Join today and have your say! It’s FREE!

Become a member today, It's free!

We will not release or resell your information to third parties without your permission.
Please Try Again
{{ error }}
By providing my email, I consent to receiving investment related electronic messages from Stockhouse.

or

Sign In

Please Try Again
{{ error }}
Password Hint : {{passwordHint}}
Forgot Password?

or

Please Try Again {{ error }}

Send my password

SUCCESS
An email was sent with password retrieval instructions. Please go to the link in the email message to retrieve your password.

Become a member today, It's free!

We will not release or resell your information to third parties without your permission.

Expect Availability Of Biogen's Newly Approved Spinraza In Just One Week

BIIB, IONS, SRPT, LLY

Biogen Inc (NASDAQ: BIIB) said its newly approved Spinraza (nusinersen) would be available in just one week time. Spinraza is approved to treat spinal muscular atrophy, a form of muscle weakness.

The company, which got the FDA approval within three months of regulatory filing, said Spinraza will be made available for shipment in the United States to healthcare providers in approximately one week. The drug was approved based on positive results from multiple clinical studies in more than 170 patients.

Biogen licensed the global rights to develop, manufacture and commercialize Spinraza from Ionis Pharmaceuticals Inc (NASDAQ: IONS).

Recent Drug Approvals Through Accelerated Pathway

Following are the recent drugs that have been approved by accelerated pathway:

  • This month, the U.S. Food and Drug Administration granted accelerated approval to Clovis Oncology Inc (NASDAQ: CLVS)'s Rubraca (rucaparib) to treat women with a certain type of ovarian cancer. At that time, Clovis said Rubraca will be available in the United States immediately.
  • In October, Eli Lilly and Co (NYSE: LLY) received accelerated for olaratumab (Lartruvo) to treat adults with advanced soft tissue sarcomas.
  • In September, Sarepta Therapeutics Inc (NASDAQ: SRPT) announced the U.S. Food and Drug Administration has granted accelerated approval for EXONDYS 51 (eteplirsen) for the treatment of Duchenne muscular dystrophy.


Get the latest news and updates from Stockhouse on social media

Follow STOCKHOUSE Today