MedPath

ALMIRALL SA

ALMIRALL SA logo
🇪🇸Spain
Ownership
Public, Subsidiary
Established
1943-01-01
Employees
1.9K
Market Cap
-
Website
http://www.almirall.com

Clinical Trials

44

Active:38
Completed:1

Trial Phases

3 Phases

Phase 1:14
Phase 3:1
Phase 4:2

Drug Approvals

114

CIMA_AEMPS:106
NMPA:5
EMA:3

Drug Approvals

Cinitapride Hydrogen Tartrate Tablets

Product Name
希笛尼
Approval Number
国药准字HJ20160477
Approval Date
Oct 29, 2024
NMPA

Cinitapride Hydrogen Tartrate Tablets

Product Name
希笛尼
Approval Number
国药准字J20171020
Approval Date
May 25, 2020
NMPA

Cinitapride Hydrogen Tartrate Tablets

Product Name
希笛尼
Approval Number
H20170099
Approval Date
Feb 25, 2020
NMPA

Ebastine Tablets

Product Name
开思亭
Approval Number
H20140856
Approval Date
May 24, 2019
NMPA

Ebastine Tablets

Product Name
开思亭
Approval Number
H20140855
Approval Date
May 24, 2019
NMPA

Clinical Trials

Distribution across different clinical trial phases (17 trials with phase data)• Click on a phase to view related trials

Phase 1
14 (82.4%)
Phase 4
2 (11.8%)
Phase 3
1 (5.9%)
No trials found

News

FDA Approves Lilly's Ebglyss (lebrikizumab-lbkz) for Moderate-to-Severe Atopic Dermatitis

The FDA has approved Ebglyss (lebrikizumab-lbkz) for adults and children 12+ with moderate-to-severe atopic dermatitis not controlled by topical treatments.

FDA Approves Lilly's Ebglyss (lebrikizumab) for Moderate-to-Severe Atopic Dermatitis

The FDA has approved Ebglyss (lebrikizumab) for adults and children 12 years and older with moderate-to-severe atopic dermatitis not well controlled by topical treatments.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.