Safety and Efficacy of PP4001 for the Treatment of Symptoms Associated With Uncomplicated Urinary Tract Infection

Exclusion Criteria

• •Clinically significant medical history or a clinically significant abnormal finding on the physical exam, vital signs or ECG at screening, including serious acute illness (e.g. pneumonia), gastrointestinal illness that would interfere with study drug absorption, or an untreated or unstable medical illness that would likely interfere with the study assessments.
• •At risk in terms of the precautions, warnings, and contraindications in the package insert for phenazopyridine hydrochloride including:
• •Known hypersensitivity to phenazopyridine hydrochloride (Defined by a history of allergic or adverse response to the drug).
• •Renal failure or insufficiency (Defined as having a history of abnormal renal function or as having a known renal disease).
• •History of hepatic disease or failure (Defined as having known liver disease or having elevated LFTs (\> 2 times the ULN) on previous laboratory testing. Patients who would not otherwise have such testing are not required to undergo special study labs).
• •Known G-6-PD (glucose-6-phosphate dehydrogenase) deficiency.
• •Prior use of a phenazopyridine product within 6 months of the first dose of study drug and throughout the study.
• •Use of any prescription analgesic medication (e.g. opioids, prescription nonsteroidal anti-inflammatory drugs (NSAID), etc.) for urinary tract pain or other pain (headache, back pain, joint pain, dental pain, sore muscles, etc) within one and a half (1.5) dosing intervals for that medication before the firs dose of study drug, and throughout the study.
• •Use of any systemic antibiotic within seven (7) days of study participation.
• •Subjects with complaint of abnormal vaginal discharge.
• •Current diagnosis or suspicion of complicated UTI or systemic infection based on one or more of the following:
• •Known presence of an anatomic or functional abnormality.
• •Presence of a urinary catheter.
• •Infection of the urinary tract requiring an intravenous pyelogram (IVP), ultrasound or cystoscopy.
• •Clinical signs of systemic infection such as fever (oral or tympanic temperature \>38 degrees Celsius), costovertebral pain or tenderness, rigors, nausea or vomiting.
• •Subjects unable to comprehend the language of the informed consent and the self evaluation scales.
• •Subjects who, in the opinion of the investigator, are not appropriate for, or are unable, or unwilling to undergo antibiotic treatment for uncomplicated urinary tract infection.
• •Subjects with complaint of abnormal vaginal bleeding defined as different from the patient's usual menstrual period flow and timing.
• •Subjects with known allergy to multivitamin or any component of the multivitamin.
• •Currently participating in a clinical trial or has received an experimental drug or used an experimental device in the last 30 days prior to admission into this study.
• •Subjects who, in the opinion of the investigator, are unsuitable for enrollment, unlikely to complete the course of study medication treatment, or unlikely to attend the End of Study visit.
• •Subjects who are unable or unwilling to comply with the use of an electronic subject diary.
• •Employees of the investigator or the institution who have direct involvement in the trial or other trials under the direction of the investigator or their associates.