“In a human whole blood assay, durvalumab did not induce the release of any cytokine”
✓ VerifiedFDA pharmacology/toxicology review, p. 63Source ↗
Biodistribution & persistence
Volume of distribution 40.5-73.0 mL/kg, consistent with residence mainly in plasma volume
“the volume of distribution is in the range of 40.5 to 73.0 mL/kg, which is expected for large protein molecules as these primarily resides in the plasma volume”
Immune-mediated toxicity: multi-organ arteritis/periarteritis and inflammatory cell infiltration (PD-L1 role in peripheral tolerance)
“Intravenous (IV) administration of durvalumab caused multi-organ arteritis/periarteritis and inflammatory cell infiltration. The immune-mediated findings were consistent with the role of PD-L1 in regulating and maintaining peripheral tolerance.”
✓ VerifiedFDA pharmacology/toxicology review, p. 4Source ↗
Anti-drug antibodies: animals
ADAs in monkeys with variable impact on PK; ADA-affected animals excluded from PK summaries
“The presence of ADA had variable impact on pharmacokinetics and PK data from animals with obvious impact of ADAs were excluded from summary statistics calculations.”
Treatment-emergent ADA 3.6% (199/5,562); 8.5% of these neutralizing
“3.6% (199/5,562) of evaluable patients tested positive for treatment-emergent anti-durvalumab antibodies, and 8.5% (17/199) of treatment-emergent ADA positive patients had neutralizing antibodies against durvalumab.”
In vitro whole-blood cytokine release far below alemtuzumab/TGN1412 controls; no effects on monkey TDAR, lymphocyte subsets or serum cytokines; ADA in some monkeys