COMPANY
Genmab
FDA-approved therapeutic company Clinical Phase 3
Timeline
- Trial start Phase 3: Study to Assess the Efficacy and Safety of Rina-S Plus Standard of Care Compared to Standard of Care Maintenance Treatment After First-line (1L) Platinum-based Chemotherapy in Participants Wi source ↗
- Trial start Phase 3: Study of Petosemtamab Plus Chemotherapy Versus Cetuximab or Bevacizumab Plus Chemotherapy in RAS and BRAF Wild Type, Recurrent, Unresectable or Metastatic Colorectal Cancer (LiGeR-CRC2) source ↗
- Trial start Phase 3: Study to Assess the Efficacy and Safety of Rina-S With or Without Bevacizumab Compared to Investigator's Choice of Platinum-based Chemotherapy With or Without Bevacizumab as Second-line Treat source ↗
- Trial start 1: A Phase 1 Trial of GEN1119 in Participants With Solid Tumors source ↗
- Trial start Phase 3: Study of Petosemtamab Plus Chemotherapy Versus Cetuximab Plus Chemotherapy in RAS and BRAF Wild-type, Unresectable or Metastatic, Left-sided Colorectal Cancer (LiGeR-CRC1) source ↗
- Trial start Phase 3: An Extension Study to Assess the Efficacy of Rina-S Compared to Treatment of Investigator's Choice in Participants With Platinum Resistant Ovarian Cancer in China source ↗
- Trial start Phase 2: Study to Assess the Efficacy and Safety of Rina-S in Participants With Advanced Gastrointestinal (GI) Cancers source ↗
- Trial start Phase 1: A Study of GEN1106 in Participants With Solid Tumors source ↗
- Trial start Phase 1: Trial to Evaluate the Safety and Preliminary Efficacy of GEN1079 in Participants With Advanced Solid Tumors source ↗
- Trial start Phase 3: Study to Assess the Efficacy and Safety of Rina-S Plus Standard of Care Compared to Standard of Care for Maintenance Treatment of Participants With Recurrent Platinum-sensitive Ovarian Cancer source ↗
- Trial start Phase 1: First-in-human (FIH) Trial of GEN3018 in Relapsed or Refractory (R/R) Acute Myeloid Leukemia (AML) or Higher-risk Myelodysplastic Syndrome (HR-MDS) source ↗
- Trial start Phase 2: Study to Assess the Efficacy and Safety of Rina-S in Participants With Non-small Cell Lung Cancer source ↗
- Trial start Phase 3: Study to Assess the Efficacy and Safety of Rina-S Compared to Treatment of Investigator's Choice in Participants With Endometrial Cancer source ↗
- Debt Debt: $1.5B (not counted as a raise), announced Nov 18, 2025. Source: company release on GlobeNewswire. source ↗
- Trial start Phase 2: Study of the Effectiveness and Safety of Acasunlimab Alone and With Pembrolizumab to Treat Advanced Melanoma of the Skin That Has Returned After Treatment With an Approved Checkpoint Inhibito source ↗
- Trial start Phase 3: Study to Assess the Efficacy of Rina-S Compared to Treatment of Investigator's Choice in Participants With Platinum Resistant Ovarian Cancer source ↗
- Trial start Phase 1/Phase 2: A First-in-Human Trial of Safety and Efficacy of GEN1078 in Participants With Solid Tumors source ↗
- Trial start Phase 3: Trial to Evaluate Acasunlimab and Pembrolizumab Combination Superiority Over Standard of Care Docetaxel in Non-Small Cell Lung Cancer (ABBIL1TY NSCLC-06) source ↗
- Trial start 1: A Phase 1/2 Study of GEN1286 in Patients With Advanced Solid Tumors source ↗
- Trial start Phase 1: Trial to Assess the Safety and Antitumor Activity of GEN1057 in Malignant Solid Tumors source ↗
- Trial start Phase 3: A Study of Subcutaneously Injected Epcoritamab Plus Oral Lenalidomide Tablets Compared to Intravenously (IV) Infused Rituximab Plus IV Infused Gemcitabine and IV Infused Oxaliplatin in Adult source ↗
- Trial start Phase 1/Phase 2: Trial to Assess the Safety and Preliminary Efficacy of GEN1055 on Malignant Solid Tumors as Monotherapy and as Combination Therapy source ↗
- Trial start Phase 3: Study of Subcutaneous Epcoritamab in Combination With Intravenous Rituximab and Oral Lenalidomide (R2) to Assess Adverse Events and Change in Disease Activity in Adult Participants With Previ source ↗
- Trial start Phase 1/Phase 2: PRO1107 in Patients With Advanced Solid Tumors source ↗
- Trial start Phase 1: A Safety Trial of GEN1042 in Japanese Subjects With Malignant Solid Tumors source ↗
Upcoming milestones
- 2027-03 (ESTIMATED) · Phase 2 · A Study to Evaluate Adverse Events of Subcutaneous (SC) Epcoritamab Administered in the Outpatient Setting in Adult Participants With Relapsed or Refractory Diffuse Large B-Cell Lymphoma and Classic F · NCT05451810
- 2027-06 (ESTIMATED) · Phase 3 · A Study to Evaluate Change in Disease Activity of Subcutaneous (SC) Epcoritamab Combined With Intravenous and Oral Rituximab, Cyclophosphamide, Doxorubicin Hydrochloride, Vincristine, and Prednisone ( · NCT05578976
- 2027-07 (ESTIMATED) · Phase 1/Phase 2 · Rinatabart Sesutecan (Rina-S, PRO1184, GEN1184) for Advanced Solid Tumors (GCT1184-01/ PRO1184-001) · NCT05579366
- Jul 30, 2027 (ESTIMATED) · Phase 3 · Trial to Evaluate Acasunlimab and Pembrolizumab Combination Superiority Over Standard of Care Docetaxel in Non-Small Cell Lung Cancer (ABBIL1TY NSCLC-06) · NCT06635824
- 2027-08 (ESTIMATED) · Phase 1 · A Safety Trial of GEN1042 in Japanese Subjects With Malignant Solid Tumors · NCT06057038
- 2027-09 (ESTIMATED) · Phase 3 · An Extension Study to Assess the Efficacy of Rina-S Compared to Treatment of Investigator's Choice in Participants With Platinum Resistant Ovarian Cancer in China · NCT07604766
- 2027-09 (ESTIMATED) · Phase 1/Phase 2 · Trial of the Safety and Efficacy of Epcoritamab in Japanese Subjects With Relapsed or Refractory (R/R) B-Cell Non-Hodgkin Lymphoma (R/R B-NHL) · NCT04542824
- Sep 30, 2027 (ESTIMATED) · Phase 1/Phase 2 · Safety and Efficacy Trial of Epcoritamab Combinations in Subjects With B-cell Non-Hodgkin Lymphoma (B-NHL) · NCT04663347
Funding
- Debt: $1.5B (not counted as a raise), announced Nov 18, 2025. Source: company release on GlobeNewswire. source ↗
Clinical trials (lead sponsor) Showing 50 of 68
| Record | Title | Phase | Status | Start | Primary completion |
|---|---|---|---|---|---|
| NCT07775287 | Study of Petosemtamab Plus Chemotherapy Versus Cetuximab or Bevacizumab Plus Chemotherapy in RAS and BRAF Wild Type, Recurrent, Unresectable or Metastatic Colorectal Cancer (LiGeR-CRC2) | Phase 3 | Recruiting | Oct 7, 2026 | Mar 30, 2029 (estimated) |
| NCT05579366 | Rinatabart Sesutecan (Rina-S, PRO1184, GEN1184) for Advanced Solid Tumors (GCT1184-01/ PRO1184-001) | Phase 1/Phase 2 | Recruiting | Dec 7, 2022 | 2027-07 (estimated) |
| NCT07564141 | Study to Assess the Efficacy and Safety of Rina-S With or Without Bevacizumab Compared to Investigator's Choice of Platinum-based Chemotherapy With or Without Bevacizumab as Second-line Treatment in Participants With Recurrent Platinum-sensitive Ovarian Cancer | Phase 3 | Recruiting | Aug 28, 2026 | 2029-12 (estimated) |
| NCT06573294 | Trial to Assess the Safety and Antitumor Activity of GEN1057 in Malignant Solid Tumors | Phase 1 | Terminated | Aug 28, 2024 | Apr 7, 2026 (actual) |
| NCT07695831 | A Phase 1 Trial of GEN1119 in Participants With Solid Tumors | 1 | Recruiting | Aug 13, 2026 | 2029-06 (estimated) |
| NCT07539311 | Study to Assess the Efficacy and Safety of Rina-S in Participants With Advanced Gastrointestinal (GI) Cancers | Phase 2 | Recruiting | May 11, 2026 | 2028-09 (estimated) |
| NCT07416123 | A Study of GEN1106 in Participants With Solid Tumors | Phase 1 | Recruiting | Apr 14, 2026 | Apr 5, 2029 (estimated) |
| NCT06635824 | Trial to Evaluate Acasunlimab and Pembrolizumab Combination Superiority Over Standard of Care Docetaxel in Non-Small Cell Lung Cancer (ABBIL1TY NSCLC-06) | Phase 3 | Active, not recruiting | Nov 25, 2024 | Jul 30, 2027 (estimated) |
| NCT07604766 | An Extension Study to Assess the Efficacy of Rina-S Compared to Treatment of Investigator's Choice in Participants With Platinum Resistant Ovarian Cancer in China | Phase 3 | Recruiting | Jun 26, 2026 | 2027-09 (estimated) |
| NCT07288177 | Study to Assess the Efficacy and Safety of Rina-S in Participants With Non-small Cell Lung Cancer | Phase 2 | Recruiting | Jan 30, 2026 | Nov 22, 2027 (estimated) |
| NCT07384715 | First-in-human (FIH) Trial of GEN3018 in Relapsed or Refractory (R/R) Acute Myeloid Leukemia (AML) or Higher-risk Myelodysplastic Syndrome (HR-MDS) | Phase 1 | Recruiting | Feb 16, 2026 | Oct 18, 2029 (estimated) |
| NCT06057038 | A Safety Trial of GEN1042 in Japanese Subjects With Malignant Solid Tumors | Phase 1 | Active, not recruiting | Nov 24, 2023 | 2027-08 (estimated) |
| NCT03625037 | First-in-Human (FIH) Trial in Patients With Relapsed, Progressive or Refractory B-Cell Lymphoma | Phase 1/Phase 2 | Active, not recruiting | Jun 26, 2018 | 2029-01 (estimated) |
| NCT04663347 | Safety and Efficacy Trial of Epcoritamab Combinations in Subjects With B-cell Non-Hodgkin Lymphoma (B-NHL) | Phase 1/Phase 2 | Active, not recruiting | Nov 3, 2020 | Sep 30, 2027 (estimated) |
| NCT04542824 | Trial of the Safety and Efficacy of Epcoritamab in Japanese Subjects With Relapsed or Refractory (R/R) B-Cell Non-Hodgkin Lymphoma (R/R B-NHL) | Phase 1/Phase 2 | Active, not recruiting | Aug 20, 2020 | 2027-09 (estimated) |
| NCT07702032 | Study of Petosemtamab Plus Chemotherapy Versus Cetuximab Plus Chemotherapy in RAS and BRAF Wild-type, Unresectable or Metastatic, Left-sided Colorectal Cancer (LiGeR-CRC1) | Phase 3 | Recruiting | Aug 11, 2026 | 2029-07 (estimated) |
| NCT07166094 | Study to Assess the Efficacy and Safety of Rina-S Compared to Treatment of Investigator's Choice in Participants With Endometrial Cancer | Phase 3 | Recruiting | Nov 28, 2025 | 2029-08 (estimated) |
| NCT04623541 | Safety and Efficacy Study of Epcoritamab in Subjects With Relapsed/Refractory Chronic Lymphocytic Leukemia and Richter's Syndrome | Phase 1/Phase 2 | Active, not recruiting | Nov 25, 2020 | 2027-12 (estimated) |
| NCT07225270 | Study to Assess the Efficacy and Safety of Rina-S Plus Standard of Care Compared to Standard of Care for Maintenance Treatment of Participants With Recurrent Platinum-sensitive Ovarian Cancer After Second-line (2L) Platinum-based Doublet Chemotherapy | Phase 3 | Recruiting | Apr 3, 2026 | 2028-10 (estimated) |
| NCT07859215 | Study to Assess the Efficacy and Safety of Rina-S Plus Standard of Care Compared to Standard of Care Maintenance Treatment After First-line (1L) Platinum-based Chemotherapy in Participants With Ovarian Cancer | Phase 3 | Not yet recruiting | 2026-11 | 2030-03 (estimated) |
| NCT06984328 | Study of the Effectiveness and Safety of Acasunlimab Alone and With Pembrolizumab to Treat Advanced Melanoma of the Skin That Has Returned After Treatment With an Approved Checkpoint Inhibitor Therapy (ABBIL1TY MELANOMA-07) | Phase 2 | Terminated | Jul 25, 2025 | May 15, 2026 (actual) |
| NCT06619236 | Study to Assess the Efficacy of Rina-S Compared to Treatment of Investigator's Choice in Participants With Platinum Resistant Ovarian Cancer | Phase 3 | Active, not recruiting | Feb 7, 2025 | Aug 18, 2026 (actual) |
| NCT05117242 | Safety and Efficacy Study of GEN1046 as a Single Agent or in Combination With Pembrolizumab for Treatment of Recurrent (Non-small Cell) Lung Cancer | Phase 2 | Terminated | Oct 27, 2021 | Dec 2, 2024 (actual) |
| NCT05451810 | A Study to Evaluate Adverse Events of Subcutaneous (SC) Epcoritamab Administered in the Outpatient Setting in Adult Participants With Relapsed or Refractory Diffuse Large B-Cell Lymphoma and Classic Follicular Lymphoma | Phase 2 | Active, not recruiting | Aug 17, 2022 | 2027-03 (estimated) |
| NCT05201248 | A Study to Evaluate Adverse Events and Change in Disease Activity of Subcutaneous (SC) Epcoritamab As Monotherapy or Combined With Standard of Care Therapies in Adult Participants in China With B-Cell Non-Hodgkin Lymphoma | Phase 1/Phase 2 | Active, not recruiting | Mar 10, 2022 | 2026-09 (estimated) |
| NCT05206357 | Study of the Adverse Events and Change in Disease State of Pediatric Participants (and Young Adults Between the Ages of 18-25) With Relapsed/Refractory Aggressive Mature B-cell Neoplasms Receiving Subcutaneous (SC) Injections of Epcoritamab | Phase 1 | Active, not recruiting | Oct 4, 2022 | 2028-11 (estimated) |
| NCT05578976 | A Study to Evaluate Change in Disease Activity of Subcutaneous (SC) Epcoritamab Combined With Intravenous and Oral Rituximab, Cyclophosphamide, Doxorubicin Hydrochloride, Vincristine, and Prednisone (R-CHOP) or R-CHOP in Adult Participants With Newly Diagnosed Diffuse Large B-Cell Lymphoma (DLBCL) | Phase 3 | Active, not recruiting | Feb 8, 2023 | 2027-06 (estimated) |
| NCT07387068 | Trial to Evaluate the Safety and Preliminary Efficacy of GEN1079 in Participants With Advanced Solid Tumors | Phase 1 | Recruiting | Apr 7, 2026 | 2031-01 (estimated) |
| NCT03917381 | GEN1046 Safety Trial in Patients With Malignant Solid Tumors | Phase 1/Phase 2 | Terminated | May 14, 2019 | Apr 1, 2025 (actual) |
| NCT05491317 | A Safety and Antitumor Activity Trial of Immunoradiotherapy Combinations as a Treatment Option for Subjects With Metastatic Solid Tumors | Phase 1/Phase 2 | Terminated | Mar 8, 2023 | Aug 11, 2025 (actual) |
| NCT06391775 | Trial to Assess the Safety and Preliminary Efficacy of GEN1055 on Malignant Solid Tumors as Monotherapy and as Combination Therapy | Phase 1/Phase 2 | Terminated | May 14, 2024 | Nov 20, 2025 (actual) |
| NCT04083599 | GEN1042 Safety Trial and Anti-tumor Activity in Participants With Malignant Solid Tumors | Phase 1/Phase 2 | Active, not recruiting | Sep 17, 2019 | Dec 30, 2025 (actual) |
| NCT06191744 | Study of Subcutaneous Epcoritamab in Combination With Intravenous Rituximab and Oral Lenalidomide (R2) to Assess Adverse Events and Change in Disease Activity in Adult Participants With Previously Untreated Follicular Lymphoma | Phase 3 | Active, not recruiting | Feb 5, 2024 | 2037-11 (estimated) |
| NCT05180474 | GEN1047 for Solid Tumors - First in Human (FIH) Trial | Phase 1/Phase 2 | Terminated | Dec 13, 2021 | Mar 25, 2026 (actual) |
| NCT06685068 | A Phase 1/2 Study of GEN1286 in Patients With Advanced Solid Tumors | 1 | Terminated | Nov 13, 2024 | Mar 30, 2026 (actual) |
| NCT05409066 | Study of Subcutaneous Epcoritamab in Combination With Intravenous Rituximab and Oral Lenalidomide (R2) to Assess Adverse Events and Change in Disease Activity in Adult Participants With Follicular Lymphoma | Phase 3 | Active, not recruiting | Sep 20, 2022 | 2029-12 (estimated) |
| NCT05283720 | A Study to Evaluate Adverse Events and Change in Disease Activity of Subcutaneous (SC) Epcoritamab in Combination With Oral and Intravenous Anti-Neoplastic Agents in Adult Participants With Non-Hodgkin Lymphoma | Phase 2 | Active, not recruiting | Jun 14, 2022 | 2032-11 (estimated) |
| NCT05660967 | Subcutaneous Epcoritamab With or Without Lenalidomide as First Line Therapy for Diffuse Large B-Cell Lymphoma | Phase 2 | Terminated | Mar 6, 2023 | Jun 10, 2026 (actual) |
| NCT06171789 | PRO1107 in Patients With Advanced Solid Tumors | Phase 1/Phase 2 | Terminated | Jan 3, 2024 | Aug 18, 2025 (actual) |
| NCT04628494 | A Phase 3 Trial of Epcoritamab vs Investigator's Choice Chemotherapy in Relapsed/Refractory (R/R) Diffuse Large B-cell Lymphoma (DLBCL) | 3 | Active, not recruiting | Jan 13, 2021 | Oct 13, 2025 (actual) |
| NCT04824794 | GEN3014 Trial in Relapsed or Refractory Hematologic Malignancies | Phase 1/Phase 2 | Terminated | Mar 9, 2021 | Jun 30, 2025 (actual) |
| NCT07226752 | A Sub-study Trial of Epcoritamab vs Investigator's Choice Chemotherapy in Relapsed/Refractory Diffuse Large B-cell Lymphoma (R/R DLBCL) in China | Phase 3 | Active, not recruiting | Oct 8, 2022 | Oct 13, 2025 (actual) |
| NCT06508658 | A Study of Subcutaneously Injected Epcoritamab Plus Oral Lenalidomide Tablets Compared to Intravenously (IV) Infused Rituximab Plus IV Infused Gemcitabine and IV Infused Oxaliplatin in Adult Participants With Relapsed or Refractory Diffuse Large B-Cell Lymphoma | Phase 3 | Active, not recruiting | Aug 13, 2024 | 2028-03 (estimated) |
| NCT05721222 | Trial of PRO1160 (GEN1160) in Relapsed or Refractory Non-Hodgkin Lymphoma (NHL) (PRO1160-001) | Phase 1/Phase 2 | Terminated | Mar 15, 2023 | Nov 5, 2025 (actual) |
| NCT06771921 | A First-in-Human Trial of Safety and Efficacy of GEN1078 in Participants With Solid Tumors | Phase 1/Phase 2 | Terminated | Jan 29, 2025 | Jun 11, 2025 (actual) |
| NCT05586321 | Study of Safety and Antitumor Activity of GEN1056 in Participants With Advanced Solid Tumors | Phase 1 | Completed | Oct 24, 2022 | Oct 23, 2025 (actual) |
| NCT06018129 | A First-in-human Trial of GEN3017 in Hodgkin Lymphoma and Non-Hodgkin Lymphoma | Phase 1/Phase 2 | Terminated | Sep 21, 2023 | Feb 5, 2025 (actual) |
| NCT04937153 | GEN1046 Safety and PK in Subjects With Advanced Solid Malignancies | Phase 1 | Completed | Jun 15, 2021 | Oct 1, 2024 (actual) |
| NCT05435339 | A Study to Evaluate Safety, Tolerability, and Preliminary Effect of the GEN1053 Antibody on Malignant Solid Tumors as Monotherapy | Phase 1/Phase 2 | Terminated | Oct 4, 2022 | May 24, 2024 (actual) |
| NCT04358458 | First-in-Human (FIH) Trial of GEN3009 in Subjects With Relapsed or Refractory B-Cell Non-Hodgkin Lymphomas | Phase 1/Phase 2 | Terminated | Mar 13, 2020 | Nov 21, 2022 (actual) |