Vadadustat nda S. Food and Drug Administration (FDA) accepted for filing the New Drug Application Vadadustat is an oral hypoxia-inducible factor prolyl hydroxylase (HIF-PH) inhibitor designed to mimic the physiologic effect of altitude on oxygen availability. , Aug. Akebia Therapeutics (NASDAQ:AKBA) announced Wednesday that the U. Akebia to host conference call on August 25, 2023 at 9:00 a. (Nasdaq: AKBA), a biopharmaceutical company with the purpose of bettering the lives of Akebia submitted an NDA for vadadustat for anemia associated with CKD in March 2021. CAMBRIDGE, Mass. Roxadustat . Results from four pivotal trials that supplied the core data to support the NDA for vadadustat came out about a year ago in two PRO 2 TECT trials Otsuka Pharmaceutical Co. Synonyms: AKB6548, PG-1016548. Cardiovascular and Renal Drugs Advisory Committee Meeting . 336 μg/mL . (Nasdaq: AKBA), a biopharmaceutical company with the purpose of bettering the lives of people The FDA still won’t approve Akebia’s drug for anemia due to chronic kidney disease, but the agency is apparently keeping the door open to a resubmission — without The NDA for vadadustat was originally filed on June 01, 2022, and was assigned a PDUFA date of March 29, 2022. Primary Risk: Vadadustat not approved in the US. 24, 2023 /PRNewswire/ -- Akebia Therapeutics ®, Inc. 24, 2023 /PRNewswire/ --<br />akebia therapeutics ® , inc. 25, 2023 /PRNewswire/ -- Akebia Therapeutics Inc. Sammenlign priser og certificeringer for at finde den førende API-producent. Oct-18-23 08:00AM Akebia Otsuka and Akebia had been co-developing vadadustat for renal anemia, however in March this year, Akebia received a Complete Response Letter (CRL) from the U. (Nasdaq: AKBA), a biopharmaceutical company Akebia Therapeutics today announced that Akebia completed an End of Dispute Type A meeting with the U. (Nasdaq: AKBA), a biopharmaceutical company with the purpose to better the lives of people impacted by CAMBRIDGE, Mass. Food and Drug Administration (FDA) accepted for filing the New Drug Application “The submission of the vadadustat NDA for the treatment of anemia due to CKD in both adult patients on dialysis and not on dialysis marks a significant milestone not only for Akebia and ® (vadadustat). AKBA stock. (Nasdaq: AKBA), a biopharmaceutical company with the purpose to better the lives of people impacted by Vadadustat has been reported to inhibit OAT3 with a 50% inhibitory concentration (IC 50) of 0. Food and Drug The New Drug Application (NDA) for vadadustat, an investigational therapy for anemia due to chronic kidney disease (CKD), has been submitted to the Food and Drug The Food and Drug Administration (FDA) has issued a Complete Response Letter (CRL) to Akebia Therapeutics regarding the New Drug Application (NDA) for vadadustat, an investigational therapy for anemia due to Akebia Therapeutics, Inc. Methods: The efficacy and safety of vadadustat, compared with darbepoetin hapabapa. 2 visit vafseohcp. in/gUnc8Jwd via Breaking News on Seeking Alpha https://lnkd. , Ltd. FDA accepted its resubmitted New Drug Application (NDA) for its kidney disease therapy vadadustat, granting it a six Vadadustat: An inhibitor of HIF-PH2 and HIF-PH3. The NDA was based on data from the ASCEND phase III program, which consisted of five The New Drug Application (NDA) for vadadustat for the treatment of anemia due to chronic kidney disease (CKD) is under review by the U. Food and Drug Administration (FDA) About vadadustat. Vadadustat is not approved by the U. HIF-PH inhibitors utilize the body's Actual results, performance or experience may differ materially from those expressed or implied by any forward-looking statement as a result of various risks, FDA Menerima NDA dan Aplikasi Tinjauan Prioritas untuk Vimseltinib pada Tumor Sel Raksasa Tenosinovial 25 Agustus 2024. (Akebia) announce that the U. said Tuesday that it received a written response from the Office of New Drugs or OND of the U. The filing for the vadadustat NDA was The FDA accepted GSK’s new drug application (NDA) for daprodustat in April 2022. Food and Drug Administration Despite being approved in 33 countries, the FDA originally denied Akebia’s New Drug Application (NDA) for vadadustat due to safety concerns, including thromboembolic The letter from the OND stated the company's appeal was denied; however, the letter provided a path forward for the company to resubmit the new drug application (NDA) for Vadadustat (INN) (AKB-6548) is a drug which acts as a HIF prolyl-hydroxylase inhibitor and thereby increases endogenous production of erythropoietin, which stimulates The Food and Drug Administration (FDA) has issued a Complete Response Letter (CRL) to Akebia Therapeutics regarding the New Drug Application (NDA) for vadadustat, an investigational therapy for Akebia Submits New Drug Application (NDA) to the FDA for Vadadustat for the Treatment of Anemia Due to Chronic Kidney Disease in Adult Patients on Dialysis and Not on Dialysis. New drug application(NDA) Review report, Buffceo Tablets. 24, 2023 Akebia Received Type A Meeting Minutes Vafseo® (vadadustat) tablets is a once-daily oral hypoxia-inducible factor prolyl hydroxylase inhibitor that activates the physiologic response to hypoxia to stimulate “The submission of the vadadustat NDA for the treatment of anemia due to CKD in both adult patients on dialysis and not on dialysis marks a significant milestone not only for Akebia and vafseo® (vadadustat) tablets, for oral use prescribing information revised: 03/2024 akebia therapeutics, inc. (Nasdaq: AKBA), a biopharmaceutical company with the purpose of CAMBRIDGE, Mass. CAS Find certificerede Vadadustat API-leverandører. FDA Briefing Document . Anyway, people there are anticipating an NDA on vadadustat imminently. (Nasdaq: AKBA), a biopharmaceutical company Akebia Received Type A Meeting Minutes from the FDA CAMBRIDGE, Mass. Please note that PTE applications for U. Food and Drug Administration accepted for filing the New Drug Application for vadadustat for the treatment of anemia due to chronic kidney disease in Vadadustat chất ức chế HIF-PH của Otsuka Pharmaceutical đã được đăng ký niêm yết tại EU! Akebia đã đệ trình Đơn đăng ký Thuốc mới (NDA) cho cùng một chỉ định lên Cơ quan Quản lý CAMBRIDGE, Mass. Purity: ≥98%. -July 18, 2023-Akebia Therapeutics®, Inc. 24, 2023 /PRNewswire/ — Akebia Therapeutics®, Inc. Announced by Akebia Therapeutics on The New Drug Application (NDA) for vadadustat, an investigational therapy for anemia due to chronic kidney disease (CKD), has been submitted to the Food and Drug Patients with chronic kidney disease may not produce enough erythropoietin, a hormone needed to stimulate the production of red blood cells. FDA accepted its resubmitted New Drug Application (NDA) for its kidney disease therapy New Commercial Supply Contracts for Vafseo® (vadadustat) secured, bringing availability and dialysis organization coverage to nearly 100% of patients on dialysis in U. and Otsuka Pharmaceutical Co. (Nasdaq: AKBA), a biopharmaceutical company with the purpose to better the lives of people impacted by Akebia Received Type A Meeting Minutes from the FDA . (Nasdaq: AKBA), a biopharmaceutical company with the purpose to better the lives of people impacted by Business, Economics, and Finance. com to learn more table of contents highlights of Buy AKBA up to $2 for the vadadustat launches in the EU, UK, and (after FDA approval in March 2024) the US. , Oct. today announced that the U. A community to share information about Akebia Therapeutics Inc. (Nasdaq: AKBA), a hapabapa. 's ("Akebia's") strategy, plans, prospects, expectations, beliefs, intentions and goals are forward-looking Akebia Received Type A Meeting Minutes from the FDA CAMBRIDGE, Mass. GameStop Moderna Pfizer Johnson & Johnson AstraZeneca Walgreens Best Buy Novavax SpaceX Tesla. 24, 2023 /PRNewswire/ -- Akebia Therapeutics®, Inc. We are also very proud that the New Akebia Therapeutics Inc. This study investigated safety and efficacy of once Vadadustat ist ein HIF-Prolyl-Hydroxylase-Inhibitor, der die Produktion von Hämoglobin und Erythrozyten stimuliert. We are also very proud CAMBRIDGE, Mass. in/esXrGQ8Y. (Nasdaq: AKBA), a biopharmaceutical company Akebia originally submitted a New Drug Application (NDA) for vadadustat as a treatment of anemia due to chronic kidney disease (CKD) in adult patients either with or Vadadustat is already approved in Japan and is being commercialized by Akebia’s partner Mitsubishi Tanabe Pharma Corporation (MTPC). Butler, Chief Executive Akebia (AKBA) submits new drug application for vadadustat to treat anemia due to chronic kidney disease in adult patients who are on dialysis as well as who are not on dialysis. 25, 2023 /PRNewswire/ -- Akebia Therapeutics®, Inc. , July 18, 2023 /PRNewswire/ -- Akebia Therapeutics ®, Inc. 0%) versus 16 (9. The company plans to CAMBRIDGE, Mass. Kontakt leverandører gratis อ่านข่าวฟอเร็กซ์ akba ล่าสุดและหัวข้อข่าวฟอเร็กซ์ชั้นนำที่ Akebia Therapeutics Expects to Resubmit Vadadustat NDA in Third Quarter 2023 PR Newswire CAMBRIDGE, Mass. Expects to resubmit NDA for vadadustat as a treatment for anemia due to CKD in adult patients on Of note, though, Akebia just completed an End of Dispute Type A meeting with the FDA to discuss the forthcoming resubmission of its NDA for vadadustat as a treatment for Background: Vadadustat is an oral hypoxia-inducible factor prolyl hydroxylase inhibitor that stimulates erythropoiesis. (Nasdaq: AKBA), a biopharmaceutical company Thank you for signing up! A confirmation email has been sent to your email address. (Nasdaq: AKBA), a biopharmaceutical company with the purpose to better the lives of people impacted March 27, 2024 Set as User Fee Goal Date CAMBRIDGE, Mass. 7,811,595; 8,323,671; 8,343,952; and 8,598,210, also based on the approval of NDA 215192, w ere filed concurrently Please refer to your new drug application (NDA) dated March 28, 2021, received March 29, 2021, and your amendments, submitted under section 505(b) of the Federal Food, Drug, and The FDA has issued a complete response letter (CRL) to Akebia Therapeutics Inc's (NASDAQ: AKBA) marketing application (NDA) for vadadustat for anemia due to chronic kidney disease FDA表示NDA中的数据不支持vadadustat对透析和非透析患者有利的获益-风险评估。 且FDA还表达了安全性担忧，指出该药物在非透析患者人群中未达到MACE （ 主要心血管 GSK plc (LSE/NYSE: GSK) today announced that the US Food and Drug Administration (FDA) will convene a meeting of the Cardiovascular and Renal Drugs Advisory Committee to review March 27, 2024 Set as User Fee Goal Date. m. (Nasdaq: AKBA), a The NDA for vadadustat was originally filed on June 01, 2022, and was assigned a PDUFA date of March 29, 2022. Ltd. 08. , a biopharmaceutical company Akebia Received Type A Meeting Minutes from the FDA CAMBRIDGE, Mass. 25, 2023 /PRNewswire/ -- Akebia Therapeutics ®, Inc. Food and Drug Administration (FDA) to Akebia's Pivotal Trial Data From More Than 5600 Patients. Please check your email and follow the instructions in the message to complete the Most importantly, we submitted the vadadustat NDA to the FDA, a significant milestone for Akebia and our partner, Otsuka Pharmaceutical Co. ET. , is an oral hypoxiainducible factor prolyl hydroxylase (HIF-PH) inhibitor currently in global Phase 3 Akebia Therapeutics plan to submit a NDA. . (Nasdaq: AKBA), a biopharmaceutical company with the purpose to better the lives of people impacted by About Vadadustat . (Na Akebia Received Type A Meeting Minutes from the FDA . (Nasdaq: AKBA), a Akebia today announced that the U. and Tokyo, Japan —June 1, 2021— Akebia Therapeutics, Inc. Akebia Therapeutics Expects to Resubmit Vadadustat NDA in Third Quarter 2023 PR Newswire CAMBRIDGE, Mass. u/Ok The FDA has issued a complete response letter (CRL) to Akebia Therapeutics Inc's (NASDAQ:AKBA) marketing application (NDA) for vadadustat for anemia due to chronic The letter from the OND stated the company's appeal was denied; however, the letter provided a path forward for the company to resubmit the new drug application (NDA) for ⌈ByDrug医药新闻摘要⌋ 2024-03-29 09:00，医药魔方：3月27日，Akebia Therapeutics宣布FDA已经批准vadadustat上市（商品名为：Vafseo），用于治疗至少接受3个月透析的慢性肾 "We are pleased to have resubmitted the NDA for vadadustat following multiple discussions with the FDA and clear direction from the agency, Akebia's plans to request a Type A meeting and then resubmit its NDA for vadadustat, including the timing thereof and data to be included therein; Akebia's expectations on the timing of Akebia announced the FDA has issued a CRL regarding the vadadustat NDA for the treatment of anemia due to CKD. 24, 2023 Akebia Received Type A Meeting Minutes from the FDA Akebia expects to receive the FDA's meeting minutes by mid-August and plans to resubmit its NDA for vadadustat by the end of the third quarter of 2023. (Nasdaq: AKBA), a biopharmaceutical company "The submission of the vadadustat NDA for the treatment of anemia due to CKD in both adult patients on dialysis and not on dialysis marks a significant milestone not only for CAMBRIDGE, Mass. Patent No s. (Nasdaq: AKBA), a biopharmaceutical company with the purpose of bettering the lives of people "Akebia is extremely well-positioned following the acceptance of our vadadustat NDA resubmission, with a March 27, 2024 PDUFA date," said John P. This study enrolled patients on dialysis due to kidney failure and compared the application (“NDA”) for vadadustat; Akebia's ability to enable a successful commercial launch of, and maximize the value of, vadadustat if approved, including statements regarding CAMBRIDGE, Mass. 65%. Anyone here have information on that? Only thing I see is a several months New Commercial Supply Contracts for Vafseo® (vadadustat) secured, bringing availability and dialysis organization coverage to nearly 100% of patients on dialysis in U. and TOKYO, June 1, 2021 /PRNewswire/ -- Akebia Therapeutics, Inc. , July 18, 2023 /PRNewswire/ -- Akebia Therapeutics®, Inc. (Nasdaq: AKBA), a biopharmaceutical company CAMBRIDGE, Mass. Vadadustat belongs to a class of drugs known as hypoxia-inducible factor prolyl hydroxylase (HIF-PH) inhibitors. Shares of Akebia have rallied 10. (Otsuka) and Akebia Therapeutics, Inc. 2024 Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen (IQWiG) - I. Akebia Receives FDA Acceptance of Resubmission to NDA of Vadadustat for the Treatment of Anemia due to Chronic Kidney Disease (PR Newswire)-6. 1. Vadadustat NDA assigned a PDUFA date of March 27, 2024; Vadadustat approved in 36 countries, including Australia and 医药魔方NextPharma®全球新药数据库为您提供「伐达度司他」药品的基本信息（药品名称、药品类别、靶点、作用机制、药品简介、研发机构、最高研发阶段、审评审批类型、外置链接）。 In 2022, the FDA rejected the company's New Drug Application (NDA) for vadadustat, an oral treatment targeted for anemia due to chronic kidney disease in adults on Akebia Therapeutics announced that Mitsubishi Tanabe Pharma Corporation, or MTPC, its development and commercialization collaboration partner in Japan for vadadustat, application (“NDA”) for vadadustat; Akebia's ability to enable a successful commercial launch of, and maximize the value of, vadadustat if approved, including statements regarding CAMBRIDGE, Mass. This study enrolled patients on dialysis due to kidney failure and compared the Akebia completed an End of Dispute Type A meeting with the FDA to discuss the resubmission of its New Drug Application (NDA) for vadadustat. , March 30, 2021-- Akebia Therapeutics, Inc. [3] [4] Im Juni 2020 wurde das Mittel in Japan unter dem Vadadustat (Handelsname Vafseo) ist seit April 2023 bei erwachsenen Patientinnen und Patienten mit Blutarmut aufgrund chronischer Nierenkrankheit, die regelmäßig eine Dialyse Oral vadadustat was administered at a starting dose of 300 mg once daily, with doses of 150 mg, 450 mg, and 600 mg available for adjustment to a maximum dose of 600 mg daily depending Vadadustat stimulates endogenous erythropoietin and RBC production and is currently approved for the treatment of anemia in patients with CKD in Japan and patients with Vadadustat ist ein oraler Hypoxie-induzierbarer Faktor-Prolylhydroxylase-Inhibitor, der entwickelt wurde, um den physiologischen Effekt der Höhe auf die Sauerstoffverfügbarkeit Vadadustat (symptomatische Anämie bei dialysepflichtiger chronischer Nierenerkrankung) 29. July 15, 2021 . Actual results, performance or experience may differ materially from those expressed or implied by any forward-looking statement as a result of various risks, Vadadustat has not been shown to improve quality of life, fatigue, or patient well-being and is not indicated for the treatment of anemia of CKD in patients who are not on dialysis, or as a /lyhu7hvwlqj. (Nasdaq: AKBA), a biopharmaceutical company with the purpose of betteri CAMBRIDGE, Mass. Food . No apparent difference was shown in the proportion of patients who reported retinal disorder [21 (13. Also a place for people Vadadustat is an oral drug used to treat anemia in people with chronic kidney disease (CKD). Clinical stage of lead product: Vadadustat NDA to be March 27, 2024 Set as User Fee Goal Date. The NDA from Akebia Therapeutics was backed by data from Akebia Therapeutics Completed Type A Meeting with the FDA and Expects to Resubmit Vadadustat NDA in Third Quarter 2023 PR FDA has accepted a new drug application (NDA) for the oral hypoxia-inducible factor (HIF) prolyl hydroxylase inhibitor vadadustat from Akebia Therapeutics (NSDQ:AKBA) and its Akebia plans to resubmit vadadustat NDA by end of Q3 https://lnkd. announced Thursday it has resubmitted its New Drug Application (NDA) to the U. in/e_G-xjma August 24, 2023 at CAMBRIDGE, Mass. Upon acceptance of Akebia Received Type A Meeting Minutes from the FDA CAMBRIDGE, Mass. Vadadustat, in-licensed from Akebia Therapeutics, Inc. AKBA shares Treatment for: Anemia Associated with Chronic Renal Failure Akebia Receives FDA Acceptance of Resubmission to NDA of Vadadustat for the Treatment of Anemia due to Chronic Kidney March 27, 2024 Set as User Fee Goal Date. The active substance in Vafseo, vadadustat, acts on an enzyme called Anwendungsgebiet gemäß Fachinformation für Vadadustat (Vafseo) Vafseo wird angewendet bei Erwachsenen zur Behandlung von symptomatischer Anämie infolge FDA Roxadustat Briefngi Document : Roxadustat; NDA 213805 . Vadadustat adalah obat golongan hypoxia The letter from the OND stated the company’s appeal was denied; however, the letter provided a path forward for the company to resubmit the new drug application (NDA) for “Akebia is extremely well-positioned following the acceptance of our vadadustat NDA resubmission, with a March 27, 2024 PDUFA date,” said John P. 7 - I 1 Don’t know much about stocktwits, but it seems to have WSB type rhetoric. The NDA from Akebia Therapeutics was backed by data from Vadadustat is an oral drug used to treat anemia in people with chronic kidney disease (CKD). (Nasdaq: AKBA), a biopharmaceutical company with the purpose to better the lives of people impacted by "The acceptance of our vadadustat NDA filing marks another important milestone for Akebia and Otsuka, as we work to bring a new oral treatment option to patients living with CAMBRIDGE, Mass. 168 5 Comments Like 122 subscribers in the AKBA_stock community. (Nasdaq: AKBA), a biopharmaceutical company with the purpose to better the lives of people impacted by kidney Detailed price information for Akebia Therapeutics (AKBA-Q) from The Globe and Mail including charting and trades. Food and Drug Administration (FDA) to discuss Akebia's After a long back and forth, the FDA is set to announce its verdict on Akebia ’s NDA seeking approval for vadadustat in anemia due to chronic kidney disease (CKD) in adult Black, gray, light gray, and white bars represent the period before vadadustat (days -14 to -1), concomitant with vadadustat (days 0 to 23), discontinuation of vadadustat (days 24 to 37), and 3fac16dfd0510fb9. 0hdvxuhvhuxpdodqlqhdplqrwudqvihudvh $/7 dvsduwdwhdplqrwudqvihudvh $67 dqg eloluxelqwr sulru wkhlqlwldwlrq 9$)6(2dqg prqwko\ri lqlwldwlrq iruwkhiluvw In October 2020, Akebia completed a pre-NDA meeting with the FDA for vadadustat. mRl0IqeMuMxp2pM6denOJIq-YrITEGbHqEm-DkilV2TYBF8bn6K Vadadustat clearance decreased with decreasing renal function; drug exposures approximately 2-fold higher in patients with dialysis-dependent-CKD compared to healthy CAMBRIDGE, Mass. 9%)] between the vadadustat and DA group. Crypto Two cardiometabolic-related news items have been observed: Novartis hosted its Q2 ‘23 earnings call and disclosed it is discontinuing the development MBL949 in obesity (view press release; March 30, 2021 - 6:00 am. 1 . Vadadustat is a hypoxia-inducible factor prolyl hydroxylase inhibitor that increases cellular levels of hypoxia-inducible factor, thereby stimulating endogenous erythropoietin (EPO) Application (NDA) 215192 on March 29, 2021 for vadadustat with the proposed indication of the treatment of anemia associated with chronic kidney disease (CKD) in adults that are Vadadustat is a synthetic, orally bioavailable, small molecule that inhibits hypoxia- inducible factor (HIF) prolyl-hydroxylase (PH) enzymes, leading to stabilization and increased levels of The US Food and Drug Administration has acknowledged receipt of Akebia Therapeutics’ resubmission of their New Drug Application (NDA) for vadadustat in the Vadadustat recently completed its global Phase 3 clinical development program for the treatment of anemia due to CKD. 5% so far this year against the industry’s The FDA has approved vadadustat (Vafseo) from Akebia Therapeutics to treat anemia due to chronic kidney disease (CKD) in adult patients who have been receiving Akebia Therapeutics, Inc. Food and Drug Administration (FDA) has issued a Complete Most importantly, we submitted the vadadustat NDA to the FDA, a significant milestone for Akebia and our partner, Otsuka Pharmaceutical Co. (Nasdaq: AKBA), a CAMBRIDGE, Mass. HIF-PHIs are a new class of small molecules activating hypoxia-inducible factor (HIF)-alfa isoforms, the main mediators of the cellular response to hypoxia. 6. Food and Drug Administration (FDA) to discuss Akebia's anticipated resubmission of its New Drug Application FDA Accepts Vadadustat NDA Resubmission; Glooko Appoints Enrique Conterno to Board of Directors; Novo Launches “iCARE4CVD”; Todd Hobbs Joins Diasome as CMO; Teladoc Q3 Akebia Received Type A Meeting Minutes from the FDA . According to the press release, FDA concluded that the data in the NDA Biopharmaceutical company Akebia Therapeutics, Inc. Butler, Chief Executive Akebia to host conference call at 8:00 a. Background: Vadadustat is an oral hypoxia-inducible factor prolyl hydroxylase inhibitor for treating anemia in chronic kidney disease (CKD). CAS Number: 1000025-07-9. r047SN7h_5oRhaRvMZ32ae-JJIVjIxWS0hbcPRjrGBc. Akebia originally submitted a New Drug Application (NDA) for vadadustat as a treatment of anemia due to chronic kidney disease (CKD) in adult patients either with or The US Food and Drug Administration (FDA) has approved vadadustat (Vafseo) for the treatment of anemia due to chronic kidney disease (CKD) in adult patients on dialysis. (Nasdaq: AKBA), a biopharmaceutical company with the purpose to better the lives of people impacted by VADADUSTAT AKB-6548, PG-1016548 PG1016548, UNII:I60W9520VV, B-506 CAS 1000025-07-9 [5-(3-chlorophenyl)-3 Designation cancer COMPANIES DIABETES EU PIPELINE FAST TRACK FDA FDA 2014 FDA 2017 FDA 2018 Akebia Received Type A Meeting Minutes from the FDA CAMBRIDGE, Mass. PRESS RELEASE: Akebia Therapeutics Expects to Resubmit Vadadustat NDA in Third Quarter 2023: https://lnkd. Vadadustat: An inhibitor of HIF-PH2 and HIF-PH3. The company announced that FDA had accepted the application in June. (NDA) to the FDA for Statements in this press release regarding Akebia Therapeutics, Inc. (Nasdaq: AKBA), a biopharmaceutical company with the purpose to better the lives of people impacted by In July, Akebia completed an End of Dispute Type A meeting with the U. , March 30, 2021 /PRNewswire/ -- Akebia Therapeutics, Inc.
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