Johnson & Johnson CDR (CAD Hedged)
- Country
- 🇺🇸United States
- Ownership
- Public
- Established
- 1886-01-01
- Employees
- 131.9K
- Market Cap
- $392.2B
- Website
- http://www.jnj.com
- Introduction
Johnson & Johnson is a holding company, which engages in the research, development, manufacture, and sale of products in the healthcare field. It operates through the Innovative Medicine and MedTech segments. The Innovative Medicine segment focuses on immunology, infectious diseases, neuroscience, oncology, cardiovascular and metabolism, and pulmonary hypertension. The MedTech segment includes a portfolio of products used in the interventional solutions, orthopaedics, surgery, and vision categories. The company was founded by Robert Wood Johnson I, James Wood Johnson, and Edward Mead Johnson Sr. in 1887 and is headquartered in New Brunswick, NJ.
Clinical Trials
8
Trial Phases
2 Phases
Drug Approvals
0
Drug Approvals
No drug approvals found
This company may not have drug approvals in our database
Clinical Trials
Distribution across different clinical trial phases (4 trials with phase data)• Click on a phase to view related trials
Blinded Dry Mouth Spray Crossover Study
- Conditions
- XerostomiaHead and Neck CancerXerostomia Following Radiotherapy
- First Posted Date
- 2020-10-29
- Last Posted Date
- 2024-02-01
- Lead Sponsor
- Jonas Johnson
- Target Recruit Count
- 129
- Registration Number
- NCT04608773
- Locations
- 🇺🇸
UPMC, Pittsburgh, Pennsylvania, United States
🇺🇸University of Pittsburgh, Pittsburgh, Pennsylvania, United States
Pilot Study to Improve Therapeutic Outcomes for Dysphagia After Radiation Therapy
- Conditions
- Oral Pharyngeal CancerDysphagia
- First Posted Date
- 2015-10-01
- Last Posted Date
- 2020-03-23
- Lead Sponsor
- Jonas Johnson
- Target Recruit Count
- 26
- Registration Number
- NCT02564887
- Locations
- 🇺🇸
UPMC, Pittsburgh, Pennsylvania, United States
News
Genmab Reports Strong Q3 2025 Results with Key Pipeline Advances and $8 Billion Merus Acquisition
Genmab achieved 21% revenue growth to $2.66 billion in the first nine months of 2025, driven primarily by increased DARZALEX and Kesimpta royalties.
Legend Biotech to Present Comprehensive CARVYKTI Data and First-in-Human Allogeneic CAR-T Results at ASH 2025
Legend Biotech will present nine abstracts on CARVYKTI (ciltacabtagene autoleucel) at the 67th ASH Annual Meeting, including two oral presentations demonstrating long-term progression-free survival benefits and improved immune fitness with earlier treatment use.
Kimberly-Clark Acquires Kenvue for $48.7 Billion, Creating Consumer Health Giant
Kimberly-Clark has agreed to acquire Tylenol maker Kenvue for approximately $48.7 billion in a cash and stock deal that will create a major consumer health company.
Johnson & Johnson Submits FDA Application for STELARA in Pediatric Ulcerative Colitis
Johnson & Johnson has submitted a supplemental Biologics License Application to the FDA seeking approval of STELARA (ustekinumab) for treating children two years and older with moderately to severely active ulcerative colitis.
HRSA Approves Eight Drug Companies for 340B Rebate Model Pilot Program Starting January 2025
The Health Resources and Services Administration has approved eight pharmaceutical companies to participate in the 340B Rebate Model Pilot Program, which will begin on January 1, 2025.
Nipocalimab Demonstrates Significant Efficacy in Phase 2 Sjögren's Disease Trial Published in The Lancet
Johnson & Johnson's nipocalimab, a first-in-class FcRn blocker, met its primary endpoint in the Phase 2 DAHLIAS study with statistically significant improvement in disease activity scores at Week 24 versus placebo.
Abivax Phase III Success Triggers 850% Stock Surge, Reignites European Biotech Rally
Abivax shares soared over 850% following positive Phase III data in ulcerative colitis, creating an "Abivax effect" that has reshaped market dynamics and reignited investor confidence in European biotech.
J&J's Rybrevant Shows 45% Response Rate in Head and Neck Cancer, Doubling Standard of Care
Johnson & Johnson's bispecific antibody Rybrevant demonstrated a 45% objective response rate in previously treated head and neck squamous cell cancer patients, doubling the response rates of current standard treatments.
Subcutaneous Amivantamab Shows 45% Response Rate in Recurrent Head and Neck Cancer
Johnson & Johnson's subcutaneous amivantamab demonstrated a 45% overall response rate in 38 patients with HPV-unrelated recurrent or metastatic head and neck squamous cell carcinoma who had progressed on checkpoint inhibitors and platinum-based chemotherapy.
Johnson & Johnson Eyes Full Acquisition of Protagonist Therapeutics Following Successful Icotrokinra Partnership
Johnson & Johnson is reportedly considering a complete acquisition of partner Protagonist Therapeutics, following years of successful collaboration on the first-in-class oral peptide icotrokinra for immune-mediated diseases.
