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Amgen, Inc.

Amgen, Inc. logo
🇺🇸United States
Ownership
Public
Established
1980-01-01
Employees
26.7K
Market Cap
$175.6B
Website
http://www.amgen.com

Clinical Trials

1.2k

Active:170
Completed:763

Trial Phases

6 Phases

Early Phase 1:2
Phase 1:365
Phase 2:256
+3 more phases

Drug Approvals

3

FDA:3

Drug Approvals

XGEVA

Approval Date
Sep 16, 2025
FDA

TEZSPIRE

Approval Date
May 26, 2023
FDA

NEUPOGEN

Approval Date
Apr 18, 2023
FDA

Clinical Trials

Distribution across different clinical trial phases (1015 trials with phase data)• Click on a phase to view related trials

Phase 1
365 (36.0%)
Phase 3
299 (29.5%)
Phase 2
256 (25.2%)
Phase 4
78 (7.7%)
Not Applicable
14 (1.4%)
Early Phase 1
2 (0.2%)
phase_1_2
1 (0.1%)

A Rollover Study Evaluating Sotorasib With or Without Panitumumab in Participants With KRAS p.G12C Mutation

Not Applicable
Not yet recruiting
Conditions
Advanced Solid Tumors
Interventions
First Posted Date
2025-09-15
Last Posted Date
2025-09-15
Lead Sponsor
Amgen
Target Recruit Count
14
Registration Number
NCT07172919

A Study to Evaluate the Effect of Maridebart Cafraglutide on Insulin Sensitivity and β-cell Function in Participants With Type 2 Diabetes Mellitus

Not Applicable
Recruiting
Conditions
Type 2 Diabetes Mellitus
Interventions
First Posted Date
2025-09-08
Last Posted Date
2025-09-25
Lead Sponsor
Amgen
Target Recruit Count
70
Registration Number
NCT07160257
Locations
🇺🇸

ProSciento, Chula Vista, California, United States

A Study to Evaluate Pharmacokinetics, Safety, and Tolerability of Teprotumumab (AMG 632) Administered Intravenously in Healthy Chinese Participants

Not Applicable
Active, not recruiting
Conditions
Healthy Volunteers
Interventions
Drug: Placebo
First Posted Date
2025-08-27
Last Posted Date
2025-09-22
Lead Sponsor
Amgen
Target Recruit Count
20
Registration Number
NCT07142642
Locations
🇨🇳

Huashan Hospital, Fudan University, Minhang, Shangai, China

Real World Evaluation of Sotorasib Among Chinese Non-Small Cell Lung Cancer Patients

Recruiting
Conditions
Non-Small Cell Lung Cancer
Interventions
First Posted Date
2025-08-27
Last Posted Date
2025-09-12
Lead Sponsor
Amgen
Target Recruit Count
115
Registration Number
NCT07143513
Locations
🇨🇳

Boao Evergrande International Hospital, Qionghai, Hainan, China

🇨🇳

Boao Super Hospital, Qionghai, Hainan, China

🇨🇳

Ruijin-Hainan Hospital Shanghai Jiao Tong University School of Medicine Hainan Boao Research Hospital, Qionghai, Hainan, China

Study Evaluating the Safety, Tolerability, and Efficacy of Xaluritamig in Combination With Androgen Receptor Pathway Inhibitors in Participants With Metastatic Hormone-sensitive Prostate Cancer

Not Applicable
Recruiting
Conditions
Metastatic Hormone-sensitive Prostate Cancer (mHSPC)
Interventions
First Posted Date
2025-08-26
Last Posted Date
2025-09-26
Lead Sponsor
Amgen
Target Recruit Count
60
Registration Number
NCT07140900
Locations
🇦🇺

Chris OBrien Lifehouse, Camperdown, New South Wales, Australia

🇦🇺

Calvary Mater Newcastle Hospital, Waratah, New South Wales, Australia

🇨🇭

Kantonsspital Graubuenden, Chur, Switzerland

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News

Crystalys Therapeutics Emerges with $205M Series A to Advance Gout Treatment Dotinurad

Crystalys Therapeutics launched with $205 million in Series A funding to develop dotinurad, a URAT1 blocker for gout treatment that is already approved in Japan, China, Philippines, and Thailand.

AstraZeneca's Tezspire Receives EU Regulatory Recommendation for Chronic Rhinosinusitis with Nasal Polyps

The European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has recommended approval of AstraZeneca and Amgen's Tezspire (tezepelumab) for treating chronic rhinosinusitis with nasal polyps in adults.

EMA Recommends Amgen's Uplizna for Rare Autoimmune Disease IgG4-RD

The European Medicines Agency's human medicines committee has recommended expanding Amgen's Uplizna (inebilizumab) indication to treat adult patients with active immunoglobulin G4-related disease (IgG4-RD).

Alnylam Pharmaceuticals Joins Alliance for Genomic Discovery to Accelerate RNAi Drug Development

Alnylam Pharmaceuticals has joined the Alliance for Genomic Discovery as the ninth member, gaining access to a comprehensive clinical genomic database containing 250,000 whole-genomes to accelerate RNA interference therapeutic development.

Ollin Biosciences Emerges with $100M to Challenge Leading Eye Disease Treatments

Ollin Biosciences launched with $100 million in Series A funding led by ARCH Venture Partners, Mubadala Capital, and Monograph Capital to develop next-generation ophthalmology treatments.

Dualitas Therapeutics Emerges from Stealth with $65M Series A to Advance Bispecific Antibody Pipeline

Dualitas Therapeutics launched from stealth with $65 million Series A funding co-led by Versant Ventures and Qiming Venture Partners USA, with participation from Eli Lilly and Company and other strategic investors.

Australian Court Denies Preliminary Injunction Against Sandoz Aflibercept Biosimilar Launch

The Federal Court of Australia denied Regeneron and Bayer's preliminary injunction application against Sandoz's aflibercept biosimilars, allowing the launch of Afqlir and Enzeevu to proceed as planned.

ALX Oncology Appoints Barbara Klencke as Interim Chief Medical Officer to Advance Cancer Pipeline

ALX Oncology has appointed Dr. Barbara Klencke as Interim Chief Medical Officer, replacing Dr. Alan Sandler who will return to the company's Board of Directors.

Samsung Biologics Secures $1.3 Billion US Manufacturing Deal Amid Trade Policy Uncertainty

Samsung Biologics has signed a $1.3 billion production contract with an unnamed US pharmaceutical company, extending through 2029.

Scenic Biotech Appoints Dr. Roland W. Bürli as Chief Scientific Officer to Advance Modifier Therapy Pipeline

Scenic Biotech has appointed Dr. Roland W. Bürli as Chief Scientific Officer, effective September 1, 2025, to lead the development of first-in-class modifier therapies for neurodegenerative and metabolic diseases.

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