Arrowhead Reports Fiscal 2015 Third Quarter Financial Results
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Fiscal 2015 Third Quarter and Recent Company Highlights
ARC-520
-
Received regulatory permission to initiate three multiple-dose Phase
2b studies in
the United States (Heparc-2004) and inGermany andHong Kong (Heparc-2002 and 2003) - Completed dosing of four cohorts in a single-dose Phase 2a study (Heparc-2001) and expanded the study to include three additional cohorts
- Completed dosing in a non-clinical study in chronically infected chimpanzees that spanned more than a year
-
Highlights of the Phase 2a and chimpanzee studies to be presented at
an analyst day planned for
September 24, 2015
ARC-AAT
- Met the dosing target for Part A of the ARC-AAT Phase 1 study in healthy volunteers, and transitioned the study into Part B which is designed to enroll patients with PiZZ genotype alpha-1 antitrypsin deficiency
-
Began dosing Part B of the Phase 1 study at one site in
Australia -
Gained regulatory clearance to expand Part B of the Phase 1 study to
allow additional sites in the
United Kingdom andNew Zealand -
Gained Orphan Drug Designation from the
United States Food and Drug Administration
Platform and Early Pipeline
- Published data on advances being made in a subcutaneously administered formulation of the Dynamic Polyconjugate (DPC) delivery system
- Presented preclinical data on ARC-F12, a potential new candidate targeting coagulation factor 12 for the potential treatment of hereditary angioedema and thromboembolic diseases
Selected Fiscal 2015 Third Quarter Financial Results
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CONSOLIDATED CONDENSED FINANCIAL INFORMATION (unaudited) | ||||||||||||||||
Three Months Ended |
Nine Months Ended |
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OPERATING SUMMARY |
2015 | 2014 | 2015 | 2014 | ||||||||||||
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REVENUE | $ | 123,750 |
$ |
43,750 |
$ | 338,250 | $ |
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OPERATING EXPENSES | ||||||||||||||||
Research and development | 7,490,400 | 6,392,200 | 36,877,925 | 14,719,739 | ||||||||||||
Acquired in-process research and development | - | - | 10,142,786 | - | ||||||||||||
Salaries and payroll-related costs | 3,570,531 | 2,454,449 | 10,262,799 | 7,634,142 | ||||||||||||
General and administrative expenses | 1,829,393 | 1,582,465 | 5,612,219 | 3,865,845 | ||||||||||||
Stock-based compensation | 2,486,074 | 2,038,682 | 6,706,009 | 3,758,264 | ||||||||||||
Depreciation and amortization | 741,058 | 276,054 | 1,480,656 | 1,075,238 | ||||||||||||
TOTAL OPERATING EXPENSES | 16,117,456 | 12,743,850 | 71,082,394 | 31,053,228 | ||||||||||||
OPERATING LOSS | (15,993,706 | ) | (12,700,100 | ) | (70,744,144 | ) | (30,921,978 | ) | ||||||||
OTHER INCOME/(EXPENSE) | 57,653 | 1,073,649 |
|
3,546,398 | (5,372,902 | ) | ||||||||||
NET LOSS | $ | (15,936,053 | ) | $ | (11,626,451 | ) | $ | (67,197,746 | ) | $ | (36,294,880 | ) | ||||
EARNINGS PER SHARE (BASIC AND DILUTED): | $ | (0.27 | ) | $ | (0.22 | ) | $ | (1.19 | ) | $ | (0.81 | ) | ||||
WEIGHTED AVERAGE SHARES OUTSTANDING | 59,492,867 | 51,931,989 | 56,631,297 | 44,565,008 | ||||||||||||
FINANCIAL POSITION SUMMARY |
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2015 | 2015 | |||||||||||||||
CASH AND CASH EQUIVALENTS | $ | 87,252,813 | $ | 96,447,301 | ||||||||||||
SHORT AND LONG-TERM INVESTMENTS | 24,365,922 | 31,922,240 | ||||||||||||||
TOTAL CASH RESOURCES (CASH, CASH EQUIVALENTS, INVESTMENTS) | 111,618,735 | 128,369,541 | ||||||||||||||
OTHER ASSETS | 33,571,590 | 34,008,917 | ||||||||||||||
TOTAL ASSETS | $ | 145,190,325 | $ | 162,378,458 | ||||||||||||
TOTAL LIABILITIES | $ | 14,445,931 | $ | 18,182,104 | ||||||||||||
TOTAL STOCKHOLDERS' EQUITY | 130,744,394 | 144,196,354 | ||||||||||||||
TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY | $ | 145,190,325 | $ | 162,378,458 | ||||||||||||
SHARES OUTSTANDING | 59,498,362 | 59,435,862 | ||||||||||||||
PROFORMA SHARES OUTSTANDING (INCLUDING CONVERSION OF PREFERRED SHARES) | 62,169,352 | 62,106,852 |
About ARC-520
Arrowhead's RNAi-based candidate ARC-520 is being investigated in the treatment of chronic HBV infection. The small interfering RNAs (siRNAs) in ARC-520 intervene at the mRNA level, upstream of the reverse transcription process where current standard of care nucleotide and nucleoside analogues act. Arrowhead is investigating ARC-520 specifically, to determine if it can be used to achieve a functional cure, which is an immune clearant state characterized by hepatitis B s-antigen negative serum with or without sero-conversion. Arrowhead has completed a Phase 1 single ascending dose study in normal volunteers and the company is conducting single dose Phase 2a studies and multiple dose Phase 2b studies in chronic HBV patients. Approximately 350-400 million people worldwide are chronically infected with the hepatitis B virus, which can lead to cirrhosis of the liver and is responsible for 80% of primary liver cancers globally.
About ARC-AAT
Arrowhead's ARC-AAT is being investigated for the treatment of liver disease associated with Alpha-1 Antitrypsin Deficiency (AATD), a rare genetic disease that severely damages the liver and lungs of affected individuals. The mean estimated prevalence of AATD in the U.S. is 1 per 3000-5000, or approximately 100,000 patients. AATD is also an important cause of pediatric liver disease with an estimated prevalence in children of approximately 20,000 patients, and 50-80% likely to manifest liver disease during childhood. It is a rare disease that appears to be frequently misdiagnosed or undiagnosed. ARC-AAT, which was granted orphan drug designation, employs a novel unlocked nucleobase analog (UNA) containing RNAi trigger molecule designed for systemic delivery using the Dynamic Polyconjugate™ delivery system. ARC-AAT is highly effective at knocking down the Alpha-1 antitrypsin (AAT) gene transcript and reducing the hepatic production of the mutant AAT (Z-AAT) protein in animal models. Reduction of liver production of the inflammatory Z-AAT protein, which is believed to be the cause of progressive liver disease in AATD patients, is important as it is expected to halt the progression of liver disease and potentially allow fibrotic tissue repair. Arrowhead is conducting a single dose Phase 1 clinical study of ARC-AAT, with part A in healthy volunteers and part B in AATD patients.
About
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Safe Harbor Statement under the Private Securities Litigation Reform Act:
This news release contains forward-looking statements within the
meaning of the "safe harbor" provisions of the Private Securities
Litigation Reform Act of 1995. These statements are based upon our
current expectations and speak only as of the date hereof. Our actual
results may differ materially and adversely from those expressed in any
forward-looking statements as a result of various factors and
uncertainties, including our ability to finance our operations, the
future success of our scientific studies, our ability to successfully
develop drug candidates, the timing for starting and completing clinical
trials, rapid technological change in our markets, and the enforcement
of our intellectual property rights.
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