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NEW PROVIDENCE, N.J. & DÜSSELDORF, Germany--(BUSINESS WIRE)--Edge Therapeutics announced today positive preliminary results from the first human use of EG-1962, the Company’s novel bioabsorbable nimodipine microparticle formulation for the prevention of delayed cerebral ischemia (DCI), a life-threatening complication of subarachnoid hemorrhage (SAH), typically resulting from a ruptured brain aneurysm or traumatic brain injury. There are approximately 90,000 patients in North America and Europe who are at risk for DCI, most of whom would be candidates for EG-1962.
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