A Non-Interventional Post-Authorization Safety Study (PASS) of Carbaglu® for the Treatment of Hyperammonemia Due to Methylmalonic Acidemia (MMA) and Propionic Acidemia (PA) in Adult and Pediatric Patient Populations

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Drug
Study Type: Observational
SUMMARY

To obtain short-term and long-term clinical safety information, in pediatric and adult patients with PA and MMA treated with Carbaglu®.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

⁃ Provision of signed and dated informed consent/assent form

⁃ Prescribed and treated with Carbaglu®

⁃ Have an established diagnosis of PA or MMA defined as follows:

∙ Diagnosed with PA by semi quantitative urine organic acid analysis, defined as presence of elevated methylcitric acid and normal methylmalonic acid levels and no evidence of biotin related disorders in the organic acid analysis; OR

‣ Diagnosed with MMA by semi quantitative urine organic acid analysis, defined as elevation of methylmalonic acid and no evidence of vitamin B12 dependent disorder on plasma amino acid analysis (vitamin B12 dependency is defined by documented vitamin B12 responsiveness).

• AND/OR

• Confirmation by molecular genetic testing

Locations
United States
Washington, D.c.
Children's National Hospital
RECRUITING
Washington D.c.
Florida
University of South Florida
RECRUITING
Tampa
Illinois
Ann & Robert H. Lurie Children's Hospital of Chicago
RECRUITING
Chicago
Indiana
Riley Children's Hospital
RECRUITING
Indianapolis
New York
Icahn School of Medicine at Mt. Sinai
RECRUITING
New York
Contact Information
Primary
Anne Marie Cesario
cesario.a@recordati.com
908-849-4907
Time Frame
Start Date: 2022-06-30
Estimated Completion Date: 2032-06-30
Participants
Target number of participants: 20
Treatments
Male and Female Adult and Pediatric Participants
Patients treated with Carbaglu for the treatment for hyperammonemia due to Methylmalonic Acidemia (MMA) and Propionic Acidemia (PA)
Sponsors
Collaborators: Target PharmaSolutions, Inc.
Leads: Recordati Rare Diseases

This content was sourced from clinicaltrials.gov