Idenix Pharmaceuticals Successfully Completes Proof-of-Concept Study of IDX184 for the Treatment of Hepatitis C Virus (HCV)
... to be a best-in-class nucleoside/tide polymerase
inhibitor with demonstrated antiviral activity and ... coming months from our non-nucleoside polymerase
inhibitor and protease
inhibitor programs, we are closer to achieving our ultimate ...
Tibotec Pharmaceuticals Announces Agreement to Develop and Commercialize a New Fixed-Dose Combination of TMC278 and Truvada(R) With Gilead Sciences
... non-nucleoside reverse transcriptase
inhibitor (NNRTI) TMC278 (rilpivirine hydrochloride 25 mg) ... with a non-nucleoside reverse transcriptase
inhibitor or a protease
inhibitor as a preferred regimen for patients initiating ...
Schering-Plough Expands Vicriviroc Phase II Study in Treatment-Naive Patients With HIV
... of the immune system, vicriviroc is an HIV entry
inhibitor designed to prevent the virus from infecting ... therapy. Atazanavir is a product in the protease
inhibitor (PI) class of HIV medications. Truvada is a ... in the nucleoside(tide) reverse transcriptase
inhibitor (NRTI) class.
The standard of care for ...
Proteolix, Inc. Drug Candidate, PR-957, Prevents Disease Progression in Rheumatoid Arthritis Models by Selective Inhibition of the Immunoproteasome
... Medicine, Proteolix's selective immunoproteasome
inhibitor PR-957 was shown to block disease progression in ... print edition in an article titled: A Selective
inhibitor of the Immunoproteasome Subunit LMP7 Blocks ... is the first highly selective, small molecule
inhibitor of the immunoproteasome. The proteasome is an ...
Proteolix Presents Phase 1b/2 Clinical Data for Carfilzomib in Advanced Solid Tumor Patients at the 2009 ASCO Annual Meeting
... activity as a highly selective and potent
inhibitor of the proteasome for treatment of solid tumor ... for carfilzomib as a promising new protease
inhibitor in hematologic and solid tumor malignancies. ... including a selective, oral proteasome
inhibitor and a selective immunoproteasome inhibitor. For ...
New Study: Antidepressants Commonly Prescribed with Tamoxifen Put Women at Much Higher Risk for Recurrent Breast Cancer
...
"We've known that these CYP2D6
inhibitor drugs block the activation of tamoxifen ... far lower levels in the blood stream when CYP2D6
inhibitor drugs are present, and it is the first study to ... that patients used tamoxifen and a CYP2D6
inhibitor concurrently was 340 days.
The analysis ...
Keryx Biopharmaceuticals Reports Single Agent Phase 2 Data of KRX-0401 (Perifosine) Further Demonstrating KRX-0401's Activity in the Treatment of Advanced Metastatic Renal Cell Cancer
... Failing Treatment Either with a VEGF Receptor
inhibitor or after Treatment with both a VEGF Receptor
inhibitor and an mTOR
inhibitor
NEW YORK, May 29 /PRNewswire-FirstCall/ -- ...
Scientific Data Relating to Cinryze(TM) Presented at 6th Annual C1 Inhibitor Deficiency Workshop
... abstracts relating to Cinryze(TM) (C1 esterase
inhibitor [human]) therapy at the 6th Annual C1
inhibitor Deficiency Workshop.
Cinryze was approved ... approved, Cinryze would be the first C1 esterase
inhibitor available for the acute treatment for this ...
Ascenta Therapeutics Announces Multiple Presentations on AT-101 at 2009 ASCO Annual Meeting
... p.m.
Min P, et al. Small molecule pan-bcl-2
inhibitor AT-101 induces apoptosis in NSCLC by upregulating ... al. Extended phase I trial of the oral pan-Bcl-2
inhibitor AT-101 by multiple dosing schedules in patients ... AT-101
AT-101 is an orally-active, pan-Bcl-2
inhibitor (including Bcl-2, Bcl-xL, Bcl-w, and Mcl-1 ...
New Study Evaluating the ADHD Medication VYVANSE(R) (lisdexamfetamine dimesylate) CII Demonstrated No Change in the Pharmacokinetic Profile of VYVANSE When Coadministered with Prilosec OTC(R) 40 mg (20 mg X 2), a Commonly Used Proton Pump Inhibitor (PPI)
... dimesylate) CII with the proton pump
inhibitor (PPI) Prilosec OTC(R) 40 mg (20 mg X 2), did not ... the first to evaluate the impact of a proton pump
inhibitor on the amphetamine pharmacokinetics of VYVANSE ... drugs; agitated states; taken a monoamine oxidase
inhibitor (MAOI) within the last 14 days.
Tell the ...
Clinical Data on Semafore's SF1126, a Vascular Targeted Pan-PI3K/mTOR Inhibitor, to be Presented at the 2009 ASCO Meeting
... for Semafore's vascular targeted pan-PI3K/mTOR
inhibitor is scheduled as follows:
Time: ... SF1126 a vascular targeted PI3K
Title:
inhibitor administered twice weekly IV in patients with
... only clinical stage vascular targeted pan-PI3K
inhibitor that selectively inhibits all PI3K class I ...
Boehringer Ingelheim to Present New Phase II Clinical Data on Two Lead Oncology Compounds at ASCO 2009
... 2992 is an orally-administered, irreversible dual
inhibitor of the epidermal growth factor receptor (EGFR) ... with a second-line or third-line reversible EGFR
inhibitor (i.e., erlotinib or gefitinib). This study ... Li D et al. "BIBW2992, an irreversible EGFR/HER2
inhibitor highlyeffective in preclinical lung cancer ....
FDA Accepts Arno Therapeutics' IND for AR-12 a PDK1 Inhibitor That Blocks the PI3K/Akt Pathway
... first-in-class, orally available, PDK1
inhibitor that blocks the PI3K/Akt pathway and induces the ... first-in-class, orally available, PDK1
inhibitor that blocks the PI3K/Akt pathway and induces the ... a potential first-in-class, orally available PDK1
inhibitor that blocks the PI3K/Akt pathway and induces the ...
Isis and Collaborators Present New Research at the ATVB Annual Conference
... research programs, one on a direct antisense
inhibitor of apoC-III, which may provide a promising new ... lower triglycerides, and a second on an antisense
inhibitor to Factor XI, which has the potential to create a ... models.
"The potential to add an apoC-III
inhibitor in the near-term to our cardiovascular pipeline, ...
Dendreon Presents Preclinical Data Demonstrating Activity of TRPM8 Agonist, D-3263, in Benign Prostatic Hyperplasia
... initiation of BPH, either D-3263, finasteride (an
inhibitor of the enzyme 5-alpha-reductase) or a combination ... of the two. While finasteride is a known
inhibitor of 5-alpha reductase, the enzyme that converts testosterone to DHT, D-3263 is not an
inhibitor of this enzyme suggesting that the two agents may ...
Ground-Breaking Combination of All-Oral Agents Demonstrates Potential as Hepatitis C Treatment Regimen
... time that the combination of an oral protease
inhibitor and an oral nucleoside polymerase
inhibitor resulted in significant HCV viral load reduction ... (ITMN-191)
R7227 is a potent, macrocyclic
inhibitor of HCV NS3/4A protease activity, and has produced ...
InterMune Reports Presentation of Triple Combination Study of ITMN-191 at European Association for the Study of the Liver (EASL)
... with HCV genotype 1. ITMN-191 is an HCV protease
inhibitor being developed in collaboration with Roche. ... 2009. A Phase 1 trial of ITMN-191 and polymerase
inhibitor R7128 (INFORM-1 Study) is currently underway.
... hepatology portfolio includes the HCV protease
inhibitor compound ITMN-191 (referred to as R7227 at Roche) ...
ANA598 Demonstrates Potent Antiviral Activity at all Dose Levels in Completed Phase Ib Study in Hepatitis C Patients
... ANA598 as a leading non-nucleoside polymerase
inhibitor in development for the treatment of HCV, and we ... of ANA598 with interferon-alpha, the protease
inhibitor telaprevir and the nucleoside polymerase
inhibitor PSI-6130 are synergistic. These studies also ...
Final Results of Boceprevir Phase II HCV SPRINT-1 Study Showed Significantly Higher SVR Rates Compared to Standard of Care in Treatment-Naive Genotype 1 Hepatitis C Patients
... care
Update on next-generation HCV protease
inhibitor SCH 900518 presented at EASL annual meeting
... study, known as HCV SPRINT-1 (HCV Serine Protease
inhibitor Therapy-1), boceprevir (800 mg TID) was evaluated ... by week 4, therefore patients have the protease
inhibitor added at a time when the backbone drug levels ...
Pharmacyclics announces Global Strategic Alliance with Les Laboratoires Servier
... an orally active, novel, small molecule
inhibitor of Pan HDAC enzymes, that is currently in Phase ... its innovative anti-cancer Pan HDAC
inhibitor agents.
"This alliance with Servier allows ... our unique and differentiated Pan HDAC
inhibitor product outside of the United States in rapid ...
Cylene to Present Advances in its Oral Inhibitor of CK2 at AACR Annual Meeting
... description of CX-4945, a first-in-class oral
inhibitor of protein kinase CK2. CK2 overexpression is ... molecular target. CX-4945 is a potent, selective
inhibitor of CK2 and modulates key survival pathways in ... 19, 2009: 8:00 AM CX-4945, a small molecule
inhibitor of CK2, inhibits angiogenesis by affecting the ...
Pharmacyclics Initiates Phase 1 Clinical Trial of Novel Oral Btk Inhibitor for Refractory B-cell Non-Hodgkin's Lymphoma
... of PCI-32765,
an orally available, selective
inhibitor of Bruton's tyrosine kinase, or Btk,
as a ... lymphoma (NHL). This is the first Btk selective
inhibitor to
be tested in humans, and is Pharmacyclics' ... Fort Collins,
CO
About Pharmacyclics' Btk
inhibitor Program
PCI-32765 is currently targeted ...
Pharmacyclics, Inc. Announces Closing of a Private Financing With the Principals of Pacific Biopharma Group, Ltd.
... This includes a leading histone deacetylase
inhibitor (PCI-24781) for multiple cancers; an
inhibitor of Factor VIIa (PCI-27483) targeting pancreatic, ... colon and breast cancers; a first in class
inhibitor of Bruton's tyrosine kinase (Btk) (PCI-32765) ...
Genaera Presents Preliminary Phase 1b Data for Trodusquemine (MSI-1436)
... (MSI-1436), the first-in-class, highly selective
inhibitor of PTP1B and Genaera's lead drug candidate for ... continues to exhibit promise as the only PTP1B
inhibitor in development to simultaneously treat both type ...
Trodusquemine is the first highly selective
inhibitor of protein tyrosine phosphatase 1B (PTP1B), an ...
Sequoia Pharmaceuticals Presents Proof of Clinical Concept of SPI-452, a Novel Pharmacokinetic Enhancer
... for use in HIV therapy is
ritonavir, a protease
inhibitor that has inherent antiviral activity. SPI-452
was designed to be a potent
inhibitor of CYP3A enzymes with no antiviral
activity and ... The first IND is for SPI-
256, an HIV protease
inhibitor in phase 1 clinical development. The second ...
FDA Grants Priority Review of a Supplemental Biologics License Application for Cinryze(TM) C1 Inhibitor (Human) as Treatment for Acute Attacks of Hereditary Angioedema (HAE)
... (FDA) has granted priority review for Cinryze C1
inhibitor (human) as a treatment for acute attacks of ... subsequent HAE attacks.
About Cinryze C1
inhibitor (human)
Cinryze is a highly purified, pasteurized and nanofiltered plasma-derived C1
inhibitor product that has been approved by FDA for routine ...
ANA598 Demonstrates Potent Antiviral Activity in an Early Clinical Study in HCV-Infected Patients
... ANA598 as a leading non-nucleoside polymerase
inhibitor in development for the treatment of HCV and we ... been reported for any other non-nucleoside HCV
inhibitor in a monotherapy study. Furthermore, the rate of ... agents, ANA598, a non-nucleoside polymerase
inhibitor and ANA773, an oral TLR7 agonist prodrug. The ...
ImQuest Submits Investigational New Product Application to the Food and Drug Administration to Initiate HIV Therapeutic Clinical Trials with IQP-0410
... trials for their lead pyrimidinedione HIV
inhibitor IQP-0410. ImQuest anticipates initiating their ... of 2009. IQP-0410 is a novel small molecule
inhibitor of HIV which primarily acts as a nonnucleoside reverse transcriptase
inhibitor (NNRTI). The compound possesses a second ...
Cylene Pharmaceuticals Initiates Phase I Trial With CX-4945 -Breakthrough First-in Class Inhibitor of CK2
... CX-4945 represents the first potent and selective
inhibitor of CK2 with a favorable safety profile and the ...
About CX-4945, an oral CK2 protein kinase
inhibitor
CX-4945 is a first-in-class small molecule ... with the objective of creating a multifunctional
inhibitor by targeting a single protein and affecting ...
Video: Femara(R) First Aromatase Inhibitor to Indicate Survival Benefit Versus Tamoxifen When Taken for Five Years After Breast Cancer Surgery
... to suggest a survival benefit for an aromatase
inhibitor versus tamoxifen in the monotherapy setting ... seeing suggested survival benefit with aromatase
inhibitor therapy for five years compared with tamoxifen ... both a head-to-head comparison of an aromatase
inhibitor with tamoxifen during the first five years ...
InterMune to Report Top-Line Results of Triple Combination Study of ITMN-191 in January 2009
... 2009
from its Phase 1b clinical trial of protease
inhibitor ITMN-191 (R7227) in
combination with ... study of ITMN-191 in
combination with polymerase
inhibitor R7128 (Roche/Pharmasset). INFORM-1 is
the first ... portfolio includes the HCV protease
inhibitor compound ITMN-191
(referred to as R7227 at Roche) ...
Video: Tasigna(R) Demonstrates Rapid Response as Initial Therapy in Life-Threatening Form of Leukemia
... Oncology.
Tasigna is a tyrosine kinase
inhibitor approved for the treatment of adult Ph+ CML ... is recommended (400 mg once daily). If the strong
inhibitor is discontinued, a washout period should be ... to the indicated dose. Tasigna is a competitive
inhibitor of CYP3A4, CYP2C8, CYP2C9, CYP2D6, and UGT1A1. ...
More Than 200 Abstracts at ASH and SABCS Reveal Potential Compelling Patient Benefits From Novartis Oncology Current and Pipeline Therapies
... 1-Year Results of TOPS (Tyrosine Kinase
inhibitor Optimization and Selectivity) Study (ASH ... Panobinostat (LBH589), a Novel Pan-Deacetylase
inhibitor (DACi) Demonstrating Efficacy in Patients with ... is metabolized by the CYP3A4 isoenzyme and is an
inhibitor of CYP3A4, CYP2D6 and CYP2C9. Dosage of Gleevec ...
Proteolix to Present Clinical and Preclinical Data at the 50th Annual Meeting of the American Society of Hematology
... characterization of its oral proteasome
inhibitor known as PR-047.
A complete list of the ... Poster II
-- The Selective Proteasome
inhibitor Carfilzomib is Well Tolerated in
... Characterization of PR-047, An
Oral
inhibitor of the 20S Proteasome (Abstract #3671)
...
Schering-Plough Highlights R&D Pipeline Progress, Innovation and Breadth of Research Projects
... and Japan);
Boceprevir, an oral protease
inhibitor for treating hepatitis C with peginterferon and ... SVR; in addition, a next-generation protease
inhibitor in Phase II for treating hepatitis C was ... Two projects for Alzheimer's -- a beta secretase
inhibitor and a gamma secretase inhibitor; and
A ...
Schering-Plough Provides Update on Boceprevir Clinical Development and Introduces Potent Next-Generation Oral HCV Protease Inhibitor for Treating Patients With Chronic Hepatitis C
... lead investigational oral hepatitis C protease
inhibitor currently in Phase III development. The company ... to be a first-in-class and best-in-class protease
inhibitor for treating chronic hepatitis C. The company ... potent next-generation oral hepatitis C protease
inhibitor that has future best-in-class potential. The ...
ViroPharma Announces Presentation of Cinryze(TM) Data in Acute Treatment of Hereditary Angioedema
... of their
family members."
About Cinryze C1
inhibitor (human)
Cinryze is a highly purified, pasteurized and nanofiltered
plasma-derived C1
inhibitor product that has been approved by FDA for
routine ... in adolescent and adult
patients with HAE. C1
inhibitor therapy has been used acutely for more than
30 ...
Tibotec Data Presented at ICAAC and HIV9 Follow Key Regulatory Approvals for Anti-HIV Compounds
... New data on PREZISTA(R)
(darunavir), a protease
inhibitor from Tibotec, will be presented at the
Ninth ... reverse transcriptase
inhibitor (NNRTI). The company
continues to research ... in combination with a boosted protease
inhibitor and other antiretroviral medicinal products, ...
Roche, InterMune and Pharmasset Announce Initiation of INFORM-1, the First Dual-Combination Clinical Trial with Oral Antivirals in Hepatitis C
... of PSI-6130, a cytidine nucleoside analog
inhibitor of HCV RNA
polymerase. A pro-drug is a chemically ... trial.
About R7227 (ITMN-191)
R7227 is an
inhibitor of HCV NS3/4A protease activity, and has ... The hepatology portfolio includes HCV
protease
inhibitor ITMN-191 (R7227) in Phase 1b, a second-generation ...
Anadys Pharmaceuticals Announces Single Dose Safety and Pharmacokinetics Results for ANA598 in Healthy Volunteers
... for Non-Nucleoside HCV Polymerase
inhibitor Being Presented at AASLD
SAN DIEGO, Nov. 1 ... Antiviral Agents that Include HCV Polymerase
inhibitor ANA598 have the
Potential to Overcome Viral ... synergistic with interferon-alpha,
the protease
inhibitor telaprevir (VX-950), and the nucleoside ...