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Sandoz Group AG

Sandoz Group AG logo
🇨🇭Switzerland
Ownership
Public
Established
1986-01-01
Employees
20K
Market Cap
$19B
Website
http://www.sandoz.com

Clinical Trials

139

Active:1
Completed:123

Trial Phases

5 Phases

Phase 1:85
Phase 2:1
Phase 3:36
+2 more phases

Drug Approvals

52

SFDA:51
FDA:1

Drug Approvals

Proventil HFA

Approval Date
Jun 14, 2023
FDA

Clinical Trials

Distribution across different clinical trial phases (133 trials with phase data)• Click on a phase to view related trials

Phase 1
85 (63.9%)
Phase 3
36 (27.1%)
Not Applicable
6 (4.5%)
Phase 4
5 (3.8%)
Phase 2
1 (0.8%)

An Efficacy and Safety Study With Integrated Pharmacokinetics (PK) and Pharmacodynamic (PD) Assessment to Compare the Proposed Ocrelizumab Biosimilar CYB704 and Ocrevus in Participants With Relapsing Multiple Sclerosis (RMS)

Phase 3
Recruiting
Conditions
Relapsing Multiple Sclerosis
Interventions
Biological: CYB704
Biological: Ocrevus-EU
Biological: Ocrevus-US
First Posted Date
2025-02-26
Last Posted Date
2025-07-29
Lead Sponsor
Sandoz
Target Recruit Count
518
Registration Number
NCT06847724
Locations
🇵🇱

Sandoz Investigational Site, Warsaw, Poland

Integrated PK/efficacy, safety, and immunogenicity study to demonstrate similarity of JPB898, a proposed biosimilar to nivolumab, to Opdivo® in combination with Yervoy®

Phase 3
Suspended
Conditions
Advanced (unresectable/metastatic) melanoma
Interventions
Drug: JPB898 (Induction and Maintenance)
Drug: Opdivo-EU (Induction)
Drug: Opdivo-US (Induction)
Drug: Yervoy-EU (Induction)
Drug: Opdivo-EU (Maintenance)
First Posted Date
2024-09-19
Last Posted Date
2025-08-07
Lead Sponsor
H e x a l AG
Target Recruit Count
302
Registration Number
2023-507865-24-00
Locations
🇨🇳

Sandoz Investigational Site, Taoyuan City, Taiwan

A Study to Compare Efficacy, Safety, and Immunogenicity of GME751 and EU-authorized Keytruda in Adult Participants With Untreated Metastatic Non-squamous Non-small Cell Lung Cancer (NSCLC)

Phase 3
Suspended
Conditions
Metastatic NSCLC
Interventions
Drug: Keytruda-EU
First Posted Date
2023-12-07
Last Posted Date
2025-07-08
Lead Sponsor
Sandoz
Target Recruit Count
720
Registration Number
NCT06159790
Locations
🇻🇳

Sandoz Investigational Site, Hà Nội, Vietnam

A PK Study to Compare GME751 (Proposed Pembrolizumab Biosimilar) and US-licensed and EU-authorized Keytruda® in Participants With Stage II and III Melanoma

Phase 1
Recruiting
Conditions
Melanoma
Interventions
First Posted Date
2023-12-01
Last Posted Date
2025-07-09
Lead Sponsor
Sandoz
Target Recruit Count
318
Registration Number
NCT06153238
Locations
🇹🇷

Sandoz Investigational Site, Yüreğir, Turkey

Study to Compare the Pharmacokinetics of Fixed-Dose Combination of Mometasone + Azelastine Nasal Spray to Mometasone and Azelastine Nasal Sprays in Adolescents and Young Adults With Seasonal Allergic Rhinitis

Phase 1
Terminated
Conditions
Seasonal Allergic Rhinitis
Interventions
First Posted Date
2023-06-05
Last Posted Date
2023-09-28
Lead Sponsor
Sandoz
Target Recruit Count
38
Registration Number
NCT05887843
Locations
🇨🇦

Sandoz Investigational Site, Toronto, Ontario, Canada

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