IT001-310 Study

What is the IT001-310 study?

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.

Who can join the IT001-310 study?

Study participants may be able to join the study if they meet the following requirements*:

* Other study requirements will apply

What will happen during the study?

Participation in the IT001-310 study lasts about 1 month. Study participants can expect the following:

Informed Consent

Review & sign the Informed Consent Form


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.