- Pharma
- 1 min read
Bayer withdraws follicular lymphoma drug after further trial fails
Based on a Phase II study, Aliqopa was granted accelerated approval by the FDA in 2017 for adults with follicular lymphoma whose disease had returned after at least two prior systemic therapies, but the go-ahead was contingent on further trials.
The decision follows discussions with the U.S. Food and Drug Administration, Bayer said in a statement.
Based on a Phase II study, Aliqopa was granted accelerated approval by the FDA in 2017 for adults with follicular lymphoma whose disease had returned after at least two prior systemic therapies, but the go-ahead was contingent on further trials.
In a follow-up study the FDA had required, the addition of Aliqopa to standard immunochemotherapy did not meet the target for progression-free survival when compared to the control group in patients on standard immunochemotherapy, Bayer added.
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