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Carna announces collaboration with J&J

June 11, 2015 11:22 am | by Business Wire | News | Comments

Carna Biosciences today announced a worldwide licensing agreement with Janssen Biotech to further develop and commercialize compounds from one of Carna Bioscience’s small molecule protein kinase inhibitor programs.

J&J opens new schizophrenia project

June 9, 2015 11:20 am | by PR Newswire | News | Comments

The project will create a new forum for collaborative analysis of Janssen's clinical trial data...

Rutgers research promises ‘revolution’ in pharmaceutical manufacturing

June 4, 2015 4:17 pm | by Meagan Parrish, Editor, Chem.Info | News | Comments

A $6 million gift from Janssen Pharmaceuticals will help spur Rutgers’ research into “...

Phase III Study with IMBRUVICA Combination Demonstrates Significant Delay in Disease Progression

March 17, 2015 8:45 am | News | Comments

Janssen has announced that a pre-planned interim analysis of the Phase 3 HELIOS study...

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Galapagos Regains Rights to GLPG1690, Ends Alliance with Janssen

March 17, 2015 8:29 am | News | Comments

Galapagos NV has announced that Janssen Pharmaceutica NV and Galapagos have mutually agreed to terminate the inflammation alliance and option agreements between the companies.

Survey: Clinical Trial Sponsors Show Improvement

March 2, 2015 11:19 am | by Andy Szal, Digital Reporter | News | Comments

Pharmaceutical companies sponsoring clinical trials showed strong improvement in their relationships with global investigative sites, according a recent survey.

FDA Grants Priority Review for Janssen’s YONDELIS

February 3, 2015 8:01 am | News | Comments

Janssen Research & Development announced today that the FDA has granted Priority Review for the New Drug Application for YONDELIS to treat patients with advanced soft tissue sarcoma, including liposarcoma and leiomyosarcoma subtypes, who have received prior chemotherapy including an anthracycline.


FDA Approves Janssen’s Schizoaffective Disorder Treatment

November 13, 2014 1:53 pm | News | Comments

Janssen Pharmaceuticals has announced that the FDA approved the supplemental New Drug Applications (sNDAs) for the once-monthly atypical long-acting antipsychotic INVEGA SUSTENNA (paliperidone palmitate) to treat schizoaffective disorder as either monotherapy or adjunctive therapy.

Big Cities Take Aim at Prescription Painkillers

September 16, 2014 2:25 pm | by MATTHEW PERRONE, AP Health Writer | News | Comments

Some of the nation's largest cities are ratcheting up their criticism of prescription painkillers, blaming the industry for a wave of addiction and overdoses that have ravaged their communities and busted local budgets.      

Cilag GmbH International Acquires Covagen AG

August 25, 2014 8:41 am | News | Comments

Cilag GmbH International, an affiliate of the Janssen Pharmaceutical Companies of Johnson & Johnson, announced today that it has acquired Covagen AG, a privately-held, biopharmaceutical company specializing in the development of multispecific protein therapeutics through the FynomAb technology platform.

Janssen Submits Supplemental New Drug Application to FDA for OLYSIOT (Simeprevir)

May 7, 2014 8:02 am | News | Comments

Janssen Research & Development, LLC has submitted a Supplemental New Drug Application (sNDA) to the U.S. Food and Drug Administration (FDA) for simeprevir, an NS3/4A protease inhibitor marketed as OLYSIOT in the United States, in combination with the nucleotide analog NS5B polymerase inhibitor sofosbuvir developed by Gilead Sciences, Inc.

J&J Says Europe Clears New Diabetes Treatment

April 25, 2014 12:37 pm | by The Associated Press | News | Comments

Johnson & Johnson said Friday that European Union regulators approved a pill that combines its diabetes drug Invokana with metformin, an older treatment for the disease. Janssen-Cilag International will market the drug under the name Vokanamet.


SIMPONI Receives FDA Approval for Ulcerative Colitis

May 16, 2013 8:17 am | News | Comments

Janssen Biotech, Inc. announced today that the U.S. Food and Drug Administration (FDA) has approved SIMPONI (golimumab) for the treatment of moderately to severely active ulcerative colitis (UC) in adult patients who have demonstrated corticosteroid dependence or who have had an inadequate response to or failed to tolerate oral aminosalicylates, oral corticosteroids, azathioprine, or 6-mercaptopurine.

The Scripps Research Institute Announces New Research and License Agreement with Janssen Pharmaceuticals

May 7, 2013 7:58 am | News | Comments

The Scripps Research Institute (TSRI) today announced a five-year agreement with Janssen Pharmaceuticals, Inc. (Janssen) to collaborate on focused research projects in the infectious disease area, with the initial project targeting the influenza virus.

Janssen Submits New Drug Application for Simeprevir

March 29, 2013 8:04 am | News | Comments

Janssen Research & Development, LLC today announced it has submitted a New Drug Application (NDA) to the FDA seeking approval for simeprevir (TMC435), an investigational NS3/4A protease inhibitor, administered as a 150 mg capsule once daily with pegylated interferon and ribavirin for the treatment of genotype 1 chronic hepatitis C in adult patients.

Janssen R & D Announces Establishment of Global Cross-Pharmaceutical Clinical Trial Investigator Databank

November 15, 2012 3:03 am | News | Comments

Janssen Research & Development, LLC today announced the establishment of a global cross-pharmaceutical Investigator Databank designed to improve efficiencies of industry-sponsored clinical trials. Merck and Eli Lilly and Company are the first two companies to join Janssen in this effort.  

FDA Grants Priority Review for XARELTO Supplemental NDAs for the Treatment of Deep Vein Thrombosis (DVT), Pulmonary Embolism (PE), and the Long-Term Prevention of Recurrent DVT and PE

July 9, 2012 4:42 am | News | Comments

Janssen Research & Development, LLC announced today the U.S. FDA has assigned a priority review designation to the supplemental New Drug Applications (sNDAs) filed on May 2, 2012 for XARELTO.


Janssen Creates new Division to Launch TMC435 and Help Conquer Hepatitis C in EMEA

April 19, 2012 4:23 am | News | Comments

Today sees the launch of Janssen Therapeutics EMEA, a division of Janssen Pharmaceutica NV, dedicated to bringing the investigational protease inhibitor TMC435 to hepatitis C patients in the EMEA region.  

Forest Labs Purchases Bystolic Royalties from Janssen Pharmaceutica NV

April 3, 2012 4:25 am | News | Comments

Forest Laboratories, Inc. today announced that Forest Laboratories Holdings Limited, its wholly owned subsidiary, and Janssen Pharmaceutica NV entered into an agreement under which Forest acquired all U.S. patents and other U.S. and Canadian intellectual property for Bystolic.

FORMA Therapeutics and Janssen Biotech to Collaborate on Cancer Research

January 11, 2012 3:20 am | News | Comments

FORMA Therapeutics has announced an exclusive alliance with Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies, in which the two companies will collaborate on the discovery, development and commercialization of novel small molecule drug candidates that target tumor metabolism mechanisms.

Shire Acquires US Rights to Resolor

January 10, 2012 3:05 am | News | Comments

Shire plc announced today that it has acquired the rights to develop and market Resolor (prucalopride) in the United States in an agreement with Janssen Pharmaceutica N.V.

NUCYNTA ER (Tapentadol Extended-Release Tablets) Receives FDA Approval for the Management of Moderate to Severe Chronic Pain

August 26, 2011 5:01 am | News | Comments

Janssen Pharmaceuticals, Inc. today announced the U.S. Food and Drug Administration (FDA) has approved NUCYNTA ER, an oral analgesic taken twice daily, for the management of moderate to severe chronic pain in adults when a continuous, around-the-clock opioid analgesic is needed for an extended period of time.

ZYTIGA Receives Health Canada Approval

July 29, 2011 4:30 am | News | Comments

Janssen Inc. announced today that after a priority review, Health Canada has approved ZYTIGA™ (abiraterone acetate), an oral medication for the treatment of men with metastatic prostate cancer.

Valeant Pharmaceuticals to Acquire Ortho Dermatologics

July 15, 2011 4:34 am | News | Comments

Valeant Pharmaceuticals has signed an agreement to acquire the assets of the Ortho Dermatologics division of Janssen Pharmaceuticals, Inc. Valeant will pay Janssen $345 million for the assets, which includes prescription brands RETIN-A MICRO, ERTACZO, and RENOVA.

Galapagos Delivers Validated Oncology Targets to Janssen

April 20, 2011 4:43 am | News | Comments

Galapagos NV announced today that its BioFocus service division has delivered a panel of validated oncology targets in its collaboration with Janssen Research & Development, a division of Janssen Pharmaceutica N.V. (Janssen). Per the agreement, Janssen retains full rights to discover, develop and commercialize novel medicines on these targets.

Eli Lilly to Buy Janssen’s Animal Health Business

March 14, 2011 4:51 am | News | Comments

INDIANAPOLIS (AP) — Eli Lilly and Co. said today it plans to buy the animal health business of Janssen Pharmaceutical NV in a deal that would give Lilly's Elanco division about 50 marketed animal health products.

Galapagos' Affiliate Argenta And Janssen Pharmaceutica Enter Into Integrated Cancer Drug Discovery Service Agreement

October 4, 2010 5:15 am | News | Comments

Galapagos NV announced today that its affiliate, Argenta Discovery 2009 Limited, has entered into a drug discovery service agreement with Janssen Pharmaceutica N.V., aimed at delivering novel cancer drug candidates.

Basilea to Withdraw Ceftobiprole from Swiss Market

September 9, 2010 4:50 am | News | Comments

Basilea Pharmaceutica Ltd. has announced that Janssen-Cilag AG, a Johnson & Johnson company, will be discontinuing sale of ceftobiprole (Zevtera) for the treatment of complicated skin and soft tissue infections (cSSTI) in Switzerland.

Mother & daughters' journey through madness

July 8, 2010 7:23 pm | by Janssen-Cilag | News | Comments

Out of the Shadow, Susan Smiley's award-winning documentary film, is now available to view on our European Psychiatry 24x7 website

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