Spinogenix receives FDA Fast Track Designation for tazbentetol in ALS
This enables expedited development following Phase 2a results showing slowed decline in patients. The company continues its Expanded Access Program.
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Biotechnology company developing synapse-restoring therapeutics for brain disorders
spinogenix.comLast updated
In short: Spinogenix advanced its pipeline with positive trial data and milestones across Alzheimer's, ALS, schizophrenia, and Fragile X.
This enables expedited development following Phase 2a results showing slowed decline in patients. The company continues its Expanded Access Program.
The study shows simultaneous EEG and cognitive improvements in FXS patients. SPG601 has FDA Fast Track and plans for Phase 2b/3 trial.
The drug demonstrates disease-modifying potential in the study.
Tazbentetol showed rapid SMMSE gains, sustained benefits in CDR-SB and ADL, favorable safety, and EEG evidence of brain activity improvement.
Spinogenix, Inc., a clinical-stage biopharmaceutical company pioneering first-in-class therapeutics designed to restore synapses to improve the lives of patients, is initiating CLARITY, a Phase 2b/3...
Spinogenix’s once-daily oral therapy has shown potential to offer disease-modifying benefits during a Phase IIa study in Alzheimer’s disease. Image credit: Nefedova Tanya via Shutterstock.com.
The MarketWatch News Department was not involved in the creation of this content. Tazbentetol, a Potential First-in-Class, Oral Synaptic Regenerative Investigational Therapy, Showed a Favorable...
Spinogenix is progressing its lead candidate, SPG302, to a registrational trial following the...
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