ATH-1105 a Phase 1, Double-Blind, Placebo-Controlled, Single-and-Multiple-Oral-Dose, Safety, Tolerability, and Pharmacokinetic Study in Healthy Male and Female Subjects
Latest Information Update: 28 Jan 2025
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At a glance
- Drugs ATH 1105 (Primary)
- Indications Amyotrophic lateral sclerosis; Frontotemporal dementia
- Focus Adverse reactions; First in man
- Sponsors Athira Pharma
- 23 Jan 2025 Status changed from recruiting to completed.
- 17 Sep 2024 According to an Athira Pharma media release, company expects to complete the full study by year-end 2024, with a goal to begin dosing ALS patients in 2025.
- 11 Jun 2024 According to an Athira Pharma media release, the company announced it has completed the first cohort of healthy volunteers in its ongoing, first-in-human, dose escalation Phase 1 clinical study evaluating ATH-1105, Completion of this trial is expected by year-end 2024.