Status:
COMPLETED
Safety and Pharmacokinetics of Kovacaine Nasal Spray (24 Hour Blood Collection)
Lead Sponsor:
St. Renatus, LLC
Collaborating Sponsors:
Triligent International
Rho, Inc.
Conditions:
Anesthesia
Eligibility:
All Genders
18-75 years
Phase:
PHASE2
Brief Summary
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...
Detailed 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 d...
Eligibility Criteria
Inclusion
- 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
- 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.
Key Trial Info
Start Date :
March 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2013
Estimated Enrollment :
24 Patients enrolled
Trial Details
Trial ID
NCT01807624
Start Date
March 1 2013
End Date
March 1 2013
Last Update
August 30 2017
Active Locations (1)
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1
Jean Brown Research
Salt Lake City, Utah, United States, 84124