LONDON -A new drug to treat benign prostatic hyperplasia was to be developed by Pfizer in a small British biotech firm.
The company that invented the drug has been working with the pharmaceutical giant to develop a way to treat the disease.
The drug is called Cialis and is being sold under the trade name "Tadalafil," although it is not yet available.
The drug, which is called Tadalista, will be sold in the UK by Pfizer, a company that makes Viagra and Cialis, and in the US by Eli Lilly. The drug has been in the pipeline since 1999.
Tadalista has been available in the UK since 1999, with the first clinical trials being in June 2007. The company said it had completed more than 1,000 clinical trials in the United States and the UK.
The drug is also being sold under the name "Tegretol," and the UK patent on the drug expires in November 2011.
Tegretol is not yet approved for clinical use in the United States, and it is not known to be a good substitute for a drug like Cialis.
The drug is also being marketed in Europe by Bayer.
Tegretol is available in a number of forms, including tablets, capsules, and liquids and as an oral suspension.
A spokeswoman for Pfizer said: "We have received several inquiries from patients and pharmacist about Cialis and Tadalista and would not comment on the final product."
She said the company would be working with other pharmaceutical companies to develop the drug.
The company will also be developing a marketing plan that will help make Cialis available in the United States.
In April this year, the British company that developed the drug and its marketing plan for Tadalista, announced it had been approached by Pfizer for approval for an experimental version.
The company said it had been working with the pharmaceutical giant to develop a way to treat benign prostatic hyperplasia (BPH) and had also entered into a marketing agreement with the company's partner, Pfizer.
Tadalista is the second drug to be approved for the treatment of BPH and the first to treat the condition.Bristol-Myers Squibb, the company that developed the drug and the marketing plan for the product, said it had not yet received any clinical trial data to confirm the drug's efficacy.
Bristol-Myers said it would have no further marketing or development activity until the product is approved. It did not respond to a request for comment from the BBC.
The British company that developed the drug and its marketing plan for the product said it had not yet received any clinical trial data to confirm its effectiveness and had not entered into a marketing agreement with Pfizer.
The company will be conducting clinical trials in the United States, and it is planning a marketing plan for the drug.
Tadalista will be available in the United States for the first time in the United States by the end of 2011.
The pharmaceutical giant that developed Tadalista and the marketing plan for it was based in London, where the company had a successful marketing campaign and development experience.
A spokeswoman for Pfizer said the company would be working with other pharmaceutical companies to develop the drug.
She said the company was aware of the challenges the drug had to the United States market, and that it was working with other companies to develop a marketing plan.
She said the company had no plans to fund its clinical trials, but that it was working with other companies to develop a marketing plan.
Bristol-Myers said it had received several inquiries from patients and pharmacist about the product and would not comment on the final product.
Tadalista is the second drug to be approved for the treatment of benign prostatic hyperplasia (BPH).
In 1998, British drug company Pfizer became the first to develop a way to treat BPH and have been testing the drug in clinical trials.
The drug's patent was expiry in November 2010, and it is expected to expire in 2011.
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