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EG-1962

microparticle formulation of nimodipine and poly(DL-lactide-co-glycolide) (PLGA) suspended in sodium hyaluronate
Networked: 5 relevant articles (0 outcomes, 4 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Etminan, Nima: 5 articles (12/2020 - 01/2015)
2. Hänggi, Daniel: 5 articles (12/2020 - 01/2015)
3. Macdonald, R Loch: 5 articles (12/2020 - 01/2015)
4. Diringer, Michael N: 4 articles (12/2020 - 01/2017)
5. Mayer, Stephan A: 4 articles (12/2020 - 01/2017)
6. Ng, David: 3 articles (12/2020 - 01/2019)
7. Faleck, Herbert J: 3 articles (01/2020 - 01/2017)
8. NEWTON Investigators: 3 articles (01/2020 - 01/2017)
9. Aldrich, E Francois: 2 articles (12/2020 - 01/2019)
10. Bleck, Thomas: 2 articles (12/2020 - 01/2020)

Related Diseases

1. Subarachnoid Hemorrhage (Aneurysmal Subarachnoid Hemorrhage)
12/15/2020 - "NEWTON-2 Cisternal (Nimodipine Microparticles to Enhance Recovery While Reducing Toxicity After Subarachnoid Hemorrhage): A Phase 2, Multicenter, Randomized, Open-Label Safety Study of Intracisternal EG-1962 in Aneurysmal Subarachnoid Hemorrhage."
01/01/2020 - "A randomized, open-label, phase 1/2a, dose-escalation study provided impetus for this study to evaluate efficacy and safety of a single intraventricular 600 mg dose of EG-1962 to patients with aneurysmal subarachnoid hemorrhage, compared with standard of care oral nimodipine. "
01/01/2019 - "Clinical Trial Protocol: Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Efficacy, and Safety Study Comparing EG-1962 to Standard of Care Oral Nimodipine in Adults with Aneurysmal Subarachnoid Hemorrhage [NEWTON-2 (Nimodipine Microparticles to Enhance Recovery While Reducing TOxicity After SubarachNoid Hemorrhage)]."
01/01/2015 - "The NEWTON (Nimodipine microparticles to Enhance recovery While reducing TOxicity after subarachNoid hemorrhage) trial is a phase 1/2a multicenter, controlled, randomized, open-label, dose-escalation, safety, tolerability, and pharmacokinetic study comparing EG-1962 and nimodipine in patients with aneurysmal SAH. "
01/01/2015 - "The PROMISE (Prolonged Release nimOdipine MIcro particles after Subarachnoid hemorrhage) trial is designed as an unblinded, nonrandomized, single-center, single-dose, dose-escalation safety and tolerability phase 1 study in patients surgically treated for aSAH and will investigate the effect of intracisternal EG-1962 administration. "
2. Brain Ischemia (Cerebral Ischemia)
3. Hypotension (Low Blood Pressure)
4. Cerebral Infarction

Related Drugs and Biologics

1. Nimodipine (Modus)
2. Delayed-Action Preparations

Related Therapies and Procedures

1. Therapeutics