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Fennec Pharmaceuticals Ord Shs T.FRX

Alternate Symbol(s):  FENC

Fennec Pharmaceuticals Inc. is a commercial-stage biopharmaceutical company focused on its product candidate PEDMARK. It sells its product through a field force, including Regional Pediatric Oncology Specialists and medical science liaisons who are helping to educate the medical communities and patients about cisplatin induced ototoxicity and its programs supporting patient access to PEDMARK. PEDMARK is a Food and Drug Administration approved therapy indicated to reduce the risk of ototoxicity associated with cisplatin treatment in pediatric patients with localized, non-metastatic, solid tumors. It is a formulation of sodium thiosulfate in single-dose, ready-to-use vials for intravenous use in pediatric patients. PEDMARK is a therapeutic agent with a dosing paradigm, across two open-label, randomized Phase 3 clinical studies, the Clinical Oncology Group (COG) Protocol ACCL0431 and SIOPEL 6. It has established Fennec HEARS, a single source program designed to connect PEDMARK patients.


TSX:FRX - Post by User

Post by IBTryinIton May 13, 2011 9:08am
327 Views
Post# 18571189

News

News

Adherex Reports Recent Developments and First Quarter March 31, 2011 Financial Results

RESEARCH TRIANGLE PARK, NORTH CAROLINA--(Marketwire - May 13, 2011) - Adherex Technologies Inc. (TSX:AHX - News; PINK SHEETS:ADHXF - News), a biopharmaceutical company focused on the development of eniluracil and 5-fluorouracil, today reported its financial results and recent developments for the first quarter ended March 31, 2011. All amounts are in U.S. dollars unless otherwise specified.

Recent Developments



-- Eniluracil Phase 2 Study Update - On April 27, 2011, Adherex announced
the enrollment of the first patient in the Phase 2 clinical trial for
Metastatic Breast Cancer comparing the oral regiment of Eniluracil + 5-
Fluorouracil (5-FU) and Leucovorin versus Capecitabine (Xeloda(R)). The
comparative study intends to enroll 140 patients at approximately 20
clinical sites in the United States and Russia in the next 12 to 14
months.

-- Rights Offering - The subscription period for the Company's previously
announced rights offering expired on March 29, 2011. The proceeds
received by the Company were approximately $2.5 million. As of April 1,
2011, at which time the proceeds from the rights offering were
collected, the Company had approximately $7.6 million in cash and
452,852,631 common shares outstanding. The Company anticipates that
available cash on hand will be sufficient to fund the Company's Phase 2
study along with related corporate expenses.

-- Annual Meeting of Shareholders - Adherex would like to invite all
shareholders to attend its Annual General and Special Meeting on
Tuesday, June 28, 2011 at 12 pm ET at the Sofitel Montreal rue
Sherbrooke, Montreal, Quebec.

"We commenced patient enrollment in our Phase 2 clinical study for Metastatic Breast Cancer. With the closing of the rights offering our capital position remains strong, we don't expect any need for raising additional capital until the conclusion of the study. We look forward to updating you on our progress in the coming quarters," said Mr. Rosty Raykov, Chief Executive Officer of Adherex.

Financial Update

The Company reported net income for the first quarter ended March 31, 2011 of $4.7 million, or net income of
.01 per share, compared to a net loss of
.4 million, or a loss of
.00 per share, in the same period in 2010. The increase in the reported net income is primarily due to an unrealized gain on the Company's derivatives. The Company reported an non-cash gain of $5.7 million on derivatives as compared to nil in the same period in 2010. Cash operating expenses totaled $1.0 million, as compared to
.4 million in the same period in 2010, as the Company increased its expenditures in preparation for the launch of the Phase 2 study and incurred costs relating to the rights offering.

Cash and cash equivalents totaled $5.0 million at March 31, 2011, compared to $5.9 million at December 31, 2010. The Company also recorded a $2.5 million subscription receivable related to proceeds received from the rights offering which were deposited on April 1, 2011. At March 31, 2011, the Company had working capital (excluding derivative liabilities) totaling approximately $7.1 million compared to $5.5 million as of December 31, 2010.

The selected financial data presented below is derived from our unaudited consolidated financial statements which were prepared in accordance with U.S. generally accepted accounting principles. The complete consolidated financial statements for the year ended March 31, 2011 and management's discussion and analysis of financial condition and results of operations will be available via www.sec.gov and www.sedar.com.

FINANCIAL CHARTS FOLLOW



Adherex Technologies Inc.
Selected Financial Data
(U.S. dollars in thousands except per share amounts)

March 31, December 31,
Consolidated Balance Sheets: 2011 2010
Assets:
Cash and cash equivalents $ 5,023 $ 5,947
Subscription receivable 2,547
Other current assets 67 46
Total assets $ 7,637 $ 5,993

Liabilities and stockholders' equity:
Current liabilities $ 556 $ 467
Derivative warrant liability 7,366 10,450
Other long-term liabilities - -
Total stockholders' equity (285 )(4,924 )
Total liabilities and stockholders' equity $ 7,637 $ 5,993



March 31, March 31,
Consolidated Statements of Operations: 2011 2010

Revenue $ - $ -

Operating expenses:
Research and development 315 163
Impairment of Capital Assets --- ---
(Gain) on Deferred Lease Inducements --- ---
General and administrative 706 203

Loss from operations (1,021 )(366 )

Other income 4 -
Gain on derivative warrants 5,680 -
Interest income 6 -

Net income (loss) and comprehensive income
(loss) $ 4,669 $ (366 )
Basic and diluted net income (loss) per
common share $ 0.01 $ (0.00 )

Except for historical information described in this press release, all other statements are forward-looking. Forward-looking statements are subject to certain risks and uncertainties inherent in the Company's business that could cause actual results to vary, including such risks that regulatory clinical and guideline developments may change, scientific data may not be sufficient to meet regulatory standards or receipt of required regulatory clearances or approvals, clinical results may not be replicated in actual patient settings, protection offered by the Company's patents and patent applications may be challenged, invalidated or circumvented by its competitors, the available market for the Company's products will not be as large as expected, the Company's products will not be able to penetrate one or more targeted markets, revenues will not be sufficient to fund further development and clinical studies, the Company may not meet its future capital needs, and its ability to obtain additional funding, as well as uncertainties relative to varying product formulations and a multitude of diverse regulatory and marketing requirements in different countries and municipalities, and other risks detailed from time to time in the Company's filings with the Securities and Exchange Commission including its Annual Report on Form 10-K for the year ended December 31, 2010. Adherex Technologies, Inc. disclaims any obligation to update these forward-looking statements except as required by law.

For a more detailed discussion of related risk factors, please refer to our public filings available at www.sec.gov and www.sedar.com.

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