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Elahere: which risks did reviewers probe?

mirvetuximab soravtansine · FRα
Immune & cytokine safety
No ADA in any monkey up to 8 mg/kg; bone marrow and lymphoid depletion; no stand-alone immunotox
“All monkeys administered mirvetuximab soravtansine at doses up to 8 mg/kg/dose tested negative for the presence of anti-drug antibodies (ADAs).”
✓ VerifiedFDA multi-discipline review, p. 38Source ↗
Biodistribution & persistence
Rat radiolabel: liver, bone marrow, lung, kidney, spleen highest; slow ocular clearance; testis penetration; brain <3%; fecal elimination
“The eye:plasma ratio increased through the duration of the study, suggesting that drug clearance from the eyes was slower than from plasma.”
✓ VerifiedFDA multi-discipline review, p. 38Source ↗
Modality-specific risk
DM4 payload ocular toxicity (corneal degeneration/keratopathy) plus myelosuppression and skin toxicity; dedicated rabbit ocular studies
“Due to ocular toxicities observed in both animal toxicity studies and in patients, the Applicant also conducted GLP compliant repeated-dose toxicity studies to evaluate ocular toxicity of mirvetuximab soravtansine in male rabbits.”
✓ VerifiedFDA multi-discipline review, p. 39Source ↗

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

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

Polivy

polatuzumab vedotin · CD79b
Surrogate ADC depleted B cells (expected pharmacology); ADA in monkeys without exposure impact

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 →