Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-26 @ 12:16 PM
Ignite Modification Date:
2025-12-26 @ 12:16 PM
NCT ID:
NCT00551200
Eligibility Criteria:
Inclusion Criteria:
* Male and female patients at least 18 years old
* Signed written informed consent by patient or patient's representative
* Diagnosis of urea cycle enzyme deficiency confirmed via enzymatic or genetic testing
* Currently treated with Buphenyl® TID for a minimum of 2 weeks prior to Visit 1
* Able to perform study activities (including the ability to collect all urine in the clinic, i.e., no patients in diapers)
* Negative pregnancy test for all females of childbearing potential. All females of childbearing potential must agree to use an acceptable method of contraception throughout the study
Exclusion Criteria:
* Use of any investigational drug within 30 days of Buphenyl® Visit 1
* Active infection (viral or bacterial) or any other condition that may increase ammonia levels
* Laboratory values outside the normal range that are determined to be clinically significant by the investigator
* Any clinical or laboratory abnormality of Grade 3 or greater severity according to the Common Terminology Criteria for Adverse Events v3.0 (CTCAE) (or for conditions not covered by the CTCAE, a severe or life-threatening toxicity); except that Grade 3 elevations in liver enzymes are allowed in an otherwise clinically stable patient
* Use of any medication known to significantly affect renal clearance (e.g., probenecid) or to increase protein catabolism (e.g., corticosteroids), or other medication (e.g., valproate) known to increase ammonia levels, within the 24 hours prior to Visit 1
* Preexisting QTc interval prolongation (\> 450 msec for males or \> 460 msec for females)
* Other severe chronic medical conditions
* Known hypersensitivity to PAA, PBA, or benzoate
* Creatinine levels equal to or greater than 1.5 × ULN
* Liver transplant
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00551200
Study Brief:
Protocol Section:
NCT00551200