Nov 07, 2006
China Biopharmaceuticals Holdings, Inc. (OTCBB: CHBP), a leading Chinese pharmaceutical company focused on the development, manufacturing and distribution of innovative drugs in China, today announced that it has completed various progress in both initiating and completing clinical trials in separate drug indications.
Completion of Clinical Trials for Torasemide Tablets and Injections
CHBP announced today that all required clinical trials for both Torasemide tablets and Injections have been completed, and the Company is waiting for final manufacturing and marketing approval from the State Food and Drug Administration of China (SFDA).
The clinical trials for Torasemide for injections and tablets were conducted in five and six hospitals respectively throughout
Both trial results will be sent to the SFDA for marketing and manufacturing approval, which is expected to be granted by the third quarter of 2007.
Torasemide is a loop diuretics. It is commonly used in conditions such as heart failure, where the pumping mechanism of the heart is less effective. Torasemide is used to relieve the symptoms of heart failure, such as the shortness of breath seen with fluid on the lungs. At higher doses, the amount of water drawn from the blood into the urine is much greater; therefore Torasemide is also used when there is reduced production of urine in patients with kidney failure, and liver failure.
Diuretics is thought as the first choice of drug treating primary hypertension. Currently, there are 160 million people suffering with hypertension in
Initiation of Clinical Trials for Flucloxacillin Magnesium
In addition, CHBP announced that it has started the clinical trials for one of its new drugs, Flucloxacillin Magnesium. The trials will be conducted in six hospitals throughout
Flucloxacillin Magnesium is a semi-synthetic penicillin derived from 6-amino-penicillanic acid and is the latest of the series of penicillinase stable penicillin. It exhibits bactericidal activity against all Gram-positive organisms (with the exception of Strep.faecalis) e.g. Haemolytic streptococci, staphylococci, streptococcus pneumonia and N. gonorrhea. Its anti-staphylococcal activity is not affected by penicillinase, and as Flucloxacillin Magnesium is active against virtually all strains of Staph. aureus (methicillin-resistant strains being the only exception), it is particularly indicated in the treatment of staphylococcal infections.
In
CHBP is the only company approved for clinical trials of this drug in
"Mr. An Lufan, CHBP President and COO, stated, "This clinical progress report further demonstrates CHBP's leading R&D capabilities, robust product pipeline and CHBP's R&D team's ability to successfully navigate the drug testing and approval process. If approved by the SFDA, these 3 drug products will have the potential to help millions of patients in
Mr. Chris Peng Mao, CHBP Chairman, further stated, "We are very excited about starting the trials for Flucioxacillin which will, if successful and approved by the SFDA, give CHBP an exclusive drug in a very large market. It also demonstrates that our R&D division is interfacing well with one of our manufacturing facilities."
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China Biopharmaceutical Holdings, Inc. (OTCBB: CHBP) is a research drive


