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Janssen Research & Development, LLC

Total Trials
12
Recruiting
12
Phases
Phase 4, Phase 1, Phase 2, Phase 2, Phase 3, Phase 3

Janssen Research & Development, LLC is the pharmaceutical research arm of Johnson & Johnson, one of the world's largest healthcare companies. Operating through the Janssen Pharmaceutical Companies — including Janssen-Cilag, Janssen Biologics, and other regional entities — J&J's pharmaceutical division runs one of the most diversified clinical trial programs in the industry, spanning oncology, immunology, neuroscience, cardiovascular and metabolism, and pulmonary hypertension.

Janssen's oncology portfolio centers on hematological malignancies, particularly multiple myeloma (daratumumab/Darzalex combinations, teclistamab bispecific, ciltacabtagene autoleucel CAR-T), prostate cancer (apalutamide/Erleada, niraparib combinations), and solid tumors. In immunology, Janssen's IL-12/23 inhibitor guselkumab (Tremfya) and IL-23 inhibitors are central to a broad pipeline in psoriatic disease, IBD, and systemic lupus. Esketamine (Spravato), an intranasal ketamine derivative for treatment-resistant depression, reflects the neuroscience program's push into rapid-onset antidepressants and suicidality intervention.

Janssen operates a global clinical development network with research sites across North America, Europe, Asia-Pacific, Latin America, and the Middle East. The company has made significant investments in decentralized and hybrid trial designs, electronic patient-reported outcomes, and real-world evidence integration. Through Johnson & Johnson's Global Public Health unit, Janssen also conducts trials on vaccines and treatments for HIV, tuberculosis, and Ebola — often in partnership with NIH, BARDA, and the Bill & Melinda Gates Foundation.

Frequently Asked Questions — Janssen Research & Development, LLC

What is daratumumab and why is Janssen running so many multiple myeloma trials?
Daratumumab (Darzalex/Darzalex Faspro) is a human CD38-targeting monoclonal antibody that has transformed the treatment of multiple myeloma. Originally approved for relapsed/refractory disease, daratumumab has demonstrated benefit in combination with virtually every active anti-myeloma regimen and has moved into frontline therapy, transplant-eligible and ineligible settings. Janssen continues to run Phase 3 trials evaluating daratumumab in earlier disease stages, maintenance settings, and newly diagnosed smoldering myeloma — one of the most active trial programs in a single disease in pharmaceutical history.
What neuroscience clinical trials does Janssen run?
Janssen's neuroscience program is anchored by esketamine (Spravato) for treatment-resistant depression and major depressive disorder with active suicidal ideation — both FDA-approved. Ongoing trials investigate esketamine in bipolar depression, post-partum depression, and adjunctive use with novel antidepressants. Janssen also has investigational programs in Alzheimer's disease (tau aggregation inhibitor seltorexant for insomnia in AD patients), schizophrenia (paliperidone palmitate 6-month injectable), and pain. J&J's acquisition of Intra-Cellular Therapies in 2025 added lumateperone (Caplyta) and expanded the neuroscience pipeline significantly.
Are Janssen global trials accessible to patients in the United States?
Yes. The majority of Janssen's Phase 2 and Phase 3 trials include US sites, typically at NCI-designated cancer centers, academic medical centers affiliated with major research universities, and large community oncology networks. US-based patients can find site-specific contact information for each trial through ClinicalTrials.gov. Janssen also operates a clinical trial matching service through its janssenclinicaltrial.com website. In some cases, expanded access (compassionate use) programs are available for patients who are ineligible for enrollment in formal trials.

Clinical Trials by Janssen Research & Development, LLC

NCT05201781 Phase 4
Recruiting

A Long-term Study for Participants Previously Treated With Ciltacabtagene Autoleucel

Multiple Myeloma
NCT07082920 Phase 1
Recruiting

A Study of JNJ-78278343 in Combination With JNJ-95298177 for Treatment of Prostate Cancer

Prostatic Neoplasms
NCT04634552 Phase 2
Recruiting

A Study of Talquetamab in Participants With Relapsed or Refractory Multiple Myeloma

Hematological Malignancies
NCT05327114 Phase 2, Phase 3
Recruiting

Efficacy and Safety Study of Nipocalimab for Adults With Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
NCT06500884 Phase 2
Recruiting

A Study to Evaluate Preventive Treatments for GPRC5D-related Oral Events

Multiple Myeloma
NCT02354014 Phase 2
Recruiting

Pharmacokinetic Study to Evaluate Anti-mycobacterial Activity of TMC207 in Combination With Background Regimen (BR) of Multidrug Resistant Tuberculosis (MDR-TB) Medications for Treatment of Children/Adolescents With Pulmonary MDR-TB

Tuberculosis, Multidrug-Resistant
NCT06449651 Phase 3
Recruiting

A Study of Nipocalimab in Reducing the Risk of Fetal and Neonatal Alloimmune Thrombocytopenia (FNAIT)

Thrombocytopenia, Neonatal Alloimmune
NCT06635148 Phase 2
Recruiting

A Long-term Extension Study of JNJ-81201887 (AAVCAGsCD59) Parent Studies in Participants With Geographic Atrophy (GA) Secondary to Age-related Macular Degeneration (AMD)

Geographic Atrophy
NCT06852222 Phase 3
Recruiting

A Study of Bleximenib, Venetoclax and Azacitidine For Treatment of Participants With Newly Diagnosed Acute Myeloid Leukemia (AML)

Leukemia, Myeloid, Acute
NCT07295951 Phase 1
Recruiting

A Study of 14C-Bleximenib (Radiolabeled) in Participants With Acute Leukemia

Acute Lymphoblastic Leukemia
NCT05265273 Phase 2, Phase 3
Recruiting

A Study of Nipocalimab in Children Aged 2 to Less Than 18 Years With Generalized Myasthenia Gravis

Myasthenia Gravis
NCT06919965 Phase 3
Recruiting

A Study to Evaluate TAR-210 Versus Intravesical Chemotherapy Treatment in Participants With High Risk Non-Muscle-Invasive Bladder Cancer

Non-Muscle Invasive Bladder Neoplasms
ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology