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Clinic Roundup
Astellas Pharma, of Tokyo, and Theravance Inc., of South San Francisco, presented data from two Phase III trials in which telavancin compared favorably to standard therapy in the treatment of patients with complicated skin and skin structure infections, including those caused by Gram-positive organismsBioWorld Today | Tuesday, April 3, 2007 -
Regeneron Signs Another Deal For A Potential $120M Payoff
The partner this time is Astellas Pharma of Toyko, which signed a deal to pay $120 million over the next five years - including $20 million upfront - for a non-exclusive license for the technologyBy Glen Harris | BioWorld Today | Monday, April 2, 2007 -
AtheroGenics Sinks On Missed Endpoint In Atherosclerosis Trial
Ltd. (now part of Tokyo-based Astellas Pharma Inc.) The company also has preclinical programs in rheumatoid arthritis and asthma.By Jennifer Boggs | BioWorld Today | Tuesday, March 20, 2007 -
FDA Submissions, Approvals And Other Actions: February 2007
Astellas Pharma US IncBioWorld Insight | Monday, March 12, 2007 -
MERLIN Study Should Expand Ranexa In Angina, But Not ACS
with Astellas Pharma US Inc., a subsidiary of Tokyo-based Astellas Pharma IncBy Aaron Lorenzo | BioWorld Today | Thursday, March 8, 2007 -
Other News To Note
Eligard is sold by Astellas Pharma Inc., of Tokyo, from which MediGene is entitled to a milestone payment of an undisclosed amountBioWorld International | Wednesday, March 7, 2007 -
Other News To Note
Eligard is sold by Astellas Pharma Inc., of Tokyo, from which MediGene is entitled to a milestone payment of an undisclosed amountBioWorld Today | Friday, March 2, 2007 -
Other News To Note
The NDA filing triggers a milestone payment of $31 million from Theravance's partner, Astellas Pharma Inc., of TokyoBioWorld Today | Thursday, February 22, 2007 -
Other News To Note
Cardiome Pharma Corp., of Vancouver, British Columbia, and Astellas Pharma US Inc., of Deerfield, Ill., said the FDA accepted for review their new drug application for the intravenous formulation of vernakalant hydrochloride, an investigational product for the acute conversion of atrial fibrillationBioWorld Today | Wednesday, February 21, 2007 -
Late-Stage RLS Drug Lands XenoPort $640M GSK Deal
Santa Clara, Calif.-based XenoPort exclusively licensed to GSK worldwide rights to XP13512, with the exception of certain Asian territories licensed in 2005 to Tokyo-based Astellas Pharma IncBy Jennifer Boggs | BioWorld Today | Friday, February 9, 2007 -
Icagen Brings In $22M Via Sale Of Stock And Warrants
Partnered preclinical programs include a compound for atrial fibrillation, with Bristol-Myers Squibb Co., of New York, and leads for memory disorders, with Astellas Pharma Inc., of TokyoBy Aaron Lorenzo | BioWorld Today | Tuesday, January 30, 2007 -
FDA Submissions, Approvals And Other Actions: December 2006
Astellas Pharma U.S. Inc. (PK:ALPMF) Vernakalant hydrochloride Intravenous formulation For the acute conversion of atrial fibrillation Resubmitted the NDA (12/19) Encysive Pharmaceuticals Inc. (ENCY) Thelin Sitaxsentan sodium Pulmonary arterial hypertension FDA informed the company that its response to the July 24 approvable letter is not complete (12/14BioWorld Insight | Monday, January 29, 2007 -
Clinical Trials Update: December 2006
Company* (Country; Symbol) Product Description Indication Status (Date) AUTOIMMUNE ChemoCentryx Inc.* Traficet-EN Orally active, anti- inflammatory agent that targets CCR9 Crohn's disease Phase II data complement earlier results showing improved clinical endpoints (12/4) Genmab A/S (Denmark; CSE:GEN) HuMax-CD20 Ofatumumab; a fully human antibody targeted at the CD20 molecule found in the cell membrane of B cells Rheumatoid arthritis Phase II data of the first 100 patients showed aBioWorld Insight | Monday, January 29, 2007 -
Cardiome Raising $84M Publicly To Boost AF Drug Development
An intravenous formulation of the drug for the acute conversion of AF demonstrated promising results in two pivotal studies, which led to the submission of an NDA by partner Astellas Pharma US in April 2006, but was followed by a refusal to file letter in May from the FDA citing "inconsistencies and omissions in the database...Astellas, a subsidiary of the Tokyo-based Astellas Pharma Inc., holds North American rights to the intravenous formulation of vernakalantBy Jennifer Boggs | BioWorld Today | Friday, January 19, 2007 -
Biotech/Big Pharma Collaborations
January | February | March | April | May | June | July | August | September | October | November | December December - 2007 Biotech Company Pharma Company Type/Product Area Terms/Details Abeome Corp. Millipore Corp. Exclusive worldwide marketing and distribution agreement for rights to Abeome's stem cell monoclonal antibody Human Embryonic Stem Cell Antigen-1 Abeome received an undisclosed up-front payment and also will receive royalties on sales by Millipore AddexBioWorld Snapshots | Wednesday, January 10, 2007 -
Milestone Payments From Corporate Partners:December 2006
TOTAL: $M54.0 Year to Date: $589.33M Company (Symbol)#* Partner (Country) Amt. (M) Triggering Event Details (Date) Cardiome Pharma Corp. (Canada; CRME) Astellas Pharma US Inc. $10 Milestone payment Triggered by Astellas' resubmission of the NDA with the FDA seeking approval of the intravenous formulation of vernakalant hydrochloride for the acute conversion of atrial fibrillation (12/18) Cerus Corp. (CERS) BioOne Corp. (Singapore) $5 Milestone payment Triggered by CE mark regulatoryBioWorld Insight | Monday, January 8, 2007 -
Other News To Note
Cardiome Pharma Corp., of Vancouver, British Columbia, said its co-development partner, Astellas Pharma U.S. Inc., of Deerfield, Ill., resubmitted the new drug application to market the intravenous formulation of vernakalant hydrochloride for the acute conversion of atrial fibrillationBioWorld Today | Wednesday, December 20, 2006 -
Theravance Submits NDA For Antibiotic Telavancin
The product is partnered with Tokyo's Astellas Pharma IncBy Aaron Lorenzo | BioWorld Today | Monday, December 11, 2006 -
Clinic Roundup
CV Therapeutics Inc., of Palo Alto, Calif., and Astellas Pharma US Inc., of Deerfield, Ill., said the second of two Phase III studies of regadenoson met its primary endpoint by showing that myocardial perfusion imaging (MPI) studies conducted with regadenoson were comparable to MPI studies conducted with Adenoscan (adenosine injectionBioWorld Today | Tuesday, December 5, 2006 -
Other News To Note
Eligard, a palliative treatment for advanced prostate cancer, will be marketed by QLT's European partner, Tokyo-based Astellas Pharma IncBioWorld Today | Monday, December 4, 2006
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