should be a non-rodent mammal before entry into human trials. Based on successful Phase 1 results in rodents, and on reviewer suggestions, in Phase 2 we shall conduct large animal testing in sheep. Sheep are recognized to have a similar ear anatomy and hearing as compared to humans, and a common animal model submitted to the FDA. We aim to: Aim 1: Select sheep noise trauma conditions based on previously published data. Aim 2: Select dose and show therapeutic effect for noise-trauma-induced hearing loss in sheep. Aim 3: Conduct a detailed safety and toxicology study in healthy (no noise trauma) sheep. We anticipate that small (Phase 1) and large animal (Phase 2) safety and therapeutic effect data in animals will support an IND (Investigational New Drug) filing to the FDA. Approval of an IND by the FDA is required to allow entry into human clinical trials.

Public Health Relevance Statement:
Project Narrative Our overall goal is to improve treatment outcomes for patients with sudden hearing loss, and other conditions of the cochlea, using a proprietary drug delivery system. Magnetic injection will be used to minimally-invasively deliver drugs to the inner ear, to improve drug concentration and uniformity and thus therapeutic effect.

Project Terms:
Acoustic Trauma; Acute; Address; Adrenal Glands; Adult; Aftercare; Anatomy; Animal Model; Animal Testing; Animals; Auditory Brainstem Responses; base; Blood; Brain; Cadaver; Caring; Chemotherapy-Oncologic Procedure; Chitosan; Cisplatin; Clinical; Clinical Trials; Cochlea; commercialization; Communication; Control Groups; Data; Dose; Drug Delivery Systems; drug distribution; Ear; Emergency Situation; experimental study; Fetus; Funding; Goals; Head; Hearing; hearing impairment; Heart; Hour; Human; improved; Inflammation; Injectable; Injection of therapeutic agent; Iron; iron oxide; Kidney; Labyrinth; Liquid substance; Literature; Liver; Magnetic nanoparticles; Magnetism; Mass Spectrum Analysis; Methods; middle ear; minimally invasive; Mus; nanomagnetic; nanoparticle; Noise; Noise-Induced Hearing Loss; Organ; Orphan; particle; Patient-Focused Outcomes; Pharmaceutical Preparations; Phase; prednisolone; Publishing; Rare Diseases; Rat-1; Rattus; Recovery; Research Design; Research Proposals; response; Rodent; Safety; safety study; Sensorineural Hearing Loss; Sheep; Small Business Innovation Research Grant; sound; Spleen; standard of care; Steroids; success; Sudden Hearing Loss; Suggestion; System; systemic toxicity; Technology; Testing; Therapeutic; Therapeutic Effect; Tinnitus; Toxic effect; Toxicology; Trauma; Treatment outcome