Glofitamab

ATC L01FX28 · 9 markets · 18 records

Glofitamab 9 markets · 18 records Forms

AU 5 records · 5 strengths

10 mg/10 mLinjectionColumvi also in GB
10 mginjectionCOLUMVI glofitamab (rch) 2.5 mg/2.5 mL concentrated solution for infusion vial also in ES unknown
2.5 mg/2.5 mLinjectionColumvi also in GB
2.5 mginjectionCOLUMVI glofitamab (rch) 2.5 mg/2.5 mL concentrated solution for infusion vial also in ES unknown

Records without a stated strength · 1 Columvi

US 2 records · 2 strengths

10 mg/10 mLliquidColumvi
2.5 mg/2.5 mLliquidColumvi

GB 2 records · 2 strengths

10 mg/10 mLinjectionColumvi 2.5mg/2.5ml concentrate for solution for infusion vials also in AU
2.5 mg/2.5 mLinjectionColumvi 2.5mg/2.5ml concentrate for solution for infusion vials also in AU

CA 2 records · 1 strengths

1 mg/1 mLliquidColumvi

ES 2 records · 2 strengths

10 mginjectionColumvi also in AU
2.5 mginjectionColumvi also in AU

HK 2 records · 1 strengths

Records without a stated strength · 1 COLUMVI CONCENTRATE FOR SOLUTION FOR INFUSION 10MG/10ML

SG 1 records · 1 strengths

1 mg/mLinjectionCOLUMVI CONCENTRATE FOR SOLUTION FOR INFUSION 1MG/ML

TW 1 records · 1 strengths

Records without a stated strength · 1 Columvi solution for infusion、利癌妥注射劑

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 Columvi

Side-by-side table

Strength / form / release	US	GB	CA	AU	SG	ES	TW	HK	EU
10 mg/10 mL injection	not recorded	Columvi 2.5mg/2.5ml concentrate for solution for infusion vials	not recorded	Columvi	not recorded	not recorded	not recorded	not recorded	not recorded
10 mg injection	not recorded	not recorded	not recorded	COLUMVI glofitamab (rch) 2.5 mg/2.5 mL concentrated solution for infusion vial	not recorded	Columvi	not recorded	not recorded	not recorded
2.5 mg/2.5 mL injection	not recorded	Columvi 2.5mg/2.5ml concentrate for solution for infusion vials	not recorded	Columvi	not recorded	not recorded	not recorded	not recorded	not recorded
2.5 mg injection	not recorded	not recorded	not recorded	COLUMVI glofitamab (rch) 2.5 mg/2.5 mL concentrated solution for infusion vial	not recorded	Columvi	not recorded	not recorded	not recorded
10 mg/10 mL liquid	Columvi	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded
2.5 mg/2.5 mL liquid	Columvi	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded
1 mg/1 mL liquid	not recorded	not recorded	Columvi	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded
1 mg/mL injection	not recorded	not recorded	not recorded	not recorded	COLUMVI CONCENTRATE FOR SOLUTION FOR INFUSION 1MG/ML	not recorded	not recorded	not recorded	not recorded
not disclosed unknown	not recorded	not recorded	not recorded	Columvi	not recorded	not recorded	not recorded	COLUMVI CONCENTRATE FOR SOLUTION FOR INFUSION 10MG/10ML	Columvi
not disclosed injection	not recorded	not recorded	not recorded	not recorded	not recorded	not recorded	Columvi solution for infusion 利癌妥注射劑	not recorded	not recorded

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Each country column shows the locally registered trade names — not translations.

3 more strength/form rows are recorded only in CA · SG · TW and are not shown in this table. Hay 3 filas de concentración/forma registradas solo en CA · SG · TW que no se muestran en esta tabla. 另有 3 个规格/剂型仅在 CA · SG · TW 有记录（未在本表显示）。另有 3 個規格/劑型僅在 CA · SG · TW 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.

Hong Kong records are name/ingredient-level only: no strength, dosage form or registration status; on the register does not prove current supply.

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.

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The same ingredient can carry completely different brand names in different countries, and the same name can point to a different ingredient. Listed by country — not interchangeable.

Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.