Nonclinical precedent Request an invite
Flexibility accepted
DARTAcceptedBeyond the letter
No embryo-fetal development study; literature and nonclinical data risk assessment instead
Why: Consistent with previous CHMP conclusions for other bispecific antibodies of this class · Class precedent · Weight of evidence
“Embryo-fetal developmental toxicology studies were not conducted with odronextamab. A risk assessment based on available nonclinical data and literature was provided. This approach is agreed and is in line with previous CHMP conclusions on other members of this class of bispecific antibodies.”
✓ VerifiedEMA assessment report, p. 37Source ↗
SpeciesVerdict not stated
Monkey, the only relevant species, binds CD3 about 100-fold more weakly than human, possibly explaining lower cytokine responses than in humans
“Whereas the binding of CD20 was within the same concentration range for both human and monkey, there was approximately a 100-fold difference with respect to human and monkey CD3. This observed difference indicates a higher affinity for human CD3 which might be the cause of the observed discrepancy between cytokine levels observed in human and in cynomolgus, respectively.”
✓ VerifiedEMA assessment report, p. 36Source ↗

Same question, other multispecifics

Bizengri

zenocutuzumab · HER2 x HER3
No reproductive or developmental toxicity studies; literature-based weight-of-evidence assessment of HER2/HER3 inhibition instead

Blincyto

blinatumomab · CD19 x CD3
Chimpanzee the only relevant species; limited non-terminal chimpanzee studies plus mouse studies with murine surrogate muS103new

Columvi

glofitamab · CD20 x CD3
No repeat-dose study longer than 4 weeks; 13-week monkey study waived

Elrexfio

elranatamab · BCMA x CD3
No reproductive or developmental toxicity studies; reproductive organs assessed in the 3-month study in sexually mature monkeys

Epkinly

epcoritamab · CD20 x CD3
No 3-month monkey study; exposure could not be maintained with repeated dosing

Hemlibra

emicizumab · FIXa x FX
No carcinogenicity studies for a chronic prophylactic antibody; written carcinogenicity assessment used instead

Imdelltra

tarlatamab · DLL3 x CD3
Monkey used as the only toxicology species although DLL3 is intracellular in normal tissues, so toxicity may be underrepresented

Kimmtrak

tebentafusp · CD3 x gp100 (TCR fusion)
No in vivo toxicology; all toxicology in vitro with human tissues and cells (no relevant species for HLA-restricted TCR and human CD3)

Korjuny

catumaxomab · EpCAM x CD3
No pharmacologically relevant species; limited single-dose studies plus partially active murine surrogate BiLu

Lunsumio

mosunetuzumab · CD20 x CD3
Monkey embryo-fetal and pre-/postnatal development study waived; weight-of-evidence assessment using other anti-CD20 antibodies

Lynozyfic

linvoseltamab · BCMA x CD3
Planned 26-week monkey study shortened after declining body condition in all dose groups; no 26-week study

Removab

catumaxomab · EpCAM x CD3
No relevant species: no repeat-dose, genotoxicity, carcinogenicity or reproductive toxicity studies submitted

Rybrevant

amivantamab · EGFR x MET
No embryo-fetal development study; weight-of-evidence assessment of reproductive and embryo-fetal risk instead

Talvey

talquetamab · GPRC5D x CD3
No cross-reactivity of talquetamab with monkey GPRC5D; pivotal monkey toxicology used a surrogate tool molecule (JNJ-64024701)

Tecvayli

teclistamab · BCMA x CD3
Only a 5-week repeat-dose monkey study; no 13-week study

Vabysmo

faricimab · VEGF-A x Ang-2
No rodent carcinogenicity studies for a chronic ophthalmic product; weight-of-evidence assessment instead

Ziihera

zanidatamab · HER2 x HER2 (biparatopic)
No reproductive and developmental toxicity studies; HER2-antibody class weight-of-evidence assessment instead

Summary across all 18 multispecifics →