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Akebia Reports Second Quarter 2020 Financial Results

CAMBRIDGE, Mass., Aug. 10, 2020 /PRNewswire/ -- Top-line data readout of global Phase 3 PRO2TECT program of vadadustat for treatment of anemia due to CKD in

articleAkebia Therapeutics, Inc.August 10, 20204/company/akebia-ther/news/akebia-reports-second-quarter-2020-financial-results
Akebia Reports Second Quarter 2020 Financial Results

About this update from Akebia Therapeutics, Inc.

[{"type":"text","content":"CAMBRIDGE, Mass., Aug. 10, 2020 /PRNewswire/ -- \n\n \n \n \n \n \n \n\n \nTop-line data readout of global Phase 3 PRO2TECT program of vadadustat for treatment of anemia due to CKD in adult patients not on dialysis on track for early September Cash runway extends beyond expected U.S. launch of vadadustatAkebia Therapeutics, Inc. (Nasdaq: AKBA), a biopharmaceutical company with the purpose of bettering the lives of people impacted by kidney disease, today reported financial results for the second quarter ended June 30, 2020. As previously announced, in lieu of a financial results and business update call, Akebia management plans to host a conference call and webcast in early September to report top-line data from PRO2TECT, the second of its two global Phase 3 cardiovascular outcomes programs. The two PRO2TECT studies evaluated the efficacy and safety of vadadustat, the Company's investigational oral hypoxia-inducible factor prolyl hydroxylase inhibitor (HIF-PHI), for the treatment of anemia due to chronic kidney disease (CKD) in adult patients not on dialysis. \n\"We had an incredible quarter in terms of advancing our vadadustat clinical development program, bringing us that much closer to achieving our purpose to better the life of each person impacted by kidney disease. We reported exciting, positive top-line data from our global Phase 3 INNO2VATE program highlighting vadadustat's potential as a new oral standard of care for treating anemia due to CKD in adult patients on dialysis, and topped off the quarter with the first regulatory approval of vadadustat in Japan,\" said John P. Butler, President and Chief Executive Officer of Akebia Therapeutics. \"The next chapter of Akebia's growth story is starting to unfold and as previously announced, we plan to share top-line data from PRO2TECT in early September.\" \nRecent Business Highlights \nIn August, the Company announced database lock for PRO2TECT and plans to report top-line data from PRO2TECT in early September. This announcement follows Akebia's earlier update provided in May that it had achieved the target number of major adverse cardiovascular events (MACE) for the PRO2TECT studies. In July, the Company announced an investigator-sponsored research study by The University of Texas Health Science Center at Houston (UTHealth) in Houston, Texas, evaluating the use of vadadusta...

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