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FibroGen Reports First Quarter 2020 Financial Results - Roxadustat U.S. NDA review and E.U. MAA filing on track - Conference Call Today at 5:00 p.m. Eastern Time/2:00 p.m. Pacific Time

Key Takeaway: FibroGen Reports First Quarter 2020 Financial Results - Roxadustat U.S. NDA review and E.U. MAA filing on track - Conference Call Today at 5:00 p.m. Eastern Time/2:00 p.m. Pacific Time SAN FRANCISCO, May 07, 2020 -- FibroGen, Inc. (NASDAQ: FGEN) today reported financial result

Full Press Release Details

FibroGen Reports First Quarter 2020 Financial Results
- Roxadustat U.S. NDA review and E.U. MAA filing on track -
Conference Call Today at 5:00 p.m. Eastern Time/2:00 p.m. Pacific Time
SAN FRANCISCO, May 07, 2020 -- FibroGen, Inc. (NASDAQ: FGEN) today reported financial results for the first quarter of 2020 and provided an update on the company's recent developments.
"During this difficult time, we continue to be inspired by our unique opportunity to leverage world-class science to benefit patients," said Enrique Conterno, Chief Executive Officer, FibroGen. "The COVID-19 pandemic has presented a number of unprecedented challenges, including in the conduct and enrollment of our clinical trials. Nevertheless, I want to reassure patients, healthcare providers, and stakeholders of our continued commitment to bring to patients our potential first-in-class medicines for the treatment of chronic and life-threatening conditions. Our strong financial position gives us sufficient runway to navigate this storm."
"We remain focused on ensuring the regulatory and commercial success of roxadustat, a potentially transformational oral medicine in anemia therapy, first demonstrated in patients with chronic kidney disease. With pamrevlumab, our monoclonal antibody targeting connective tissue growth factor (CTGF), we are implementing a comprehensive plan to accelerate development across the three indications of idiopathic pulmonary fibrosis (IPF), locally advanced unresectable pancreatic cancer (LAPC), and Duchenne muscular dystrophy (DMD) once the situation with COVID-19 improves. Finally, we continue to advance the innovation of our hypoxia-inducible factor (HIF) and CTGF platforms."
Key Events in Recent Months and Other Developments
Corporate and Financial
Conference Call and Webcast Details
FibroGen will host a conference call and webcast today, Thursday, May 7, 2020, at 5:00 p.m. Eastern Time (2:00 p.m. Pacific Time) to discuss financial results and provide a business update. A live audio webcast of the call may be accessed in the investor section of the company's website, www.fibrogen.com. To participate in the conference call by telephone, please dial 1 (877) 658-9081 (U.S. and Canada) or 1 (602) 563-8732 (international), reference the FibroGen first quarter 2020 financial results conference call, and use passcode 9946439. A replay of the webcast will be available shortly after the call for a period of two weeks. To access the replay, please dial (855) 859-2056 (domestic) or (404) 537-3406 (international) and use passcode 9946439.
Roxadustat is a first-in-class, orally administered small molecule HIF-PH inhibitor that promotes erythropoiesis through increasing endogenous production of erythropoietin, and improved iron absorption, transport and mobilization. Roxadustat is approved in China for the treatment of anemia in CKD patients on dialysis and patients not on dialysis, and is approved in Japan for the treatment of anemia in CKD patients on dialysis, and a supplemental NDA for the treatment of anemia in CKD patients not on dialysis is under regulatory review. The roxadustat NDA for the treatment of anemia in CKD is under review by the U.S. FDA with a Prescription Drug User Fee Act date of December 20, 2020. Our partner Astellas expects the Marketing Authorization Application filing for roxadustat for the treatment of anemia in CKD in the second quarter of 2020. Roxadustat is also in clinical development for anemia associated with myelodysplastic syndromes (MDS) and for chemotherapy-induced anemia.
Astellas and FibroGen are collaborating on the development and commercialization of roxadustat for the treatment of anemia in territories including Japan and Europe. AstraZeneca and FibroGen are collaborating on the development and commercialization of roxadustat for the treatment of anemia in the U.S., China, and other markets.
Pamrevlumab is a first-in-class antibody developed by FibroGen that inhibits the activity of connective tissue growth factor (CTGF), a common factor in fibrotic and proliferative disorders. Pamrevlumab is in Phase 3 clinical development for the treatment of idiopathic pulmonary fibrosis (IPF) and locally advanced unresectable pancreatic cancer (LAPC), and in Phase 2 clinical development for the treatment of Duchenne muscular dystrophy (DMD). For information about pamrevlumab studies currently recruiting patients, please visit www.clinicaltrials.gov.
FibroGen, Inc. is a biopharmaceutical company committed to discovering, developing and commercializing a pipeline of first-in-class therapeutics. The company applies its pioneering expertise in hypoxia-inducible factor (HIF) and connective tissue growth factor (CTGF) biology to advance innovative medicines to treat unmet needs. The Company is currently developing and commercializing roxadustat, an oral small molecule inhibitor of HIF prolyl hydroxylase activity, for anemia associated with chronic kidney disease (CKD). Roxadustat is also in clinical development for anemia associated with myelodysplastic syndromes (MDS) and for chemotherapy-induced anemia. Pamrevlumab, an anti-CTGF human monoclonal antibody, is in clinical development for the treatment of idiopathic pulmonary fibrosis (IPF), locally advanced unresectable pancreatic cancer, and Duchenne muscular dystrophy (DMD). For more information, please visit www.fibrogen.com.
Forward-Looking Statements
This release contains forward-looking statements regarding our strategy, future plans and prospects, including statements regarding the development and commercialization of the company's product candidates, our financial results, the potential safety and efficacy profile of our product candidates, our clinical programs and regulatory events, and those of our partners. These forward-looking statements include, but are not limited to, statements about our plans, objectives, representations and contentions and are not historical facts and typically are identified by use of terms such as "may," "will", "should," "on track," "could," "expect," "plan," "anticipate," "believe," "estimate," "predict," "potential," "continue" and similar words, although some forward-looking statements are expressed differently. Our actual results may differ materially from those indicated in these forward-looking statements due to risks and uncertainties related to the continued progress and timing of our various programs, including the enrollment and results from ongoing and potential future clinical trials, and other matters that are described in our Annual Report on Form 10-K for the fiscal year ended December 31, 2019 and our Quarterly Report on Form 10-Q for quarter ended March 31, 2020 filed with the Securities and Exchange Commission (SEC), including the risk factors set forth therein. Investors are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this release, and we undertake no obligation to update any forward-looking statement in this press release, except as required by law.
Condensed Consolidated Balance Sheets
March 31, 2020 December 31, 2019
(Unaudited) (1)
Assets
Current assets:
Cash and cash equivalents $ 121,560 $ 126,266
Short-term investments 413,869 407,491
Accounts receivable, net 58,540 28,455
Inventory 8,408 6,887
Prepaid expenses and other current assets 134,028 133,391
Total current assets 736,405 702,490
Restricted time deposits 2,072 2,072
Long-term investments 223 61,118
Property and equipment, net 40,058 42,743
Finance lease right-of-use assets 37,017 39,602
Other assets 8,602 9,372
Total assets $ 824,377 $ 857,397
Liabilities, stockholders' equity and non-controlling interests
Current liabilities:
Accounts payable $ 2,865 $ 6,088
Accrued and other liabilities 42,309 83,816
Deferred revenue 8,531 490
Finance lease liabilities, current 12,396 12,351
Total current liabilities 66,101 102,745
Long-term portion of lease obligations 1,040 1,141
Product development obligations 16,536 16,780
Deferred revenue, net of current 139,404 99,449
Finance lease liabilities, non-current 34,545 37,610
Other long-term liabilities 89,122 64,266
Total liabilities 346,748 321,991
Total stockholders' equity 458,358 516,135
Non-controlling interests 19,271 19,271
Total equity 477,629 535,406
Total liabilities, stockholders' equity and non-controlling interests $ 824,377 $ 857,397
Condensed Consolidated Statements of Operations
(In thousands, except per share data)
Three Months Ended March 31,
2020 2019
(Unaudited)
Revenue:
License revenue $ - $ -
Development and other revenue 19,446 23,863
Product revenue, net 4,955 -
Total revenue 24,401 23,863
Operating costs and expenses:
Cost of goods sold 970 -
Research and development 54,902 50,496
Selling, general and administrative 49,603 22,210
Total operating costs and expenses 105,475 72,706
Loss from operations (81,074 ) (48,843 )
Interest and other, net:
Interest expense (633 ) (770 )
Interest income and other, net 3,165 4,177
Total interest and other, net 2,532 3,407
Loss before income taxes (78,542 ) (45,436 )
Benefit from income taxes (194 ) (25 )
Net loss $ (78,348 ) $ (45,411 )
Net loss per share - basic and diluted $ (0.89 ) $ (0.53 )
Weighted average number of common shares used to calculate net loss per share - basic and diluted 88,219 85,704
Contact: FibroGen, Inc.
Corporate Strategy / Investor Relations
Last updated: May 7, 2020