Pernix Therapeutics Holdings, Inc. ("Pernix" or the "Company") (NYSE
Amex: PTX), a specialty pharmaceutical company, today announced
financial results for the quarter and year ended December 31, 2011.
Financial Results
For the fourth quarter of 2011, net revenues increased by 74% to $21.4
million, compared to $12.3 million for the fourth quarter of 2010. The
increase in net revenues was due primarily to higher volume of product
sales resulting from the launch of the Company's new CEDAX product
formulation, NATROBA, and certain generic products.
Net income for the fourth quarter of 2011 was $3.9 million, or $0.15 per
basic and diluted share, compared to $1.5 million, or $0.07 per basic
and diluted share, for the fourth quarter of 2010. Excluding a $0.4
million impairment charge on land owned by Pernix based on an updated
appraisal, net income for the quarter ended December 31, 2011 was $4.3
million, or $0.16 per diluted share.
Adjusted earnings before interest, taxes, depreciation and amortization
(adjusted EBITDA, a non-GAAP measure) increased 94% to $7.0 million for
the fourth quarter of 2011, compared to $3.6 million for the fourth
quarter of 2010. See the table at the end of this press release for a
reconciliation of EBITDA and adjusted EBITDA to net income.
Selling, general and administrative ("SG&A") expenses in the fourth
quarter of 2011 increased to $7.0 million, compared to $5.3 million for
the fourth quarter of 2010. The increase was primarily due to the
addition of several key management positions, bonuses, commissions,
incentives and stock compensation expense. The increase included the
$0.4 million impairment charge on the land owned by Pernix. Depreciation
and amortization expense was $0.6 million for the fourth quarter of
2011, compared to $0.7 million for the fourth quarter of 2010. The
Company recognized an income tax expense of $2.1 million for the fourth
quarter of 2011, compared to $1.4 million in the fourth quarter of 2010.
Cooper Collins, President and Chief Executive Officer of Pernix, said,
"We achieved significant growth in net revenues and adjusted EBITDA
during the fourth quarter and full year 2011, despite a soft cough and
cold season. This strong growth was primarily due to the launches of the
new CEDAX 180 mg formulation in January 2011, several generic products
throughout 2011, and NATROBA in August 2011. The management team remains
focused on expanding our branded prescription and generic product
portfolios and launching our new gastroenterology product by mid-year
2012. We expect to continue to execute on our growth strategy, which
includes the horizontal integration of our branded prescription,
generic, and over-the-counter (OTC) businesses."
For the year ended December 31, 2011, net revenues increased by 82% to
$60.6 million, compared to $33.2 million for the prior year period,
which is attributed to the new product launches described above.
Net income for the year ended December 31, 2011 was $8.3 million, $0.35
per basic and $$0.34 per diluted share, compared to $9.3 million, or
$0.40 per basic and diluted share, for the prior year period. Excluding
a $0.4 million impairment charge related to land owned by Pernix based
on an updated appraisal, net income for the year ended December 31, 2011
was $8.7 million, or $0.36 per diluted share. For the year ended
December 31, 2011, the Company recognized an income tax expense of $4.6
million (effective tax rate of 35%), compared to an income tax expense
of $1.5 million (effective tax rate of 14%) for the prior year period.
Adjusted EBITDA increased 45% to $15.8 million for the year ended
December 31, 2011, compared to $10.9 million for the prior year period.
See the table at the end of this press release for a reconciliation of
EBITDA and adjusted EBITDA to net income.
SG&A expenses for the year ended December 31, 2011 increased to $22.5
million, compared to $15.2 million for the year ended December 31, 2010.
The increase was primarily due to the non-recurring impairment charge on
the land, the addition of several key management positions, bonuses,
commissions, incentives and stock compensation expense. Depreciation and
amortization expenses increased to $2.3 million for the year ended
December 31, 2011, compared to $1.2 million for the prior year period.
The Company also recognized $0.8 million in expenses related to its
joint venture with SEEK for the development of Theobromine during the
year ended December 31, 2011.
Business Update
New Gastroenterology Product Launch On Track for Mid-Year of 2012
In January 2012, Pernix entered into a license and supply agreement with
a private company for a new FDA-approved prescription product to treat
gastroenterology disease. Under the terms of the agreement, Pernix paid
an up-front license fee of $2.0 million to obtain exclusive marketing
rights to this gastroenterology product in the United States. Pernix
also expects to pay an additional fee of $2.0 million upon commercial
launch of the product. This new product will be positioned as a
first-line therapy in a niche market of more than $100 million annually
in the U.S. As previously announced, Pernix remains on track to launch
the product in mid-year of 2012. Prior to launching the product, the
Company plans to establish a sales force of up to 30 representatives
dedicated to gastroenterology.
Generic Products
Pernix markets generic products through its wholly-owned subsidiary,
Macoven Pharmaceuticals. In 2011, the generic product portfolio made a
significant contribution to the Company's consolidated net revenue
growth. Sales of generic products represented 32% of the consolidated
net revenues of Pernix for the year ended December 31, 2011.
Natroba™ (spinosad) Topical Suspension, 0.9%
Under the exclusive co-promotion agreement with ParaPRO, LLC, Pernix
launched Natroba™ with its pediatric sales force in August 2011.
NATROBA™ received U.S. Food and Drug Administration (FDA) approval in
January 2011 as a prescription medication indicated for the topical
treatment of head lice infestations in patients four years of age and
older. In March 2012, Pernix introduced a nationwide Point-of-Sale (POS)
coupon for NATROBA.
Theobromine (BC 1036)
In March 2011, Pernix and its joint venture partner SEEK, a leading U.K.
drug discovery and development group, appointed a financial advisor in
connection with an auction of Theobromine (BC 1036), a non-codeine,
non-narcotic, antitussive drug candidate in late-stage development for
the treatment of persistent cough. While the joint venture has not
received an offer to purchase the Theobromine assets that was acceptable
by its Board of Directors, the joint venture continues to evaluate
opportunities and expects to continue discussions with interested
parties to maximize the value of this asset. The joint venture is
currently planning to initiate its pivotal Phase III trial in the
European Union in the first half of 2012, and is currently evaluating
over-the-counter strategies in the United States.
Guidance
In 2012, the Company plans to invest in the launch of its
Gastroenterology product, which includes establishing a new
gastroenterology sales force of up to 30 sales representatives.
Additionally, the Company plans to invest in the development of
Theobromine and the recently announced prescription product in
development for the pediatric market. The Company expects these
investments along with the expansion of the corporate infrastructure
will increase operating expenses in the range of $12 to $15 million for
the full year 2012. In terms of revenue, the Company expects that 2012
quarterly revenues will have a similar percentage relationship to the
full year 2012 revenues as was experienced in 2011. For example, in 2011
the third and fourth quarters comprised 63% of total net revenues. The
Company anticipates similar quarterly net revenue percentages in 2012.
Financial Position
As of December 31, 2011, the Company had $34.6 million of cash and cash
equivalents.
In February 2012, Pernix initiated an At-the-Market (ATM) equity
offering sales program. Under the ATM sales agreement, Pernix may from
time to time offer and seek to sell up to $25 million of its common
stock through Cantor Fitzgerald & Co. at prevailing market prices, at
prices related to prevailing market prices, or at negotiated prices. As
of March 23, 2012, the Company has sold 264,000 shares of common stock
under its ATM program for total net proceeds of approximately $2.5
million.