Clinical trial
A Phase 2 Double Blinded, Randomized, Placebo Controlled Dose Escalation Study to Evaluate the Efficacy and the Safety of GM602 in Patients With Acute Middle Cerebral Artery Ischemic Stroke Within an 18-hour Treatment Window
NCT01221246 is registered in ClinicalTrials.gov with Genervon Biopharmaceuticals, LLC as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase 2 Double Blinded, Randomized, Placebo Controlled Dose Escalation Study to Evaluate the Efficacy and the Safety of GM602 in Patients With Acute Middle Cerebral Artery Ischemic Stroke Within an 18-hour Treatment Window
- Lead sponsor
- Genervon Biopharmaceuticals, LLC
- Phase
- Phase 2
- Overall status
- Completed
- Start date
- March 8, 2011
- Completion date
- July 7, 2016
- Enrollment
- 34 (actual)
- Sites
- 8
Conditions
As the registry lists them; a condition with its own page is linked.