AEON Biopharma Doses First Patient in Phase 2 Trial of ABP-450 for the Treatment of Cervical Dystonia
Retrieved on:
Monday, April 5, 2021
The first patient dosed in our cervical dystonia study represents an important milestone as we advance our development programs for the therapeutic uses of ABP-450, said Marc Forth, Chief Executive Officer of AEON Biopharma.
Key Points:
- The first patient dosed in our cervical dystonia study represents an important milestone as we advance our development programs for the therapeutic uses of ABP-450, said Marc Forth, Chief Executive Officer of AEON Biopharma.
- Botulinum toxin is the standard of care for the treatment of cervical dystonia, helping to improve pain, posture, and disability.
- The Phase 2 trial will evaluate the efficacy and safety of ABP-450 in adults with a clinical diagnosis of cervical dystonia.
- AEON Biopharma is a biopharmaceutical company focused on developing ABP-450 (prabotulinumtoxinA) injection for the treatment of debilitating medical conditions.