http://www.twitter.comTwitter is a service for friends, family, and co-workers to communicate and stay connected through the exchange of quick, frequent answers to one simple question: What are you doing?
View Older Stories View More Recent Stories
-
Ethicon Showcases Leading Edge Solutions Beyond The O.R. To Empower Patients And Providers In Fight Against Obesity At ObesityWeek™ 2017
-
Janssen (JNJ) Announces FDA Approval for New 10 mg Dosing for XARELTO to Reduce Continued Risk of VTE
-
FDA Approves New 10 mg Dosing for XARELTO® (rivaroxaban) to Reduce the Continued Risk of Venous Thromboembolism (VTE)
-
Janssen (JNJ) Says Darunavir-Based Single-Tablet Regimen Shows Positive Results in Previously Untreated HIV Patients in Pivotal Phase 3 AMBER Clinical Trial
-
Investigational Darunavir-Based Single-Tablet Regimen Shows Positive Results in Previously Untreated HIV Patients in Pivotal Phase 3 AMBER Clinical Trial
-
First General Surgery Virtual Residency Program To Allow Training Anytime, Anywhere Launched In Collaboration With Ethicon
-
Janssen (JNJ) Receives Two U.S. FDA Approvals For SIMPONI ARIA For Treatment of Adults With Active PsA or Active Ankylosing Spondylitis
-
Janssen Receives Two U.S. FDA Approvals For SIMPONI ARIA® (golimumab) For The Treatment Of Adults With Active Psoriatic Arthritis Or Active Ankylosing Spondylitis
-
BabyCenter® Launches Channel On The Roku Platform To Expand Access To Best-In-Class Videos On Pregnancy And Parenthood
-
Janssen (JNJ) Announces U.S. FDA Approval Of STELARA For The Treatment Of Adolescents With Moderate To Severe Plaque Psoriasis
-
Janssen Announces U.S. FDA Approval Of STELARA® (ustekinumab) For The Treatment Of Adolescents With Moderate To Severe Plaque Psoriasis
-
Janssen (JNJ) Submits U.S. NDA for Apalutamide (ARN-509) to Treat Men with Non-Metastatic Castration-Resistant Prostate Cancer
-
Janssen Submits New Drug Application to U.S. FDA for Apalutamide (ARN-509) to Treat Men with Non-Metastatic Castration-Resistant Prostate Cancer
-
Janssen Research & Development Establishes First-of-Its-Kind Mobile Medication and Data Management Technology Platform for Industry Use
-
Janssen (JNJ) Says EMERALD 48-week Safety and Efficacy Results published in The Lancet HIV, to be Presented at IDWeek
-
Janssen Announces Pivotal Phase 3 Study Results for Investigational Darunavir-Based Single-Tablet Regimen for the Treatment of HIV-1 Infection in Adults Switching from Boosted Protease Inhibitors Plus
-
Janssen (JNJ) Says NAVIGATE ESUS Study Stopped Early Due to Futility
-
NAVIGATE ESUS Study Stopped Early Due to Comparable Efficacy in Treatment Arms
-
Janssen (JNJ) Submits U.S. NDA for First Darunavir-Based Single Tablet Regimen for the Treatment of HIV-1
-
Janssen Submits New Drug Application to U.S. Food and Drug Administration for the First Darunavir-Based Single Tablet Regimen for the Treatment of HIV-1
-
Janssen (JNJ) Receives CRL From U.S. FDA For Sirukumab Biologics License
-
Janssen Receives Complete Response Letter From U.S. FDA For Sirukumab Biologics License Application
-
Johnson & Johnson (JNJ) Subsidiary Janssen Research Reports New Two-Year TREMFYA (Guselkumab) Data
-
New Two-Year TREMFYA™ (guselkumab) Data Show Patients With Moderate To Severe Plaque Psoriasis Achieved Consistent Rates Of Skin Clearance
-
Janssen (JNJ) Submits sNDA to FDA for ZYTIGA to Treat Men with Earlier Stages of Metastatic Prostate Cancer
-
Janssen Submits Supplemental New Drug Application to U.S. FDA for ZYTIGA® (abiraterone acetate) to Treat Men with Earlier Stages of Metastatic Prostate Cancer
-
Multiple Myeloma Patients and Supporters Embark on Cross-Country Journey to Raise Awareness and Accelerate Cancer Research
-
Ethicon Reports Major Progress On Multi-Year Initiative To Fill Clinical And Economic Evidence Gaps And Expand Access To Bariatric Surgery
-
Ethicon Launches ProxiSure™ Suturing Device Designed To Improve Precision In Minimally-Invasive Surgery
-
President Trump Announces End of Strategic & Policy Forum and Manufacturing Council on Twitter
-
Janssen (JNJ) Confirms FDA Advisory Committee Does Not Recommend Approval of Sirukumab to Treat RA
-
FDA Advisory Committee Does Not Recommend Approval Of Sirukumab For The Treatment Of Moderately To Severely Active Rheumatoid Arthritis
-
Johnson & Johnson (JNJ) Announces FDA Approval for IMBRUVICA in Adults with cGVHD
-
U.S. FDA Approves IMBRUVICA® (ibrutinib) as First and Only Approved Treatment for Adult Patients with Chronic Graft-Versus-Host-Disease (cGVHD) After Failure of One or More Lines of Systemic Therapy
-
Johnson & Johnson (JNJ) Janssen Gains FDA Approval for Plaque Psoriasis Treatment TREMFYA
-
Janssen Announces U.S. FDA Approval Of TREMFYA™ (Guselkumab) For The Treatment Of Moderate To Severe Plaque Psoriasis
-
Endangered Baby Names 2017
-
Johnson & Johnson Releases 2016 Health for Humanity Report
-
Janssen Biotech (JNJ) Granted FDA Approval for DARZALEX (daratumumab) in Combination with Pomalidomide & Dexamethasone
-
DARZALEX® (daratumumab) Approved by the U.S. FDA in Combination with Pomalidomide and Dexamethasone for Patients with Multiple Myeloma Who Have Received At Least Two Prior Therapies
-
Johnson & Johnson (JNJ) Completes Acquisition of Actelion
-
Johnson & Johnson Announces Completion of Acquisition of Actelion
-
Johnson & Johnson Announces Expected Settlement of Actelion Tender Offer on June 16, 2017
-
Johnson & Johnson (JNJ) Subsidiary, Ethicon Granted FDA Approval for SURGICEL Powder Absorbable Hemostat
-
Ethicon Announces FDA Approval For SURGICEL Powder Absorbable Hemostat
-
Janssen (JNJ) Announces Daratumumab Combination Therapy Improved Clinical Outcomes Regardless of Cytogenetic Risk for Previously-Treated Patients with Multiple Myeloma
-
Janssen (JNJ) Reports Abiraterone Acetate Provided Significant Clinical Benefit in Patients with High-Risk Metastatic Hormone-Naive Prostate Cancer (mHNPC)
-
Janssen (JNJ) Says Data at ASCO Show Consistent Progression-Free Survival Benefit in R/R CLL/SLL Patients Treated with Ibrutinib
-
Data at ASCO Show Consistent Progression-Free Survival Benefit in Relapsed/Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma Patients Treated with Ibrutinib, Including Those with High
-
Daratumumab Combination Therapy Improved Clinical Outcomes Regardless of Cytogenetic Risk for Previously-Treated Patients with Multiple Myeloma

