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Polivy: which risks did reviewers probe?

polatuzumab vedotin · CD79b
Immune & cytokine safety
Surrogate ADC depleted B cells (expected pharmacology); ADA in monkeys without exposure impact
“Anti-drug-antibodies to polatuzumab vedotin or the surrogate ADC did not appear to impact exposure at any dose level and the toxicokinetic (TK) profiles were similar between ADA-positive and ADA-negative animals.”
✓ VerifiedFDA pharmacology/toxicology review, p. 12Source ↗
Biodistribution & persistence
Rat: non-specific distribution to highly perfused tissues peaking ~2 h; MMAE eliminated >95% in feces
“In a combined distribution and elimination study, MMAE and MMAE-related catabolites of polatuzumab vedotin were primarily eliminated through the hepatobiliary pathway in rats: >95% in feces, ~5% in urine.”
✓ VerifiedFDA pharmacology/toxicology review, p. 11Source ↗
Modality-specific risk
MMAE payload toxicity: myelosuppression, hepatotoxicity, testicular toxicity, genotoxicity; target-mediated B-cell depletion
“Toxicity of polatuzumab vedotin and MMAE observed in rats and Cynomolgus monkeys is consistent with the expected toxicity of a tubulin-binding agent, causing arrest of the cell cycle and apoptosis especially in rapidly dividing tissues.”
✓ VerifiedEMA assessment report, p. 55Source ↗

Same question, other ADCs

Adcetris

brentuximab vedotin · CD30
Anti-drug antibodies (PAHA) in monkeys reduced ADC exposure but increased MMAE exposure without added toxicity

Besponsa

inotuzumab ozogamicin · CD22
Low ADA incidence in rats (10-13%); no ADA detected in monkeys

Datroway

datopotamab deruxtecan · Trop-2
ADA in 5/6 monkeys at 10 mg/kg reducing exposure; minimal in vitro cytokine release; transient CRP increases

Decnupaz

pivekimab sunirine · CD123
ADA in monkeys reduced exposure; thymic lymphoid depletion and lymphopenia; ADCC present in vitro

Elahere

mirvetuximab soravtansine · FRα
No ADA in any monkey up to 8 mg/kg; bone marrow and lymphoid depletion; no stand-alone immunotox

Emrelis

telisotuzumab vedotin · c-Met
No substantial cytokine release from human PBMC; no ADA in 13-week monkey study; low C1q, no complement activation

Enhertu

fam-trastuzumab deruxtecan · HER2
No treatment-emergent ADA in rat or monkey studies; ADCC activity retained in vitro

Kadcyla

ado-trastuzumab emtansine · HER2
No ADA detected after single dose in monkey safety pharmacology study; ADA assessed across monkey studies

Mylotarg

gemtuzumab ozogamicin · CD33
ADA in rats (reduced exposure) and some monkeys; marked eosinophilia and hypersensitivity reactions in monkeys

Padcev

enfortumab vedotin · Nectin-4
ADA in rats and monkeys reduced exposure on repeat dosing; no ADCC/CDC, ADCP activity in vitro

Tivdak

tisotumab vedotin · Tissue factor
ADA in most monkeys after repeat dosing, reduced exposure in some; immunotoxic potential minimal

Trodelvy

sacituzumab govitecan · Trop-2
ADA in all monkeys at all doses in 13-week study, reducing low-dose exposure; reduced thymic/lymphoid cellularity

Zynlonta

loncastuximab tesirine · CD19
Pro-inflammatory responses (WBC, fibrinogen, multi-organ inflammation) typical of PBD ADCs; ADA in few monkeys

Summary across all 14 ADCs →