COMPANY
Amgen
FDA-approved therapeutic company FDA-cleared device company Clinical Phase 3
Hiring
| Title | Location (from posting) | Employer posted | First seen |
|---|---|---|---|
| オンコロジー事業本部 固形がん領域MR | Japan - Tokyo | Oct 22, 2026 | Oct 9, 2026 |
| Order-to-Cash Product Execution | India - Hyderabad | Oct 22, 2026 | Oct 9, 2026 |
| Associate Director, Biomedical Data Stewardship (Standards Lead) | India - Hyderabad | Oct 22, 2026 | Oct 9, 2026 |
| Sr. Data Scientist – AI Driven Operations Research | India - Hyderabad | Oct 22, 2026 | Oct 9, 2026 |
| Maintenance Manager | Ireland - Dublin | Oct 22, 2026 | Oct 16, 2026 |
Trial and FDA signals
- New trial + clinical hiring Started a Phase 3 trial (NCT07778316, actual start Aug 28, 2026) (+5 other new trials); 102 clinical-operations roles open. ClinicalTrials.gov NCT07778316 (Aug 28, 2026)
Evidence (6 events)
- Aug 28, 2026 · ClinicalTrials.gov NCT07778316
leadSponsor.name='Amgen'; phases=['PHASE3']; overallStatus=RECRUITING; startDateStruct={date:2026-08-28,type:ACTUAL}; studyFirstPostDate=2026-08-21; briefTitle='Phase 3 Trial of Tarlatamab (SC vs IV) in Extensive-Stage Small Cell Lung Cancer After Platinum Based First-line Chemotherapy (ES-SCLC)' - Jul 29, 2026 · ClinicalTrials.gov NCT07684144
leadSponsor.name='Amgen'; phases=['PHASE3']; overallStatus=RECRUITING; startDateStruct={date:2026-07-29,type:ACTUAL}; studyFirstPostDate=2026-07-06; briefTitle='Extension Trial to Evaluate the Long-term Efficacy, Safety, and Tolerability of Maridebart Cafraglutide (MARITIME-2-EXTENSION)' - Jul 23, 2026 · ClinicalTrials.gov NCT07684235
leadSponsor.name='Amgen'; phases=['PHASE3']; overallStatus=RECRUITING; startDateStruct={date:2026-07-23,type:ACTUAL}; studyFirstPostDate=2026-07-06; briefTitle='Extension Trial to Evaluate the Long-term Efficacy, Safety, and Tolerability of Maridebart Cafraglutide (MARITIME-1-EXTENSION)' - Jul 21, 2026 · ClinicalTrials.gov NCT06987539
leadSponsor.name='Amgen'; phases=['PHASE2']; overallStatus=RECRUITING; startDateStruct={date:2026-07-21,type:ACTUAL}; studyFirstPostDate=2025-05-23; briefTitle='A Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of Inebilizumab in Children With Generalized Myasthenia ' - Sep 22, 2026 · ClinicalTrials.gov NCT07811999
leadSponsor.name='Amgen'; phases=['PHASE1']; overallStatus=RECRUITING; startDateStruct={date:2026-09-22,type:ACTUAL}; studyFirstPostDate=2026-09-10; briefTitle='Comparing the Extent to Which Romosozumab (AMG 785) is Made Available in the Body When Administered as a Single SC Injection or as 2 SC Inje' - Aug 7, 2026 · ClinicalTrials.gov NCT07745907
leadSponsor.name='Amgen'; phases=['PHASE1']; overallStatus=RECRUITING; startDateStruct={date:2026-08-07,type:ACTUAL}; studyFirstPostDate=2026-08-04; briefTitle='A Phase 1 Trial of AMG 691 in Healthy Chinese and Japanese Volunteers'
- Aug 28, 2026 · ClinicalTrials.gov NCT07778316
Timeline
- Trial start Phase 3: A Study Evaluating Subcutaneous Versus Intravenous Blinatumomab in Newly Diagnosed Adults With B-cell Precursor Acute Lymphoblastic Leukaemia source ↗
- Trial start Phase 4: A Trial Assessing the Effectiveness of Evolocumab in Reducing the Plaque Burden in Participants With Subclinical Atheroma source ↗
- Trial start Phase 3: Maridebart Cafraglutide Versus Semaglutide in Participants With Type 2 Diabetes source ↗
- Trial start —: Observational Safety Study in Women With Neuromyelitis Optica Spectrum Disorder (NMOSD) Exposed to UPLIZNA® During Pregnancy source ↗
- Trial start Phase 1: Comparing the Extent to Which Two Maridebart Cafraglutide Drug Products Are Made Available in the Body After a Single Subcutaneous Dose source ↗
- Board tracked Radar started tracking this company’s job board (1,747 open jobs at last check). source ↗
- Trial start 3: A Phase 3 Study of Inebilizumab in Participants With Primary Membranous Nephropathy source ↗
- Trial start Phase 1: Comparing the Extent to Which Romosozumab (AMG 785) is Made Available in the Body When Administered as a Single SC Injection or as 2 SC Injections source ↗
- Trial start 3: Phase 3 Trial of Tarlatamab (SC vs IV) in Extensive-Stage Small Cell Lung Cancer After Platinum Based First-line Chemotherapy (ES-SCLC) source ↗
- Trial start Phase 3: A Study of Romiplostim Plus Predniso(lo)ne vs. Predniso(lo)ne Alone for the Treatment of Previously Untreated Primary Immune Thrombocytopenia (ITP) source ↗
- Trial start Phase 3: Extension Trial to Evaluate the Long-term Efficacy, Safety, and Tolerability of Maridebart Cafraglutide (MARITIME-2-EXTENSION) source ↗
- Trial start Phase 3: Extension Trial to Evaluate the Long-term Efficacy, Safety, and Tolerability of Maridebart Cafraglutide (MARITIME-1-EXTENSION) source ↗
- Trial start Phase 2: A Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of Inebilizumab in Children With Generalized Myasthenia Gravis (gMG) source ↗
- Trial start Phase 3: A Study to Evaluate Efficacy, Safety, and Immunogenicity With ABP 938 8 mg Versus EYLEA® HD (Aflibercept) in Participants With Neovascular Age-related Macular Degeneration source ↗
- Trial start Phase 3: Efficacy, Safety and Tolerability of Switching From Glucagon-like Peptide-1 Receptor Agonists (GLP-1RA) to Maridebart Cafraglutide in Adults With Obesity or Overweight (MARITIME-SWITCH) source ↗
- Trial start Phase 1: Trial of Xaluritamig in Adults With Metastatic Castration-resistant Prostate Cancer source ↗
- Trial start Phase 1: Comparing the Extent to Which Two Evolocumab Drug Products Are Made Available in the Body After a Single Subcutaneous Dose. source ↗
- Trial start Phase 1: Evaluation of Xaluritamig in Adults, Adolescents and Children With Relapsed or Refractory Ewing Sarcoma (EWS) source ↗
- Trial start Phase 1: AMG 436 as Monotherapy and Combination Therapy in Participants With MSI-H/dMMR Solid Tumors source ↗
- Trial start Phase 2: A Trial to Evaluate Efficacy and Safety of Maridebart Cafraglutide in Adults Living With Elevated Liver Fat and Obesity or Overweight source ↗
- Trial start Phase 3: A Double-blind, Randomized Controlled Trial to Investigate the Efficacy, Safety, and Pharmacokinetics of Pegloticase Administration Via Subcutaneous and Intravenous Routes Both With Methotrex source ↗
- Trial start Phase 3: Maridebart Cafraglutide Versus Placebo in Adult Participants With Obstructive Sleep Apnea on Positive Airway Pressure Therapy source ↗
- Trial start Phase 1/Phase 2: A Study of Subcutaneous Blinatumomab in Children With R/R and and MRD+ B-Cell Precursor Acute Lymphoblastic Leukemia source ↗
- Trial start Phase 3: A Study of Xaluritamig Plus Abiraterone Versus Investigator's Choice in Participants With Chemotherapy-naïve Metastatic Castration-resistant Prostate Cancer source ↗
- Trial start Phase 3: Maridebart Cafraglutide Versus Placebo in Adult Participants With Obstructive Sleep Apnea Not on Positive Airway Pressure (PAP) Therapy source ↗
Upcoming milestones
- Jan 14, 2027 (ESTIMATED) · Phase 1 · Comparing the Extent to Which Romosozumab (AMG 785) is Made Available in the Body When Administered as a Single SC Injection or as 2 SC Injections · NCT07811999
- Jan 21, 2027 (ESTIMATED) · Phase 3 · Evaluation of Maridebart Cafraglutide in Adult Participants Without Type 2 Diabetes Mellitus Who Have Obesity or Are Overweight · NCT06858839
- Mar 13, 2027 (ESTIMATED) · Phase 1 · Evaluation of Xaluritamig in High-Risk, Biochemically Recurrent, Non-metastatic Castrate-sensitive Prostate Cancer · NCT06555796
- Mar 23, 2027 (ESTIMATED) · Phase 1 · Comparing the Extent to Which Two Maridebart Cafraglutide Drug Products Are Made Available in the Body After a Single Subcutaneous Dose · NCT07832799
- Apr 19, 2027 (ESTIMATED) · Phase 3 · Comparison Between ABP 692 and Ocrevus® (Ocrelizumab) · NCT06700343
- Jun 30, 2027 (ESTIMATED) · Phase 3 · A Study Evaluating Sotorasib Platinum Doublet Combination Versus Pembrolizumab Platinum Doublet Combination as a Front-Line Therapy in Participants With Stage IV or Advanced Stage IIIB/C Nonsquamous N · NCT05920356
- Jul 31, 2027 (ESTIMATED) · Phase 3 · A Study to Evaluate Efficacy, Safety, and Immunogenicity With ABP 938 8 mg Versus EYLEA® HD (Aflibercept) in Participants With Neovascular Age-related Macular Degeneration · NCT07614776
- Aug 20, 2027 (ESTIMATED) · Phase 3 · Maridebart Cafraglutide Versus Placebo in Adult Participants With Obstructive Sleep Apnea on Positive Airway Pressure Therapy · NCT07225686
Open jobs 1,746
| Title | Location (from posting, not HQ) | Employer posted | First seen | Level |
|---|---|---|---|---|
| オンコロジー事業本部 固形がん領域MR | Japan - Tokyo | Oct 22, 2026 | Oct 9, 2026 | Mid |
| Order-to-Cash Product Execution | India - Hyderabad | Oct 22, 2026 | Oct 9, 2026 | Not stated |
| Associate Director, Biomedical Data Stewardship (Standards Lead) | India - Hyderabad | Oct 22, 2026 | Oct 9, 2026 | Senior |
| Sr. Data Scientist – AI Driven Operations Research | India - Hyderabad | Oct 22, 2026 | Oct 9, 2026 | Senior |
| Maintenance Manager | Ireland - Dublin | Oct 22, 2026 | Oct 16, 2026 | Not stated |
| Senior Data Scientist – Perturbation Biology & AI | India - Hyderabad | Oct 22, 2026 | Oct 22, 2026 | Not stated |
| Biopharmaceutical Representative-Cardiology | Bulgaria - Sofia | Oct 22, 2026 | Oct 22, 2026 | Not stated |
| Specialist HR Systems & Solutions- Payroll Configuration | India - Hyderabad | Oct 22, 2026 | Oct 22, 2026 | Not stated |
| Sr. Associate - Technology Project Controller | India - Hyderabad | Oct 22, 2026 | Oct 22, 2026 | Not stated |
| Associate Software Engineer | India - Hyderabad | Oct 22, 2026 | Oct 22, 2026 | Not stated |
| Specialist Quality Assurance (Technical Support) | Singapore Manufacturing - Tuas | Oct 22, 2026 | Oct 22, 2026 | Not stated |
| Sr Biopharmaceutical Rep-Repatha-Zhengzhou | China - Zhengzhou | Oct 22, 2026 | Oct 22, 2026 | Not stated |
| Commercial Forecasting Senior Associate | Portugal - Lisbon | Oct 21, 2026 | Oct 9, 2026 | Mid |
| Process Development Associate Scientist | US - California - Thousand Oaks | Oct 21, 2026 | Oct 9, 2026 | Mid |
| Mgr, Maintenance I | US - North Carolina - Holly Springs | Oct 21, 2026 | Oct 9, 2026 | Not stated |
| Orchestration Engine, Associate Director | 2 locations, including Thousand Oaks, California, US | Oct 21, 2026 | Oct 9, 2026 | Senior |
| Area Network Marketing Manager | Japan - Tokyo | Oct 21, 2026 | Oct 9, 2026 | Mid |
| Director, Scientific and Operations Intelligence, Obesity | US - California - Thousand Oaks | Oct 21, 2026 | Oct 9, 2026 | Senior |
| Executive Director, Research Oncology | US - California - South San Francisco | Oct 21, 2026 | Oct 9, 2026 | Executive |
| Manufacturing Associate | US - California - Thousand Oaks | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| EH&S Sr Mgr | US - California - Thousand Oaks | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Associate Manufacturing - Days | US - Rhode Island - West Greenwich | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Process Development Associate Scientist | US - Massachusetts - Cambridge | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Mfg Process Technician - Days | US - Rhode Island - West Greenwich | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Associate Manufacturing-Nights | US - Rhode Island - West Greenwich | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Scientist – Inflammation Research | US - California - Thousand Oaks | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Digital Engagement Manager | Netherlands - Breda | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| EH&S Manager - Risk Management | US - North Carolina - Holly Springs | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Patient Access & Reimbursement Marketing Manager,- Biosimilar | US - California - Thousand Oaks | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| International Tax Manager | Ireland - Dublin | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Manufacturing Training Specialist – Manufacturing Support | US - North Carolina - Holly Springs | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Amgen Graduate Opportunities 2027 | Ireland - Dun Laoghaire | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Learning and Performance Senior Manager - Rest of World | Portugal - Lisbon | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Product Specialist Oncology - Veneto Orientale | Italy - Milan | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Sr Biopharmaceutical Rep-Tongliao | China - Tongliao | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Brand Engagement Manager, Cardiovascular | Japan - Tokyo | Oct 21, 2026 | Oct 22, 2026 | Not stated |
| Senior Process Engineer - CIP/SIP/Autoclaves | US - North Carolina - Holly Springs | Oct 20, 2026 | Oct 9, 2026 | Senior |
| Global Value & Access Senior Manager (Flexible Location: Argentina, Brazil, Colombia, Mexico City) | 4 locations, including Bogota, Colombia | Oct 20, 2026 | Oct 9, 2026 | Senior |
| SIEM Engineer | Portugal - Lisbon | Oct 20, 2026 | Oct 9, 2026 | Mid |
| Senior Director, Consumer Pricing & Non-Reimbursed Channels, Obesity and Related Conditions (OaR) | United States - Remote | Oct 20, 2026 | Oct 9, 2026 | Senior |
| Senior Maintenance Technician – Utilities (Waste Water Treatment) – Day Shift | US - North Carolina - Holly Springs | Oct 20, 2026 | Oct 9, 2026 | Senior |
| Clinical Development Medical Director, Early Development Oncology | United States - Remote | Oct 20, 2026 | Oct 9, 2026 | Senior |
| Associate Paralegal | US - California - Thousand Oaks | Oct 20, 2026 | Oct 9, 2026 | Mid |
| Specialty/Senior Specialty Representative - Cardiovascular - Springfield, Il | US - Missouri - St. Louis | Oct 20, 2026 | Oct 16, 2026 | Not stated |
| Sr. Medical Science Liaison - Obesity and Related Conditions - Camden, NJ | US - New Jersey - Camden | Oct 20, 2026 | Oct 19, 2026 | Not stated |
| Scientist, Integrated Computational and Experimental Inflammation Discovery | US - California - South San Francisco | Oct 20, 2026 | Oct 22, 2026 | Not stated |
| Specialty/Senior Specialty Representative - Cardiovascular - Springfield, Il | US - Illinois - Springfield | Oct 20, 2026 | Oct 22, 2026 | Not stated |
| Administrative Coordinator – CV Cardio-Metabolic and Bone TA | United States - Remote | Oct 20, 2026 | Oct 22, 2026 | Not stated |
| Process Development Senior Associate | US - California - Thousand Oaks | Oct 20, 2026 | Oct 22, 2026 | Not stated |
| Manager, Value & Access Analytics - GTN Forensics - U.S. Remote | United States - Remote | Oct 20, 2026 | Oct 22, 2026 | Not stated |
Clinical trials (lead sponsor) Showing 50 of 1,043
| Record | Title | Phase | Status | Start | Primary completion |
|---|---|---|---|---|---|
| NCT07037433 | Evaluating the Impact of Maridebart Cafraglutide on Cardiovascular Outcomes in Participants With Atherosclerotic Cardiovascular Disease and Overweight or Obesity | Phase 3 | Recruiting | Jul 25, 2025 | Jun 30, 2028 (estimated) |
| NCT07575399 | Efficacy, Safety and Tolerability of Switching From Glucagon-like Peptide-1 Receptor Agonists (GLP-1RA) to Maridebart Cafraglutide in Adults With Obesity or Overweight (MARITIME-SWITCH) | Phase 3 | Recruiting | May 11, 2026 | Jan 3, 2028 (estimated) |
| NCT07866066 | Maridebart Cafraglutide Versus Semaglutide in Participants With Type 2 Diabetes | Phase 3 | Not yet recruiting | Nov 2, 2026 | Sep 4, 2028 (estimated) |
| NCT06585462 | Single and Multiple Ascending Dose Study of AMG 513 in Participants With Obesity | Phase 1 | Completed | Sep 9, 2024 | Sep 16, 2026 (actual) |
| NCT07225686 | Maridebart Cafraglutide Versus Placebo in Adult Participants With Obstructive Sleep Apnea on Positive Airway Pressure Therapy | Phase 3 | Active, not recruiting | Dec 19, 2025 | Aug 20, 2027 (estimated) |
| NCT06745323 | A Phase 2, Open-label, Randomized, Multicenter Study of Tarlatamab Dosing Regimens in Subjects With SCLC | 2 | Active, not recruiting | Feb 26, 2025 | Aug 10, 2029 (estimated) |
| NCT07684235 | Extension Trial to Evaluate the Long-term Efficacy, Safety, and Tolerability of Maridebart Cafraglutide (MARITIME-1-EXTENSION) | Phase 3 | Recruiting | Jul 23, 2026 | Dec 26, 2027 (estimated) |
| NCT04804553 | Apremilast Pediatric Study in Children With Active Juvenile Psoriatic Arthritis | Phase 3 | Recruiting | Mar 17, 2022 | Mar 21, 2028 (estimated) |
| NCT07134088 | A Study of Subcutaneous Blinatumomab in Children With R/R and and MRD+ B-Cell Precursor Acute Lymphoblastic Leukemia | Phase 1/Phase 2 | Active, not recruiting | Dec 8, 2025 | Mar 6, 2031 (estimated) |
| NCT07811999 | Comparing the Extent to Which Romosozumab (AMG 785) is Made Available in the Body When Administered as a Single SC Injection or as 2 SC Injections | Phase 1 | Recruiting | Sep 22, 2026 | Jan 14, 2027 (estimated) |
| NCT06570798 | A Phase 2 Master Protocol Assessing Inebilizumab and Blinatumomab in Autoimmune Diseases | 2 | Recruiting | Jul 16, 2025 | Aug 6, 2028 (estimated) |
| NCT07684144 | Extension Trial to Evaluate the Long-term Efficacy, Safety, and Tolerability of Maridebart Cafraglutide (MARITIME-2-EXTENSION) | Phase 3 | Recruiting | Jul 29, 2026 | Dec 26, 2027 (estimated) |
| NCT06987539 | A Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of Inebilizumab in Children With Generalized Myasthenia Gravis (gMG) | Phase 2 | Recruiting | Jul 21, 2026 | Mar 13, 2030 (estimated) |
| NCT07545226 | Comparing the Extent to Which Two Evolocumab Drug Products Are Made Available in the Body After a Single Subcutaneous Dose. | Phase 1 | Completed | Apr 21, 2026 | Sep 2, 2026 (actual) |
| NCT05565560 | A Study to Assess the Efficacy and Safety of Apremilast in Japanese Pediatric Participants With Moderate to Severe Plaque Psoriasis | Phase 3 | Completed | Jan 25, 2023 | Nov 20, 2025 (actual) |
| NCT07851220 | A Phase 3 Study of Inebilizumab in Participants With Primary Membranous Nephropathy | 3 | Recruiting | Oct 1, 2026 | Sep 27, 2031 (estimated) |
| NCT06072482 | A Study to Evaluate Avacopan in Participants With ANCA-associated Vasculitis | Phase 4 | Recruiting | Feb 7, 2024 | Dec 31, 2036 (estimated) |
| NCT07226765 | Maridebart Cafraglutide Versus Placebo in Adult Participants With Obstructive Sleep Apnea Not on Positive Airway Pressure (PAP) Therapy | Phase 3 | Active, not recruiting | Nov 25, 2025 | Aug 30, 2027 (estimated) |
| NCT07614776 | A Study to Evaluate Efficacy, Safety, and Immunogenicity With ABP 938 8 mg Versus EYLEA® HD (Aflibercept) in Participants With Neovascular Age-related Macular Degeneration | Phase 3 | Recruiting | May 27, 2026 | Jul 31, 2027 (estimated) |
| NCT07441252 | A Trial to Evaluate Efficacy and Safety of Maridebart Cafraglutide in Adults Living With Elevated Liver Fat and Obesity or Overweight | Phase 2 | Active, not recruiting | Mar 5, 2026 | Aug 25, 2027 (estimated) |
| NCT05920356 | A Study Evaluating Sotorasib Platinum Doublet Combination Versus Pembrolizumab Platinum Doublet Combination as a Front-Line Therapy in Participants With Stage IV or Advanced Stage IIIB/C Nonsquamous Non-Small Cell Lung Cancers (CodeBreaK 202) | Phase 3 | Recruiting | Nov 16, 2023 | Jun 30, 2027 (estimated) |
| NCT07037758 | A Study of Tarlatamab in Combination With AB248 in Participants With Extensive Stage Small Cell Lung Cancer (DeLLphi-311) | Phase 1 | Recruiting | Sep 16, 2025 | Mar 18, 2028 (estimated) |
| NCT07297979 | Evaluation of Xaluritamig in Adults, Adolescents and Children With Relapsed or Refractory Ewing Sarcoma (EWS) | Phase 1 | Recruiting | Apr 8, 2026 | May 26, 2030 (estimated) |
| NCT07229157 | Effect of Maridebart Cafraglutide on the Heart's Electrical Activity | Phase 1 | Completed | Oct 22, 2025 | Aug 27, 2026 (actual) |
| NCT07213674 | A Study of Xaluritamig Plus Abiraterone Versus Investigator's Choice in Participants With Chemotherapy-naïve Metastatic Castration-resistant Prostate Cancer | Phase 3 | Recruiting | Nov 28, 2025 | Jan 7, 2030 (estimated) |
| NCT06700343 | Comparison Between ABP 692 and Ocrevus® (Ocrelizumab) | Phase 3 | Active, not recruiting | Jan 13, 2025 | Apr 19, 2027 (estimated) |
| NCT07832799 | Comparing the Extent to Which Two Maridebart Cafraglutide Drug Products Are Made Available in the Body After a Single Subcutaneous Dose | Phase 1 | Not yet recruiting | Oct 12, 2026 | Mar 23, 2027 (estimated) |
| NCT03836040 | Efficacy and Safety of Erenumab in Pediatric Participants With Episodic Migraine | Phase 3 | Active, not recruiting | Jul 19, 2019 | Nov 19, 2025 (actual) |
| NCT07803679 | A Trial Assessing the Effectiveness of Evolocumab in Reducing the Plaque Burden in Participants With Subclinical Atheroma | Phase 4 | Not yet recruiting | Jan 31, 2027 | Apr 30, 2029 (estimated) |
| NCT07403721 | AMG 436 as Monotherapy and Combination Therapy in Participants With MSI-H/dMMR Solid Tumors | Phase 1 | Recruiting | Apr 8, 2026 | Jan 1, 2030 (estimated) |
| NCT07778316 | Phase 3 Trial of Tarlatamab (SC vs IV) in Extensive-Stage Small Cell Lung Cancer After Platinum Based First-line Chemotherapy (ES-SCLC) | 3 | Recruiting | Aug 28, 2026 | Sep 24, 2027 (estimated) |
| NCT06229145 | A Trial to Investigate the Non-inferiority of Pegloticase Administered Every 4 Weeks (Q4W) With MTX Compared With Every 2 Weeks (Q2W) With MTX in Participants With Uncontrolled Refractory Gout | Phase 4 | Completed | Mar 18, 2024 | Jul 30, 2025 (actual) |
| NCT06858839 | Evaluation of Maridebart Cafraglutide in Adult Participants Without Type 2 Diabetes Mellitus Who Have Obesity or Are Overweight | Phase 3 | Active, not recruiting | Mar 12, 2025 | Jan 21, 2027 (estimated) |
| NCT07700238 | A Study of Romiplostim Plus Predniso(lo)ne vs. Predniso(lo)ne Alone for the Treatment of Previously Untreated Primary Immune Thrombocytopenia (ITP) | Phase 3 | Recruiting | Aug 21, 2026 | Sep 14, 2029 (estimated) |
| NCT07037459 | Maridebart Cafraglutide in Heart Failure With Preserved or Mildly Reduced Ejection Fraction and Obesity | Phase 3 | Recruiting | Jun 25, 2025 | Jun 30, 2028 (estimated) |
| NCT07493512 | Trial of Xaluritamig in Adults With Metastatic Castration-resistant Prostate Cancer | Phase 1 | Recruiting | Apr 28, 2026 | Jul 30, 2030 (estimated) |
| NCT07223190 | A Study Evaluating Subcutaneous Versus Intravenous Blinatumomab in Newly Diagnosed Adults With B-cell Precursor Acute Lymphoblastic Leukaemia | Phase 3 | Not yet recruiting | Jun 30, 2028 | Dec 30, 2031 (estimated) |
| NCT06590051 | AMG 335 Expanded Access Program for IgG4-Related Disease | Not listed | Approved for marketing | Not listed | Not listed |
| NCT06104124 | A Study to Evaluate the Efficacy and Safety of Dazodalibep in Participants With Sjögren's Syndrome (SS) With Moderate-to-severe Systemic Disease Activity | Phase 3 | Completed | Jan 24, 2024 | Jul 23, 2026 (actual) |
| NCT06468826 | A Study of Avacopan in Participants With Normal Renal Function and Participants With End-Stage Renal Disease (ESRD) | Phase 1 | Completed | Jun 18, 2024 | Oct 5, 2024 (actual) |
| NCT03747939 | Efficacy, Safety, and Tolerability Study of Apremilast to Treat Early Oligoarticular Psoriatic Arthritis. | Phase 4 | Completed | Dec 31, 2018 | Dec 19, 2022 (actual) |
| NCT06660173 | A Study of Maridebart Cafraglutide in Adult Participants With Type 2 Diabetes Mellitus (T2DM) | Phase 2 | Active, not recruiting | Nov 7, 2024 | Oct 6, 2025 (actual) |
| NCT05111626 | Bemarituzumab Plus Chemotherapy and Nivolumab Versus Chemotherapy and Nivolumab for FGFR2b Overexpressed Untreated Advanced Gastric and Gastroesophageal Junction Cancer. | Phase 3 | Terminated | Mar 14, 2022 | Oct 14, 2025 (actual) |
| NCT05361395 | First-Line Tarlatamab in Combination With Carboplatin, Etoposide, and PD-L1 Inhibitor in Subjects With Extensive Stage Small Cell Lung Cancer (ES-SCLC) | Phase 1 | Active, not recruiting | Aug 24, 2022 | May 30, 2030 (estimated) |
| NCT07005128 | A Study Comparing Tarlatamab, Durvalumab, Carboplatin, and Etoposide Versus Durvalumab, Carboplatin, and Etoposide in First-line Extensive Stage Small-Cell Lung Cancer (ES-SCLC) | Phase 3 | Active, not recruiting | Aug 18, 2025 | Jan 4, 2029 (estimated) |
| NCT06555796 | Evaluation of Xaluritamig in High-Risk, Biochemically Recurrent, Non-metastatic Castrate-sensitive Prostate Cancer | Phase 1 | Active, not recruiting | Sep 23, 2024 | Mar 13, 2027 (estimated) |
| NCT06295679 | A Study Assessing Repatha® in Combination With Standard of Care (SOC) Compared With SOC on Major Cardiovascular Events in Chinese Participants With Atherosclerotic Cardiovascular Disease | Not listed | Active, not recruiting | Dec 19, 2022 | Dec 19, 2028 (estimated) |
| NCT07388498 | A Double-blind, Randomized Controlled Trial to Investigate the Efficacy, Safety, and Pharmacokinetics of Pegloticase Administration Via Subcutaneous and Intravenous Routes Both With Methotrexate in Participants With Uncontrolled Gout | Phase 3 | Recruiting | Feb 9, 2026 | Jun 18, 2028 (estimated) |
| NCT06252649 | Study of Sotorasib, Panitumumab and FOLFIRI Versus FOLFIRI With or Without Bevacizumab-awwb in Treatment-naïve Participants With Metastatic Colorectal Cancer With KRAS p.G12C Mutation | Phase 3 | Recruiting | Jul 17, 2024 | Sep 25, 2028 (estimated) |
| NCT05909761 | Observational Safety Study in Women With Neuromyelitis Optica Spectrum Disorder (NMOSD) Exposed to UPLIZNA® During Pregnancy | Not listed | Recruiting | Oct 15, 2026 | Oct 31, 2032 (estimated) |
FDA records (last 2 years)
- FDA New indication / efficacy supplement: IMDELLTRA (tarlatamab-dlle) — BLA761344/1, Nov 19, 2025. Applicant at approval: Amgen Inc. source ↗
- FDA Original approval: OTEZLA; OTEZLA XR (apremilast) — NDA210745, Aug 29, 2025. Applicant at approval: Amgen Inc. source ↗
- FDA Original approval: OTEZLA; OTEZLA XR (apremilast) — NDA210745/ORIG2, Aug 29, 2025. Applicant at approval: Amgen Inc. source ↗
- FDA New indication / efficacy supplement: OTEZLA (apremilast) — NDA205437/14, Jul 23, 2025. Applicant at approval: Amgen Inc. source ↗
- FDA New indication / efficacy supplement: PROLIA; XGEVA (denosumab) — BLA125320/219, May 22, 2025. Applicant at approval: Amgen Inc. source ↗
- FDA New indication / efficacy supplement: AMJEVITA (adalimumab-atto) — BLA761024/21, May 20, 2025. Applicant at approval: Amgen Inc. Biosimilar. source ↗
- FDA New indication / efficacy supplement: AMJEVITA (adalimumab-atto) — BLA761024/23, Apr 7, 2025. Applicant at approval: Amgen, Inc. Biosimilar. source ↗
- FDA New indication / efficacy supplement: LUMAKRAS (sotorasib) — NDA214665/9, Jan 16, 2025. Applicant at approval: Amgen Inc. source ↗
- FDA New indication / efficacy supplement: VECTIBIX (panitumumab) — BLA125147/213, Jan 16, 2025. Applicant at approval: Amgen Inc. source ↗
- FDA New indication / efficacy supplement: WEZLANA (ustekinumab-auub) — BLA761285/1, Dec 26, 2024. Applicant at approval: Amgen Inc. Biosimilar. source ↗
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