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Priya Life Science Compound trial record
Compound · clinical trials

Darzalex clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 23 trials in our USA, France, China, UK, Germany, Spain, Canada, Japan, South Korea, Italy, Australia, Israel, Poland, Brazil, Taiwan, Netherlands, Norway, Turkey, Belgium, Sweden, Austria, Czechia, Mexico, India and Egypt registers that name Darzalex as an intervention. Synced 10 Nov 2026
23Current trials
13Recruiting now
21Lead sponsors
25Country registers
At a glance

Darzalex is named as an intervention in 23 current clinical trials in our USA, France, China, UK, Germany, Spain, Canada, Japan, South Korea, Italy, Australia, Israel, Poland, Brazil, Taiwan, Netherlands, Norway, Turkey, Belgium, Sweden, Austria, Czechia, Mexico, India and Egypt registers. 13 are recruiting patients now. The most common phase is Phase 3. The sponsor with the most trials is Regeneron Pharmaceuticals (3). The most-studied condition is Multiple Myeloma.

Patient leaflets for Darzalex

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Trials by status

  • Recruiting1357%
  • Not yet open29%
  • Active, closed835%

Trials by phase

  • Phase 3730%
  • Phase 2730%
  • Phase 1/2417%
  • Phase 1313%
  • Phase 2/314%
  • Phase 414%
01

Clinical trials of Darzalex

23 trials
StudyPhaseStatusLead sponsorRegisters
Treatment of High-risk Newly Diagnosed Multiple Myeloma With Minimal Residual Disease Detection
NCT06409702 · ClinicalTrials.gov ↗ · Newly Diagnosed, High Risk, MRD
Phase 4 Recruiting The First Affiliated Hospital of Soochow University China
Lenalidomide, and Dexamethasone With or Without Daratumumab in Treating Patients With High-Risk Smoldering Myeloma
NCT03937635 · ClinicalTrials.gov ↗ · Smoldering Plasma Cell Myeloma
Phase 3 Recruiting ECOG-ACRIN Cancer Research Group Egypt
A Study to Learn About the Study Medicine Elranatamab Alone and With Daratumumab in People With Multiple Myeloma Who Have Received Other Treatments
NCT05020236 · Multiple Myeloma
Phase 3 Recruiting Pfizer UK, USA, China, Germany, France, Spain, Italy, Netherlands, Belgium, Sweden, Poland, Austria, Czechia, Norway, Turkey, Canada, Brazil, Mexico, Japan, South Korea, Taiwan, Australia
Elranatamab/Lenalidomide Consolidation and/or Elranatamab Maintenance Versus Standard of Care After D-VRd Induction in Transplant-eligible NDMM Patients
NCT06918002 · ClinicalTrials.gov ↗ · Multiple Myeloma, Newly Diagnosed
Phase 3 Recruiting Intergroupe Francophone du Myelome France, Belgium
A Study to Compare Linvoseltamab Monotherapy and Linvoseltamab + Carfilzomib Combination Therapy With Standard-of-Care Combination Regimens in Adult Participants With Relapsed/Refractory Multiple Myeloma (RRMM)
NCT07222761 · Relapsed and/or Refractory Multiple Myeloma (RRMM)
Phase 3 Recruiting Regeneron Pharmaceuticals UK, USA, Turkey, Brazil, South Korea, Taiwan, Australia
A Study Comparing AZD0120, a Dual-targeted CAR-T Against B-cell Maturation Antigen (BCMA) and CD19, Versus Standard Regimens in Participants With Relapsed Refractory Multiple Myeloma (DURGA-4)
NCT07391657 · Relapsed Refractory Multiple Myeloma
Phase 3 Recruiting AstraZeneca UK, USA, China, Germany, France, Spain, Italy, Poland, Norway, Canada, Brazil, Japan, South Korea, Taiwan, Australia
A Study to Compare Linvoseltamab and Daratumumab Treatment in High-Risk Smoldering Multiple Myeloma (HR-SMM)
NCT07393282 · High Risk Smoldering Multiple Myeloma (HR-SMM)
Phase 3 Recruiting Regeneron Pharmaceuticals UK, USA, France, Poland, Japan, South Korea
Study to Evaluate the Safety and Efficacy of Daratumumab and Carfilzomib-based Induction/Consolidation/Maintenance Therapy in Transplant-eligible, Ultra High-risk, Newly Diagnosed Multiple Myeloma
NCT06140966 · ClinicalTrials.gov ↗ · Multiple Myeloma, Primary Plasma Cell Leukemia, Extramedullary Multiple Myeloma
Phase 2 Recruiting Union Hospital, Tongji Medical College, Huazhong University of Science and Technology China
Use of a New Medicine "Daratumumab" to Treat Left-over Cancer in a Blood Cancer Called "T Acute Lymphoblastic Leukemia"
NCT07021677 · ClinicalTrials.gov ↗ · T Acute Lymphoblastic Leukemia
Phase 2 Recruiting Tata Memorial Centre India
Selinexor and Backbone Treatments of Multiple Myeloma Patients
NCT02343042 · Multiple Myeloma
Phase 1/2 Recruiting Karyopharm Therapeutics Inc USA, Canada
IDP-023 as a Single Agent and in Combination With Antibody Therapies in Patients With Advanced Hematologic Cancers
NCT06119685 · NHL, Multiple Myeloma, Blood Cancer
Phase 1/2 Recruiting Indapta Therapeutics, INC USA
A Study to Examine the Effects of Novel Therapy Linvoseltamab in Combination With Other Cancer Treatments for Adult Participants With Multiple Myeloma That is Resistant to Current Standard of Care Treatments
NCT05137054 · Multiple Myeloma
Phase 1 Recruiting Regeneron Pharmaceuticals USA, France, Spain, Israel
Escalation of Doses of Daratumumab in Combination With Chemotherapy (Idarubicin and Cytarabine or CPX-351) in Patients of 60 Years Old or More With Adverse Risk Acute Myeloblastic Leukemia (AML) (DARALAM)
NCT05749276 · ClinicalTrials.gov ↗ · Adult Patients With Adverse Risk Acute Myeloblastic Leukemia
Phase 1 Recruiting Nantes University Hospital France
A Study to Evaluate the Efficacy and Safety of HLX15-IV Versus DARZALEX® in Combination with Lenalidomide-Dexamethasone (Rd) in Transplant-ineligible Patients with Newly Diagnosed Multiple Myeloma
NCT06895512 · ClinicalTrials.gov ↗ · Newly Diagnosed Multiple Myeloma
Phase 3 Not yet open Shanghai Henlius Biotech China
New Therapeutic Target for Toxic Epidermal Necrolysis (TEN) Using Anti-CD38+ Monoclonal Antibodies.
NCT07110662 · ClinicalTrials.gov ↗ · Toxic Epidermal Necrolysis, Immunotherapy, Cutaneous Adverse Drug Reactions (CADR)
Phase 1/2 Not yet open Hospices Civils de Lyon France
Safety and Efficacy of Daratumumab in Patients With Anti-Aquaporin 4 Antibody Positive Neuromyelitis Optica Spectrum Disorders
NCT05403138 · ClinicalTrials.gov ↗ · Neuromyelitis Optica, Neuromyelitis Optica Spectrum Disorder, NMO Spectrum Disorder
Phase 2/3 Active, closed Tianjin Medical University General Hospital China
Phase II Study of the CD38 Antibody Daratumumab in Patients With High-Risk MGUS and Low-Risk Smoldering Multiple Myeloma
NCT03236428 · ClinicalTrials.gov ↗ · Monoclonal Gammopathy, Smoldering Multiple Myeloma
Phase 2 Active, closed Dana-Farber Cancer Institute Israel
A Trial for Relapsed and Relapsed/Refractory Multiple Myeloma Patients
NCT04124497 · ClinicalTrials.gov ↗ · Multiple Myeloma, Deletion 17P Syndrome
Phase 2 Active, closed Fondazione EMN Italy Onlus Italy
Daratumumab, Carfilzomib, Pomalidomide, Dexamethasone In MM
NCT04176718 · Multiple Myeloma, Refractory Multiple Myeloma, Multiple Myeloma in Relapse
Phase 2 Active, closed Andrew Yee, MD Israel
Daratumumab for First Line Treatment of Transplant-ineligible Myeloma Patients Followed by Daratumumab Re-treatment at First Relapse
NCT04656951 · ClinicalTrials.gov ↗ · Multiple Myeloma
Phase 2 Active, closed University of Cologne Germany
Study of Selinexor Plus DRd for Newly Diagnosed Multiple Myeloma
NCT04782687 · Multiple Myeloma, Myeloma Multiple, Kahler Disease
Phase 2 Active, closed US Oncology Research USA
A Study to Determine Dose, Safety, Tolerability and Efficacy of CC-220 Monotherapy, and in Combination With Other Treatments in Subjects With Multiple Myeloma
NCT02773030 · Multiple Myeloma
Phase 1/2 Active, closed Celgene UK, USA, Germany, France, Spain, Italy, Netherlands, Canada, Japan, Australia, Israel
A Study of Subcutaneous Daratumumab Regimens in Combination With Bispecific T Cell Redirection Antibodies for the Treatment of Participants With Multiple Myeloma
NCT04108195 · Multiple Myeloma
Phase 1 Active, closed Janssen Research & Development, LLC USA, Germany, Spain, Netherlands, Canada

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with Darzalex

32 conditions
Multiple Myeloma12High Risk Smoldering Multiple Myeloma (HR-SMM)1Relapsed Refractory Multiple Myeloma1Relapsed and/or Refractory Multiple Myeloma (RRMM)1NHL1Blood Cancer1Refractory Non-Hodgkin Lymphoma1Myeloma Multiple1Kahler Disease1Myeloma, Plasma Cell1T Acute Lymphoblastic Leukemia1Neuromyelitis Optica1
All 32 conditions
Condition (as registered)Trials
Multiple Myeloma12
High Risk Smoldering Multiple Myeloma (HR-SMM)1
Relapsed Refractory Multiple Myeloma1
Relapsed and/or Refractory Multiple Myeloma (RRMM)1
NHL1
Blood Cancer1
Refractory Non-Hodgkin Lymphoma1
Myeloma Multiple1
Kahler Disease1
Myeloma, Plasma Cell1
T Acute Lymphoblastic Leukemia1
Neuromyelitis Optica1
Neuromyelitis Optica Spectrum Disorder1
NMO Spectrum Disorder1
Primary Plasma Cell Leukemia1
Extramedullary Multiple Myeloma1
Newly Diagnosed Multiple Myeloma1
Newly Diagnosed1
High Risk1
MRD1
Toxic Epidermal Necrolysis1
Immunotherapy1
Cutaneous Adverse Drug Reactions (CADR)1
Adult Patients With Adverse Risk Acute Myeloblastic Leukemia1
Multiple Myeloma, Newly Diagnosed1
Deletion 17P Syndrome1
Monoclonal Gammopathy1
Smoldering Multiple Myeloma1
Refractory Multiple Myeloma1
Multiple Myeloma in Relapse1
Relapse1
Smoldering Plasma Cell Myeloma1
05

Related compounds

06

Questions about Darzalex trials

How many clinical trials are testing Darzalex?

23 current trials in our USA, France, China, UK, Germany, Spain, Canada, Japan, South Korea, Italy, Australia, Israel, Poland, Brazil, Taiwan, Netherlands, Norway, Turkey, Belgium, Sweden, Austria, Czechia, Mexico, India and Egypt registers name Darzalex as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are Darzalex trials recruiting patients?

Yes. 13 of the 23 trials are recruiting: 7 with sites in USA, 6 with sites in France, 4 with sites in China, 4 with sites in UK, 2 with sites in Germany, 3 with sites in Spain, 3 with sites in Canada, 3 with sites in Japan, 4 with sites in South Korea, 2 with sites in Italy, 3 with sites in Australia, 1 with sites in Israel, 3 with sites in Poland, 3 with sites in Brazil, 3 with sites in Taiwan, 1 with sites in Netherlands, 2 with sites in Norway, 2 with sites in Turkey, 2 with sites in Belgium, 1 with sites in Sweden, 1 with sites in Austria, 1 with sites in Czechia, 1 with sites in Mexico, 1 with sites in India and 1 with sites in Egypt. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Darzalex clinical trials?

Regeneron Pharmaceuticals (3), AstraZeneca (1), Celgene (1) and Pfizer (1), among 21 lead sponsors in total. The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Darzalex works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how Darzalex works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Darzalex (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 10 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.