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Janssen Research & Development, LLC

Total Trials
9
Recruiting
9
Phases
Phase 3, Phase 1, Phase 2, Phase 2, Phase 1

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

NCT05552222 Phase 3
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

Multiple Myeloma
NCT07227025 Phase 1, Phase 2
Recruiting

A Study of Amivantamab and Olomorasib Combination Therapy in Participants With Metastatic Non-Small Cell Lung Cancer

Carcinoma, Non-Small-Cell Lung
NCT07602088
Recruiting

A Real-world Study of Ibrutinib and Venetoclax (I+V) First-Line Treatment Given for Fixed-duration of Time in Participants With Chronic Lymphocytic Leukemia

Leukemia, Lymphocytic, Chronic, B-Cell
NCT07573176 Phase 3
Recruiting

A Study of Seltorexant as Monotherapy in Adults and Elderly Participants With Major Depressive Disorder

Depressive Disorder, Major
NCT06750094 Phase 3
Recruiting

A Study of Amivantamab and FOLFIRI Versus Cetuximab/Bevacizumab and FOLFIRI in Participants With KRAS/NRAS and BRAF Wild-type Colorectal Cancer Who Have Previously Received Chemotherapy

Colorectal Neoplasms
NCT05923073 Phase 3
Recruiting

A Study of Guselkumab in Pediatric Participants With Moderately to Severely Active Crohn's Disease

Crohn's Disease
NCT07589634 Phase 2
Recruiting

A Study Evaluating the Prophylactic Use of Tocilizumab to Prevent Cytokine Release Syndrome With Ramantamig Administration in Participants With Relapsed/Refractory Multiple Myeloma

Multiple Myeloma
NCT07524855 Phase 1
Recruiting

A Study of JNJ-101684362 (HLD-0117) in Patients With Metastatic Breast Cancer

Metastatic Breast Cancer
NCT07438496 Phase 3
Recruiting

A Study of Nipocalimab in Adults With Moderate to Severe Systemic Lupus Erythematosus

Lupus Erythematosus, Systemic
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: November 2026  ·  Data Methodology