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STADA Arzneimittel AG

STADA Arzneimittel AG logo
🇩🇪Germany
Ownership
Subsidiary
Established
1895-01-01
Employees
11.6K
Market Cap
-
Website
http://www.stada.com

Clinical Trials

2

Active:2
Completed:0

Trial Phases

1 Phases

Phase 1:2

Drug Approvals

34

CIMA_AEMPS:19
EMA:11
PHILIPPINES:4

Drug Approvals

Uzpruvo

Authorization Status
Authorised
Approval Date
Jan 5, 2024
EMA

Ximluci

Authorization Status
Authorised
Approval Date
Nov 9, 2022
EMA

Kinpeygo

Authorization Status
Authorised
Approval Date
Jul 15, 2022
EMA

Hukyndra

Authorization Status
Authorised
Approval Date
Nov 15, 2021
EMA

Hukyndra

Authorization Status
Authorised
Approval Date
Nov 15, 2021
EMA

Libmyris

Authorization Status
Authorised
Approval Date
Nov 12, 2021
EMA

Libmyris

Authorization Status
Authorised
Approval Date
Nov 12, 2021
EMA

Libmyris

Authorization Status
Authorised
Approval Date
Nov 12, 2021
EMA

Oyavas

Authorization Status
Authorised
Approval Date
Mar 26, 2021
EMA

Movymia

Authorization Status
Authorised
Approval Date
Jan 11, 2017
EMA
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Clinical Trials

Distribution across different clinical trial phases (2 trials with phase data)• Click on a phase to view related trials

Phase 1
2 (100.0%)
No trials found

News

Alvotech Appoints Linda Jónsdóttir as Chief Financial Officer

Alvotech, a global biosimilar medicines company, has appointed Linda Jónsdóttir as Chief Financial Officer, bringing 15 years of senior leadership experience from Marel food processing technology company.

Alvotech Acquires Swiss Packaging Specialist Ivers-Lee to Expand Biosimilar Manufacturing Capacity

Alvotech has acquired Ivers-Lee Group, a Swiss family-owned pharmaceutical packaging company founded in 1947, to expand its assembly and packaging capabilities ahead of three new biosimilar launches in 2025.

Alvotech Expands European Presence with Successful Nasdaq Stockholm Listing

Alvotech's Swedish Depository Receipts (SDRs) offering was multiple times oversubscribed, attracting over 3,000 new shareholders and raising approximately SEK 39 million.

EMA Accepts Bio-Thera's Marketing Application for BAT2506, First Chinese-Developed Golimumab Biosimilar

Bio-Thera Solutions achieves milestone as the European Medicines Agency accepts marketing application for BAT2506, marking the first golimumab biosimilar from a Chinese company submitted for EU approval.

EMA Accepts Alvotech's Biosimilar AVT03 for Prolia and Xgeva

The European Medicines Agency (EMA) has accepted Alvotech's Marketing Authorization Application for AVT03, a biosimilar candidate to Prolia and Xgeva.

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