Daratumumab
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Also known as Daratumumab component of darzalex fasproDaratumumab-fihjDarzalexHUMAX-CD 38HUMAXCD38HuMax-CD38
Summary
Daratumumab (CHEMBL1743007) is an approved antibody (ATC L01FC01) targeting CD38; indicated across 46 conditions including plasma cell myeloma and neoplasm.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Antibody
- ATC class: L01FC01
- Targets: 1 (CD38)
- Indications: 46 conditions
- Clinical trials: 314
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1743007 |
| Name | Daratumumab |
| Type | Antibody |
| Max phase | 4 |
| ATC | L01FC01 |
Also known as: Daratumumab, Daratumumab component of darzalex faspro, Daratumumab-fihj, Darzalex, HUMAX-CD 38, HUMAXCD38, HuMax-CD38, DARATUMUMAB
Targets
Targets
Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| CD38 | CD38 | Antagonist | 8.22 | 0% | P28907 |
Bioactivity
No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).
Target pathways
Aggregated over 1 target gene(s): CD38.
Top Reactome pathways
4 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| Metabolism | 1 | CD38 |
| Nicotinate metabolism | 1 | CD38 |
| Metabolism of water-soluble vitamins and cofactors | 1 | CD38 |
| Metabolism of vitamins and cofactors | 1 | CD38 |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| response to hypoxia | 1 |
| signal transduction | 1 |
| positive regulation of cytosolic calcium ion concentration | 1 |
| female pregnancy | 1 |
| response to xenobiotic stimulus | 1 |
| negative regulation of neuron projection development | 1 |
| artery smooth muscle contraction | 1 |
| positive regulation of cell growth | 1 |
| positive regulation of B cell proliferation | 1 |
| positive regulation of insulin secretion | 1 |
| response to estradiol | 1 |
| response to retinoic acid | 1 |
| response to progesterone | 1 |
| response to hydroperoxide | 1 |
| B cell proliferation | 1 |
Indications & clinical
Indications
46 indications (3 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| plasma cell myeloma | 4 | MONDO:0009693 | EFO:0001378 |
| neoplasm | 4 | MONDO:0005070 | EFO:0000616 |
| amyloidosis | 3 | MONDO:0019065 | EFO:1001875 |
| smoldering plasma cell myeloma | 3 | MONDO:0005235 | EFO:0003073 |
| hereditary amyloidosis | 3 | MONDO:0018634 | MONDO:0019438 |
| lymphoma | 2 | MONDO:0005062 | EFO:0000574 |
| B-cell chronic lymphocytic leukemia | 2 | MONDO:0004948 | EFO:0000095 |
| myelodysplastic syndrome | 2 | MONDO:0018881 | EFO:0000198 |
| monoclonal gammopathy | 2 | MONDO:0004960 | EFO:0000203 |
| acute lymphoblastic leukemia | 2 | MONDO:0004967 | EFO:0000220 |
| acute myeloid leukemia | 2 | MONDO:0018874 | EFO:0000222 |
| diffuse large B-cell lymphoma | 2 | MONDO:0018905 | EFO:0000403 |
| non-small cell lung carcinoma | 2 | MONDO:0005233 | EFO:0003060 |
| mantle cell lymphoma | 2 | MONDO:0018876 | EFO:1001469 |
| colorectal carcinoma | 2 | MONDO:0024331 | EFO:1001951 |
| plasma cell leukemia | 2 | MONDO:0018689 | EFO:0006475 |
| Waldenstrom macroglobulinemia | 2 | MONDO:0100280 | EFO:0009441 |
| plasmacytoma | 2 | MONDO:0005615 | EFO:0006738 |
| autoimmune thrombocytopenic purpura | 2 | MONDO:0008558 | EFO:0007160 |
| POEMS syndrome | 2 | MONDO:0017364 | EFO:1001115 |
| follicular lymphoma | 2 | MONDO:0018906 | MONDO:0018906 |
| T-cell acute lymphoblastic leukemia | 2 | MONDO:0004963 | EFO:0000209 |
| lupus nephritis | 2 | MONDO:0005556 | EFO:0005761 |
| neuromyelitis optica | 2 | MONDO:0019100 | EFO:0004256 |
| Alzheimer disease | 2 | MONDO:0004975 | MONDO:0004975 |
| membranoproliferative glomerulonephritis | 2 | MONDO:0002461 | MONDO:0018904 |
| nephrotic syndrome | 2 | MONDO:0005377 | EFO:0004255 |
| glomerulonephritis | 2 | MONDO:0002462 | MONDO:0002462 |
| systemic lupus erythematosus | 2 | MONDO:0007915 | MONDO:0007915 |
| leukemia | 2 | MONDO:0005059 | EFO:0000565 |
| lymphoid leukemia | 2 | MONDO:0005402 | EFO:0004289 |
| male reproductive organ cancer | 2 | MONDO:0005836 | EFO:0007355 |
| sickle cell disease | 2 | MONDO:0011382 | MONDO:0011382 |
| Hodgkins lymphoma | 1 | MONDO:0004952 | EFO:0000183 |
| prostate adenocarcinoma | 1 | MONDO:0005082 | EFO:0000673 |
| non-Hodgkin lymphoma | 1 | MONDO:0018908 | EFO:0005952 |
| mycosis fungoides | 1 | MONDO:0009691 | EFO:1001051 |
| graft versus host disease | 1 | MONDO:0013730 | EFO:0004599 |
| glioblastoma | 1 | MONDO:0018177 | EFO:0000519 |
| non-autoimmune hemolytic anemia | 1 | MONDO:0021559 | EFO:0005558 |
| immune system disorder | 1 | MONDO:0005046 | EFO:0000540 |
| aplastic anemia | 1 | MONDO:0015909 | HP:0001915 |
| primary cutaneous T-cell non-Hodgkin lymphoma | 1 | MONDO:0000607 | EFO:0002913 |
| clear cell renal carcinoma | 0 | MONDO:0005005 | EFO:0000349 |
2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 314.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE2 | 142 |
| PHASE1 | 52 |
| PHASE3 | 50 |
| PHASE1/PHASE2 | 37 |
| Not specified | 16 |
| PHASE4 | 7 |
| PHASE2/PHASE3 | 7 |
| EARLY_PHASE1 | 3 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT03829371 | PHASE4 | ACTIVE_NOT_RECRUITING | STUDY COMPARING TWO STANDARD TREATMENTS IN AUTOLOGOUS STEM CELL TRANSPLANTATION INELIGIBLE POPULATION AFFECTED BY MULTIPLE MYELOMA |
| NCT05849740 | PHASE4 | RECRUITING | An Exploratory Study of Cluster of Differentiation 38 (CD38) Monoclonal Antibody Combined Corticosteroid in Acquired Hemophilia A |
| NCT05888870 | PHASE4 | RECRUITING | ITI Using SCT800 Alone or Combining Daratumumab in Hemophilia A Adolescents and Adults With High Titer Inhibitor |
| NCT06409702 | PHASE4 | RECRUITING | Treatment of High-risk Newly Diagnosed Multiple Myeloma With Minimal Residual Disease Detection |
| NCT07274462 | PHASE4 | ACTIVE_NOT_RECRUITING | DARA-MVI Study (Daratumumab for Microvascular Inflammation in Kidney Transplantation) |
| NCT03768960 | PHASE4 | COMPLETED | A Study of DARZALEX (Daratumumab) In Indian Participants With Relapsed and Refractory Multiple Myeloma, Whose Prior Therapy Included a Proteasome Inhibitor and an Immunomodulatory Agent |
| NCT05511428 | PHASE4 | COMPLETED | Home Based Daratumumab Administration for Patients With Multiple Myeloma |
| NCT03651128 | PHASE3 | ACTIVE_NOT_RECRUITING | Efficacy and Safety Study of bb2121 Versus Standard Regimens in Subjects With Relapsed and Refractory Multiple Myeloma (RRMM) |
| NCT03652064 | PHASE3 | ACTIVE_NOT_RECRUITING | A Study Comparing Daratumumab, VELCADE (Bortezomib), Lenalidomide, and Dexamethasone (D-VRd) With VELCADE, Lenalidomide, and Dexamethasone (VRd) in Participants With Untreated Multiple Myeloma and for Whom Hematopoietic Stem Cell Transplant is Not Planned as Initial Therapy |
| NCT03710603 | PHASE3 | ACTIVE_NOT_RECRUITING | Daratumumab, VELCADE (Bortezomib), Lenalidomide and Dexamethasone Compared to VELCADE, Lenalidomide and Dexamethasone in Subjects With Previously Untreated Multiple Myeloma |
| NCT03742297 | PHASE3 | ACTIVE_NOT_RECRUITING | Treatment for Elderly Fit Newly Diagnosed Multiple Myeloma Patients Aged Between 65 and 80 Years |
| NCT03836014 | PHASE3 | ACTIVE_NOT_RECRUITING | Study Comparing Continuous Versus Fixed Duration Therapy With Daratumumab, Lenalidomide, and Dexamethasone for Relapsed Multiple Myeloma |
| NCT03901963 | PHASE3 | ACTIVE_NOT_RECRUITING | A Study of Daratumumab Plus Lenalidomide Versus Lenalidomide Alone as Maintenance Treatment in Participants With Newly Diagnosed Multiple Myeloma Who Are Minimal Residual Disease Positive After Frontline Autologous Stem Cell Transplant |
| NCT03937635 | PHASE3 | RECRUITING | Lenalidomide, and Dexamethasone With or Without Daratumumab in Treating Patients With High-Risk Smoldering Myeloma |
| NCT04071457 | PHASE3 | ACTIVE_NOT_RECRUITING | S1803, Lenalidomide +/- Daratumumab/rHuPh20 as Post-ASCT Maintenance for MM w/MRD to Direct Therapy Duration |
| NCT04181827 | PHASE3 | ACTIVE_NOT_RECRUITING | A Study Comparing JNJ-68284528, a CAR-T Therapy Directed Against B-cell Maturation Antigen (BCMA), Versus Pomalidomide, Bortezomib and Dexamethasone (PVd) or Daratumumab, Pomalidomide and Dexamethasone (DPd) in Participants With Relapsed and Lenalidomide-Refractory Multiple Myeloma |
| NCT04246047 | PHASE3 | ACTIVE_NOT_RECRUITING | Evaluation of Efficacy and Safety of Belantamab Mafodotin, Bortezomib and Dexamethasone Versus Daratumumab, Bortezomib and Dexamethasone in Participants With Relapsed/Refractory Multiple Myeloma |
| NCT04513639 | PHASE2/PHASE3 | RECRUITING | The Relapse from MRD Negativity As Indication for Treatment (REMNANT) Study |
| NCT04566328 | PHASE3 | RECRUITING | Testing the Use of Combination Therapy in Adult Patients With Newly Diagnosed Multiple Myeloma, the EQUATE Trial |
| NCT04975997 | PHASE3 | ACTIVE_NOT_RECRUITING | Open-label Study Comparing Iberdomide, Daratumumab and Dexamethasone (IberDd) Versus Daratumumab, Bortezomib, and Dexamethasone (DVd) in Participants With Relapsed or Refractory Multiple Myeloma (RRMM) |
| NCT05020236 | PHASE3 | RECRUITING | A Study to Learn About the Study Medicine Elranatamab Alone and With Daratumumab in People With Multiple Myeloma Who Have Received Other Treatments |
| NCT05083169 | PHASE3 | ACTIVE_NOT_RECRUITING | A Study of Teclistamab in Combination With Daratumumab Subcutaneously (SC) (Tec-Dara) Versus Daratumumab SC, Pomalidomide, and Dexamethasone (DPd) or Daratumumab SC, Bortezomib, and Dexamethasone (DVd) in Participants With Relapsed or Refractory Multiple Myeloma |
| NCT05257083 | PHASE3 | ACTIVE_NOT_RECRUITING | A Study of Daratumumab, Bortezomib, Lenalidomide and Dexamethasone (DVRd) Followed by Ciltacabtagene Autoleucel Versus Daratumumab, Bortezomib, Lenalidomide and Dexamethasone (DVRd) Followed by Autologous Stem Cell Transplant (ASCT) in Participants With Newly Diagnosed Multiple Myeloma |
| NCT05403138 | PHASE2/PHASE3 | ACTIVE_NOT_RECRUITING | Safety and Efficacy of Daratumumab in Patients With Anti-Aquaporin 4 Antibody Positive Neuromyelitis Optica Spectrum Disorders |
| NCT05438043 | PHASE3 | RECRUITING | A Study of Daratumumab |
| NCT05455320 | PHASE3 | ACTIVE_NOT_RECRUITING | A Study Comparing Talquetamab in Combination With Daratumumab or in Combination With Daratumumab and Pomalidomide Versus Daratumumab in Combination With Pomalidomide and Dexamethasone in Participants With Multiple Myeloma That Returns After Treatment or is Resistant to Treatment |
| NCT05552222 | PHASE3 | RECRUITING | A Study of Teclistamab in Combination With Daratumumab and Lenalidomide (Tec-DR) and Talquetamab in Combination With Daratumumab and Lenalidomide (Tal-DR) in Participants With Newly Diagnosed Multiple Myeloma |
| NCT05561387 | PHASE3 | RECRUITING | Comparing Combinations of Drugs to Treat Newly Diagnosed Multiple Myeloma (NDMM) When a Stem Cell Transplant is Not a Medically Suitable Treatment |
| NCT05623020 | PHASE3 | RECRUITING | A Study to Learn About the Effects of the Combination of Elranatamab, Daratumumab and Lenalidomide Compared With Daratumumab, Bortezomib, Lenalidomide, and Dexamethasone in Patients With Newly Diagnosed Multiple Myeloma Who Are Not Candidates for Transplant |
| NCT06022939 | PHASE3 | RECRUITING | Comparing Dara-VCD Chemotherapy Plus Stem Cell Transplant to Dara-VCD Chemotherapy Alone for People Who Have Newly Diagnosed AL Amyloidosis |
| NCT06182774 | PHASE3 | RECRUITING | Fixed Duration vs Continuous Anti-CD38 Antibody Therapy Among Transplant Ineligible Older Adults With Newly-Diagnosed Multiple Myeloma |
| NCT06187441 | PHASE3 | RECRUITING | FeAsiBility of a Treatment Free Interval in Newly Diagnosed MM Patients Treated With Daratumumab-lenalidomide-dexamethasone (HOVON174MM) |
| NCT06296121 | PHASE3 | RECRUITING | A Study of the Efficacy and Safety of Monotherapy With BCD-264 and Darzalex in Subjects With Relapsed and Refractory Multiple Myeloma |
| NCT06413498 | PHASE3 | RECRUITING | A Study Comparing Anitocabtagene Autoleucel to Standard of Care Therapy in Participants With Relapsed/ Refractory Multiple Myeloma |
| NCT06464991 | PHASE3 | RECRUITING | A Phase III Study of Eque-cel in Subjects With Len-refractory RRMM (FUMANBA-03) |
| NCT06615479 | PHASE3 | RECRUITING | A Study to Compare the Efficacy and Safety of BMS-986393 Versus Standard Regimens in Adult Participants With Relapsed or Refractory and Lenalidomide-exposed Multiple Myeloma (QUINTESSENTIAL-2) |
| NCT06679101 | PHASE3 | RECRUITING | A Study of Belantamab Mafodotin Administered in Combination With Lenalidomide and Dexamethasone (BRd) Versus Daratumumab, Lenalidomide, and Dexamethasone (DRd) in Participants With Newly Diagnosed Multiple Myeloma (NDMM) Who Are Ineligible for Autologous Stem Cell Transplantation (TI-NDMM) |
| NCT06742138 | PHASE3 | NOT_YET_RECRUITING | To Evaluate the Efficacy and Safety of QL2109 and DARZALEX FASPRO® in Multiple Myeloma |
| NCT06868654 | PHASE3 | ACTIVE_NOT_RECRUITING | China Subpopulation: Evaluation of Efficacy and Safety of Belantamab Mafodotin, Bortezomib and Dexamethasone Versus Daratumumab, Bortezomib and Dexamethasone in Participants With Relapsed/Refractory Multiple Myeloma |
| NCT06868667 | PHASE3 | ACTIVE_NOT_RECRUITING | Japan Expansion Cohort: Evaluation of Efficacy and Safety of Belantamab Mafodotin, Bortezomib and Dexamethasone Versus Daratumumab, Bortezomib and Dexamethasone in Participants With Relapsed/Refractory Multiple Myeloma |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.
3 molecules share ≥1 primary target. Top 3 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| QUERCETIN | ChEMBL + PubChem | Phase 3 (approved) | CD38 |
| LUTEOLIN | ChEMBL | Phase 2 | CD38 |
| Resveratrol | PubChem | Approved | CD38 |
Related Atlas pages
- Genes: CD38
- Diseases: plasma cell myeloma, neoplasm, amyloidosis, smoldering plasma cell myeloma, hereditary amyloidosis
- Drugs: Quercetin, Resveratrol