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FDA Accepts Repros' Phase 3 Efficacy Protocol for Androxal(R) Under a Special Protocol Assessment Agreement

THE WOODLANDS, Texas, July 9, 2012 (GLOBE NEWSWIRE) -- Repros Therapeutics Inc.® (Nasdaq:RPRX) today announced it has reached agreement with the FDA for the design of the pivotal efficacy studies fo...

Analysis Software for USB Protocol Analyzers

Agilent Technologies Inc. has introduced a new analysis software suite for the U4611A, U4611B, and U4612A family of USB protocol analyzers. The suite features MegaZoom technology, offering USB device...

Protocol Stems Postpartum Bleeds (CME/CE)

SAN FRANCISCO (MedPage Today) -- A comprehensive protocol for treating maternal hemorrhage reduced transfusions and hysterectomies, researchers found.

[Comment] SPIRIT 2013: new guidance for content of clinical trial protocols

The protocol is an important document that details the background, methods, ethical considerations, and administration of a clinical trial. The information contained in the protocol is useful for seve...

Abortions, Not Euthanasia, Increased After Protocol Enacted

Reported cases of euthanasia declined after the Groningen Protocol was published in 2005. Medscape Medical News

DKA Improves with Isotonic Fluid Protocol (CME/CE)

WASHINGTON (MedPage Today) -- Rates of death and disability were much lower among children with diabetic ketoacidosis (DKA) when they were treated with a consistent protocol that supplied high leve...

Teva to Initiate Third Phase III Trial of Oral Laquinimod for the Treatment of Relapsing ...

The clinical trial protocol has been granted a Special Protocol Assessment agreement by the Food and Drug Administration

Terumo BCT Launches Mononuclear Cell Collection Protocol

LAKEWOOD, Colo.--Terumo BCT announced today that the Spectra Optia system mononuclear cell (MNC) collection protocol is now cleared by the U.S. Food and Drug Administration (FDA) and available for use...

Autologous transplantation in multiple myeloma with an augmented conditioning protocol.

Abstract We compared the tolerability and anti-myeloma effect of 2 conditioning regimens for auto-SCT in consecutive groups of patients. Protocol 1 was the earlier and consisted of the combination of...

Evaluation of the University of Florida lomustine, vincristine, procarbazine, and prednisone chemotherapy protocol for the treatment of relapsed lymphoma in dogs: 33 cases (2003-2009).

Objective-To evaluate the toxicity and efficacy of a modification of a previously evaluated combination of lomustine, vincristine, procarbazine, and prednisone (LOPP) as a rescue protocol for refracto...

Body weight-tailored contrast material injection protocol for 64-detector row computed tomography coronary angiography.

PURPOSE: The aim of this study was to assess the body weight-tailored contrast material injection protocol for 64-detector computed tomography (CT) to maintain optimal coronary CT attenuation. MATERIA...

Evaluation of factors associated with recruitment in hematological clinical trials: a retrospective cohort study.

The objectives of this study were to measure the recruitment, to study characteristics associated with recruitment, and to explore reasons for non-recruitment in clinical trials for malignant hematolo...

A pre-validation transferability study of the GreenScreen HC GADD45a-GFP assay with a metabolic activation system (S9).

A new protocol has recently been developed and validated for the GreenScreen HC GADD45a-GFP genotoxicity reporter assay, enabling the incorporation of an S9 metabolic activation system into the assay....