Safety and Pharmacokinetics of Kovacaine Nasal Spray (24 Hour Blood Collection)

St. Renatus

Status and phase

Completed

Phase 2

Conditions

Anesthesia

Treatments

Drug: Tetracaine HCl 3% and Oxymetazoline HCl 0.05%

Study type

Interventional

Funder types

Industry

Identifiers

NCT01807624

SR 2-06

Details and patient eligibility

About

The purpose of this study is to determine the pharmacokinetics/pharmacodynamics and safety of a nasal spray containing the anesthetic drug tetracaine in combination with oxymetazoline with blood draws over 24 hours.

Full description

The purpose of this study is to determine the pharmacokinetics and safety of tetracaine, para- butylaminobenzoic acid (PBBA), and oxymetazoline after intranasal administration of the highest Phase 3 dose of Kovacaine Mist (Tetracaine Hydrochloride with Oxymetazoline Hydrochloride) to healthy volunteers.

This is an open-label, single-treatment, single-dose study in healthy volunteers in which all subjects will receive the highest Phase 3 dose of Kovacaine Mist on one occasion. No randomization is necessary for this single treatment, single dose study. A single study center will participate.

Each subject will receive a single dose of Kovacaine Mist (3% tetracaine HCl with 0.05% oxymetazoline HCl) consisting of 3 sprays (each 0.2 mL) in one nostril not taking longer than 8 minutes, for a total 0.6 mL dose containing 18 mg tetracaine HCl and 0.3 mg oxymetazoline HCl.

The total dosing period will be 8 minutes. Subjects will be required to fast 10 hours prior to dosing and for four (4) hours after dosing. Water will be allowed ad lib during the study except for one (1) hour prior through one (1) hour after dose administration. Subjects will be admitted to the study unit no later than 2100 hours of the evening prior to drug administration and will remain in the unit until the 24 hour blood sample is collected and discharge procedures are completed.

Enrollment

24 patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Male or non-pregnant, non-breast-feeding female subjects between the ages of 18 and 75 years (inclusive).
Can understand and sign the informed consent document, can communicate with the investigator, and can understand and comply with the requirements of the protocol.
Body mass index between 18 and 35 BMI.
Sufficiently healthy as determined by the investigator to receive the test medications and undergo the scheduled study procedure.
Can breathe through both nostrils.
Screening BP ≤ 140/90 mm Hg.

Exclusion criteria

History of clinically significant respiratory, gastrointestinal, renal, hepatic, neurologic, hematologic, endocrine, oncologic, pulmonary, immunologic, psychiatric, or cardiovascular disease, including cardiac arrhythmia, narrow angle glaucoma and benign prostatic hypertrophy (in men), uncontrolled thyroid disease (including Hashimoto's Thyroiditis and lymphocytic thyroiditis), uncontrolled diabetes mellitus or any other condition which, in the opinion of the Principal Investigator, would jeopardize the safety of the subject or impact the validity of the study results.
Has clinically significant abnormal findings on the physical examination, medical history, electrocardiogram (ECG), or clinical laboratory evaluation during screening. This includes current upper respiratory infections.
Currently experiencing seasonal or perennial allergic rhinitis, recurrent nose-bleeds or asthma, or has a significant history of these conditions, in the opinion of the Investigator.
Current, including the last 30 days, sinusitis or other upper respiratory infections.
Nasal polyps, significant nasal or sinus surgery or other abnormality that may interfere with the dose administration.
History of allergic or adverse responses to tetracaine, other ester local anesthetics, PBBA, oxymetazoline and its preservatives, or para-aminobenzoic acid as found in PABA containing sunscreens or any comparable or similar product.
Donation of blood or plasma within 30 days of the first dose of Study Drug.
Participation in a clinical trial within 30 days prior to the first dose of Study Drug.
Use of any new over-the-counter (OTC) medication, including topical anesthetic creams or gels, vitamins, within seven days prior to the first dose of the Study Drug or during the study unless approved by the Principal Investigator.
Any prescription medication, whose dose is not stable at the time of screening, as determined by the Principal Investigator.
Treatment with any known enzyme altering drugs such as barbiturates, phenothiazines, cimetidine, carbamazepine, etc., within 30 days prior to the first dose of Study Drug or during the study.
Smoking or use of tobacco products within 6 months prior to the first dose of Study Drug or during the study.
Female trying to conceive, is pregnant, suspected of being pregnant, or is lactating. (Females of child-bearing potential will be required to take a serum pregnancy test at screening (up to 21 days prior to the start of the study, including the day of the study), as well as a urine pregnancy test at check-in to rule out pregnancy.)
Positive serum pregnancy test at screening or urine pregnancy test at check-in for all women of childbearing potential.
Positive blood screen for HIV, Hepatitis B surface antigen (HbSAg), or Hepatitis C, or a positive urine screen for alcohol, drugs of abuse, or cotinine.
Have a history of pseudocholinesterase deficiency or previous prolonged paralysis with succinylcholine or difficulty waking up from general anesthesia.
Have a history of alcoholism and/or drug abuse.
Have taken a monoamine oxidase inhibitor or vasopressor drug within the past 3 weeks.