The IT001-310 clinical research study is for adult women experiencing a UTI. The goal of the study is to compare the effectiveness of the study medication to amoxicillin/clavulanate in women with an active UTI.
Study participants may be able to join the study if they meet the following requirements*:
- Female 18 years of age or older
- Experiencing UTI symptoms, including:
- Frequent/urgent urination
- Painful or burning urination
- Pain above the pubic region - Symptoms that have lasted between 1-4 days
- Have not taken antibiotics for a UTI within the past week
* Other study requirements will apply
Participation in the IT001-310 study lasts about 1 month. Study participants can expect the following:
Informed Consent
Review & sign the Informed Consent Form
Screening
Receive study health assessments to confirm if you qualify for the study
Treatment Period
Take your assigned study medication as instructed and visit the study clinic 4 times for study assessments. You will also complete a daily diary with information about when you take the assigned medication
Participation in a clinical study is voluntary. You can ask any questions you have and may leave the study at any time, for any reason.
