MedPath

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

1.1k

Active:168
Completed:759

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
Jan 12, 2024
FDA

TEZSPIRE

Approval Date
May 26, 2023
FDA

NEUPOGEN

Approval Date
Apr 18, 2023
FDA

Clinical Trials

Distribution across different clinical trial phases (1009 trials with phase data)• Click on a phase to view related trials

Phase 1
365 (36.2%)
Phase 3
299 (29.6%)
Phase 2
256 (25.4%)
Phase 4
78 (7.7%)
Not Applicable
8 (0.8%)
Early Phase 1
2 (0.2%)
phase_1_2
1 (0.1%)

AMG 410 Alone and in Combination With Other Agents in Participants With KRAS Altered Advanced or Metastatic Solid Tumors

Not Applicable
Not yet recruiting
Conditions
KRAS Altered Advanced or Metastatic Solid Tumors
Interventions
First Posted Date
2025-07-30
Last Posted Date
2025-07-30
Lead Sponsor
Amgen
Target Recruit Count
434
Registration Number
NCT07094113

Real World Study to Describe the Effectiveness and Safety of Teprotumumab Among Thyroid Eye Disease Patients

Recruiting
Conditions
Thyroid Eye Disease
Interventions
First Posted Date
2025-07-25
Last Posted Date
2025-07-25
Lead Sponsor
Amgen
Target Recruit Count
10
Registration Number
NCT07085117
Locations
🇨🇳

Boao Vanguard Hospital, Qionghai, Hainan, China

Olpasiran Expanded Access Program

First Posted Date
2025-07-23
Last Posted Date
2025-07-23
Lead Sponsor
Amgen
Registration Number
NCT07079267

Maridebart Cafraglutide in Heart Failure With Preserved or Mildly Reduced Ejection Fraction and Obesity

Phase 3
Recruiting
Conditions
Heart Failure With Preserved Ejection Fraction
Heart Failure With Mildly Reduced Ejection Fraction
Obesity
Interventions
First Posted Date
2025-06-25
Last Posted Date
2025-07-25
Lead Sponsor
Amgen
Target Recruit Count
5056
Registration Number
NCT07037459
Locations
🇺🇸

SEC Clinical Research, Dothan, Alabama, United States

🇺🇸

National Heart Institute, Beverly Hills, California, United States

🇺🇸

National Institute of Clinical Research, Huntington Beach, California, United States

and more 19 locations

A Study of Tarlatamab in Combination With AB248 in Participants With Extensive Stage Small Cell Lung Cancer (DeLLphi-311)

Phase 1
Not yet recruiting
Conditions
Extensive Stage Small Cell Lung Cancer
Interventions
First Posted Date
2025-06-25
Last Posted Date
2025-06-25
Lead Sponsor
Amgen
Target Recruit Count
380
Registration Number
NCT07037758
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News

Kyowa Kirin to Present Phase 3 Rocatinlimab Results for Atopic Dermatitis at EADV 2025

Kyowa Kirin will present results from the Phase 3 ROCKET IGNITE trial of rocatinlimab, an investigational anti-OX40 monoclonal antibody for moderate-to-severe atopic dermatitis, at the EADV 2025 Annual Meeting in Paris.

Leveragen and Propeller Bio Form Strategic Partnership to Advance Next-Generation Antibody Discovery Platform

Leveragen, a Boston-based biotech company, has announced a strategic collaboration with newly launched Propeller Bio to advance antibody and protein-based therapeutics development.

TCG Labs Soleil Raises $400M to Build Single-Asset Biotech Startups for Strategic Partnerships

TCG Labs Soleil, a venture firm collaborating with The Column Group, has raised $400 million to continue launching single-drug biotechnology startups focused on achieving proof-of-concept data for strategic partnerships.

BioVie Strengthens Board with Neuroscience and Finance Veterans as Bezisterim Advances Through Phase 2 Trials

BioVie Inc. appointed Amy S. Chappell, MD, FAAN, and Kameel D. Farag to its Board of Directors to support the company's neurological and liver disease drug development programs.

FDA Appoints Biotech Veteran George Tidmarsh to Lead Drug Regulation Center Amid Agency Restructuring

The FDA has appointed Dr. George Tidmarsh, a former pharmaceutical executive and cancer specialist, to direct the Center for Drug Evaluation and Research, the agency's largest division responsible for reviewing drug safety and effectiveness.

Crescent Biopharma Appoints Jan Pinkas as Chief Scientific Officer to Advance Oncology Pipeline

Crescent Biopharma has appointed Jan Pinkas, Ph.D., as chief scientific officer, bringing over two decades of oncology drug development experience including expertise in antibody-drug conjugates.

Oxford BioTherapeutics and Boehringer Ingelheim Advance Third Oncology Drug Candidate to IND-Enabling Studies

Oxford BioTherapeutics announced that Boehringer Ingelheim has selected a third drug candidate targeting OB33 to advance into IND-enabling studies under their ongoing collaboration.

EPO and UPC Reach Opposite Conclusions on Amgen's PCSK9 Antibody Patent Validity

The European Patent Office (EPO) Opposition Division upheld Amgen's PCSK9 antibody patent EP 3666797, finding it inventive, while the Unified Patent Court (UPC) Central Division revoked the same patent for lacking inventive step.

bluebird bio Strengthens Leadership Team with Three Key Executive Appointments

bluebird bio, a pioneer in gene therapies for severe genetic diseases, has appointed three new executives to strengthen its leadership team as the company focuses on commercial execution.

Sandoz Invests $1.1 Billion in European Biosimilar Manufacturing Hub to Capture $222 Billion Market Opportunity

Sandoz has broken ground on a $440 million biosimilar manufacturing facility in Brnik, Slovenia, bringing total planned investment in the country to over $1.1 billion by 2029.

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