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Case study provided by: Raja Zabaneh, MD, FACP, FASN – Northwest Louisiana Nephrology, Shreveport, LA
This case study is provided for general medical education purposes only and is not a substitute for independent clinical medical judgment. The intent of this case study is to present the experience of an individual patient, which may not represent outcomes in the overall patient population. Response to treatment may vary from patient to patient.
Asian man, age 49, with a medical history of hepatitis B found to have elevated UPCR and creatinine levels on a routine wellness exam
ACE=angiotensin-converting enzyme; MMF=mycophenolate mofetil; UPCR=urine protein/creatinine ratio.
*MMF is not FDA-approved to treat IgAN.
After treatment with Acthar Gel, UPCR was reduced by more than 40%
UPCR levels during treatment course and the following 9 months:
UPCR dropped from 2.27 mg/dL to 1.34 mg/dL
Patient continued experiencing improvements 9 months after stopping treatment with Acthar Gel
Clinical outcomes may not be solely attributable to Acthar Gel.
Commonly reported postmarketing adverse reactions for Acthar include injection site reaction, asthenic conditions (including fatigue, malaise, asthenia, and lethargy), fluid retention (including peripheral swelling), insomnia, headache, and blood glucose increased.
Dosage should be individualized according to the medical condition of each patient. Frequency and dose of the drug should be determined by considering the severity of the disease and the initial response of the patient.
Sudden withdrawal of Acthar Gel after prolonged use may lead to adrenal insufficiency or recurrent symptoms. It may be necessary to taper the dose and increase the injection interval to gradually discontinue the medication.
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