Abstract: A liposome composition and method for delivery of a nucleic acid in vivo or ex vivo is described. The liposomes in the composition are comprised of (i) a cationic lipid and (ii) a lipid joined to a hydrophilic polymer by a releasable linkage. The liposomes are associated with a nucleic acid for delivery to a cell.
Abstract: The present invention provides a reusable spring driven autoinjector. The drive mechanism of the autoinjector of the present invention includes one or more drive springs formed of a shape memory alloy. Therefore, by alternating the shape memory alloy forming the one or more drive springs between austenite phase before an injection and a martensite phase after injection, the reusable autoinjector of the present invention is capable of providing an injection force that is higher than the compressive force required to cock the drive mechanism in preparation for a subsequent injection operation.
Abstract: An osmotic delivery system flow modulator assembly, an osmotic delivery system with a flow modulator assembly, and a method of assembling an osmotic delivery system. The osmotic delivery system flow modular assembly includes a body having a hole located through the body and communicating two opposing ends of the body. The use of the osmotic delivery system flow modulator assembly lessens the chance that air or gas pockets will form in the enclosure of the osmotic delivery system during assembly of the system. Because less air is within the osmotic delivery system, performance of the system is enhanced. Use of the flow modulator assembly also lessens the chance that beneficial agent will be wasted during assembly of the osmotic delivery system.
Type:
Application
Filed:
September 16, 2007
Publication date:
March 20, 2008
Applicant:
ALZA CORPORATION
Inventors:
Lewis Peterson, Fred Maruyama, Houdin Dehnad, Lawton Hom, Kevin Sly, Craig Davis, John Peery
Abstract: The present invention includes an expandable osmotic layer and a coating suspension for providing an expandable osmotic layer, both of which are useful for the manufacture of controlled release dosage forms. The expandable osmotic layer of the present invention may be produced using the coating suspension of the present invention. Advantageously, the coating suspension of the present invention can be used to coat expandable osmotic layers under both wet and dry process conditions without sacrificing the quality of the expandable osmotic layers produced, and therefore provides a relatively robust coating suspension that facilitates commercial production of controlled release dosage forms including a coated expandable osmotic layer.
Type:
Grant
Filed:
June 28, 2003
Date of Patent:
March 4, 2008
Assignee:
ALZA Corporation
Inventors:
Shaoling Li, Liang-Chang Dong, Padmaja Shivanand, Patrick S. L. Wong
Abstract: An apparatus and method for transdermally delivering a biologically active agent to prevent or treat osteopenia, comprising a delivery system having a microprojection member (or system) that includes a plurality of microprojections (or array thereof) that are adapted to pierce through the stratum corneum into the underlying epidermis layer, or epidermis and dermis layers. In one embodiment, the PTH-based agent is contained in a biocompatible coating that is applied to the microprojection member.
Type:
Application
Filed:
March 15, 2007
Publication date:
February 14, 2008
Applicant:
ALZA CORPORATION
Inventors:
Mahmoud Ameri, Michel Cormier, Yuh-Fun Maa, Marika Kamberi, Peter Daddona
Abstract: An implant retention trocar includes a cannula for puncturing the skin of an animal and an obturator for delivering the implant beneath the skin of the animal. The implant retention trocar has a cannula distal tip design which causes a minimum of trauma and tearing of tissue during implant insertion. A spring element received within the cannula prevents an implant which is to be inserted into an animal from falling out of the cannula during the implant insertion process. The spring element includes a longitudinal leg which is folded with a zigzag-shaped bend. When the spring element is inserted into the cannula, the zigzag-shaped bend of the longitudinal leg retains the implant within the cannula.
Abstract: Composition of matter for application to a body surface or membrane to administer warfarin by permeation through the body surface or membrane, the composition comprising warfarin to be administered, at a therapeutically effective rate, alone or in combination with a permeation enhancer or mixture. Also disclosed are drug delivery devices containing the warfarin or warfarin and enhancer composition and methods for the transdermal administration of the warfarin and warfarin/enhancer composition.
Abstract: A composition and a dosage form are disclosed comprising oxybutynin alone/or accompanied by another drug indicated for therapy. A method is disclosed for administering oxybutynin alone/or accompanied by a different drug or for administering oxybutynin and a different drug according to a therapeutic program for the management of incontinence alone, and for other therapy.
Type:
Application
Filed:
July 25, 2007
Publication date:
January 24, 2008
Applicant:
Alza Corporation
Inventors:
George Guittard, Francisco Jao, Susan Marks, David Kidney, Fernando Gumucio, Suneel Gupta, Gayatri Sathyan
Abstract: Electrotransport drug delivery devices, systems and methods for delivery of lofentanil or carfentanil are disclosed. The lofentanil or carfentanil may be provided as a water soluble salt (e.g., lofentanil or carfentanil hydrochloride), such as in a hydrogel formulation. A transdermal, electrotransport delivered dose of lofentanil or carfentanil is provided which is sufficient to induce analgesia in (e.g., adult) human patients suffering from chronic, acute and/or breakthrough pain.
Type:
Application
Filed:
June 26, 2007
Publication date:
January 10, 2008
Applicant:
ALZA Corporation
Inventors:
Robert Gale, Rama Padmanabhan, Joseph Phipps
Abstract: Apparatus, systems and methods for stimulation of a vagus nerve of a patient are disclosed. An element that can be deployed and retained inside the patient's stomach without surgery and having a power supply and electrodes is associated with the expandable element. The electrodes are capable of stimulating the vagus nerve while the expandable element remains in the stomach for an extended period of time.
Type:
Application
Filed:
June 26, 2007
Publication date:
January 3, 2008
Applicant:
ALZA Corporation
Inventors:
Rolfe Anderson, Pedro E. de la Serna, Laura Maurer
Abstract: A transdermal drug delivery system with microprojections for disrupting a body surface to an individual. At least some of the microprojections arise from a first microprojection layer and at least some of the microprojections arise from a second microprojection layer. The first and second microprojection layers are stacked together.
Type:
Application
Filed:
April 25, 2007
Publication date:
December 27, 2007
Applicant:
ALZA CORPORATION
Inventors:
Keith Chan, Rajan Patel, Peter Daddona, Cedric Wright, Neha Agarwal
Abstract: A transdermal drug delivery system with microprojections for disrupting a body surface to an individual. At least some of the microprojections form groups in a microprojection array. There are repeated units of such groups in the microprojection array.
Type:
Application
Filed:
April 25, 2007
Publication date:
December 20, 2007
Applicant:
ALZA CORPORATION
Inventors:
Keith Chan, Rajan Patel, Peter Daddona, Cedric Wright, Neha Agarwal
Abstract: A transdermal drug delivery system with microprojections for disrupting a body surface to an individual. At least some of the microprojections have a depression for increasing drug loading by a drug coating.
Type:
Application
Filed:
April 25, 2007
Publication date:
December 20, 2007
Applicant:
ALZA CORPORATION
Inventors:
Keith Chan, Rajan Patel, Peter Daddona, Cedric Wright, Neha Agarwal
Abstract: An osmotic delivery system flow modulator includes an outer shell constructed and arranged for positioning in an opening, an inner core inserted in the outer shell, and a fluid channel having a spiral shape defined between the outer shell and the inner core. The fluid channel is adapted for delivery of an active agent formulation from the reservoir of the osmotic delivery system.
Type:
Application
Filed:
May 30, 2007
Publication date:
December 6, 2007
Applicant:
ALZA CORPORATION
Inventors:
Scott D. Lautenbach, Pedro E. de la Serna, Pauline C. Zamora, Michael A. DesJardin
Abstract: Methods for administering mitomycin C to a multi-drug resistant cell and for reducing the toxicity of the compound are described. In the methods, mitoymic C is provided in the form of a prodrug conjugate, where the drug is linked to a hydrophobic moiety, such as a lipid, through a cleavable dithiobenzyl linkage. The dithiobenzyl linkage is susceptible to cleavage by mild thiolysis, resulting in release of mitomycin C in its original form. The linkage is stable under nonreducing conditions. The prodrug conjugate can be incorporated into liposomes for administration in vivo and release of mitomycin C in response to endogenous in vivo reducing conditions or in response to administration of an exogenous reducing agent.
Type:
Grant
Filed:
November 14, 2003
Date of Patent:
December 4, 2007
Assignees:
Alza Corporation, Yissum Research Development Company of the Hebrew University of Jerusalem
Abstract: The invention provides an improved electrotransport drug delivery system for analgesic drugs, namely fentanyl and sufentanil. The fentanyl/sufentanil is provided as a water soluble salt (e.g., fentanyl hydrochloride), preferably in a hydrogel formulation, for use in an electrotransport device (10). In accordance with the present invention, a transdermal electrotransport delivered dose of fentanyl/sufentanil is provided which is sufficient to induce analgesia in (e.g., adult) human patients suffering from moderate-to-severe pain associated with major surgical procedures.
Type:
Grant
Filed:
October 28, 2005
Date of Patent:
November 27, 2007
Assignee:
ALZA Corporation
Inventors:
Mary Southam, Keith J. Bernstein, Henk Noorduin
Abstract: A transdermal drug delivery system with a high barrier retainer for holding a microprojection member for disrupting a body surface to an individual. The retainer is made of a high barrier material (such as metal) that is easily sterilizable, such as by heat, and can be used for keeping out contamination and maintaining the environment of the microprojection member.
Abstract: An electrotransport reservoir housing which contains, integrally formed therein, at least one region of conductive material which allows for a liquid and moisture tight barrier, while at the same time providing a means for conducting an electric current therethrough.
Abstract: The present invention provides methods and devices for the non-invasive, transdermal administration by electrotransport of nesiritide, or pharmaceutically acceptable nesiritide salts, to patients in need of treatment with nesiritide. The present invention also provides methods for the treatment of congestive heart failure that involve the administration of nesiritide, or pharmaceutically acceptable nesiritide salts, by electrotransport to patients that suffer from congestive heart failure.
Type:
Application
Filed:
March 26, 2007
Publication date:
October 25, 2007
Applicant:
ALZA CORPORATION
Inventors:
Rama V. Padmanabhan, Joseph Bradley Phipps