Kite’s Yescarta (axicabtagene ciloleucel) Receives the US FDA’s Approval for New Label Update in all Approved Indications
Shots:
- The update was based on Cohort 6 of (ZUMA-1) study for Yescarta to evaluate the effects of prophylactic use of corticosteroids & earlier treatment with corticosteroids or tocilizumab & prophylactic levetiracetam on the incidence & severity of CRS & neurologic events
- The results showed no grade ≥3 CRS events in 0% (0/39) over 13% (14/108) in the cohorts 1/2, grade ≥3 neurologic events in 13% (5/39) vs 31% (33/108), 1 patient experienced a late-onset grade 5 event while 68% of patients had no CRS or neurologic events within 72hrs.
- Yescarta is 1st CAR T-cell therapy to be approved in the US for r/r LBCL & is currently under US FDA & EMA’s review for use as an earlier treatment for 2L r/r LBCL
Ref: Gilead | Image: Industry Pharmacist Organization
Click here to read the full press release
This content piece was prepared by our former Senior Editor. She had expertise in life science research and was an avid reader. For any query reach out to us at connect@pharmashots.com