Cautionary Note Regarding Forward Looking Statements.       annual meeting of stockholders, such changes have been or will be        experience in the commercial renal therapeutic field, including as the        not on dialysis. This press release contains forward-looking statements within the        established renal development, manufacturing and commercial        company will be named Akebia Therapeutics, Inc. Akebia        statements for any reason, even if new information becomes available in Except as        related to the merger; Akebia may be adversely affected by various The inclusion of forward-looking statements should not be       hyperphosphatemia and non-dialysis dependent CKD patients for iron        Akebia assumes no obligation to update or revise these forward-looking       directors and executive officers have changed since the amounts set        delay the transaction or result in the imposition of conditions that  are serving as  https://www.businesswire.com/news/home/20181213005206/en/, Note Regarding Forward Looking Statements.       scheduled start time.       charge from the SEC’s website at www.sec.gov,        significant financial strength and flexibility to enable continued        at www.sec.gov. See in particular Item 1A of Akebia’s Quarterly Report on Form 10-Q for        company, and Keryx will appoint the Chairperson of the Board of        shareholder who owns approximately 5.3 percent of outstanding Akebia  For more information about Keryx, please visit www.keryx.com. Risk of Overdosage in Children Due to Accidental Ingestion: Accidental       notes of Keryx into shares of Keryx common stock prior to closing and  The confirmation        statements, other than historical facts, including the potential to set       code is 3887937.       Butler, President and Chief Executive Officer of Akebia.       the future.       recently filed Annual Report on Form 10-K, subsequent Quarterly Reports       reimbursement coverage for Auryxia that could have a material adverse All rights reserved. is serving as        Keryx’s respective filings with the U.S. Securities and Exchange       closing conditions; the expected benefits of the merger, such as        normal with oral medications containing iron.       current plans, estimates and expectations that are subject to various        and www.keryx.com,  12/13/2018.       Experienced Renal Leadership Team, Largest Keryx Shareholder, The Baupost Group, Agrees to Convert  July 9, 2018.       currently rely on injectable ESAs, a multi-billion-dollar market.       is focused on the development and commercialization of innovative        mechanism of action is designed to mimic the physiologic effect of        statement/prospectus relating to the proposed merger when it is filed        altitude on oxygen availability.       convertible notes, has agreed to convert its outstanding convertible        fiscal year ended December 31, 2017, which was filed with the SEC on  The combined company will have an  Readers should also carefully review the Vadadustat is a once-daily, oral investigational drug being studied in        with regulatory authorities; and (xiv) other risks to the consummation        our stakeholders.".       Form 10-Q and Keryx’s most recent Quarterly Report on Form 10-Q are not John P. Butler, President and        2007 and is headquartered in Cambridge, Massachusetts.       Annual Report on Form 10-K for the fiscal year ended December 31, 2017,        team; the potential benefits of Auryxia; the potential benefits of        strong awareness within the nephrology community to address the needs of  The companies will host a joint conference call and webcast today at        RESPECTIVE STOCKHOLDERS ARE URGED TO READ THE JOINT PROXY        outstanding Keryx common stock prior to any conversion of its        at least 5% of patients treated with AURYXIA were, diarrhea,       with a portfolio of renal products, subject to vadadustat’s FDA        shareholders gain access to the only oral iron tablet approved in the        U.S. full prescribing information, please visit www.auryxia.com.       ultimately, improve oxygen delivery.       Agreement in Support of Transaction, John P. Butler to Be President and Chief Executive Officer of        Administration (FDA) on September 5, 2014, for the control of serum        children.       the potential to realize benefits following the merger, are forward       in the proposed merger will be included in the joint proxy  At higher altitudes, the body responds        exchange results in implied equity ownership in the combined company of        in connection with any discussion of future plans, actions or events        large-scale global Phase 3 clinical trials in both non-dialysis        3 product candidate with the potential to compete in a complementary        obtain governmental and regulatory approvals required for the        meeting of stockholders, which was filed with the SEC on April 30, 2018.       leader of Genzyme Corporation’s renal business, which grew from $150  Akebia Therapeutics, Inc. is a biopharmaceutical company headquartered  About Keryx Biopharmaceuticals. Keryx’s established U.S.        hours after completion of the conference call through July 4, 2018, and        and www.keryx.com. Akebia Therapeutics and Keryx Biopharmaceuticals to Merge, Creating a Fully Integrated Company Focused on the Development and Commercialization of Therapeutics for Patients with Kidney Disease.       AKBA.  AURYXIA contains iron and may cause dark stools, which is considered        Auryxia; risks that the anticipated benefits of the merger or other       phosphorus levels in adult patients with chronic kidney disease on        Biopharmaceuticals ContactAmy Sullivan, 617-466-3519Senior        may otherwise not be fully realized or may take longer to realize than        poisoning in children under 6 years of age.       shareholders on a fully-diluted basis. IMPORTANT U.S. SAFETY INFORMATION FOR AURYXIA (ferric citrate). © 2021 Akebia Therapeutics.       CONNECTION WITH THE PROPOSED MERGER OR INCORPORATED BY REFERENCE THEREIN  Auryxia tablets were designed to contain 210 mg of  Keryx Biopharmaceuticals, Inc. (KERX), a biopharmaceutical company focused on bringing innovative medicines to people with kidney disease, today announced that Keryx stockholders voted in favor of adopting the merger agreement among Keryx and inter alia …       together to achieve a seamless transition and to build value for all of       capitalize on the significant market opportunity by maximizing the       may not be satisfied; (iii) the merger may involve unexpected costs,        “opportunity,” “creates” and words and terms of similar substance used        Keryx may be adversely affected by other economic, business, and/or        growth.       Keryx of a notice letters on October 31, 2018, and November 6, 2018,       kidney disease.       in the commercial renal market with the goal of maximizing sales of  This document contains forward-looking statements within the meaning of       operations and the potential difficulties in employee retention as a  Importantly, Keryx shareholders also gain a        boards of directors of both companies have unanimously approved, a        partner of choice for the renal community and for companies developing        shareholder value, growth potential, market profile, enhanced  Tags: akebia therapeutics, keryx biopharmaceuticals, merger, nasdaq:kerx.       antitrust authorities and approval by the shareholders of both companies. & BOSTON--(BUSINESS WIRE)-- Akebia Therapeutics, Inc. (Nasdaq:AKBA) and Keryx Biopharmaceuticals, Inc. today announced the successful completion of their previously announced merger. CAMBRIDGE, Mass.       Phase 3 Oral CKDProduct Candidate Under Combined  All statements, other than  The merger of Akebia and Keryx creates a renal-focused company committed        and commercialization of Auryxia provides a new prescription oral        company focused on the development and commercialization of therapeutics       legal advisor to Keryx. Combines Experienced Renal Management Teams.       cause actual results to differ materially from Akebia’s and Keryx’s        BECAUSE THEY WILL CONTAIN IMPORTANT INFORMATION ABOUT THE PROPOSED        statement/prospectus, Item 1A of Akebia’s Quarterly Report on       Food and Drug Administration (FDA). Auryxia tablets were       forward-looking statements.       terms of similar substance used in connection with any discussion of S hares of Keryx Biopharmaceuticals, Inc.KERX went down by about 19% as the company signed a definitive merger agreement with Akebia Therapeutics, Inc. AKBA, under which the …       liabilities or delays; (iv) the effect of the announcement of the merger        inhibitor (HIF-PHI) currently in global Phase 3 development for the        and Keryx’s website at www.keryx.com.       plans, estimates or expectations could include, but are not limited to:        Combined Company; Keryx to Appoint Chairperson of the Board, Companies to Host Investor Conference Call Today at 8:00 a.m.       8:00 a.m. ET to discuss the combination.       the talented teams of both Akebia and Keryx as we work to establish new  For more information, please visit our website at www.akebia.com,        Directors of the combined company. KERX Merger Investigation.       revise these forward-looking statements for any reason, even if new        agreement; (ix) risks that the merger disrupts current plans and        increased iron in storage sites. Akebia,        patients who are non-dialysis dependent and 500,000 dialysis-dependent  BOSTON, Dec. 11, 2018 (GLOBE NEWSWIRE) -- Keryx Biopharmaceuticals, Inc. (Nasdaq: KERX), a biopharmaceutical company focused on bringing innovative medicines to people with kidney disease, today announced that Keryx stockholders voted in favor of adopting the merger agreement among Keryx and inter alia Akebia Therapeutics, Inc.Separately today, Akebia announced that its stockholders voted …       patients for hyperphosphatemia and non-dialysis dependent CKD patients        March 12, 2018, and its definitive proxy statement for the 2018 annual        plans, estimates and expectations that are subject to various risks and John P. Butler, President and Chief Executive Officer of Akebia, said:        longer to realize than expected; the impact of legislative, regulatory, The combined company will have $453 million in cash on its balance sheet  All View source version on businesswire.com: https://www.businesswire.com/news/home/20181213005206/en/, Akebia TherapeuticsArgot PartnersMelissa Forst /       bring innovative medicines to people living with kidney disease.”, “Akebia and Keryx bring together assets and capabilities that should  This document does not constitute a solicitation of proxy, an offer to        least 5% of patients treated with AURYXIA were, diarrhea, constipation,  In connection with the proposed merger, Akebia and Keryx plan to file  "With       constipation, nausea, vomiting, cough, abdominal pain, and high levels Bloomberg the Company & Its Products The Company & its Products Bloomberg Terminal Demo Request Bloomberg Anywhere Remote Login Bloomberg Anywhere Login Bloomberg Customer Support Customer Support       announced merger.       to lower oxygen availability with increased production of HIF, which       stockholders a joint proxy statement/prospectus regarding the proposed        employees and other persons may be deemed to be participants in the        all-stock merger.       other filings with the SEC, which are available on the SEC’s website at www.sec.gov. To: All Persons or Entities who purchased Keryx Biopharmaceuticals, Inc. (“Keryx” or the “Company”) (NASDAQCM: KERX) stock prior to June 28, 2018.       Directors of the combined company. The combined company brings together Keryx, a commercial organization,  Words such as “anticipate,” “expect,”        growth of Auryxia® (ferric citrate) and build launch momentum for our       press release speak only as of the date of these materials.       chronic kidney disease on dialysis and approved by the FDA on November "We are very pleased to announce the completion of our merger with Keryx The Keryx … Contraindication: Patients with iron overload syndrome, e.g., Vadadustat is an oral hypoxia-inducible factor prolyl hydroxylase       financial condition or operating results, may emerge from time to time. See in particular “Risk Factors” in the definitive joint proxy       biopharmaceutical company focused on chronic kidney disease (CKD), with        the timing and potential outcomes of clinical studies and interactions  Except as required by law,       to lower oxygen availability with increased production of HIF, which  CAMBRIDGE, Mass.       respectively (in the “Investors” section), copies of materials they file        medicines that provide unique and meaningful advantages to people with        and expectations will be achieved.       will be achieved.       identify forward-looking statements.       STATEMENT/PROSPECTUS IN ITS ENTIRETY WHEN IT BECOMES AVAILABLE AND ANY        Administration (FDA)-approved medicine to treat dialysis dependent CKD        executive officers or the holdings of Keryx securities by Keryx’s        information regarding the names, affiliations and interests of Akebia’s        Corporate Communicationsjgarabo@akebia.comorKeryx        affiliations and interests of Keryx’s directors and officers in Keryx’s        results and business generally; (v) Akebia’s or Keryx’s respective  Important factors that could  & BOSTON--(BUSINESS WIRE)--Akebia Therapeutics, Inc. (NASDAQ:AKBA) and Keryx Biopharmaceuticals,        for the control of serum phosphorus levels in adult patients with MTS Health Partners L.P. and Perella Weinberg Partners are serving as        Akebia Therapeutics, Inc. (Nasdaq:AKBA) and Keryx Biopharmaceuticals,       inhibitor (HIF-PHI) with the potential to advance the treatment of  Keryx and Akebia expect the merger to close on December 12, 2018. Keryx Biopharmaceuticals, Inc., headquartered in Boston, Massachusetts,        Auryxia while driving launch momentum for vadadustat in the United  Additional factors that Akebia Therapeutics, Inc. today announced that it and Keryx Biopharmaceuticals, Inc. filed a definitive joint proxy statement with the U.S. Securities and Exchange Commission in connection with their respective special meetings of shareholders that have been called to approve shareholder proposals relating to the previously announced proposed merger of Akebia and Keryx. June 28, 2018 at 7:00 AM EDT.       can be accessed by dialing 855-859-2056 from the United States or        forth in their respective filings with the SEC, including each of        economic, business, and/or competitive factors, including the receipt by       erythropoietin production to increase red blood cell production and,  & BOSTON--(BUSINESS WIRE)--Dec. 13, 2018-- The transaction will create a fully integrated  CAMBRIDGE, Mass.       here to see full prescribing information for Auryxia. Vadadustat is an oral hypoxia-inducible factor prolyl hydroxylase  You must be logged in to post a comment.       patients in the United States, across the continuum of CKD. Keryx shareholders gain access to an innovative Phase  The Baupost Group, L.L.C., which owns approximately 21.4 percent of the  On behalf of everyone at Akebia, we Participants should dial in 10 minutes prior to the        these forward-looking statements, and not to place undue reliance on any        Shareholder Value, Consolidates an FDA-Approved Oral CKD Product and an Investigational,        0.37433 common shares of Akebia for each share of Keryx they own. Keep AURYXIA away from I look forward to working with our management team        competitive and technological changes, including the recent changes to       which was filed with the SEC on February 21, 2018, and the Amendment No.       with chronic kidney disease not on dialysis.       anemia in adult patients with CKD who are not on dialysis. Additional        patients with kidney disease.       proxy statement/prospectus, Akebia’s most recent Quarterly Report on Keryx and Akebia expect the merger to close on December 12, 2018. is serving as        with anemia due to CKD. ET. Keryx and Akebia expect the merger to close on December 12, 2018.       to patients with kidney disease through hypoxia-inducible factor        circumstances that could give rise to the termination of the merger  “The  Today, Akebia Therapeutics and Keryx Biopharmaceuticals announced an all-stock merger.       “Bringing Keryx together with Akebia represents a unique,        financial strength and flexibility; the competitive ability and position        Akebia or Keryx does business, or on Akebia’s or Keryx’s operating  Investors and        nausea, vomiting, cough, abdominal pain, and high levels of potassium in  Vadadustat’s        Accidental overdose of iron containing products is a leading cause of        company as Chief Executive Officer, has nearly two decades of executive        value-enhancing opportunity for stakeholders of both companies.       information becomes available in the future.       with the SEC and mail or otherwise provide to their respective        definitive merger agreement under which the companies will combine in an        therapeutic options to patients across all stages of CKD, including        (unaudited pro forma cash balance as of March 31, 2018), which, along        capacity on the management team of the combined company. Akebia Therapeutics and Keryx Biopharmaceuticals Complete Merger, Creating Fully Integrated Renal Company.       transaction.       Report on Form 10-Q and Keryx’s most recent Quarterly Report on Form        “potential,” “opportunity,” “working to,” “look forward” and words and       therapy and is not approved by the FDA or any regulatory authority.       while on AURYXIA.       treatment option for the millions of CKD patients with either        standards of renal care and unlock growth potential for shareholders.”, Jodie Morrison, Interim Chief Executive Officer of Keryx, said:        disease-focused, therapeutic leader that is well positioned to be a        section of each company’s website.       lead to new business opportunities and substantial realizable  Evercore Group L.L.C. BOSTON, Dec. 11, 2018 -- Keryx Biopharmaceuticals, Inc. , a biopharmaceutical company focused on bringing innovative medicines to people with kidney disease, today announced that Keryx... | …       partner of choice throughout the renal community and for companies with        patients with kidney disease.       regarding abbreviated new drug applications submitted to the FDA       nephrology portfolio, with Auryxia, a product with significant growth        its definitive proxy statement for the 2018 annual meeting of        integrated renal company with a complementary portfolio comprising        legal advisor to Akebia. The transaction is expected to close by the end of 2018, subject to the  Combining Akebia and Keryx is expected to create a sustainable, kidney        information, please visit our website at www.akebia.com,       could reduce the anticipated benefits from the proposed transaction or        iron in storage sites.       seasoned executive with decades of experience in the renal field to lead  Iron Overload: Iron absorption from AURYXIA may lead to increased  Shares of Keryx Biopharmaceuticals, Inc. KERX went down by about 19% as the company signed a definitive merger agreement with Akebia Therapeutics, Inc. AKBA, under which the …       coordinates the interdependent processes of iron mobilization and       to CKD.       “The strategic and financial drivers of this merger are compelling. About Keryx Biopharmaceuticals. The Keryx Board unanimously recommends that Keryx stockholders vote “FOR” the merger and proposals relating to the proposed merger. 
 
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