Amgen forecast darkens as FDA review looms

The FDA couldn't have scheduled today's meeting on the risks posed by Amgen's anemia drugs at a worse time. With the market opening to a new raft of chilly economic reports, analysts covering Amgen were in a particularly dour mood about Amgen's chances. Christopher Raymond at Robert W. Baird predicted more restrictions on the use of its multibillion-dollar drugs, which would further eat into the biotech company's revenue. And FBR Capital's Jim Reddoch wouldn't even rule out a vote to remove Aranesp from the market--a worst-case scenario that would inflict major damage at a company that has been working to build up a pipeline of new therapies needed to rescue its bottom line.

Amgen officials, though, will fight this battle over the $6 billion market to the bitter finish.

"ESAs provide an unequivocal treatment benefit for cancer patients undergoing chemotherapy by reducing the need for blood transfusions," said Roger M. Perlmutter, Amgen's executive vice president of research and development.

- see Amgen's release
- read the story from CNN
-
and check out the Dow Jones report

Related Articles:
Epogen/Aranesp--Top 10 Warnings and Recalls. Report
FDA's worst-case anemia scenario. Report
Do anemia warnings signal new limits? Report
Study: Anemia meds hike death risk 10%. Report
FDA: More risks from anemia drugs. Report

Suggested Articles

Janssen’s BCMA-targeting CAR-T therapy eliminated tumors in 69% of patients with advanced multiple myeloma in a small phase 1 study.

In a study, BMS' CAR-T therapy banished tumors in more than half and shrank tumors in nearly three-quarters of relapsed blood cancer patients.

Novartis unveiled more data showing how its asthma combo QMF149 fared against the standard of care: a combination of the same types of drugs.