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Clinical Trials
Cardiovascular Systems’ Predator 360° Data Demonstrates Favorable 12-Month Results Treating Peripheral Arterial Disease PDF Print E-mail
Wednesday, 19 October 2011 01:27

Data from Cardiovascular Systems’ (CSI) (Nasdaq: CSII) Predator 360° prospective single-center clinical study titled, Use of Orbital Treatment in a High Volume Clinical Practice Modifies Non-Compliant Plaque to Deliver Durable Long-Term Results, presented today affirmed the procedural safety and efficacy, as well as the long-term durability, of the Predator 360® PAD System in treating peripheral arterial disease (PAD), or blockages in leg arteries.

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EORTC, BIG, and Agendia Announce Completion of Patient Recruitment for International MINDACT Study PDF Print E-mail
Tuesday, 18 October 2011 05:30

The EORTC, BIG, and Agendia, a commercial-stage molecular cancer diagnostics company, today announced the completion of patient registration for the EORTC 10041/BIG3-04 MINDACT (Microarray In Node negative and 1-3 positive lymph node Disease may Avoid Chemotherapy Trial) study.

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Takeda Initiates Phase 3 Clinical Trial Program in the United States, Latin America, and Europe for Investigational Type 2 Diabetes Therapy TAK-875 PDF Print E-mail
Tuesday, 18 October 2011 05:26
Takeda Pharmaceutical Company Limited ("Takeda") and its wholly-owned subsidiaries, Takeda Global Research & Development Center, Inc. ("TGRD U.S."), and Takeda Global Research & Development Centre (Europe), Ltd. ("TGRD Europe"), announced today the initiation of the Company's Phase 3 clinical trial program for TAK-875, an investigational therapy for type 2 diabetes.
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Dendreon Begins Enrollment in Phase 2 Neu-ACT Trial for Second Active Cellular Immunotherapy Product Candidate, DN24-02 PDF Print E-mail
Monday, 17 October 2011 20:25

Dendreon Corporation (Nasdaq: DNDN) today announced that the company has begun enrolling patients into a Phase 2 trial for DN24-02, Dendreon’s investigational active cellular immunotherapy being evaluated for the treatment of HER2 positive cancer.

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Multi-center Clinical Trial Shows ParaPRO’s Spinosad Eradicates Head Lice and Nits PDF Print E-mail
Monday, 17 October 2011 20:22

ParaPRO, LLC, announced that researchers have presented data showing the effectiveness of Natroba™ (spinosad) Topical Suspension, 0.9% against head lice and nits following one treatment without nit combing.

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Innavirvax Announces Phase I/IIa Clinical Trial Authorization Granted by AFSSAPS for its VAC-3S Vaccine for the Treatment of HIV Infections PDF Print E-mail
Saturday, 15 October 2011 16:51
InnaVirVax, a biopharmaceutical company dedicated to the development of therapeutic and diagnostic solutions in pathologies associated with immune dysregulation, declared today that it has obtained authorization from the French drug agency (AFSSAPS) to start a Phase I/IIa clinical study of its therapeutic vaccine VAC-3S for the treatment of HIV infections.
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ViroMed Takes One Step Closer to Finding a Cure for Diabetic Neuropathy through US Clinical Trial I/II PDF Print E-mail
Saturday, 15 October 2011 16:48
ViroMed Co., Ltd. (KOSDAQ: 084990) today announced that the results of the Phase I/II study on its diabetic neuropathy therapeutic drug (VM202-DPN) were presented at ‘BIO KOREA 2011 Conference & Exhibition’ held at COEX (Seoul, Korea) from 28th to 30th Sept., and showed the world the possibility of an innovative treatment method completely different from the currently available diabetic neuropathy treatments.
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Baxter Initiates Phase III Trial of Investigational BAX 111 For the Treatment of von Willebrand Disease PDF Print E-mail
Friday, 14 October 2011 01:43

Baxter International Inc. today announced initiation of a Phase III clinical trial to evaluate the safety and effectiveness of BAX 111, Baxter’s investigational recombinant von Willebrand factor (rVWF), for the treatment and prevention of bleeding episodes in patients with von Willebrand disease.

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Renessa® Treatment for Stress Incontinence: Three Year Clinical Results Presented PDF Print E-mail
Friday, 14 October 2011 01:40
Novasys Medical, Inc., a developer of innovative therapies in women's health, announced today that a poster describing results from a prospective three year clinical trial of its non-surgical Renessa® treatment for stress urinary incontinence (SUI) in women was presented at two professional society meetings in September 2011: the annual national Scientific Meeting of the American Urogynecologic Society (AUGS) and the South Central Section of the American Urological Association.
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Shield Therapeutics Initiates AEGIS 1 And AEGIS 2 Phase 3 Studies Of ST10 PDF Print E-mail
Thursday, 13 October 2011 01:26
Two pivotal trials initiated for treatment of iron deficiency anaemia associated with ulcerative colitis and Crohn's disease -

Shield Therapeutics (Shield), the independent specialty pharmaceutical company focused on the development and commercialisation of late-stage, mineral-derived hospital pharmaceuticals which address areas of high unmet medical need, today announced that the first patients have been treated in the two Phase 3 clinical studies of ST10 for the treatment of iron deficiency anaemia (IDA) in subjects with inflammatory bowel disease (IBD).

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CTRI Confirms Leading Indian CRO Supports Majority of Hemophilia Trials in India PDF Print E-mail
Tuesday, 18 October 2011 05:33
Max Neeman International is the only CRO in India to manage hemophilia trials according to the Clinical Trials Registry-India (CTRI).
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Halozyme Announces Positive Results from Roche's Subcutaneous Herceptin Phase 3 Trial PDF Print E-mail
Tuesday, 18 October 2011 05:28
Halozyme Therapeutics, Inc. (NASDAQ: HALO), a biopharmaceutical company developing and commercializing products targeting the extracellular matrix for the diabetes, cancer, dermatology and drug delivery markets, today announced that the Phase 3 HannaH trial, conducted by Roche, showed that women with HER2-positive early breast cancer who received a new, investigational subcutaneous (SC) injection of Herceptin® (trastuzumab), experienced comparable results to Herceptin given as an intravenous (IV) infusion.
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Infinity Completes Enrollment in Phase 2 Trial of IPI-926, an Oral Smoothened Antagonist, in Pancreatic Cancer and Provides Additional Program Updates PDF Print E-mail
Monday, 17 October 2011 20:26

Infinity Pharmaceuticals, Inc. (NASDAQ: INFI) today announced updates to its development program for IPI-926, including that the company has completed enrollment of its Phase 2 trial of IPI-926 in patients with previously untreated pancreatic cancer.

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AB Science Announces Recruitment of First Patient in Phase 3 Study of Masitinib in Multiple Myeloma PDF Print E-mail
Monday, 17 October 2011 20:23

AB Science SA (Paris:AB)(NYSE Euronext - FR0010557264 - AB), a pharmaceutical company specializing in the research, development and commercialization of protein kinase inhibitors (PKIs), announced today recruitment of the first patient in the phase 3 study of masitinib in the treatment of patients with relapsing multiple myeloma who received one previous therapy.

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Roche (RHHBY)'s Experimental Alzheimer's Drug Gantenerumab Looks Promising in Phase I PDF Print E-mail
Saturday, 15 October 2011 16:53

Roche (SIX: RO, ROG; OTCQX: RHHBY) today announced the publication of a study demonstrating that its monoclonal antibody gantenerumab removes amyloid plaques from the brain of patients with Alzheimer's disease.

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Ampio Pharmaceuticals, Inc. (AMPE) Completes Treatment Phase of the Ampion(TM) -in-Knee Clinical Trial for Osteoarthritis PDF Print E-mail
Saturday, 15 October 2011 16:50

Ampio Pharmaceuticals, Inc. (NASDAQ: AMPE) ("Ampio" or the "Company"), a company that discovers and develops new uses for previously approved drugs and new molecular entities ("NMEs"), today announced that it has completed the treatment phase of the Ampion-in-Knee (AIK) trial.

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Atrium’s COBEST Trial Results Published PDF Print E-mail
Saturday, 15 October 2011 00:21
Atrium Medical Corporation (Hudson, NH) announced that Principal Investigator Prof. Bibombe Patrice Mwipatayi, MMed (Surg), published results from the COBEST (Covered Versus Balloon-Expandable Stent Trial) trial online ahead of print in the Journal of Vascular Surgery.
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Phase 1/2 Clinical Trial Results of Perifosine Plus Bortezomib and Dexamethasone in Patients with Relapsed/Refractory Multiple Myeloma Published in the Journal of Clinical Oncology PDF Print E-mail
Friday, 14 October 2011 01:41
Aeterna Zentaris Inc. (NASDAQ: AEZS) (TSX: AEZ) (the "Company") today announced that a manuscript entitled "Perifosine Plus Bortezomib and Dexamethasone in patients with Relapsed/Refractory Multiple Myeloma Previously Treated with Bortezomib: Results of a Multicenter Phase 1/2 Trial" reporting Phase 1/2 combination activity of perifosine in the treatment of advanced multiple myeloma (MM) patients, was selected for publication in the October 10, 2011 online edition of the Journal of Clinical Oncology (JCO).
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Merck’s ISENTRESS® (raltegravir) in Combination Therapy Demonstrated Virological and Immunological Efficacy Versus the Efavirenz Regimen at 192 Weeks of Treatment in Previously Untreated Adults with HIV-1 PDF Print E-mail
Friday, 14 October 2011 01:18

Merck (NYSE: MRK), known as MSD outside the United States and Canada, today announced results of new exploratory pre-specified analyses from the ongoing STARTMRK Phase III study of its integrase inhibitor ISENTRESS® (raltegravir) Tablets in combination therapy compared to efavirenz in combination therapy in previously untreated (treatment-naïve) adult HIV-1-infected patients.

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Pfizer Negotiates Global Rights to GlycoMimetics’ Phase II Sickle Cell Crisis Drug PDF Print E-mail
Thursday, 13 October 2011 00:50

Pfizer negotiated exclusive worldwide rights to develop GlycoMimetics’ pan-selectin antagonist GMI-1070, in a deal which could be worth $340 million to GlycoMimetics in up-front and development, regulatory, and commercialization milestones, plus additional sale royalties. 

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