Akebia Reports Third Quarter 2020 Financial Results and Recent Business Updates
CAMBRIDGE, Mass., Nov. 5, 2020 /PRNewswire/ -- Akebia 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 third quarter ended September 30, 2020 and provided business updates, including confirming completion of a pre-NDA meeting with the U.S. Food and Drug Administration (FDA) for vadadustat. Vadadustat is Akebia's investigational oral hypoxia-inducible factor prolyl hydroxylase inhibitor (HIF-PHI) in development for the treatment of anemia due to chronic kidney disease (CKD) in adult patients on dialysis and not on dialysis.
"We recently completed our pre-NDA meeting with the FDA. This was an important milestone for our vadadustat development program, and we remain on track to submit an NDA to the FDA as early as possible next year. A key component of this NDA is the positive data from our global Phase 3 INNO(2)VATE program for the treatment of anemia due to CKD in adult patients on dialysis, which we shared most recently at ASN Kidney Week. These data were clear and consistent, and showed that vadadustat achieved both the primary and key secondary efficacy endpoints, as well as the primary and key secondary safety endpoints of the program for patients on dialysis. Based on our pre-NDA meeting, we remain confident that these results support the potential approval of vadadustat for the treatment of anemia due to CKD in adult patients on dialysis," said John P. Butler, President and Chief Executive Officer of Akebia Therapeutics. "Subject to regulatory review and approval, we believe vadadustat has the potential to be a new oral standard of care to help address the unmet needs of adult patients on dialysis, including both incident and prevalent dialysis patients. We believe this could translate into a potential $2 billion market opportunity in the U.S., alone. Together with our collaborator, Otsuka, we look forward to bringing this innovative therapy to patients on dialysis globally, if approved."
Butler continued, "The pre-NDA meeting also allowed us the opportunity to clarify key questions regarding data from PRO(2)TECT, our global Phase 3 program for the treatment of anemia due to CKD in adult patients not on dialysis, and we look forward to working with the FDA in their review of these data. While the PRO(2)TECT data showed that vadadustat achieved both the primary and key secondary efficacy endpoints, it did not meet the program's primary safety endpoint for patients not on dialysis, and we remain appropriately cautious in our outlook for potential approval of vadadustat in patients not on dialysis. Importantly, we believe the PRO(2)TECT data will not adversely impact the potential approvability of vadadustat for the treatment of anemia due to CKD in adult patients on dialysis."
Akebia plans to submit a New Drug Application (NDA) to the FDA for vadadustat as early as possible in 2021 for two indications: (1) the treatment of anemia due to CKD in adult patients on dialysis, and (2) the treatment of anemia due to CKD in adult patients not on dialysis. In addition, Akebia and its collaborator, Otsuka Pharmaceutical Co. Ltd., are working in close collaboration to prepare a Marketing Authorization Application (MAA) for submission to the European Medicines Agency (EMA) next year.
Recent Business Highlights
-- In October, the Company presented data from its global Phase 3 program
at American Society of Nephrology Kidney Week 2020 Reimagined (ASN
Kidney Week). Akebia's global Phase 3 program consists of two programs
that evaluated the efficacy and safety of vadadustat versus darbepoetin
alfa for the treatment of anemia due to CKD in adult patients on
dialysis (INNO(2)VATE) and not on dialysis (PRO(2)TECT).
-- Highlights of INNO(2)VATE ASN Kidney Week Presentation: As
previously reported in May 2020, vadadustat achieved the primary and
key secondary efficacy endpoints and the primary safety endpoint of
the INNO(2)VATE program, defined as non-inferiority of vadadustat
versus darbepoetin alfa in time to first occurrence of a major
adverse cardiovascular event (MACE), which is the composite of
all-cause mortality, non-fatal myocardial infarction (MI), or
non-fatal stroke, across both INNO(2)VATE studies. Newly presented
INNO(2)VATE data showed that vadadustat also achieved
non-inferiority to darbepoetin alfa on key secondary safety
endpoints including expanded MACE, cardiovascular MACE,
cardiovascular mortality, and all-cause mortality.
-- Highlights of PRO(2)TECT ASN Kidney Week Presentation: As previously
reported in September 2020, vadadustat achieved the primary and key
secondary efficacy endpoints of the PRO(2)TECT program, but did not
meet the primary safety endpoint. Newly presented pre-specified
regional analyses of the PRO(2)TECT program showed vadadustat
demonstrated no clinically meaningful increase in cardiovascular
risk compared to darbepoetin alfa in analyses of MACE, expanded MACE
and all-cause mortality in U.S. patients treated to a target
hemoglobin (Hb) range of 10 to 11 g/dL, consistent with U.S.
treatment guidelines.
-- In October, Akebia and Otsuka launched Balancing Anemia Due to CKD, a
campaign and website designed to increase awareness and education of
anemia due to CKD among healthcare providers with the goal of improving
the management of this disease for patients.
-- In August, the Company announced the launch of vadadustat in Japan by
Mitsubishi Tanabe Pharma Corporation (MTPC), Akebia's partner in Japan,
as a treatment for anemia due to CKD in both adult patients on dialysis
and not on dialysis under the trade name VAFSEO(TM).
-- 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 vadadustat as a potential
therapy to prevent and lessen the severity of acute respiratory distress
syndrome (ARDS), a complication of COVID-19. The study is currently
underway and actively enrolling patients.
Third Quarter Financial Results
-- Revenues: Total revenue was $60.0 million for the third quarter of 2020
compared to $92.0 million for the third quarter of 2019. The decline
versus the prior year period was driven by lower collaboration revenue
consistent with the Company completing the INNO(2)VATE and PRO(2)TECT
studies.
-- Collaboration revenue was $25.6 million for the third quarter of
2020 compared to $62.0 million in the third quarter of 2019, and
included $0.4 million in royalty revenue related to the commercial
sale of vadadustat (VAFSEO(TM)) in Japan from MTPC.
-- Net product revenue for Auryxia(®) (ferric citrate) was $34.4
million for the third quarter of 2020 compared with $30.0 million in
the third quarter of 2019, an increase of 14.6 percent.
-- COGS: Cost of goods sold was $30.3 million for the third quarter of 2020
compared to $38.3 million for the third quarter of 2019 and includes the
impact of $9.9 million in non-cash inventory write-downs largely related
to a previously disclosed manufacturing quality issue related to
Auryxia.
-- R&D Expenses: Research and development expenses were $46.9 million for
the third quarter of 2020 compared to $74.5 million for the third
quarter of 2019. The decline versus the prior year period was primarily
driven by a decrease in costs consistent with the Company completing the
INNO(2)VATE and PRO(2)TECT studies.
-- SG&A Expenses: Selling, general and administrative expenses were $40.2
million for the third quarter of 2020 compared to $34.2 million for the
third quarter of 2019. The increase was primarily a result of higher
professional service fees related to marketing and pre-commercialization
activities for vadadustat and legal fees.
-- Net Loss: Net loss was $60.0 million for the third quarter of 2020
compared to $54.6 million for the third quarter of 2019. The increase in
net loss compared to the prior year period was due primarily to lower
total revenue and more specifically, lower collaboration revenue,
partially offset by lower operating expenses.
-- Cash Position: Cash, cash equivalents and available-for-sale securities
as of September 30, 2020 were $269.3 million. The Company expects its
cash resources to fund its current operating plan beyond the expected
U.S. launch of vadadustat, assuming regulatory approval.
Conference Call
Akebia will host a conference call at 9:00 a.m. Eastern Time today, Thursday, November 5th, to discuss its third quarter financial results and recent business highlights. To listen to the conference call, please dial (877) 458-0977 (domestic) or (484) 653-6724 (international) using conference ID number 2860285. The call will also be webcast LIVE and can be accessed via the Investors section of the Company's website at http://ir.akebia.com.
A replay of the conference call will be available two hours after the completion of the call through November 11, 2020. To access the replay, dial (855) 859-2056 (domestic) or (404) 537-3406 (international) and reference conference ID number 2860285. An online archive of the conference call can be accessed via the Investors section of the Company's website at http://ir.akebia.com.
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. For more information, please visit our website at www.akebia.com, which does not form a part of this release.
About Vadadustat
Vadadustat is an oral hypoxia-inducible factor prolyl hydroxylase (HIF-PH) inhibitor designed to mimic the physiologic effect of altitude on oxygen availability. At higher altitudes, the body responds to lower oxygen availability with stabilization of hypoxia-inducible factor, which can lead to increased red blood cell production and improved oxygen delivery to tissues. Vadadustat recently completed its global Phase 3 development program for the treatment of anemia due to CKD. Vadadustat is not approved by the U.S. Food and Drug Administration (FDA) or any regulatory authority with the exception of Japan's Ministry of Health, Labour and Welfare (MHLW). In Japan, vadadustat is approved as a treatment for anemia due to CKD in both dialysis-dependent and non-dialysis dependent adult patients.
About Anemia due to Chronic Kidney Disease (CKD)
Anemia is a condition in which a person lacks enough healthy red blood cells to carry adequate oxygen to the body's tissues. It commonly occurs in people with CKD because their kidneys do not produce enough erythropoietin (EPO), a hormone that helps regulate production of red blood cells. Anemia due to CKD can have a profound impact on a person's quality of life as it can cause fatigue, dizziness, shortness of breath and cognitive dysfunction. Left untreated, anemia leads to deterioration in health and is associated with increased morbidity and mortality in people with CKD.
IMPORTANT U.S. SAFETY INFORMATION FOR AURYXIA(® )(ferric citrate) 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
Most common adverse reactions with AURYXIA 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 at 1-844-445-3799.
Please see full Prescribing Information
Forward-Looking Statements
Statements in this press release regarding Akebia's strategy, plans, prospects, expectations, beliefs, intentions and goals are forward-looking statements within the meaning of the U.S. Private Securities Litigation Reform Act of 1995, as amended, including but not limited to statements regarding the potential for obtaining approval of vadadustat in dialysis and the potential for vadadustat to be a new oral standard of care in dialysis; the potential indications for and benefits of vadadustat; submitting filings for marketing approval of vadadustat, and the timing thereof; the market and clinical opportunity for vadadustat; the belief that the PRO(2)TECT data will not adversely impact the potential approvability of vadadustat for the treatment of anemia due to CKD in adult patients on dialysis; the expectation regarding the Company's cash resources; and the timing of our cash runway in relation to the expected timing of the U.S. launch of vadadustat. The terms "believe," "confident," "expect," "look forward," "on track," "plan," "potential," "will," "working" and similar references are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Each forward-looking statement is subject to risks and uncertainties that could cause actual results to differ materially from those expressed or implied in such statement, including the timing and content of advice given and decisions made by health authorities, including approval and labeling decisions; the actual time it takes to make regulatory submissions for vadadustat to health authorities, including the submission of the NDA to the FDA and the submission of the MAA to the EMA; risks associated with the Priority Review Voucher for vadadustat; the potential direct or indirect impact of the COVID-19 pandemic on our business, operations, and the markets and communities in which we and our partners, collaborators, vendors and customers operate; manufacturing and quality risks; risks associated with management and key personnel changes and transitional periods; the actual funding required to continue to commercialize our commercial product, to develop and commercialize vadadustat, and to operate the Company; market acceptance and coverage and reimbursement of our commercial product and vadadustat, if approved; the risks associated with potential generic entrants for our commercial product and vadadustat, if approved; early termination of any of Akebia's collaborations; Akebia's and its collaborators' ability to satisfy their obligations under Akebia's collaboration agreements; the competitive landscape for our commercial product and vadadustat; the scope, timing, and outcome of any legal, regulatory and administrative proceedings; changes in the economic and financial conditions of the businesses of Akebia and its collaborations partners and vendors; and Akebia's ability to obtain, maintain and enforce patent and other intellectual property protection for our commercial product, vadadustat and any other product candidates. Other risks and uncertainties include those identified under the heading "Risk Factors" in Akebia's Quarterly Report on Form 10-Q for the quarter ended June 30, 2020 and other filings that Akebia may make with the U.S. Securities and Exchange Commission in the future. These forward-looking statements (except as otherwise noted) speak only as of the date of this press release, and Akebia does not undertake, and specifically disclaims, any obligation to update any forward-looking statements contained in this press release.
Investor Contact:
Kristen K. Sheppard, Esq.
ir@akebia.com
AKEBIA THERAPEUTICS, INC.
Consolidated Statements of Operations
(in thousands, except share and per share data)
(unaudited)
Three Months Ended
Nine Months Ended
---
September 30, September 30, September 30, September 30,
2020 2019 2020 2019
---
Revenues:
Product revenue, net $
34,392 $
30,004 $
94,297 $
82,204
License, collaboration and
other revenue 25,596 61,973 144,311 183,242
Total revenues 59,988 91,977 238,608 265,446
Cost of goods sold:
Product 24,239 29,162 92,840 79,888
Amortization of intangibles 6,106 9,101 24,307 27,301
Impairment of intangible asset - 115,527
Total cost of goods sold 30,345 38,263 232,674 107,189
Operating expenses:
Research and development 46,857 74,512 180,907 242,557
Selling, general and
administrative 40,171 34,178 113,636 104,537
License expense 710 929 2,430 2,560
Total operating expenses 87,738 109,619 296,973 349,654
Operating loss (58,095) (55,905) (291,039) (191,397)
Other income (expense), net (1,864) 43 (5,418) 1,342
Net loss before income taxes (59,959) (55,862) (296,457) (190,055)
Benefit from income taxes - (1,277) (4,879)
Net loss $
(59,959) $
(54,585) $
(296,457) $
(185,176)
Net loss per share -basic and
diluted $
(0.42) $
(0.46) $
(2.18) $
(1.57)
Weighted-average number of
common shares - basic and
diluted 143,314,729 118,863,063 136,230,889 118,071,674
---
AKEBIA THERAPEUTICS, INC.
Selected Balance Sheet Data
(in thousands)
(unaudited)
September 30, 2020
December 31, 2019
---
Cash,
cash
equivalents
and
available
for
sale
securities $269,255 $147,694
Working
capital 209,542 101,415
Total
assets 676,143 771,201
Total
stockholders'
equity 317,962 394,757
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SOURCE Akebia Therapeutics
