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Compound · clinical trials

Elotuzumab clinical trials

Also listed in trial records as Empliciti
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 7 trials in our USA, UK, China and India registers that name Elotuzumab as an intervention. Synced 26 Sep 2026
7Current trials
4Recruiting now
7Lead sponsors
4Country registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards
At a glance

Elotuzumab is named as an intervention in 7 current clinical trials in our USA, UK, China and India registers. 4 are recruiting patients now. The most common phase is Phase 3. The sponsor with the most trials is Regeneron Pharmaceuticals (1). The most-studied condition is Multiple Myeloma. The EU clinical trials register (CTIS) separately lists 2 authorised or ongoing trials.

Trials by status

  • Recruiting457%
  • Active, closed343%

Trials by phase

  • Phase 3571%
  • Phase 1/2229%
01

Clinical trials of Elotuzumab

7 trials
StudyPhaseStatusLead sponsorRegisters
A Trial to Learn How Well Linvoseltamab Works Compared to the Combination of Elotuzumab, Pomalidomide and Dexamethasone for Adult Participants With Relapsed/Refractory Multiple Myeloma
NCT05730036 · ClinicalTrials.gov ↗ · Relapsed Refractory Multiple Myeloma (RRMM)
Phase 3 Recruiting Regeneron Pharmaceuticals UK, USA
MagnetisMM-32: A Study to Learn About the Study Medicine Called Elranatamab in People With Multiple Myeloma (MM) That Has Come Back After Taking Other Treatments (Including Prior Treatment With an Anti-CD38 Antibody and Lenalidomide)
NCT06152575 · ClinicalTrials.gov ↗ · Multiple Myeloma
Phase 3 Recruiting Pfizer UK, USA, China
Cevostamab in Combination With Pomalidomide and Dexamethasone Versus Standard of Care in Participants With Previously Treated Multiple Myeloma
NCT07555938 · Multiple Myeloma
Phase 3 Recruiting Hoffmann-La Roche USA, China
Selinexor and Backbone Treatments of Multiple Myeloma Patients
NCT02343042 · ClinicalTrials.gov ↗ · Multiple Myeloma
Phase 1/2 Recruiting Karyopharm Therapeutics Inc USA
Study Assessing Activity of Intravenous (IV) Etentamig Monotherapy Versus Standard Available Therapies in Adult Participants With Relapsed or Refractory Multiple Myeloma
NCT06158841 · ClinicalTrials.gov ↗ · Multiple Myeloma
Phase 3 Active, closed AbbVie UK, USA, China
A Study Comparing Talquetamab Plus Pomalidomide, Talquetamab Plus Teclistamab, and Elotuzumab, Pomalidomide, and Dexamethasone or Pomalidomide, Bortezomib, and Dexamethasone in Participants With Relapsed or Refractory Myeloma Who Have Received an Anti-CD38 Antibody and Lenalidomide
NCT06208150 · ClinicalTrials.gov ↗ · Multiple Myeloma
Phase 3 Active, closed Janssen Research & Development, LLC UK, USA, India, China
A Study to Determine the Recommended Dose and Regimen and to Evaluate the Safety and Preliminary Efficacy of CC-92480 in Combination With Standard Treatments in Participants With Relapsed or Refractory Multiple Myeloma (RRMM) and Newly Diagnosed Multiple Myeloma (NDMM)
NCT03989414 · Multiple Myeloma
Phase 1/2 Active, closed Celgene USA

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

Elotuzumab in the EU trials register (CTIS)

2 trials

Authorised or ongoing trials in the EU Clinical Trials Information System that list a product containing Elotuzumab. Many trials are registered in both CTIS and ClinicalTrials.gov, so these are shown separately rather than added to the count above. Trials with a site in Ireland are listed first.

StudyPhaseStatusSponsorCountries
A Phase III, Randomized, Open-Label, Multicenter Study Evaluating the Efficacy and Safety of Cevostamab in Combination with Pomalidomide and Dexamethasone Versus Standard of Care in Patients with Multiple Myeloma who Have Received One to Three Prior Lines of Therapy
2025-524028-23-00 · CTIS ↗ · Neoplasms
Phase 3 Ongoing F. Hoffmann-La Roche AG France, Germany, Italy + 5 more
HO183 CAR T: A phase III randomized trial comparing academically produced BCMA-directed CAR T-cells (ARI0002h) with standard of care regimen in patients with relapsed/refractory multiple myeloma
2025-524876-43-00 · CTIS ↗ · Neoplasms
Phase 3 Authorised Universitair Medisch Centrum Groningen Netherlands
03

Elotuzumab across our data

Ireland · EU · US

The same active substance in our other registers, matched by its exact name. Each entry links to the register record it comes from.

Licensed in Ireland (HPRA)

2 single-substance products containing Elotuzumab on the HPRA medicines list.

All 2 Irish products →

Supply shortages

No entry for Elotuzumab in the EMA, FDA or German BfArM shortage lists we track.

04

Conditions studied with Elotuzumab

2 conditions
Multiple Myeloma6Relapsed Refractory Multiple Myeloma (RRMM)1
05

Sponsors

lead sponsor per trial
Lead sponsorTrials
Regeneron Pharmaceuticals1
Janssen Research & Development, LLC1
AbbVie1
Pfizer1
Celgene1
Hoffmann-La Roche1
Karyopharm Therapeutics Inc1
06

By country register

RegisterTrialsRecruiting
Clinical trials in USA74
Clinical trials in UK42
Clinical trials in China42
Clinical trials in India10
EU register (CTIS)2—

A trial with sites in more than one country appears in each of those registers. CTIS does not publish a recruiting flag; its trials may also appear in the registers above.

07

Related compounds

08

Questions about Elotuzumab trials

How many clinical trials are testing Elotuzumab?

7 current trials in our USA, UK, China and India registers name Elotuzumab as a drug or biological intervention, as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are Elotuzumab trials recruiting patients?

Yes. 4 of the 7 trials are recruiting: 4 with sites in USA, 2 with sites in UK and 2 with sites in China. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Elotuzumab clinical trials?

Regeneron Pharmaceuticals (1), Janssen Research & Development, LLC (1), AbbVie (1) and Pfizer (1), among 7 lead sponsors in total. The number in brackets is how many trials each organisation leads.

Is Elotuzumab licensed in Ireland?

Yes. The HPRA medicines list includes 2 single-substance products containing Elotuzumab, for example Empliciti 300 mg powder for concentrate for solution for infusion. (Bristol-Myers Squibb Pharma EEIG). A licence does not mean a product is currently marketed or reimbursed; see each product's record.

Is there a Elotuzumab shortage?

Not in the lists we track: Elotuzumab has no entry in the EMA, FDA or German BfArM shortage registers as of their latest sync.

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 Elotuzumab 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 โ€” it is not written from memory, and nothing here describes how Elotuzumab 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 Elotuzumab (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 26 Sep 2026.

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 โ€” 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 โ€” we correct promptly and log it.