auryxia
auryxia: developed by 2 companies · 1 FDA decision.
auryxia evidence translation
What we can confirm
1 FDA record
What it means
What to watch
Prepared research question
What is verified about auryxia, and what remains unknown?
Traceable citations · Unknowns marked
See linked entities and source evidence2 indications · 0 study sponsors
Related indications
Study sponsors
No additional listed-company sponsor is linked.
Development Pipeline (2)
| Company | Phase |
|---|---|
| Akebia Therapeutics, Inc. (AKBA) Control of serum phosphorus levels in adult patients with di… | Phase 3 |
| KERYX BIOPHARMACEUTICALS INC (KERYX) Treatment of iron deficiency anemia in adults with CKD, not … | Approved |
FDA Decisions1 records
Frequently asked questions
Who is developing auryxia?
auryxia is being developed by Akebia Therapeutics, Inc., KERYX BIOPHARMACEUTICALS INC.
What is auryxia's latest FDA decision?
The most recent tracked FDA decision for auryxia is Approval for 1 INDICATIONS AND USAGE Ferric citrate tablets are a phosphate binder indicated for the control of serum phosphorus levels in adult patients with chronic kidney disease on dialysis. ( 1 ) Ferric citrate tablets are an iron replacement product indicated for the treatment of iron deficiency anemia in adult patients with chronic kidney disease not on dialysis. ( 1 ) 1.1 Hyperphosphatemia in Chronic Kidney Disease on Dialysis Ferric citrate tablets are indicated for the control of serum phosphorus levels in adult patients with chronic kidney disease on dialysis. 1.2 Iron Deficiency Anemia in Chronic Kidney Disease Not on Dialysis Ferric citrate tablets are indicated for the treatment of iron deficiency anemia in adult patients with chronic kidney disease not on dialysis., dated September 5, 2014.