Glybera
alipogene tiparvovec · LPL (AAV1)Not explicitly justified; clinical 1x10^12 gc/kg lies within active range in LPL-/- mice (10^11-10^13); tox covered 10x
The public FDA and EMA reviews of Zevaskyn don't say how the first human dose was chosen. That rationale is in the IND, which is confidential, so it is missing for most approved products.
FDA expects preclinical proof-of-concept and toxicology studies to identify active dose levels and support the choice of starting dose and escalation. The 2013 guidance gives no numeric formula or scaling rule for the starting dose.
NOAEL / key findings: No gross or histopathological findings in any tissue, including explanted products; no NOAEL stated (FDA summary basis for approval, p. 13)