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Celgene clinical trials

Also registered as Celgene Corp
Source: ClinicalTrials.gov, U.S. National Library of Medicine and the EU Clinical Trials Information System (CTIS) — current trials in our USA, UK, China, India, Ireland and EU (CTIS) registers with Celgene as lead sponsor. Synced 26 Sep 2026
24Current trials
8Recruiting now
39Drugs in these trials
6Trial registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 — Top 14 finalist
Compiled from ClinicalTrials.gov and CTIS registry records · Last verified · Editorial standards
At a glance

Celgene is the lead sponsor of 24 current clinical trials in our USA, UK, China, India, Ireland and EU (CTIS) registers. 8 are recruiting patients now. The most common phase is Phase 3. The drugs named most often in its trials are Cyclophosphamide, Rituximab and Dexamethasone. The most-studied condition is Multiple Myeloma.

Company profiles on this site (news, sites, medicines, approvals): Bristol Myers Squibb (US) →Bristol Myers Squibb (IE) →

ClinicalTrials.gov trials by status

  • Recruiting836%
  • Not yet open15%
  • Active, closed1359%

Trials by phase

  • Phase 3941%
  • Phase 2523%
  • Phase 1/2523%
  • Phase 129%
  • Phase 2/315%
01

Clinical trials sponsored by Celgene

22 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
A Study to Evaluate Mezigdomide, Bortezomib and Dexamethasone (MEZIVd) Versus Pomalidomide, Bortezomib and Dexamethasone (PVd) in Participants With Relapsed or Refractory Multiple Myeloma (RRMM)
NCT05519085 · Relapsed or Refractory Multiple Myeloma
Phase 3 Recruiting 2022-09 Ireland, UK, USA, India, China
Study of Safety & PK of Luspatercept (ACE-536) in Pediatric Participants With Beta (β)-Thalassemia
NCT04143724 · Beta-Thalassemia
Phase 2 Recruiting 2019-11 USA, India, China
A Study to Compare the Efficacy and Safety of Golcadomide in Combination With Rituximab (Golca + R) vs Investigator's Choice in Participants With Relapsed/Refractory Follicular Lymphoma Who Have Received at Least 1 Prior Line of Systemic Therapy (GOLSEEK-4)
NCT06911502 · ClinicalTrials.gov ↗ · Follicular Lymphoma
Phase 3 Recruiting 2025-07 UK, USA, India, China
A Study to Determine the Recommended Dose and Schedule, and Evaluate the Safety and Preliminary Efficacy of Mezigdomide in Combination With Elranatamab in Participants With Relapsed and/or Refractory Multiple Myeloma
NCT06988488 · Multiple Myeloma
Phase 1/2 Recruiting 2025-10 UK, USA, China
Long-Term Follow-up Protocol for Participants Treated With Gene-Modified T Cells
NCT03435796 · ClinicalTrials.gov ↗ · Neoplasms
Phase 2/3 Recruiting 2018-07 UK, USA
A Study to Evaluate Long-term Safety in Participants Who Have Participated in Other Luspatercept (ACE-536) Clinical Trials
NCT04064060 · ClinicalTrials.gov ↗ · Myelodysplastic Syndromes (MDS), Beta-thalassemia, Myeloproliferative Neoplasm(MPN)-Associated Myelofibrosis
Phase 3 Recruiting 2019-08 UK, USA, China
Study to Evaluate the Efficacy, Safety, and Tolerability of BMS-986368, for the Treatment of Agitation in Participants With Alzheimer's Disease
NCT06808984 · Agitation, Alzheimer Disease
Phase 2 Recruiting 2025-06 USA, China
A Study to Evaluate the Efficacy, Safety and Tolerability of BMS-986368 in Participants With Multiple Sclerosis Spasticity
NCT06782490 · ClinicalTrials.gov ↗ · Multiple Sclerosis Spasticity
Phase 2 Recruiting 2025-06 USA
A Study to Assess the Relative Bioavailability of Irafamdastat (BMS-986368) and to Assess the Food Effect on the Pharmacokinetics of Irafamdastat in Healthy Adult Participants
NCT07837115 · ClinicalTrials.gov ↗ · Healthy Volunteers
Phase 1 Not yet open 2026-10 USA
Open-label Study Comparing Iberdomide, Daratumumab and Dexamethasone (IberDd) Versus Daratumumab, Bortezomib, and Dexamethasone (DVd) in Participants With Relapsed or Refractory Multiple Myeloma (RRMM)
NCT04975997 · Multiple Myeloma
Phase 3 Active, closed 2022-06 Ireland, UK, USA, India, China
A Study to Evaluate the Efficacy and Safety of Golcadomide in Combination With Rituximab in Participants With Newly Diagnosed Advanced Stage Follicular Lymphoma
NCT06425302 · Lymphoma, Follicular
Phase 2 Active, closed 2024-08 UK, USA
A Study to Compare the Efficacy and Safety of BMS-986365 Versus the Investigator's Choice of Therapy in Participants With Metastatic Castration-resistant Prostate Cancer
NCT06764485 · ClinicalTrials.gov ↗ · Metastatic Castration-resistant Prostate Cancer
Phase 3 Active, closed 2025-03 Ireland, UK, USA, China
Study to Compare the Effectiveness and Safety of Golcadomide Plus R-CHOP vs Placebo Plus R-CHOP in Participants With Previously Untreated High-risk Large B-cell Lymphoma
NCT06356129 · ClinicalTrials.gov ↗ · Large B-cell Lymphoma
Phase 3 Active, closed 2024-06 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 2019-09 USA
An Efficacy and Safety Study of Luspatercept (ACE-536) Versus Placebo in Subjects With Myeloproliferative Neoplasm-Associated Myelofibrosis on Concomitant JAK2 Inhibitor Therapy and Who Require Red Blood Cell Transfusions
NCT04717414 · ClinicalTrials.gov ↗ · Myeloproliferative Disorders, Myelofibrosis, Primary Myelofibrosis
Phase 3 Active, closed 2021-02 Ireland, UK, USA, China
A Study to Compare the Efficacy and Safety of Luspatercept (ACE-536) Versus Epoetin Alfa for the Treatment of Anemia Due to IPSS-R Very Low, Low, or Intermediate Risk Myelodysplastic Syndromes (MDS) Participants Who Require Red Blood Cell Transfusions and Are ESA Naïve
NCT03682536 · Myelodysplastic Syndromes
Phase 3 Active, closed 2019-01 UK, 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 · ClinicalTrials.gov ↗ · Multiple Myeloma
Phase 1/2 Active, closed 2016-10 UK, USA
Study of Safety and Efficacy of Iberdomide (CC-220) and CC-99282 Combined With R-CHOP to Treat Lymphoma
NCT04884035 · Lymphoma, B-Cell
Phase 1 Active, closed 2021-09 USA
A Study to Assess the Safety and Efficacy of Two Combinations of Isocitrate Dehydrogenase (IDH) Mutant Targeted Therapies Plus Azacitidine in Participants With Newly Diagnosed Acute Myeloid Leukemia (AML) Harboring IDH Mutations Who Are Not Candidates to Receive Intensive Induction Chemotherapy
NCT02677922 · ClinicalTrials.gov ↗ · Leukemia, Myeloid, Acute
Phase 1/2 Active, closed 2016-06 UK, USA
A Safety and Preliminary Efficacy Study of CC-99282, Alone and in Combination With Anti-lymphoma Agents in Participants With Relapsed or Refractory Non-Hodgkin Lymphomas (R/R NHL)
NCT03930953 · ClinicalTrials.gov ↗ · Lymphoma, Non-Hodgkin
Phase 1/2 Active, closed 2019-05 UK, USA, China
A Study to Evaluate the Efficacy and Safety of JCAR017 in Adult Subjects With Relapsed or Refractory Indolent B-cell Non-Hodgkin Lymphoma (NHL)
NCT04245839 · ClinicalTrials.gov ↗ · Lymphoma, Non-Hodgkin
Phase 2 Active, closed 2020-07 UK, USA
A Study to Compare the Efficacy and Safety of Idecabtagene Vicleucel With Lenalidomide Maintenance Therapy Versus Lenalidomide Maintenance Therapy Alone in Adult Participants With Newly Diagnosed Multiple Myeloma Who Have Suboptimal Response After Autologous Stem Cell Transplantation
NCT06045806 · ClinicalTrials.gov ↗ · Multiple Myeloma
Phase 3 Active, closed 2023-10 UK, 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. Titles and statuses are copied from the registry as published.

02

Celgene in the EU trials register (CTIS)

2 trials

Authorised or ongoing trials in the EU Clinical Trials Information System with Celgene as sponsor. Some are the same study as a ClinicalTrials.gov record above; the two registries share no common ID. Trials with a site in Ireland are listed first.

StudyPhaseStatusCountries
A Phase 2, Multicenter, Open-Label Study of Zolacabtagene Autoleucel (BMS-986353), CD19-Targeted NEX-T CAR T Cells, in Participants with Chronic Immune Thrombocytopenia (cITP) and Autoimmune Hemolytic Anemia (AIHA) (Breakfree-AiCE)
2025-524993-41-00 · Immune System Diseases
Phase 2 Authorised Germany, Denmark
A Phase 3, Randomized, Open-label, Multicenter Study to Compare the Efficacy and Safety of BMS-986353, CD19-targeted NEX-T CAR T Cells, Versus Standard of Care in Participants with Active Systemic Sclerosis (Breakfree-SSc)
2025-524337-11-00 · CTIS ↗ · Immune System Diseases
Phase 3 Authorised Spain, Germany, France + 2 more
03

Drugs in Celgene trials

39 compounds

Drugs and biologicals named as interventions in these trials, with the number of this sponsor's trials that name each one. Placebos and generic comparators are excluded.

04

Conditions in Celgene trials

23 conditions
Multiple Myeloma5Lymphoma, Non-Hodgkin2Relapsed or Refractory Multiple Myeloma1Metastatic Castration-resistant Prostate Cancer1Myeloproliferative Disorders1Myelofibrosis1Primary Myelofibrosis1Post-Polycythemia Vera Myelofibrosis1Lymphoma, Follicular1Myelodysplastic Syndromes1Neoplasms1Leukemia, Myeloid, Acute1Follicular Lymphoma1Myelodysplastic Syndromes (MDS)1Beta-thalassemia1Myeloproliferative Neoplasm(MPN)-Associated Myelofibrosis1Lymphoma, B-Cell1Beta-Thalassemia1Agitation1Alzheimer Disease1Large B-cell Lymphoma1Multiple Sclerosis Spasticity1Healthy Volunteers1
05

By trial register

RegisterTrialsRecruiting
Clinical trials in USA228
Clinical trials in UK155
Clinical trials in China116
Clinical trials in India53
Clinical trials in Ireland41
EU register (CTIS)2—

A trial with sites in more than one country appears in each of those registers.

06

Other sponsors in Multiple Myeloma

SponsorTrials
Janssen Research & Development24
AbbVie13
GlaxoSmithKline13
Pfizer8
Zhujiang Hospital4
Regeneron Pharmaceuticals3
European Myeloma Network3
Nanjing IASO Biotechnology3
Genrix (Shanghai) Biopharmaceutical3
Xuzhou Medical University3

Sponsors with the most current trials registered for this condition.

07

Questions about Celgene trials

How many clinical trials does Celgene sponsor?

Celgene is the lead sponsor of 22 current trials on ClinicalTrials.gov in our USA, UK, China, India and Ireland registers, and 2 authorised or ongoing trials in the EU register (CTIS), as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are Celgene trials recruiting?

Yes. 8 of its 22 ClinicalTrials.gov trials are recruiting. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Which drugs is Celgene testing?

Its current trials name 39 drugs and biologicals as interventions. The most frequent are Cyclophosphamide (7), Rituximab (6), Dexamethasone (5), Golcadomide (5) and Bortezomib (4). The number in brackets is how many of its trials name each drug.

Does Celgene have clinical trials in Ireland?

Yes. 4 trials in our Ireland register (ClinicalTrials.gov). Some may be the same study registered in both. See the Irish clinical trials register for sites and contacts.

Where does this information come from?

Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.

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How this page is built

Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. 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 trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. 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 the registries 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 — 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.