AkebiaShares Program: Current Approaches for Managing Hyperphosphatemia and Caring for Patients via Telehealth
Akebia Therapeutics (Nasdaq: AKBA) announced a virtual panel scheduled for December 16, 2020, aimed at discussing hyperphosphatemia management in patients with chronic kidney disease (CKD) on dialysis. The panel will feature insights from kidney care professionals and emphasize the importance of a multidisciplinary care approach and telehealth monitoring. Akebia's AURYXIA® (ferric citrate) is FDA-approved for controlling serum phosphorus levels in CKD patients on dialysis and treating iron deficiency anemia in CKD patients not on dialysis.
- Scheduled virtual panel on December 16, 2020, focusing on CKD management.
- Discussion to include telehealth monitoring and multidisciplinary care, enhancing patient management strategies.
- AURYXIA® is FDA-approved for managing hyperphosphatemia and iron deficiency anemia.
- None.
CAMBRIDGE, Mass., Dec. 9, 2020 /PRNewswire/ -- Akebia Therapeutics, Inc. (Nasdaq: AKBA), a biopharmaceutical company with the purpose to better the lives of people impacted by kidney disease, today announced the latest scheduled program of AkebiaShares, a peer-to-peer educational series for the kidney community. The upcoming virtual panel, scheduled for Wednesday, December 16, 2020 at 7:30 p.m. EST, will feature a discussion among kidney care professionals who will share their insights and experiences managing hyperphosphatemia in people with chronic kidney disease (CKD) on dialysis. AkebiaShares aims to bring together kidney professionals to share information and best practices on topics related to providing care to people with CKD.
Hyperphosphatemia is a condition in which a person's phosphorus levels are too high, potentially causing serious damage to the body. It is a primary hallmark of CKD, particularly in people with end-stage renal disease and on dialysis. The panelists will share information on hyperphosphatemia in people on dialysis, and discuss management including the value of a multidisciplinary care team, ongoing patient engagement and monitoring via telehealth, and the use of phosphate binders as a treatment option.
To register for the complimentary event visit: http://dwa.adobeconnect.com/endruu01ne5s/event/registration.html?campaign-id=akebia5.
The discussion will be moderated by German Hernandez, M.D., nephrologist at El Paso Kidney Specialists and Karen Robertson, DNP, ANP, nurse practitioner at Carolina Nephrology. Joining the discussion will be Beth Morlang, RD, renal dietitian at Central Florida Kidney Centers, Inc.
Akebia markets AURYXIA® (ferric citrate), a phosphate binder that contains iron, which is approved by the U.S. Food and Drug Administration (FDA) and marketed for two indications in the U.S.: the control of serum phosphorus levels in adult patients with CKD on dialysis (the Hyperphosphatemia Indication), and the treatment of iron deficiency anemia (IDA) in adult patients with CKD not on dialysis (the IDA Indication).
About Akebia Therapeutics
Akebia Therapeutics, Inc. is a fully integrated biopharmaceutical company with the purpose to better the lives of people impacted by kidney disease. The Company was founded in 2007 and is headquartered in Cambridge, Massachusetts.
About Auryxia® (ferric citrate) Tablets
Auryxia (ferric citrate) was approved by the FDA on September 5, 2014 for the control of serum phosphorus levels in adult patients with CKD on dialysis and approved by the FDA on November 6, 2017 for the treatment of iron deficiency anemia in adult patients with CKD not on dialysis. For more information about Auryxia and the U.S. full prescribing information, please visit www.auryxia.com.
IMPORTANT SAFETY INFORMATION CONTRAINDICATION
AURYXIA® (ferric citrate) is contraindicated in patients with iron overload syndromes, e.g., hemochromatosis
WARNINGS AND PRECAUTIONS
- Iron Overload: Increases in serum ferritin and transferrin saturation (TSAT) were observed in clinical trials with AURYXIA in patients with chronic kidney disease (CKD) on dialysis treated for hyperphosphatemia, which may lead to excessive elevations in iron stores. Assess iron parameters prior to initiating AURYXIA and monitor while on therapy. Patients receiving concomitant intravenous (IV) iron may require a reduction in dose or discontinuation of IV iron therapy
- Risk of Overdosage in Children Due to Accidental Ingestion: Accidental ingestion and resulting overdose of iron-containing products is a leading cause of fatal poisoning in children under 6 years of age. Advise patients of the risks to children and to keep AURYXIA out of the reach of children
ADVERSE REACTIONS
The most common adverse reactions reported with AURYXIA in clinical trials were:
- Hyperphosphatemia in CKD on Dialysis: Diarrhea (
21% ), discolored feces (19% ), nausea (11% ), constipation (8% ), vomiting (7% ) and cough (6% ) - Iron Deficiency Anemia in CKD Not on Dialysis: Discolored feces (
22% ), diarrhea (21% ), constipation (18% ), nausea (10% ), abdominal pain (5% ) and hyperkalemia (5% )
SPECIFIC POPULATIONS
- Pregnancy and Lactation: There are no available data on AURYXIA use in pregnant women to inform a drug-associated risk of major birth defects and miscarriage. However, an overdose of iron in pregnant women may carry a risk for spontaneous abortion, gestational diabetes and fetal malformation. Data from rat studies have shown the transfer of iron into milk, hence, there is a possibility of infant exposure when AURYXIA is administered to a nursing woman
To report suspected adverse reactions, contact Akebia Therapeutics, Inc. at 1-844-445-3799
Please see full Prescribing Information.
Akebia Therapeutics Contact
Kristen K. Sheppard, Esq
ir@akebia.com
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SOURCE Akebia Therapeutics
FAQ
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