Full Press Release Details
Pharmaceuticals Reports 2016 Financial Results and Provides 2017 Business Update
Q4 2016 marked by positive data from Phase 2 study of JBT-101 for the treatment of systemic sclerosis showing clear signal of
Topline data for Phase 2 cystic fibrosis study expected to be reported by the end of Q1 2017-
Company has sufficient capital to fund its operations into the fourth quarter 2018 -
MA (March 9, 2017) - Corbus Pharmaceuticals Holdings, Inc. (NASDAQ: CRBP) ("Corbus" or the "Company"),
a clinical stage drug development company targeting rare, chronic, serious inflammatory and fibrotic diseases, announced today
its financial results for the year ended December 31, 2016.
Company also provided an update to its corporate progress, clinical status and anticipated milestones for JBT-101 ("Resunab"),
its novel synthetic oral endocannabinoid-mimetic drug that is designed to resolve chronic inflammation and halt fibrosis.
November 2016, the Company reported positive topline data results from a Phase 2 study in diffuse cutaneous systemic sclerosis
("systemic sclerosis"). Corbus recently completed a Phase 2 study of JBT-101 for the treatment of cystic fibrosis
("CF") with topline data to be announced by the end of March 2017. JBT-101 is also being evaluated in a third
Phase 2 study in skin-predominant dermatomyositis. A fourth Phase 2 study in systemic lupus erythematosus ("SLE")
is planned to commence in the second quarter of 2017. Additionally, twelve month open-label extension studies are being conducted
in systemic sclerosis and skin-predominant dermatomyositis.
Corporate Highlights
| Reported positive topline results showing clear signal of clinical benefit with JBT-101 in a Phase 2 study of systemic sclerosis; | ||
| Conducted an end of Phase 2 meeting with the FDA in late February 2017 to discuss a proposed Phase 3 clinical program in systemic sclerosis; | ||
| Filed for Breakthrough Therapy Designation with the FDA for JBT-101 in the treatment of systemic sclerosis; | ||
| Completed a $27.2 million registered direct offering on March 3, 2017; | ||
| Announced the completion of Phase 2 clinical study of JBT-101 in CF supported by a $5 million development award from Cystic Fibrosis Foundation Therapeutics, Inc .; | ||
| Reported preclinical data demonstrating JBT-101 reduces inflammation in alveolar macrophages from CF patients ; | ||
| Reported data from a clinical research model demonstrating JBT-101 inhibited neutrophil infiltration and resolved inflammation in the skin of healthy volunteers; | ||
| Commenced a one-year open-label extension to the ongoing Phase 2 study of JBT-101 in dermatomyositis; and | ||
| Received Orphan Designation for JBT-101 in the treatment of CF and systemic sclerosis in the European Union. |
are very pleased with the progress we have made over the recent quarters and I am proud to report that in 2016, we achieved many
significant corporate milestones and successfully advanced JBT-101 through important regulatory and clinical milestones, including
the positive clinical data from our Phase 2 study of systemic sclerosis," stated Yuval Cohen, Ph.D., Chief Executive
Officer of the Company.
Near-Term Milestones
| Report topline results of the Phase 2 first in patient safety study of JBT-101 for the treatment of CF by the end of Q1 2017; | ||
| Submit a clinical protocol to the FDA for a Phase 3 clinical program in systemic sclerosis; | ||
| Complete enrollment of Phase 2 clinical study in dermatomyositis in Q1 2017; | ||
| Continue open-label extension studies in systemic sclerosis and dermatomyositis; and | ||
| Launch the Phase 2 clinical study in SLE expected in the second quarter of 2017, in collaboration with the NIH. |
are prepared for an important year ahead as we seek to move JBT-101 into a Phase 3 clinical program in systemic sclerosis. We
are moving forward from a position of financial strength enabling us to remain focused on our commitment to clinically advance
JBT-101 as a potential therapy for individuals with serious inflammatory and fibrotic diseases. We look forward to reporting topline
data from our Phase 2 first in patient safety study of JBT-101 in CF by the end of this month," concluded Dr. Cohen.
of Financial Results for 2016
the year ended December 31, 2016, the Company reported a net loss of approximately $19,999,000, or a net loss per diluted share
of $0.49, compared to a net loss of approximately $8,851,000, or a net loss per diluted share of $0.28 for the year ended December
revenue for the year increased by approximately $1.3 million to $1.9 million due to revenue recognized from the $5 million development
award received from the Cystic Fibrosis Foundation Therapeutics, Inc. Operating expenses increased by approximately $12.4 million
to $21.9 million due to increased spending for clinical studies, manufacturing costs to produce JBT-101 for clinical studies and
Company's cash and cash equivalents balance at December 31, 2016 was approximately $15.0 million and increased by $2.7 million
during 2016. The Company received net proceeds of approximately $16.6 million from the issuance of common stock during fiscal
March 2, 2017, the Company reported $39.4 million of cash on hand including the proceeds from the $27.2 million registered direct
financing. The Company expects the cash on hand to fund operations into the fourth quarter of 2018, based on current planned expenditures.
is a novel synthetic oral endocannabinoid-mimetic drug that preferentially binds to the cannabinoid receptor type 2 (CB2) expressed
on activated immune cells and fibroblasts. CB2 activation triggers endogenous pathways that resolve inflammation and halt fibrosis.
Preclinical and Phase 1 studies have shown JBT-101 to have a favorable safety, tolerability and pharmacokinetic profile. It has
also demonstrated promising potency in preclinical models of inflammation and fibrosis. JBT-101 is designed to trigger the production
of "Specialized Pro-resolving Lipid Mediators" that activate an endogenous cascade responsible for the resolution
of inflammation and fibrosis, while reducing production of multiple inflammatory mediators. In effect, JBT-101 triggers endogenous
pathways to turn "off" chronic inflammation and fibrotic processes, without causing immunosuppression.
Pharmaceuticals Holdings, Inc. is a clinical stage pharmaceutical company focused on the development and commercialization of
novel therapeutics to treat rare, chronic, and serious inflammatory and fibrotic diseases. The Company's lead product candidate,
JBT-101, is a novel synthetic oral endocannabinoid-mimetic drug designed to resolve chronic inflammation, and fibrotic processes.
In November 2016, Corbus reported positive topline data results from a Phase 2 study in diffuse cutaneous systemic sclerosis,
showing clear signal of clinical benefit with JBT-101. The Company recently completed a Phase 2 study of JBT-101 for the treatment
of cystic fibrosis with topline data expected to be announced by the end of the first quarter of 2017. Additionally, JBT-101 is
being evaluated in a Phase 2, 12-month open-label extension study in systemic sclerosis, a Phase 2 study in skin-predominant dermatomyositis,
with a 12-month open-label extension study in dermatomyositis and another Phase 2 study in systemic lupus erythematosus planned
to commence in the second quarter of 2017.
more information, please visit www.CorbusPharma.com and connect with the Company on Twitter, LinkedIn, Google+
press release contains certain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and
Section 21E of the Securities Exchange Act of 1934 and Private Securities Litigation Reform Act, as amended, including those relating
to the Company's product development, clinical and regulatory timelines, market opportunity, competitive position, possible
or assumed future results of operations, business strategies, potential growth opportunities and other statement that are predictive
in nature. These forward-looking statements are based on current expectations, estimates, forecasts and projections about the
industry and markets in which we operate and management's current beliefs and assumptions.
statements may be identified by the use of forward-looking expressions, including, but not limited to, "expect," "anticipate,"
"intend," "plan," "believe," "estimate," "potential," "predict,"
"project," "should," "would" and similar expressions and the negatives of those terms. These
statements relate to future events or our financial performance and involve known and unknown risks, uncertainties, and other
factors which may cause actual results, performance or achievements to be materially different from any future results, performance
or achievements expressed or implied by the forward-looking statements. Such factors include those set forth in the Company's
filings with the Securities and Exchange Commission. Prospective investors are cautioned not to place undue reliance on such forward-looking
statements, which speak only as of the date of this press release. The Company undertakes no obligation to publicly update any
forward-looking statement, whether as a result of new information, future events or otherwise.
Pharmaceuticals Holdings, Inc.
Statements of Operations
| For the Years Ended December 31, | ||||||||
| 2016 | 2015 | |||||||
| Collaboration revenue | $ | 1,911,424 | $ | 648,382 | ||||
| Operating expenses: | ||||||||
| Research and development | 15,436,735 | 5,888,659 | ||||||
| General and administrative | 6,459,747 | 3,613,416 | ||||||
| Total operating expenses | 21,896,482 | 9,502,075 | ||||||
| Operating loss | (19,985,058 | ) | (8,853,693 | ) | ||||
| Other income (expense): | ||||||||
| Interest income, net | 477 | 977 | ||||||
| Foreign currency exchange gain (loss) | (14,094 | ) | 1,977 | |||||
| Other income (loss), net | (13,617 | ) | 2,954 | |||||
| Net loss | $ | (19,998,675 | ) | $ | (8,850,739 | ) | ||
| Net loss per share, basic and diluted | $ | (0.49 | ) | $ | (0.28 | ) | ||
| Weighted average number of common shares outstanding, basic and diluted | 41,137,518 | 31,350,145 |
Pharmaceuticals Holdings, Inc.
Consolidated Balance Sheets
| December 31, | ||||||||
| 2016 | 2015 | |||||||
| ASSETS | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 14,992,257 | $ | 12,338,275 | ||||
| Restricted cash | 150,000 | - | ||||||
| Grants receivable | 1,000,000 | - | ||||||
| Stock subscriptions receivable | 330,413 | - | ||||||
| Prepaid expenses | 930,261 | 376,515 | ||||||
| Total current assets | 17,402,931 | 12,714,790 | ||||||
| Restricted cash | 50,000 | 36,375 | ||||||
| Property and equipment, net | 435,251 | 124,138 | ||||||
| Total assets | $ | 17,888,182 | $ | 12,875,303 | ||||
| LIABILITIES AND STOCKHOLDERS' EQUITY | ||||||||
| Current liabilities: | ||||||||
| Notes payable | $ | 271,757 | $ | 162,019 | ||||
| Accounts payable | 3,419,921 | 1,314,377 | ||||||
| Accrued expenses | 3,256,455 | 562,279 | ||||||
| Deferred revenue, current | 1,940,195 | 1,591,358 | ||||||
| Deferred rent, current | 10,263 | - | ||||||
| Total current liabilities | 8,898,591 | 3,630,033 | ||||||
| Deferred revenue, noncurrent | - | 260,260 | ||||||
| Deferred rent, noncurrent | 65,724 | - | ||||||
| Other liabilities | 4,632 | - | ||||||
| Total liabilities | 8,968,947 | 3,890,293 | ||||||
| Commitments and Contingencies | ||||||||
| Stockholders' equity | ||||||||
| Preferred Stock $0.0001 par value:10,000,000shares authorized, no shares issued andoutstanding at December 31, 2016 and 2015 | - | - | ||||||
| Common stock, $0.0001 par value; 150,000,000shares authorized, 44,681,745 and 37,605,134shares issued and outstanding at December 31, 2016 and 2015 | 4,468 | 3,761 | ||||||
| Additional paid-in capital | 42,191,256 | 22,259,063 | ||||||
| Accumulated deficit | (33,276,489 | ) | (13,277,814 | ) | ||||
| Total stockholders' equity | 8,919,235 | 8,985,010 | ||||||
| Total liabilities and stockholders' equity | $ | 17,888,182 | $ | 12,875,303 |
Thomas Communications, LLC
Corbus Pharmaceuticals Holdings, Inc.