Relfovetmab

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Relfovetmab
Monoclonal antibody
TypeWhole antibody
TargetNerve growth factor (NGF)
Clinical data
Trade namesPortela
Other namesZTS-00084768
Routes of
administration
Subcutaneous
ATCvet code
Legal status
Legal status
Identifiers
CAS Number
UNII
E number{{#property:P628}}
CompTox Dashboard (EPA)
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Chemical and physical data
FormulaC6580H10118N1760O2038S46
Molar mass147964.37 g·mol−1

Relfovetmab, sold under the brand name Portela, is a felinized monoclonal antibody for the alleviation of pain associated with osteoarthritis in cats.[3] Relfovetmab targets nerve growth factor.[3] Nerve growth factor binds to TrkA receptors located on immune cells to elicit the release of additional proinflammatory mediators, including nerve growth factor itself.[2] These inflammatory mediators lead to further peripheral sensitization involved in pain perception.[2] The inhibition of nerve growth factor was demonstrated to provide relief from pain associated with osteoarthritis.[2]

Relfovetmab was authorized for veterinary use in the European Union in October 2025,[4] and in Canada in December 2025.[5]

Medical uses

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Relfovetmab is indicated for the alleviation of pain associated with osteoarthritis in cats.[6]

Society and culture

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In September 2025, the Committee for Veterinary Medicinal Products of the European Medicines Agency adopted a positive opinion, recommending the granting of a marketing authorization for the veterinary medicinal product Portela, solution for injection, intended for cats.[2] The applicant for this veterinary medicinal product is Zoetis Belgium.[2] Relfovetmab was authorized for veterinary use in the European Union in October 2025.[4]

Relfovetmab was authorized for veterinary use in Canada in December 2025.[5]

Names

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Relfovetmab is the international nonproprietary name.[7]

Relfovetmab is sold under the brand name Portela.[4][5]

References

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  2. ^ a b c d e f Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value). Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
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