LONDON (Reuters) - Ablynx, a Belgian biotech company using llama DNA to develop a new class of drugs, has signed a deal worth up to $212.5 million with U.S. healthcare group Wyeth, the two companies said on Monday.
The agreement will allow Wyeth to develop a new generation of anti-TNF treatments for diseases such as rheumatoid arthritis using ultra-small antibodies.
Ablynx is pioneering medicines called nanobodies, which it believes could treat conditions including arthritis, thrombosis, cancer and Alzheimer's disease. It expects to start testing them on humans early in 2007.
Esperance Pharmaceuticals Inc., of Baton Rouge, whose nanoparticles target and kill some of the most common types of cancer cells, has secured $9 million in financing from three venture capital firms.
In deciding whether pharmaceuticals are fit for prescribing to patients, the Food and Drug Administration uses agency scientists to review the voluminous submissions from sponsoring companies. For about a third of new drugs,[1] the agency also convenes a meeting of an advisory committee comprised of outside experts whose opinions are expected to be impartial and in the interests of the public health.
Bristol-Myers Squibb Co., one of the nation's biggest drugmakers, said Thursday that its third-quarter earnings plunged 65 percent because two key drugs struggled with generic competition and results a year-ago were swelled by a one-time gain. It also raised earnings guidance for the year and said one of the government investigations into a patent deal has been expanded.
Pfizer Inc.'s potential blockbuster drug torcetrapib may be delayed until 2011, clouding plans to replace top-selling cholesterol medicine Lipitor when its patent expires.
FORMER junior biotech Pharmaxis took its biggest step towards becoming a fully-fledged pharmaceutical company yesterday, winning a Swedish licence for its asthma drug Aridol.