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FibroGen Reports Fourth Quarter and Full Year 2017 Financial Results

Roxadustat U.S. Phase 3 Program in CKD Anemia Enrollment Completion and Data Readout in 2018

Pamrevlumab Phase 2 IPF Study Achieves Statistically Significant Attenuation of Lung Fibrosis as Measured by Quantitative HRCT

Conference Call and Webcast to be Held Today at 5:00 p.m. Eastern Time/2:00 p.m. Pacific Time

SAN FRANCISCO, Feb. 27, 2018 (GLOBE NEWSWIRE) -- FibroGen, Inc. (NASDAQ:FGEN), a science-based biopharmaceutical company, today reported financial results for the fourth quarter and full year 2017 and provided an update on the company’s recent developments.

“In 2017, we continued to make significant progress on key clinical and regulatory milestones. Our first NDA submission for roxadustat was accepted for review by the China Food and Drug Administration. With our partners, we are advancing the roxadustat Phase 3 CKD anemia programs to completion with plans to file for market approvals in the U.S., Europe, and Japan. In our fibrosis program, pamrevlumab has demonstrated tremendous potential in multiple indications. In a randomized double-blind, placebo-controlled Phase 2b study in IPF, pamrevlumab was well-tolerated and achieved statistical significance in the primary endpoint of FVC % predicted, in FVC, and in the secondary endpoints of quantitative changes of lung fibrosis, disease progression, and patient-reported outcomes,” said Thomas B. Neff, FibroGen’s Chief Executive Officer. “We are intensely focused on the execution of critical activities for our CKD anemia, idiopathic pulmonary fibrosis, and pancreatic cancer programs as these approach important new milestones in 2018.”

Recent Developments and Highlights
Roxadustat for CKD Anemia in U.S./ROW

  • With our partner AstraZeneca, we have agreed to a timeline for Phase 3 enrollment completion in the second quarter of 2018 and data readout in the fourth quarter of 2018 to support U.S. regulatory submission in the first half of 2019
  • DSMB recommended Phase 3 clinical studies to continue under current protocols with no changes

Roxadustat for CKD Anemia in China

  • Positive efficacy and safety results reported from two Phase 3 trials
  • New Drug Application accepted for filing by the CFDA  

Roxadustat for CKD Anemia in Japan

  • Our partner Astellas has completed three of six Phase 3 trials 
  • Topline positive Phase 3 results reported in peritoneal dialysis study

Roxadustat for MDS Anemia

  • Enrollment commenced in our first U.S./Europe Phase 3 study for the treatment of anemia in myelodysplastic syndromes (MDS)

Pamrevlumab for Idiopathic Pulmonary Fibrosis (IPF)

  • Statistically significant high-resolution computed tomography (HRCT) results achieved in our randomized double-blind, placebo-controlled Phase 2b study  
  • Positive Phase 2b study results presented at European Respiratory Society (ERS) International Congress 2017       

Pamrevlumab for Pancreatic Cancer

  • Reported positive interim Phase 2 open-label results at 2017 ASCO-GI conference showing a majority of pamrevlumab-treated patients converted from unresectable to resectable cancer; all resection evaluations complete and results continue to be favorable for pamrevlumab

Corporate and Financial

  • Net loss for the fourth quarter of 2017 was $22.1 million, or $0.27 per share, compared to $34.0 million, or $0.54 per share one year ago
  • Net loss for the year ended December 31, 2017, was $126.2 million, or $1.73 per share, compared to $61.7 million, or $0.98 per share one year ago
  • At December 31, 2017, FibroGen had $762.2 million in cash, restricted time deposits, cash equivalents, investments, and receivables  
    • Received a $15.0 million milestone payment from AstraZeneca in the fourth quarter of 2017 upon roxadustat NDA submission to CFDA 
    • Completed financings in April 2017 and in August 2017 with net proceeds of $115.1 million and $356.2 million, respectively

 2018 Outlook

  • U.S. Phase 3 CKD anemia enrollment completion in the second quarter of 2018
  • U.S. Phase 3 CKD anemia data readout in the fourth quarter of 2018 to support U.S. regulatory submission in the first half of 2019
  • NDA approval decision expected in China for CKD anemia by the end of 2018
  • Expect to confirm plans with our partner Astellas for regulatory submissions in Europe and Japan
  • Anticipate data readout from two Japan Phase 3 hemodialysis studies, a long-term conversion study and a correction (ESA-naïve) study, in the first quarter of 2018
  • Anticipate initiation of roxadustat Phase 2/3 clinical study in China for anemia associated with MDS in first half of 2018
  • Expect to present HRCT and health-related quality-of-life results from the IPF Phase 2b trial at an upcoming scientific conference
  • Design pivotal trials for IPF and locally advanced pancreatic cancer

Conference Call and Webcast Details 
FibroGen will host a conference call and webcast today, February 27, 2018, at 5:00 p.m. Eastern (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 (888) 771-4371 (U.S. and Canada) or 1 (847) 585-4405 (international), reference the FibroGen fourth quarter and full year 2017 financial results conference call, and use passcode 46307822#. A replay of the webcast will be available shortly after the call for a period of two weeks. To access the replay, please dial (888) 843-7419 (domestic) or (630) 652-3042 (international), and use passcode 46307822#.

About Roxadustat
Roxadustat is a first-in-class oral therapeutic in global Phase 3 clinical development as a treatment for anemia associated with chronic kidney disease (CKD) with the potential to offer a safer and more effective, convenient, and accessible treatment than current therapies. Roxadustat, a hypoxia-inducible factor prolyl hydroxylase inhibitor (HIF-PHI), promotes erythropoiesis, or the production of red bloods, by increasing endogenous erythropoietin, improving iron regulation, and reducing hepcidin, including in the presence of inflammation and without need for supplemental intravenous iron.

The roxadustat Phase 3 program is the largest Phase 3 clinical program in anemia to date, and is supported by extensive Phase 2 results demonstrating correction and maintenance of hemoglobin levels in anemia in multiple subpopulations of CKD dialysis and non-dialysis patients. A New Drug Application (NDA) has been accepted for review by the China Food and Drug Administration (CFDA), and enrollment completion and data readout for the Phase 3 program are expected in 2018. Roxadustat is also in Phase 3 clinical development in the U.S. and Europe, and expected to shortly enter Phase 2/3 development in China, for anemia associated with myelodysplastic syndromes (MDS). For information about roxadustat studies currently recruiting patients, please visit www.clinicaltrials.gov.

About Pamrevlumab
Pamrevlumab is a first-in-class antibody developed by FibroGen to inhibit the activity of connective tissue growth factor (CTGF), a common factor in fibrotic and proliferative disorders characterized by persistent and excessive scarring that can lead to organ dysfunction and failure. Pamrevlumab is advancing towards Phase 3 clinical development for the treatment of idiopathic pulmonary fibrosis (IPF) and pancreatic cancer, and is currently in a Phase 2 trial for Duchenne muscular dystrophy (DMD). Pamrevlumab has been well tolerated in a number of Phase 2 clinical studies to date, with a good safety and tolerability profile. For information about pamrevlumab studies currently recruiting patients, please visit www.clinicaltrials.gov.

About FibroGen
FibroGen, Inc., headquartered in San Francisco, CA with subsidiary offices in Beijing and Shanghai, PRC, is a leading science-based biopharmaceutical company discovering and developing 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 and clinical development to advance innovative medicines for the treatment of anemia, fibrotic disease, and cancer. Roxadustat, the company’s most advanced product candidate, is an oral small molecule inhibitor of HIF prolyl hydroxylase activity in worldwide Phase 3 clinical development for the treatment of anemia in chronic kidney disease (CKD) with the exception of China, where a New Drug Application is currently under review by the CFDA for regulatory approval. Roxadustat is in Phase 3 clinical development in the U.S. and Europe, and expected to shortly enter Phase 2/3 development in China, for anemia associated with myelodysplastic syndromes (MDS). Pamrevlumab, a fully-human monoclonal anti-CTGF antibody, is advancing towards Phase 3 clinical development for the treatment of idiopathic pulmonary fibrosis (IPF) and pancreatic cancer, and is currently in a Phase 2 trial for Duchenne muscular dystrophy (DMD).  FibroGen is also developing a biosynthetic cornea in China. 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 of the company's product candidates pamrevlumab and roxadustat, the potential safety and efficacy profile of our product candidates, and our clinical, regulatory, and commercial plans, 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,” “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, 2017, 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
(In thousands)

  December 31, 2017     December 31, 2016  
  (Unaudited)     (1)
 
Assets              
Current assets:              
Cash and cash equivalents $ 673,658     $ 173,782    
Short-term investments   62,060       79,397    
Accounts receivable   8,452       10,448    
Prepaid expenses and other current assets   4,800       2,889    
Total current assets   748,970       266,516    
               
Restricted time deposits   5,181       6,217    
Long-term investments   10,506       71,010    
Property and equipment, net   129,476       123,657    
Other assets   4,517       2,152    
Total assets $ 898,650     $ 469,552    
               
Liabilities, stockholders' equity and non-controlling interests              
Current liabilities:              
Accounts payable $ 5,509     $ 6,223    
Accrued liabilities   63,781       50,914    
Deferred revenue   7,968       7,988    
Total current liabilities   77,258       65,125    
               
Long-term portion of lease financing obligations   97,763       97,352    
Product development obligations   17,244       14,854    
Deferred rent   3,657       4,212    
Deferred revenue, net of current   112,231       106,709    
Other long-term liabilities   8,047       6,191    
Total liabilities   316,200       294,443    
               
Total stockholders’ equity   563,179       155,838    
Non-controlling interests   19,271       19,271    
Total equity   582,450       175,109    
Total liabilities, stockholders' equity and non-controlling interests $ 898,650     $ 469,552    

(1) The condensed consolidated balance sheet amounts at December 31, 2016 are derived from audited financial statements.


Condensed Consolidated Statements of Operations
(In thousands, except per share data)

  Three Months Ended December 31,     Years Ended December 31,  
  2017     2016     2017     2016  
    (Unaudited)       (Unaudited)       (1)
 
Revenue:                                      
License and milestone revenue $   35,126     $   23,551     $   96,056     $   137,352    
Collaboration services and other revenue     7,383         8,362         29,612         42,225    
Total revenue     42,509         31,913         125,668         179,577    
Operating expenses:                                      
Research and development     52,469         50,607         196,517         187,206    
General and administrative     13,851         12,585         51,760         46,025    
Total operating expenses     66,320         63,192         248,277         233,231    
Loss from operations     (23,811 )       (31,279 )       (122,609 )       (53,654  
Interest and other, net:                                      
Interest expense     (1,806 )       (2,750 )       (9,706 )       (10,725  
Interest income and other, net     3,651         217         6,433         2,628    
Total interest and other, net     1,845         (2,533 )       (3,273 )       (8,097  
Loss before income taxes     (21,966 )       (33,812 )       (125,882 )       (61,751  
Provision for (benefit from) income taxes     156         189         321         (71  
Net loss $   (22,122 )   $   (34,001 )   $   (126,203 )   $   (61,680  
                                       
Net loss per share - basic and diluted   $ (0.27 )     $ (0.54 )     $ (1.73 )     $ (0.98  
Weighted average number of common shares used to calculate net loss per share - basic and diluted     82,151         63,345         72,987         62,744    

(1) The condensed consolidated statements of operations amounts for the year ended December 31, 2016 are derived from audited financial statements.

Contact
FibroGen, Inc.
Karen L. Bergman
Vice President, Investor Relations and Corporate Communications
1 (415) 978-1433
kbergman@fibrogen.com

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