Clinical trial
Efficacy and Safety of Bumetanide Oral Liquid Formulation in Children Aged From 2 to Less Than 7 Years Old With Autism Spectrum Disorder. A 6-month Randomised, Double-blind, Placebo Controlled Multicentre Parallel Group Study to Evaluate Efficacy and Safety of Bumetanide 0.5mg Twice a Day Followed by an Open Label Active 6-month Treatment Period With Bumetanide (0.5mg Twice a Day) and a 6 Weeks Discontinuation Period After Treatment Stop.
NCT03715153 is registered in ClinicalTrials.gov with Institut de Recherches Internationales Servier as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Efficacy and Safety of Bumetanide Oral Liquid Formulation in Children Aged From 2 to Less Than 7 Years Old With Autism Spectrum Disorder. A 6-month Randomised, Double-blind, Placebo Controlled Multicentre Parallel Group Study to Evaluate Efficacy and Safety of Bumetanide 0.5mg Twice a Day Followed by an Open Label Active 6-month Treatment Period With Bumetanide (0.5mg Twice a Day) and a 6 Weeks Discontinuation Period After Treatment Stop.
- Lead sponsor
- Institut de Recherches Internationales Servier
- Phase
- Phase 3
- Overall status
- Terminated
- Start date
- October 4, 2018
- Completion date
- October 26, 2021
- Enrollment
- 211 (actual)
- Sites
- 50
Conditions
As the registry lists them; a condition with its own page is linked.
autism spectrum disorder (asd)