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Janssen Pharmaceuticals, Inc.
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Agreement
Genmab Signs Agreement with Janssen for Next-Generation CD38 Antibody, HexaBody®-CD38
PR-M06-19-NI-007
Drug Development
Janssen Submits Application to U.S. FDA Seeking Approval of ERLEADA® (apalutamide) for Patients with Metastatic Castration-Sensitive Prostate Cance
PR-M05-19-NI-001
FDA Approval
U.S. FDA Approves DARZALEX® (daratumumab) Split-Dosing Regimen
PR-M02-19-NI-028
Phase 3
New DARZALEX® (daratumumab) Phase 3 Study Shows Efficacy and Safety Data of Anti-CD38 Monoclonal Antibody in Patients with Newly Diagnosed Multiple Myeloma
PR-M12-18-NI-019
Depression
New Data Presented at Psych Congress 2018 Sheds Light on the Significant Economic Burden of Treatment-Resistant Depression Amongst U.S. Veterans
PR-M10-18-NI-104
Clinical Data
Janssen Announces New Three-Year TREMFYA® (Guselkumab) Data Demonstrates Stably Maintained Rates of Skin Clearance in Patients with Moderate to Severe Plaque Psoriasis
PR-M10-18-NI-073
RNA
Janssen Collaborates on RNA Therapy
PAO-M10-18-NI-008
New Drug Application
Janssen Submits New Drug Application to U.S. FDA Seeking Approval of Erdafitinib for the Treatment of Metastatic Urothelial Cancer
PR-M09-18-NI-083
Study Results
Janssen Reports Positive Topline Results for ATLAS Phase III Study of a Novel, Long Acting Injectable Two-Drug Regimen for the Treatment of HIV-1
PR-M09-18-NI-045
Regulatory
Janssen Submits U.S. & EU Regulatory Applications Seeking Approval of DARZALEX® (daratumumab) Split Dosing Regimen
PR-M08-18-NI-093
Positive Opinion
Janssen Receives Positive CHMP Opinion for Darzalex®▼ (daratumumab) as Frontline Treatment for Newly Diagnosed Patients with Multiple Myeloma
PR-M08-18-NI-007
FDA Approval
Janssen Announces U.S. FDA Approval of SYMTUZA™ (D/C/F/TAF), the First and Only Complete Darunavir-Based Single-Tablet Regimen for the Treatment of HIV-1 Infection
PR-M07-18-NI-061
Janssen Announces Initiation of Phase 1b/2 Clinical Development Program Evaluating JNJ-68284528 CAR-T Cells for the Treatment of Multiple Myeloma
PR-M06-18-NI-005
Real-World Study
New Real-World Study Finds Long-Term XARELTO® (rivaroxaban) Use Resulted in Fewer Strokes and Systemic Emboli
PR-M05-18-NI-101
Commission Approval
Janssen Announces European Commission Approval of JULUCA®▼ (dolutegravir/rilpivirine), the First Two-Drug Regimen, Once-Daily, Single-Pill for the Treatment of HIV-1
PR-M05-18-NI-088
Data Presentation
Janssen to Present Data in Treatment-Resistant Mental Ilnesses
PR-M05-18-NI-029
Acquisition
Janssen to Acquire BeneVir Biopharm to Advance Immunotherapy Regimens
PR-M05-18-NI-021
Study
Real-World Study Shows INVOKANA® (canagliflozin) 300mg Demonstrates Better Blood Glucose Control Than Farxiga® (dapagliflozin) 10mg in Patients with Type 2 Diabetes
PR-M05-18-NI-010
Cardiovascular
Janssen Announces Worldwide Development and Commercialization Collaboration with Bristol-Myers Squibb to Advance a Next-Generation Therapy for Cardiovascular Diseases
PR-M04-18-NI-72
Biologics
Next Generation Biologics, Janssen's Tremfya, Eli Lilly's Taltz, and Novartis' Cosentyx, Raising the Bar in Psoriasis Management
PR-M03-18-NI-040
FDA Approval
FDA approves new treatment for a certain type of prostate cancer using novel clinical trial endpoint
PR-M02-18-NI-77
Capacity Expansion
Janssen Expands Biomanufacturing Capabilities in Ireland
PAO-M10-17-NI-031
Collaboration
Collaboration Targets Vaccine Technologies to Wipe out HIV-1 and Hep-B
PAO-M08-17-NI-013