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ALEXION PHARMACEUTICALS AUSTRALASIA PTY LTD

🇦🇺Australia
Ownership
-
Employees
-
Market Cap
-
Website

Clinical Trials

3

Active:1
Completed:0

Trial Phases

1 Phases

Phase 2:3

Drug Approvals

16

TGA:16

Drug Approvals

VOYDEYA 50 + 100 mg film-coated tablets, composite bottle pack (416091)

Product Name
VOYDEYA 50 + 100 mg film-coated tablets, composite bottle pack
Approval Date
Nov 25, 2024
TGA

VOYDEYA 50 + 100 mg film-coated tablets, composite blister pack (416092)

Product Name
VOYDEYA 50 + 100 mg film-coated tablets, composite blister pack
Approval Date
Nov 25, 2024
TGA

VOYDEYA danicopan 100 mg film-coated tablets, bottle (416090)

Product Name
VOYDEYA danicopan 100 mg film-coated tablets, bottle
Approval Date
Nov 25, 2024
TGA

VOYDEYA danicopan 100 mg film-coated tablets, blister pack (416093)

Product Name
VOYDEYA danicopan 100 mg film-coated tablets, blister pack
Approval Date
Nov 25, 2024
TGA

KOSELUGO selumetinib 25 mg capsule bottle (345972)

Product Name
KOSELUGO selumetinib 25 mg capsule bottle
Approval Date
Dec 2, 2021
TGA

KOSELUGO selumetinib 10 mg capsule bottle (345973)

Product Name
KOSELUGO selumetinib 10 mg capsule bottle
Approval Date
Dec 2, 2021
TGA

ULTOMIRIS ravulizumab rch 300 mg in 3 mL (100 mg/mL) concentrated solution for injection by intravenous infusion vial (330566)

Product Name
ULTOMIRIS ravulizumab rch 300 mg in 3 mL (100 mg/mL) concentrated solution for injection by intravenous infusion vial
Approval Date
Mar 23, 2021
TGA

ULTOMIRIS ravulizumab rch 1100 mg in 11 mL (100 mg/mL) concentrated solution for injection by intravenous infusion vial (336710)

Product Name
ULTOMIRIS ravulizumab rch 1100 mg in 11 mL (100 mg/mL) concentrated solution for injection by intravenous infusion vial
Approval Date
Mar 23, 2021
TGA

ULTOMIRIS ravulizumab rch 10 mg/mL concentrated solution for intravenous infusion vial (311926)

Product Name
ULTOMIRIS ravulizumab rch 10 mg/mL concentrated solution for intravenous infusion vial
Approval Date
Oct 17, 2019
TGA

KANUMA sebelipase alfa rce 2 mg/mL injection intravenous infusion vial (274498)

Product Name
KANUMA sebelipase alfa rce 2 mg/mL injection intravenous infusion vial
Approval Date
May 18, 2017
TGA
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Clinical Trials

Distribution across different clinical trial phases (3 trials with phase data)• Click on a phase to view related trials

Phase 2
3 (100.0%)
No trials found

News

No news found

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