FDA fast-tracks Abbvie's lung cancer drug

The investigational drug against non-small cell lung cancer can look forward to special treatment by the FDA, which has granted the drug Breakthrough Therapy Designation.
Photo: Abbvie / PR
Photo: Abbvie / PR
by MIKKEL AABENHUS HEMMINGSEN, translated by daniel pedersen

Abbvie starts out 2022 with positive news, as the US Food and Drug Administration (FDA) sees big potential in Abbvie's investigational antibody-drug conjugate, telisotuzumab vedotin.

Already a subscriber?Log in here

Read the whole article

Get access for 14 days for free. No credit card is needed, and you will not be automatically signed up for a paid subscription after the free trial.

With your free trial you get:

  • Access all locked articles
  • Receive our daily newsletters
  • Access our app
!
!
Must contain at least 6 characters
!
Must contain at least 2 characters
!
Must contain at least 2 characters

Get full access for you and your coworkers

Start a free company trial today

Sign up for our newsletter

Stay ahead of development by receiving our newsletter on the latest sector knowledge.

!
Newsletter terms

Front page now

Further reading