Tikcro Technologies Reports 2011 First Quarter Results

TEL AVIV, Israel--(BUSINESS WIRE)-- Tikcro Technologies Ltd. (OTC PK: TIKRF) today reported results for the first quarter ended March 31, 2011.

Net loss for the first quarter was $30,000 or $(0.00) per diluted share.

Tikcro holds approximately 25% of BioCancell, taking into account the conversion of a convertible note and exercise of warrants, and approximately 18% on a fully diluted basis. Shares of BioCancell are traded on the Tel Aviv Stock Exchange (TASE). The valuation of the holding in BioCancell is influenced, among other factors, by the share price of BioCancell on TASE.

BioCancell is a clinical stage biotechnology company focused on developing targeted cancer therapies for solid cancer tumors. The Company’s lead drug-candidate, BC-819, is progressing toward a US FDA Phase IIb clinical trial for pancreatic cancer. The Phase IIb clinical trial follows recently published one-year, multi-center Phase I/IIa results, addressing patients with non-resectable (inoperable) pancreatic cancer, with no metastases.

Following three months of treatment with BC-819 in the Phase I/IIa trial, five out of nine patients showed significant tumor reduction or stability, and two out of six patients in the higher dosage group became resectable (operable).

Approximately 80% of patients with pancreatic cancer die within a year of diagnosis and 95% within five years. BC-819 uses the H19 gene to synthesize Diphtheria Toxin in cancerous cells only, in order to destroy the cells. BC-819 is also undergoing Phase IIb testing for bladder cancer and Phase I/IIa testing for ovarian cancer.

As of March 31, 2011, the Company had net cash and marketable securities totaling $7.3 million.

About Tikcro Technologies:

Tikcro has holdings in BioCancell Therapeutics, Inc., a clinical-stage biopharmaceutical company operating in the area of cancer treatment. BioCancell's leading drug, BC-819, is a double stranded DNA plasmid construct that incorporates the gene for diphtheria toxin (DTA) under the regulation of the promoter sequence for H19 gene. Pursuant to U.S. FDA approved protocols, BioCancell concluded a phase I/IIa clinical trial for the treatment of pancreatic cancer and is conducting a phase IIb clinical trial for the treatment of superficial bladder carcinoma cancer and a Phase I/IIa clinical trial for the treatment of ovarian cancer.

For more information, visit Tikcro website at www.tikcro.com.

Safe Harbor Statement

Certain of the statements contained herein may be considered forward-looking statements that involve risks and uncertainties including, but not limited to, risks related to our ability to raise financing and the business of BioCancell, including, but not limited to, the development, testing, regulatory approval and commercialization of its products, its intellectual property rights, its funding, its competition, its exposure to lawsuits and its dependence on key suppliers and personnel. Such risks and uncertainties are set forth in the Company's SEC reports, including the Company's Form 20-F. Actual results may materially differ. Results of operations in any past period should not be considered indicative of the results to be expected for future periods. We undertake no duty to update any forward-looking information.

Tikcro Technologies Ltd.

Balance Sheet

(US dollars in thousands)

       
March 31, December 31,
2011 2010
Assets
Current assets
Cash and short-term marketable securities $ 7,259 $ 7,308
Other receivables   187   118
Total current assets 7,446 7,426
 
Investment in BioCancell – stock, convertible note and warrant 5,604 5,625
 
Total assets $ 13,050 $ 13,051
 
Liabilities and Shareholders' Equity
Current liabilities
Other current liabilities $ 338 $ 318
 
Shareholders' equity   12,712   12,733
 
Total liabilities and shareholders' equity $ 13,050 $ 13,051
   
 
Three Months Ended
March 31,
2011 2010
Selling, marketing, general and administrative expenses $ 81   $ 71  
 
Total operating expenses   81     71  
 
Operating loss (81 ) (71 )
 
Financial income (expenses), net   51     2,006  
 
Net income (loss) $ (30 ) $ 1,935  
   
Basic net earnings (loss) per share $ (0.00 ) $ 0.23  
 
Diluted net earnings (loss) per share $ (0.00 ) $ 0.23  
 
Basic weighted average shares   8,544     8,430  
 
Diluted weighted average shares   8,544     8,430  



CONTACT:

Investor Relations
KCSA Strategic Communications
Jeff Corbin / Marybeth Csaby
212-896-1214 / 1236
[email protected] / [email protected]

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