Mirvetuximab Soravtansine
ATC L01FX26 · 8 markets · 9 records
AU 2 records · 2 strengths
- 100 mginjectionELAHERE mirvetuximab soravtansine 100 mg/20 mL concentrate solution for intravenous infusion vial
Records without a stated strength · 1 ELAHERE
US 1 records · 1 strengths
- 5 mginjectionELAHERE
GB 1 records · 1 strengths
- 100 mg/20 mLinjectionElahere 100mg/20ml concentrate for solution for infusion vials
CA 1 records · 1 strengths
- 5 mg/1 mLliquidELAHERE
SG 1 records · 1 strengths
- 100 mg/20 mLinjectionELAHERE CONCENTRATE FOR SOLUTION FOR INFUSION 100MG/20ML
ES 1 records · 1 strengths
- 5 mg/1 mLinjectionELAHERE
TW 1 records · 1 strengths
- 5 mginjectionELAHERE solution for infusion 5 mg/mL艾樂延靜脈輸注液5 mg/mL
EU 1 records · 1 strengths
EU centralised authorisation (EMA) — Authorised at EU level — not a record of sale in any single country. The EU register carries no strength, dosage form or pack size.
Records without a stated strength · 1 ELAHERE
| Strength / form / release | US | GB | CA | AU | SG | ES | TW | EU |
|---|---|---|---|---|---|---|---|---|
| 5 mg injection | ELAHERE | ELAHERE solution for infusion 5 mg/mL 艾樂延靜脈輸注液5 mg/mL | ||||||
| 100 mg/20 mL injection | Elahere 100mg/20ml concentrate for solution for infusion vials | ELAHERE CONCENTRATE FOR SOLUTION FOR INFUSION 100MG/20ML | ||||||
| 5 mg/1 mL liquid | ELAHERE | |||||||
| 100 mg injection | ELAHERE mirvetuximab soravtansine 100 mg/20 mL concentrate solution for intravenous infusion vial | |||||||
| 5 mg/1 mL injection | ELAHERE | |||||||
unknown | ELAHERE | ELAHERE |
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Each country column shows the locally registered trade names — not translations.
3 more strength/form rows are recorded only in GB · CA · SG · ES and are not shown in this table. Hay 3 filas de concentración/forma registradas solo en GB · CA · SG · ES que no se muestran en esta tabla. 另有 3 个规格/剂型仅在 GB · CA · SG · ES 有记录(未在本表显示)。 另有 3 個規格/劑型僅在 GB · CA · SG · ES 有記錄(未在本表顯示)。
“not disclosed” means the source does not publish the strength — it does not mean the product has none.
Australia ARTG data has no registration-status column, so status is shown as unknown; being on the register does not mean currently marketed.
EU centralised authorisation (EMA) — Authorised at EU level — not a record of sale in any single country. The EU register carries no strength, dosage form or pack size.
Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.