Tuesday, August 21, 2012

Reuters: Regulatory News: UPDATE 1-FDA extends review for Pfizer arthritis drug by three months

Reuters: Regulatory News
Reuters.com is your source for breaking news, business, financial and investing news, including personal finance and stocks. Reuters is the leading global provider of news, financial information and technology solutions to the world's media, financial institutions, businesses and individuals. // via fulltextrssfeed.com
UPDATE 1-FDA extends review for Pfizer arthritis drug by three months
Aug 21st 2012, 13:13

Tue Aug 21, 2012 9:13am EDT

* FDA sets new review deadline of Nov. 21

* Pfizer says trial results still favor drug's approval

* Shares little changed

Aug 21 (Reuters) - The U.S. Food and Drug Administration extended by three months its review of Pfizer Inc's experimental rheumatoid arthritis treatment tofacitinib, one of the most promising new drugs in the company's pipeline.

In July, Pfizer disclosed that the FDA sought a "routine" analysis of clinical trial data for the drug that could delay a decision by three months or more beyond the agency's Aug. 21 deadline.

If approved, the pill could offer a more convenient alternative to Abbott Laboratories Inc's $8 billion-a-year injectable medication Humira.

The FDA now views the additional analysis as a major amendment to Pfizer's application for approval, and set a new Nov. 21 deadline for reviewing the drug, the company said on Tuesday. It did not give more details of the data analysis it provided.

Pfizer said it still believes trial results favor the drug's use, and is working with the FDA, as well as regulators in Europe, Japan and other countries, to bring it to market.

Rheumatoid arthritis, a chronic inflammatory autoimmune disease, affects about 1.6 million Americans and 23.7 million people worldwide, the company said.

Tofacitinib blocks signals that activate immune and inflammatory responses in the body, and is the first in a new class of drugs called Janus kinase (JAK) inhibitors.

A panel of outside advisers to the FDA recommended the agency approve the drug during a May meeting, though many said it should be used only after patients had tried other treatments. Safety concerns included possible infections, such as pneumonia, or malignancies.

Wall Street analysts estimate that tofacitinib could reap up to $3 billion in annual sales if approved.

Pfizer shares rose 2 cents to $23.91 in premarket trading.

  • Link this
  • Share this
  • Digg this
  • Email
  • Reprints

You are receiving this email because you subscribed to this feed at blogtrottr.com.

If you no longer wish to receive these emails, you can unsubscribe from this feed, or manage all your subscriptions

0 comments:

Post a Comment

 
Great HTML Templates from easytemplates.com.