Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Amzell
Age
0–2
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Participant has been diagnosed with IS within 6 weeks prior to Screening. Diagnostic criteria include both clinical spasms and an EEG pattern consistent with hypsarrhythmia or significant abnormality compatible with IS
Participant has normal renal function as defined by an estimated glomerular filtration rate (eGFR) greater than \[\>\] 60 milliliter/minute (mL/min)/1.73 m\^2, calculated as eGFR = 0.413 × (height \[Centimeter (cm)\]/serum creatinine \[milligrams per deciliter {mg/dL}\])
Participant's legally authorized representative (that is \[i.e.\], parent or guardian) must provide written informed consent obtained per Institutional Review Board (IRB) policy and requirements, consistent with the International Council for Harmonisation (ICH)
Participant's parent/guardian is able to understand and willing to comply with study procedures and restrictions
You may not be if
Participant has been diagnosed with tuberous sclerosis
Participant has acute illness considered clinically significant by the Investigator within 30 days prior to Screening
Participant has a diagnosis of recent systemic fungal infection; history of ocular herpes simplex; history of or current peptic ulcer; uncontrolled hypertension or congestive heart failure; or any other condition that would be significantly impacted by the study drug
Participant has a preplanned surgery or procedure(s) that would interfere with the conduct of the study
Participant has received any prior treatment for IS
Participant has been previously treated with adrenocorticotropic hormone (ACTH), corticosteroids, or Vigabatrin for seizures;
Participant has been previously treated with a course of corticosteroids for an indication other than seizures within 30 days prior to Screening
Participant has a known or suspected allergy to ACTH or Vigabatrin or any component of AMZ002 or Vigabatrin
Participant has used any other investigational drug within 30 days or 5 half-lives prior to the first dose of AMZ002 or Vigabatrin (whichever is longer)
Participant' s parent/guardian is unable to provide written informed consent and/or to complete the daily diary
Participant has any other disease, condition, or therapy that, in the opinion of the Investigator, might compromise safety or compliance, preclude the participant from successfully completing the study, or interfere with the interpretation of the results
Clareo Health | A Study to Evaluate Safety and Efficacy of AMZ002 Treatment, Compared With Vigabatrin in Participants With Infantile Spasms
