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A Phase II multicenter, placebo-controlled, proof-of-concept study evaluating the safety, and efficacy of intratympanic STR001 thermogel to preserve residual hearing in adults undergoing cochlear implant surgery

A Phase II multicenter, placebo-controlled, proof-of-concept study evaluating the safety, and efficacy of intratympanic STR001 thermogel to preserve residual hearing in adults undergoing cochlear implant surgery

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2015-002672-25-DE
Enrollment
110
Registered
2015-09-21
Start date
2015-11-18
Completion date
Unknown
Last updated
2019-01-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prevention of Hearing Loss after Cochlear Implant Surgery

Interventions

Product Name: STR001 thermogel Product Code: STR001 Pharmaceutical Form: Gel for injection INN or Proposed INN: not available Current Sponsor code: STR001 Concentration unit: % (W/W) percent weight/we

Sponsors

Strekin AG
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Males or females aged between =18 years and = 80 years 2. Patients with a diagnosis of moderate to severe hearing loss with = 80 dB by average Pure Tone Audiometry measured at the frequencies of 125, 250, 500 and 750Hz, eligible for cochlear implant surgery (average up to 82.5 will be rounded down to 80 i.e. will be considered eligible) 3. Patients must be willing and capable to perform all study procedures 4. Patients have understood the patient Information documents and have provided informed consent 5. Females must have a negative Serum pregnancy test or must be post-menopausal Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 110 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 110

Exclusion criteria

Exclusion criteria: 1. Malformation or cochlear ossification 2. Developmental disabilities or psychiatric diseases such as severe depression 3. History of Meniere’s disease 4. Acute or chronic middle ear inflammatory disease 5. Use of thiazolidinedione (e.g. pioglitazone, rosiglitazone) in the last 6 months prior to baseline 6. Chronic (i.e. at least 3 continuous months) oral steroids in the last 6 months prior to baseline 7. Daily nasal/pulmonary steroid in the last month prior to baseline 8. Fibrates (e.g. gemfibrozil, fenofibrate) in the last 6 months prior to baseline 9. Patients with known hypersensitivity to STR001 or any formulation component 10. Initiation of treatment with lipophilic statins (e.g. atorvastatin, pitavastatin, lovastatin, fluvastatin or simvastatin) in the last month prior to inclusion in the study. Patients on stable doses of lipophilic statins should continue therapy during the study. 11. Any drug-based therapy for inner ear hearing loss that is ongoing or was performed in the past month prior to baseline

Design outcomes

Primary

MeasureTime frame
Main Objective: To evaluate the safety and tolerability of STR001 thermogel in patients receiving cochlear implants To assess the efficacy of STR001 thermogel in preserving hearing 6 weeks after cochlear implant surgery as determined by average Pure Tone Audiometry (aPTA) values ;Secondary Objective: To evaluate secondary efficacy parameters of hearing on average Bone Conduction Threshold Audiometry (aBCTA) and individual frequencies by BCTA and PTA. To evaluate the systemic exposure of STR001 after STR001 thermogel administration ;Primary end point(s): Efficacy: Average Pure Tone Audiometry Treshold (aPTA) at 125, 250, 500 and 750 Hz of implanted ear at Week 6. Safety: The incidence and severity of adverse events, serious adverse events, deaths, as well as drug and study discontinuations; The incidence of laboratory abnormalities, based on hematology, clinical chemistry, and urinalysis test results; ECGs; Physical examination; Vital signs ;Timepoint(s) of evaluation of this end point: 6 weeks after CI surgery

Secondary

MeasureTime frame
Secondary end point(s): Efficacy (key): BCTA of the implanted ear as the average of the following frequencies: 250, 500 and 750 Hz at Week 6. Efficacy (other): Pure Tone Audiometry will also be assessed at each individual frequency at 125, 250, 500 and 750 Hz at Week 6. BCTA will also be assessed at each individual frequency at 250, 500 and 750 Hz at Week 6. BCTA will also be assessed at each frequency: 250, 500 and 750 Hz at Week 6. Pharmacokinetics: STR001 and its main metobolites (M-III and M-IV) Plasma concentrations. ;Timepoint(s) of evaluation of this end point: Efficay: 6 weeks after CI surgery Pharmacokinetics: At baseline, prior to surgery and after the surgery (4 samples/Patient)

Countries

Germany, Spain

Contacts

Public ContactCEO

Strekin AG

Alexander.bausch@strekin.com0041797888252

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026