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Extensive published preclinical research, primarily from rat and mouse models

Typical cycle: 48 weeks

View FDA listings: AVE Continues to Update FDA Listings AVE has completed FDA establishment registration (Registration Number: 3031915160)

We agree with the RUC and we proposed naming changes for the following supplies and equipment items: EQ392: We proposed to rename the heart failure patient physiologic monitoring equipment package to patient physiologic monitoring equipment package

RGN-352 was shown to be safe and well-tolerated with no serious drug-related adverse events reported (PMID: 20536472) Phase 2 AMI trial (incomplete): RegeneRx designed a Phase 2 proof-of-concept trial (NCT01311518) to evaluate RGN-352 in approximately 75 patients with acute ST-segment elevation myocardial infarction (heart attack)

Improved Mood and Focus: Adequate B12 levels are associated with better cognitive function and mood regulation