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WB confirmed the upregulated p-Akt

Adverse reactions for the 1.28 mg dose (11.6 mg/vial formulation) of EGRIFTA WR are expected to be similar to those observed with the 2 mg dose (1 mg/vial formulation) of EGRIFTA [see Clinical Pharmacology (12.3)]

Follow-up testing usually occurs 612 weeks after initial dosing

The NAD connection: sustained NAD availability from NNMT inhibition has downstream effects that are not fully mapped across cell types

Everything the B12 injection does, plus fat metabolism support, liver function optimization, and insulin sensitization

Multi-route: After reconstitution, the resulting mixture can be administered IV, IM, or SC per the drugs instructions