Annovis Bio Announces New Data from Phase III Parkinson’s Study Highlighting Improvements in Unified Parkinson's Disease Rating Scale (MDS-UPDRS) and Cognition after Treatment with Buntanetap
Changes in MMSE after treatment with 10mg or 20mg buntanetap compared to baseline and placebo Figure 1. Changes in MDS-UPDRS after treatment with 10mg or 20mg buntanetap in patients with a PD diagnosis over 3 years compared to baseline and placebo Figure 2. Changes in MDS-UPDRS after treatment with 10mg or 20mg buntanetap in patients with PIGD Figure 3. Buntanetap showed dose-dependent and statistically significant improvements in cognition in the overall enrolled PD population. Parkinson’s pati
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“We are very pleased to see improvements in many of our patients over such a short course of treatment. These compelling data reinforce our commitment to advancing buntanetap into a longer study, which will allow us not only to verify observed symptomatic improvements but also to explore buntanetap’s disease-modifying properties.”
Maria Maccecchini, Ph.D., Founder, President and CEO of Annovis Bio