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SAN FRANCISCO, Aug. 13, 2015 (GLOBE NEWSWIRE) -- FibroGen, Inc. (NASDAQ:FGEN) ("FibroGen"), a research-based biopharmaceutical company, today reported financial results for the quarter ended June 30, 2015.
"FibroGen continues to make advancements across multiple programs, including anemia, idiopathic pulmonary fibrosis, pancreatic cancer, and Duchenne muscular dystrophy," said Thomas B. Neff, chief executive officer of FibroGen. "Through FibroGen's joint effort with our partners, AstraZeneca and Astellas, the Phase 3 development of roxadustat remains on track. We continue to expect to file the roxadustat regulatory submissions in 2016 for China and 2018 for the United States."
"As previously announced, our first roxadustat Phase 2 publication appeared on line last week. The article breaks new ground as the first peer-reviewed article ever to feature clinical evidence of hemoglobin correction by a hypoxia inducible factor prolyl hydroxylase inhibitor in anemic patients. Additional manuscripts on roxadustat Phase 2 studies have been submitted for editorial review. We expect this body of scientific literature will reinforce the first-in-class and best-in-class potential of roxadustat for the treatment of anemia in patients with chronic kidney disease."
"In our fibrosis programs, the FDA cleared our Investigational New Drug application for the study of FG-3019 in Duchenne muscular dystrophy. We plan to begin evaluating the potential anti-fibrotic activity of FG-3019 in non-ambulatory boys with this disease later this year. In addition, we are evaluating expansion of enrollment in our Phase 2 idiopathic pulmonary fibrosis study to include FG-3019 as a combination treatment with approved therapy. Our open label study of FG-3019 in pancreatic cancer continues to advance and we look forward to evaluating potential program expansion once we have sufficient preliminary data from the study."
Anemia in Chronic Kidney Disease (CKD) - Roxadustat (FG-4592)
Idiopathic Pulmonary Fibrosis - FG-3019
Pancreatic Cancer – FG-3019
Duchenne Muscular Dystrophy – FG-3019
Other Financial Highlights
Conference Call Details
FibroGen will host a conference call and webcast today, August 13, 2015 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 (800) 708-4540 (U.S. and Canada) or (847) 619-6397 (international), reference the FibroGen Second Quarter 2015 conference call, and use the confirmation number 40444300. To ensure timely connection, it is recommended that listeners register 15 minutes before the scheduled start time. A replay of the webcast will be archived on the FibroGen website and accessible approximately two hours after the event.
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 inhibitor of HIF prolyl hydroxylases (HIF-PHs), 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 liver fibrosis.
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 IND filing for planned clinical trials for FG-3019 in idiopathic pulmonary fibrosis and pancreatic cancer, and Duchenne muscular dystrophy, respectively; 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, 2014 filed with the Securities and Exchange Commission ("SEC") on March 26, 2015 and our Quarterly Report on Form 10-Q for the quarter ended March 31, 2015 filed with the SEC on May 12, 2015, including the risk factors set forth in that filing, as well as the Quarterly Report on Form 10-Q for the quarter ended June 30, 2015, which we expect to file on August 13, 2015 with the SEC. 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|
|June 30, 2015||December 31, 2014|
|Cash and cash equivalents||$ 236,536||$ 165,455|
|Prepaid expenses and other current assets||2,731||4,966|
|Total current assets||263,579||198,238|
|Property and equipment, net||130,451||132,171|
|Total assets||$ 541,395||$ 483,528|
|Liabilities and equity|
|Accounts payable||$ 3,915||$ 4,551|
|Total current liabilities||63,502||62,754|
|Long-term portion of lease financing obligations||96,929||96,818|
|Product development obligations||15,186||16,465|
|Deferred revenue, net of current||87,273||60,988|
|Other long-term liabilities||702||696|
|Total stockholders' equity||253,615||221,405|
|Total liabilities and equity||$ 541,395||$ 483,528|
|(1) The condensed consolidated balance sheet amounts at December 31, 2014 are derived from audited financial statements.|
|Condensed Consolidated Statements of Operations|
|(In thousands, except per share data, unaudited)|
|Quarter Ended June 30,||Six Months Ended June 30,|
|License and milestone revenue||$ 106,879||$ 82,463||$ 118,385||$ 97,148|
|Collaboration services and other revenue||13,671||7,495||18,463||10,686|
|Research and development||51,555||33,269||102,094||58,919|
|General and administrative||9,680||7,516||20,162||13,948|
|Total operating expenses||61,235||40,785||122,256||72,867|
|Income from operations||59,315||49,173||14,592||34,967|
|Interest and other income, net||707||383||1,550||1,075|
|Income before income taxes||57,260||46,831||10,622||30,591|
|Provision (benefit) from income taxes||205||--||(66)||--|
|Net income||$ 57,055||$ 46,831||$ 10,688||$ 30,591|
|Net income per share:|
|Basic||$ 0.95||$ 1.36||$ 0.18||$ 0.74|
|Weighted average number of common shares used to calculate net income per share:|
|(2) On November 10, 2014, we effected a 1-for-2.5 reverse split of our common stock. All of the outstanding common stock share numbers (including shares of common stock which our outstanding preferred stock shares were convertible into), common stock warrants have been adjusted on a retroactive basis, to reflect this 1-for-2.5 reverse stock split for the quarter and six months ended June 30, 2014.|
|Reconciliation of Non-GAAP Financial Measures|
June 30, 2014
Six Months Ended
June 30, 2014
|GAAP weighted average shares outstanding - basic||13,347||13,279|
|Shares sold in initial public offering||9,315||9,315|
|Concurrent private placement - AstraZeneca||1,111||1,111|
|Conversion of preferred shares upon initial public offering||33,920||33,920|
|Conversion of European subsidiary shares||959||959|
|Effect of potentially dilutive securities||8,022||7,959|
|Non-GAAP weighted average shares outstanding - diluted||66,674||66,543|
|GAAP net income||$ 46,831||$ 30,591|
|Non-GAAP net income per diluted share||$ 0.70||$ 0.46|
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 – diluted and non-GAAP net income per diluted share for the quarter and six months ended June 30, 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 income per diluted share as GAAP net income for the quarter and six months ended June 30, 2014 divided by the non-GAAP weighted average shares outstanding – diluted for the quarter and six months ended June 30, 2014. Non-GAAP weighted average shares outstanding – diluted is based on GAAP weighted average shares outstanding – basic plus the issuance of and conversion into shares of our common stock upon the closing of our initial public offering. This includes issuance of 9.3 million shares in our initial public offering, issuance of 1.1 million shares in our concurrent private placement, conversion of all outstanding shares of our preferred stock into 33.9 million shares and conversion of FibroGen Europe preferred stock into 1.0 million shares. Non-GAAP weighted average shares outstanding – diluted also includes the effect of any potentially dilutive securities during the periods. We believe the presentation of non-GAAP net income per diluted share provides useful information to investors regarding comparability of net income per diluted share amounts between periods.
CONTACT: Greg Mann, 415-978-1433 FibroGen, Inc. firstname.lastname@example.orgNEXT ARTICLE
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