Full Press Release Details
FibroGen Announces Fiscal 2015 Financial Results
-- Webcast Conference Call Scheduled for 4:30pm EST Today -
SAN FRANCISCO-February 29, 2016 -- FibroGen, Inc. (NASDAQ: FGEN) ("FibroGen"), a research-based biopharmaceutical company, today reported financial results for the year ended December 31, 2015.
"2015 was a year that marked significant progress for FibroGen and our clinical-stage programs in anemia, idiopathic pulmonary fibrosis, pancreatic cancer, and Duchenne muscular dystrophy," said Thomas B. Neff, chief executive officer of FibroGen. "In partnership with Astellas and AstraZeneca, our roxadustat Phase 3 development program has strong momentum and remains on track, with regulatory submissions expected in 2016 for China and in 2018 for the United States. Additionally, now that we have reached the cap on FibroGen's development cost contributions for roxadustat, our partners will cover all development costs through product launch outside of China."
Anemia in Chronic Kidney Disease (CKD) - Roxadustat (FG-4592)
Anti-Connective Tissue Growth Factor (CTGF) - (FG-3019)
Financial Highlights
Conference Call Details
FibroGen will host a conference call and webcast today, February 29, 2016, at 4:30 p.m. Eastern Time (1:30 p.m. Pacific Time), to discuss financial results and provide a business update. Interested parties may access a live audio webcast of the conference call via the investor section of the FibroGen website, www.fibrogen.com. To access the conference call by telephone, please dial (888) 771-4371 (U.S. and Canada) or (847) 585-4405 (international), reference the FibroGen Year-End 2015 conference call, and use the confirmation number 41794315. It is recommended that listeners register 15 minutes before the scheduled start time to ensure a timely connection. A replay of the webcast will be available shortly after the call for a period of four weeks. To access the replay, please dial (888) 843-7419 (domestic) or (630) 652-3042 (international), and use the confirmation number 41794315.
FibroGen is a research-based biopharmaceutical company focused on the discovery, development and commercialization of novel therapeutics to treat serious unmet medical needs. We have capitalized on our extensive experience in fibrosis and hypoxia-inducible factor (HIF) biology to generate multiple programs targeting various therapeutic areas. Our most advanced product candidate, roxadustat, or FG-4592, is an oral small molecule HIF prolyl hydroxylase (HIF-PH) inhibitor in Phase 3 clinical development for the treatment of anemia in chronic kidney disease (CKD). Our second product candidate, FG-3019, is a monoclonal antibody in Phase 2 clinical development for the treatment of idiopathic pulmonary fibrosis (IPF), pancreatic cancer, and Duchenne muscular dystrophy. For more information about FibroGen, please visit www.fibrogen.com.
Forward-Looking Statements
This release contains forward-looking statements, including statements regarding our milestones, clinical plans and financial projections. Our actual results may differ materially from those indicated in these forward-looking statements due to risks and uncertainties, including the continued progress and timing of our various clinical programs, including the timing of enrollment of the Phase 3 clinical trials for roxadustat in CKD and the initiation and enrollment in ongoing and planned clinical trials for FG-3019 in IPF, pancreatic cancer, DMD, and liver fibrosis; the continued progress of our plans and programs in China; and other matters that are described in our Annual Report on Form 10-K for the year ended December 31, 2015, 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
| December 31, 2015 | December 31, 2014 | ||||||||
| (Unaudited) | (1) | ||||||||
| Assets | |||||||||
| Current assets: | |||||||||
| Cash and cash equivalents | $ | 153,324 | $ | 165,455 | |||||
| Short-term investments | 27,847 | 14,364 | |||||||
| Accounts receivable | 15,405 | 13,453 | |||||||
| Prepaid expenses and other current assets | 3,988 | 4,966 | |||||||
| Total current assets | 200,564 | 198,238 | |||||||
| Restricted cash | 7,254 | 7,254 | |||||||
| Long-term investments | 131,720 | 144,269 | |||||||
| Property and equipment, net | 129,020 | 132,171 | |||||||
| Other assets | 2,016 | 1,596 | |||||||
| Total assets | $ | 470,574 | $ | 483,528 | |||||
| Liabilities, stockholders' equity and non-controlling interests | |||||||||
| Current liabilities: | |||||||||
| Accounts payable | $ | 6,521 | $ | 4,551 | |||||
| Accrued liabilities | 47,932 | 48,985 | |||||||
| Deferred revenue | 12,728 | 9,218 | |||||||
| Total current liabilities | 67,181 | 62,754 | |||||||
| Long-term portion of lease financing obligations | 97,042 | 96,818 | |||||||
| Product development obligations | 15,085 | 16,465 | |||||||
| Deferred rent | 4,702 | 5,131 | |||||||
| Deferred revenue, net of current | 85,132 | 60,988 | |||||||
| Other long-term liabilities | 4,607 | 696 | |||||||
| Total liabilities | 273,749 | 242,852 | |||||||
| Total stockholders' equity | 177,554 | 221,405 | |||||||
| Non-controlling interests | 19,271 | 19,271 | |||||||
| Total equity | 196,825 | 240,676 | |||||||
| Total liabilities, stockholders' equity and non-controlling interests | $ | 470,574 | $ | 483,528 |
Condensed Consolidated Statements of Operations
(In thousands, except per share data, unaudited)
| Years Ended December 31, | ||||||||||
| 2015 | 2014 | |||||||||
| (Unaudited) | (1) | |||||||||
| Revenue: | ||||||||||
| License and milestone revenue | $ | 148,093 | $ | 117,191 | ||||||
| Collaboration services and other revenue | 32,735 | 20,410 | ||||||||
| Total revenue | 180,828 | 137,601 | ||||||||
| Operating expenses: | ||||||||||
| Research and development | 214,089 | 150,794 | ||||||||
| General and administrative | 44,364 | 36,909 | ||||||||
| Total operating expenses | 258,453 | 187,703 | ||||||||
| Loss from operations | (77,625 | ) | (50,102 | ) | ||||||
| Interest and other, net: | ||||||||||
| Interest expense | (11,033 | ) | (11,108 | ) | ||||||
| Interest income and other, net | 3,121 | 1,706 | ||||||||
| Total interest and other, net | (7,912 | ) | (9,402 | ) | ||||||
| Loss before income taxes | (85,537 | ) | (59,504 | ) | ||||||
| Provision for income taxes | 242 | - | ||||||||
| Net loss | $ | (85,779 | ) | $ | (59,504 | ) | ||||
| Net loss per share - basic and diluted | $ | (1.42 | ) | $ | (3.17 | ) | ||||
| Weighted average number of common shares used to calculate net loss per share - basic and diluted | 60,337 | 18,775 | (2) |
Reconciliation of Non-GAAP Financial Measures
(In thousands, except per share data, unaudited)
| Year Ended December 31, 2014 | |||
| GAAP weighted average shares outstanding | 18,775 | ||
| Shares sold in initial public offering | 8,218 | ||
| Concurrent private placement - AstraZeneca | 980 | ||
| Conversion of preferred shares upon initial public offering | 29,924 | ||
| Conversion of European subsidiary shares | 846 | ||
| Non-GAAP weighted average shares outstanding | 58,743 | ||
| GAAP net loss | $ | (59,504 | ) |
| Non-GAAP net loss per basic and diluted share | $ | (1.01 | ) |
About Non-GAAP Financial Measures
To supplement our condensed consolidated financial statements, which are prepared and presented in accordance with U.S. generally accepted accounting principles ("GAAP"), we present non-GAAP weighted average shares outstanding and non-GAAP net loss per basic and diluted share for the year ended December 31, 2014. The presentation of this financial information is not intended to be considered in isolation or as a substitute for, or superior to, the financial information prepared and presented in accordance with GAAP.
We define non-GAAP net loss per basic and diluted share as GAAP net loss for the year ended December 31, 2014 divided by the non-GAAP weighted average shares outstanding for the year ended December 31, 2014. Non-GAAP weighted average shares outstanding is based on GAAP weighted average shares outstanding plus the impacts from reflecting full year weight for the issuance of and conversion into shares of our common stock upon the closing of our initial public offering on November 19, 2014. This includes 8.2 million additional weighted shares related to issuance of 9.3 million shares in our initial public offering, 1.0 million additional weighted shares related to issuance of 1.1 million shares in our concurrent private placement, 29.9 million additional weighted shares related to conversion of all outstanding shares of our preferred stock into 33.9 million shares, and 0.8 million additional weighted shares related to conversion of FibroGen Europe preferred stock into 1.0 million shares. We believe the presentation of non-GAAP net loss per basic and diluted share provides useful information to investors regarding comparability of net loss per basic and diluted share amounts between periods presented.