Amgen, Inc.

- Country
- 🇺🇸United States
- Ownership
- Public
- Established
- 1980-01-01
- Employees
- 26.7K
- Market Cap
- $175.6B
- Website
- http://www.amgen.com
Clinical Trials
1.2k
Trial Phases
6 Phases
Drug Approvals
3
Clinical Trials
Distribution across different clinical trial phases (1015 trials with phase data)• Click on a phase to view related trials
A Rollover Study Evaluating Sotorasib With or Without Panitumumab in Participants With KRAS p.G12C Mutation
- 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
- Conditions
- Type 2 Diabetes Mellitus
- Interventions
- Drug: Placebo
- First Posted Date
- 2025-09-08
- Last Posted Date
- 2025-09-08
- 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
- Conditions
- Healthy Volunteers
- Interventions
- Drug: Placebo
- First Posted Date
- 2025-08-27
- Last Posted Date
- 2025-08-27
- Lead Sponsor
- Amgen
- Target Recruit Count
- 20
- Registration Number
- NCT07142642
Real World Evaluation of Sotorasib Among Chinese Non-Small Cell Lung Cancer Patients
- 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
- Conditions
- Metastatic Hormone-sensitive Prostate Cancer (mHSPC)
- Interventions
- First Posted Date
- 2025-08-26
- Last Posted Date
- 2025-08-26
- Lead Sponsor
- Amgen
- Target Recruit Count
- 60
- Registration Number
- NCT07140900
- Prev
- 1
- 2
- 3
- 4
- 5
- 182
- Next
News
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.
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.
Hengrui Licenses Heart Disease Drug HRS-1893 to Braveheart Bio for $65M Upfront, Potential $1B+ Total
Jiangsu Hengrui Pharmaceuticals has licensed its selective myosin blocker HRS-1893 to Delaware-based startup Braveheart Bio for $65 million upfront plus potential milestone payments exceeding $1 billion.
Merck KGaA Appoints David Weinreich as Global Head of R&D to Revitalize Healthcare Pipeline
Merck KGaA has appointed David Weinreich as Global Head of R&D and Chief Medical Officer for its Healthcare business sector, bringing over 20 years of experience and leadership in developing 15 approved drugs worldwide.
Amgen Secures Expanded FDA Approval for Repatha® in Cardiovascular Risk Management
Amgen received expanded FDA approval for Repatha®, broadening its use for adults at risk of major cardiovascular events.
FDA Expands Repatha Indication to Include Adults at High Risk for Cardiovascular Events Without Prior Disease Diagnosis
The FDA has expanded Repatha's (evolocumab) indication to include adults at increased risk for major adverse cardiovascular events due to uncontrolled LDL cholesterol, removing the requirement for prior cardiovascular disease diagnosis.
I-Mab Strengthens Leadership Team with Three New Board Appointments and R&D Committee Formation
I-Mab appointed three seasoned biotech executives to key leadership positions, including Dr. Robert Lenz and Ms. Xin Liu to the Board of Directors and Dr. Ken Takeshita to the Scientific Advisory Board.
Royalty Pharma Acquires $950 Million IMDELLTRA Royalty Rights from BeOne Medicines
Royalty Pharma acquired BeOne Medicines' royalty rights to IMDELLTRA (tarlatamab-dlle) for up to $950 million, with $885 million paid upfront and an option for additional $65 million within 12 months.
Johnson & Johnson Commits $55 Billion to U.S. Manufacturing Expansion in Strategic Reshoring Initiative
Johnson & Johnson announced a $55 billion U.S. manufacturing initiative in March 2025, representing 25% more capital allocation to domestic operations than the previous four years.