Tobira Therapeutics
Aug 9, 2016

Tobira Therapeutics Reports Second Quarter 2016 Financial and Business Results

-Guest Speaker Arun Sanyal, M.D. to Speak on CENTAUR Study and NASH Landscape-

-Conference Call to be Held Today at 4:30 p.m. Eastern Time-

SOUTH SAN FRANCISCO, Calif.--(BUSINESS WIRE)-- Tobira Therapeutics, Inc. (NASDAQ: TBRA) a clinical-stage biopharmaceutical company focused on developing and commercializing therapies for non-alcoholic steatohepatitis (NASH) and other liver diseases, today reported business highlights and financial results for the three months ended June 30, 2016.

"We are excited about the results of the CENTAUR trial, which we believe is the first study to prospectively meet an endpoint recommended for Phase 3 studies to support marketing authorization, namely ‘an improvement in fibrosis by at least one stage without worsening of NASH.' This is an important milestone as fibrosis is a key predictor of mortality and liver-related events. We are confident about our path forward, and we look forward to discussing the Phase 3 study with regulators and presenting the CENTAUR data at a medical meeting later this year," said Laurent Fischer, M.D., chief executive officer of Tobira. "On the strength of the fibrosis data, we are also advancing our NASH program with a Phase 1 trial of cenicriviroc in combination with evogliptin, which is targeted at the metabolic abnormalities implicated in NASH and complements CVC."

Recent Progress

Upcoming Target Milestones

Second Quarter 2016 Financial Results

2016 Six-Month Results

Cash, Cash Equivalents & Restricted Cash

As of June 30, 2016, Tobira had cash, cash equivalents, and restricted cash of $41.0 million.

Conference Call Information

The company will host a conference call today to review Tobira's business highlights and financial results for the first quarter of 2016 beginning at 1:30 p.m. Pacific Time / 4:30 p.m. Eastern Time. Analysts and investors can participate in the conference call by dialing +1 (855) 638-8858 for domestic callers and +1 (707) 294-1299 for international callers, using the conference ID# 59149594. The webcast can be accessed live on the Investor Relations page of Tobira's website, and will be available for replay for 30 days following the call.

About the CENTAUR Study

The CENTAUR study (NCT02217475) is a Phase 2b multinational, randomized, double-blind study comparing CVC to placebo for the treatment of NASH in adults with liver fibrosis. The trial enrolled 289 patients, all with moderate to advance fibrosis (F1-F3). The primary endpoint was improvement of NAFLD Activity Score at the one year time point. The two key secondary endpoints included: ‘complete resolution of steatohepatitis and no worsening of fibrosis' (worsening defined as progression of NASH CRN fibrosis stage) and ‘improvement in liver fibrosis by at least one stage with no worsening of steatohepatitis' (no worsening of lobular inflammation or hepatocellular ballooning grade). In July 2016, Tobira announced that CENTAUR met the key secondary endpoint of improvement in liver fibrosis by at least one stage with no worsening of steatohepatitis after one year of treatment, which was recommended by regulators as an endpoint for Phase 3 studies to support a marketing application. The CENTAUR study continues for a second year analysis of endpoints, which is expected in the third quarter of 2017.

CENTAUR exclusively enrolled adults at increased risk of progression to cirrhosis. Of the 289 patients enrolled the majority (67%) had moderate (F2) to severe fibrosis (F3), the population that currently evaluate in contemporary Phase 3 studies.

About Cenicriviroc (CVC)

CVC is an oral, once-daily, potent immunomodulator that blocks two chemokine receptors, CCR2 and CCR5, which are intricately involved in the inflammatory and fibrogenic pathways in NASH that cause liver damage and often lead to cirrhosis, liver cancer, or liver failure. Because of this unique mechanism of action, targeting two of the main engines driving NASH, CVC has the potential to play a differentiated role in the management of NASH and may form the cornerstone of NASH combination treatment strategies, both as a single agent and in combination with other agents targeting metabolic pathways. CVC has been granted Fast Track status in patients with NASH and liver fibrosis, the patient population at highest risk of progression to cirrhosis.

In addition to CENTAUR, CVC is also being evaluated in the PERSEUS study (identifier NCT02653625), a Phase 2 proof-of-concept study of CVC in patients with primary sclerosing cholangitis, a rare inflammatory liver disease.

About Non-Alcoholic Steatohepatitis (NASH)

NASH is a severe type of non-alcoholic fatty liver disease (NAFLD), which is characterized by the accumulation of fat in the liver with no other apparent causes. NASH occurs when the accumulation of liver fat is accompanied by inflammation and cellular damage. The inflammation can lead to fibrosis (scarring) of the liver and eventually progress to cirrhosis, portal hypertension, liver cancer, and eventual liver failure.

NASH is an emerging health crisis impacting 3% to 5% of the U.S. population and 2% to 4% globally, and is the fastest growing cause of liver cancer and liver transplant in the U.S. The increasing prevalence of NASH is attributed to the growing obesity epidemic and the disease is often diagnosed in patients who have diabetes, high cholesterol or high triglycerides. There is currently no approved treatment for NASH.

About Tobira Therapeutics

Tobira is a clinical-stage biopharmaceutical company focused on the development and commercialization of therapies for non-alcoholic steatohepatitis (NASH) and other liver diseases. The company's lead product candidate, cenicriviroc (CVC), is a first-in-class immunomodulator and dual inhibitor of CCR2 and CCR5 in late-stage development for the treatment of NASH, a serious liver disease that can progress to cirrhosis, liver cancer and liver failure. CVC is also being investigated to address primary sclerosing cholangitis (PSC), a disease which causes inflammation and scarring of the bile ducts, eventually leading to serious liver damage. Tobira's pipeline also includes evogliptin, a selective DPP-4 inhibitor, which it plans to develop for NASH in combination with CVC. Learn more about Tobira at

Tobira® is a registered trademark owned by Tobira Therapeutics, Inc.

©2016 Tobira Therapeutics, Inc. All Rights Reserved.

Forward Looking Statements

This release contains forward-looking statements made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Forward-looking statements reflect management's current knowledge, assumptions, judgment and expectations regarding future performance or events. Although management believes that the expectations reflected in such statements are reasonable, they give no assurance that such expectations will prove to be correct and you should be aware that actual results could differ materially from those contained in the forward-looking statements. Forward-looking statements are subject to a number of risks and uncertainties including, but not limited to, the company's clinical development of cenicriviroc (CVC) and evogliptin (EVO); the potential timing and outcomes of clinical studies of Tobira's product candidates undertaken now or in the future; the ability of the company to timely source adequate supply of its development products from third party manufacturers on whom the company depends; the company's limited cash reserves and its ability to obtain additional capital on acceptable terms, or at all; the company's ability to successfully progress, partner or complete further development of its programs; the uncertainties inherent in clinical testing; the timing, cost and uncertainty of obtaining regulatory approvals; the company's ability to protect its intellectual property; competition; changes in the regulatory landscape or the imposition of regulations that affect the company's products; and other factors listed under "Risk Factors" in the company's other filings with the Securities and Exchange Commission.




(In thousands)

June 30, December 31,

2015 (1)



Current assets:
Cash and cash equivalents $ 40,692 $ 62,431
Other current assets   1,702   802
Total current assets 42,394 63,233
Restricted cash 334 334
Other assets   1,913   1,841
Total assets $ 44,641 $ 65,408
Liabilities and Stockholders' Equity
Current liabilities:
Accounts payable $ 4,232 $ 3,089
Accrued expenses and other liabilities 5,267 4,263
Term loan 2,523
Other current liabilities   80   71
Total current liabilities 12,102 7,423
Term loan 12,624 15,013
Other liabilities   157   201
Total liabilities 24,883 22,637
Total stockholders' equity   19,758   42,771
Total liabilities and stockholders' equity $ 44,641 $ 65,408
(1) Derived from audited financial statements




(In thousands, except share and per share data)

Three Months Ended Six Months Ended
June 30, June 30,
2016     2015 2016     2015
License and collaboration revenue $ 1,058 $ $ 1,165 $
Operating expenses:
Research and development 10,880 6,616 19,559 12,287
General and administrative   3,128   3,119   6,469   5,271
Total operating expenses   14,008   9,735   26,028   17,558
Loss from operations (12,950 ) (9,735 ) (24,863 ) (17,558 )
Other income (expense), net:
Interest expense, net (310 ) (1,190 ) (618 ) (2,435 )
Change in fair value of preferred stock warrant liabilities     (97 )     1,939
Loss before income tax (expense) benefit (13,260 ) (11,022 ) (25,481 ) (18,054 )
Income tax benefit (expense)   (83 )   35   (83 )   35
Net loss and comprehensive loss $ (13,343 ) $ (10,987 ) $ (25,564 ) $ (18,019 )
Net loss per common share, basic and diluted $ (0.71 ) $ (0.99 ) $ (1.36 ) $ (3.14 )
Weighted-average common shares outstanding, basic and diluted   18,815,689   11,124,751   18,815,689   5,733,406

Tobira Investor & Media Contact:
Ian Clements, Ph.D., +1 650-351-5013
BrewLife Media Contact:
Kelly Boothe, Ph.D., +1 415-946-1076

Source: Tobira Therapeutics, Inc.

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