Patents Assigned to NeuroSystec Corporation
  • Patent number: 8298176
    Abstract: Drug solutions (or other combinations of vehicle with entrained drug) are prepared by removing drug from one or more masses of a solid form of the drug. The solid form of the drug may be sparingly soluble or insoluble in water. Examples of devices for holding solid drug and facilitating delivery of such drug to targeted regions are also described.
    Type: Grant
    Filed: July 19, 2010
    Date of Patent: October 30, 2012
    Assignee: NeuroSystec Corporation
    Inventors: Thomas J. Lobl, Anna Imola Nagy, Jacob E. Pananen, John V. Schloss
  • Patent number: 8267905
    Abstract: Implantable drug delivery systems target delivery of small volumes of drugs to specific tissues. In some cases, a drug delivery system includes an implantable osmotic pump connected to a drug-containing housing, with that housing connected to a needle, cochlear implant or other type of component for ultimate delivery to the target tissue. In some implementations, a subcutaneous port receives a fluid from an external pump. The port is connected to a needle or other component for delivery of one or more drugs to the target tissue. Both solid and liquid drug formulations can be used. In embodiments using solid drugs, a separate drug vehicle (such as saline) can be used to dissolve a portion of the solid drug, with the drug-loaded vehicle then delivered to the target tissue.
    Type: Grant
    Filed: May 1, 2006
    Date of Patent: September 18, 2012
    Assignee: NeuroSystec Corporation
    Inventors: Thomas J. Lobl, Stephen J. McCormack, Anna Imola Nagy, Jacob E. Pananen, John V. Schloss
  • Publication number: 20120208848
    Abstract: Improved formulations of gacyclidine for direct administration to the inner or middle ear.
    Type: Application
    Filed: April 25, 2012
    Publication date: August 16, 2012
    Applicant: NEUROSYSTEC CORPORATION
    Inventors: Thomas Jay Lobl, John Vinton Schloss, Jacob E. Pananen
  • Publication number: 20120208851
    Abstract: Colloidal suspensions comprising a therapeutic agent and squalene. Squalene binds to certain compounds, such as gacyclidine, much more tightly than other drug carriers, such as polylactic glycolic acid. Including squalene in the particulate phase sequesters the therapeutic agent and provides superior stability at room or body temperature.
    Type: Application
    Filed: June 18, 2009
    Publication date: August 16, 2012
    Applicant: NEUROSYSTEC CORPORATION
    Inventors: John Vinton Schloss, Thomas Jay Lobl
  • Publication number: 20110136870
    Abstract: Improved formulations of gacyclidine for direct administration to the inner or middle ear.
    Type: Application
    Filed: February 4, 2011
    Publication date: June 9, 2011
    Applicant: NEUROSYSTEC CORPORATION
    Inventors: Thomas Jay Lobl, John Vinton Schloss, Stephen Joseph McCormack, Anna Imola Nagy, Jacob E. Pananen
  • Publication number: 20110071493
    Abstract: Drug solutions (or other combinations of vehicle with entrained drug) are prepared by removing drug from one or more masses of a solid form of the drug. The solid form of the drug may be sparingly soluble or insoluble in water. Examples of devices for holding solid drug and facilitating delivery of such drug to targeted regions are also described.
    Type: Application
    Filed: July 19, 2010
    Publication date: March 24, 2011
    Applicant: NEUROSYSTEC CORPORATION
    Inventors: Thomas J. Lobl, Anna Imola Nagy, Jacob E. Pananen, John V. Schloss
  • Patent number: 7803148
    Abstract: Drug solutions (or other combinations of vehicle with entrained drug) are prepared by removing drug from one or more masses of a solid form of the drug. The solid form of the drug may be sparingly soluble or insoluble in water. Examples of devices for holding solid drug and facilitating delivery of such drug to targeted regions are also described.
    Type: Grant
    Filed: June 7, 2007
    Date of Patent: September 28, 2010
    Assignee: NeuroSystec Corporation
    Inventors: Thomas J. Lobl, Anna Imola Nagy, Jacob E. Pananen, John V. Schloss
  • Publication number: 20090209945
    Abstract: A drug-delivery unit suitable for implantation into a patient body may include a valveless impedance pump. In some implementations the unit may include an actuator, control electronics and a battery, and may communicate with an external patient interface unit. The patient interface unit can be used to control operation of the implant and to download data from the implant. The patient interface unit can also be used to charge the implant and/or a separate charger can be used. In other implementations, a drug-delivery implant unit may lack internal electronics and instead rely on an externally-supplied magnetic field to actuate the pump.
    Type: Application
    Filed: January 19, 2009
    Publication date: August 20, 2009
    Applicant: NEUROSYSTEC CORPORATION
    Inventors: Thomas J. Lobl, Jacob E. Pananen, David L. Canfield, Anna I. Nagy, Adrian L. Krag
  • Publication number: 20080152694
    Abstract: Devices, systems and techniques for delivering drugs to an ocular tissue are described. In at least some embodiments, a terminal component (e.g., a needle or open end of a catheter) is implanted in an ocular tissue and used to deliver one or more drugs. The delivered drugs may come from a source which is also implanted, or may be introduced from an external source (e.g., via a port). Both solid and liquid drug formulations can be used. Ocular implants can alternatively include a thin film coating that releases a drug into an ocular tissue.
    Type: Application
    Filed: July 20, 2007
    Publication date: June 26, 2008
    Applicant: NEUROSYSTEC CORPORATION
    Inventors: Thomas J. Lobl, Anna Imola Nagy, Jacob E. Pananen, John V. Schloss
  • Publication number: 20080145439
    Abstract: A suspension of nanoparticles in a liquid medium provides a mechanism for delivery of gacyclidine base or other drug that is substantially insoluble in the liquid medium.
    Type: Application
    Filed: July 31, 2007
    Publication date: June 19, 2008
    Applicant: NEUROSYSTEC CORPORATION
    Inventors: Thomas J. Lobl, John V. Schloss, Anna Imola Nagy, Jacob E. Pananen
  • Publication number: 20080065002
    Abstract: A drug-compatible, biocompatible, drug-delivery catheter can include multi-lumen tubing attached to an end fitting, with the end fitting having an internal fluid chamber and a fluid exit region. The catheter can also include multi-lumen tubing having one or more needles attached at a distal end.
    Type: Application
    Filed: September 5, 2007
    Publication date: March 13, 2008
    Applicant: NEUROSYSTEC CORPORATION
    Inventors: Thomas J. Lobl, John V. Schloss, Anna Imola Nagy, Jacob E. Pananen
  • Publication number: 20070287984
    Abstract: Drug solutions (or other combinations of vehicle with entrained drug) are prepared by removing drug from one or more masses of a solid form of the drug. The solid form of the drug may be sparingly soluble or insoluble in water. Examples of devices for holding solid drug and facilitating delivery of such drug to targeted regions are also described.
    Type: Application
    Filed: June 7, 2007
    Publication date: December 13, 2007
    Applicant: NEUROSYSTEC CORPORATION
    Inventors: Thomas J. Lobl, Anna Imola Nagy, Jacob E. Pananen, John V. Schloss
  • Publication number: 20070255237
    Abstract: Implantable drug delivery systems target delivery of small volumes of drugs to specific tissues. In some cases, a drug delivery system includes an implantable osmotic pump connected to a drug-containing housing, with that housing connected to a needle, cochlear implant or other type of component for ultimate delivery to the target tissue. In some implementations, a subcutaneous port receives a fluid from an external pump. The port is connected to a needle or other component for delivery of one or more drugs to the target tissue. Both solid and liquid drug formulations can be used. In embodiments using solid drugs, a separate drug vehicle (such as saline) can be used to dissolve a portion of the solid drug, with the drug-loaded vehicle then delivered to the target tissue.
    Type: Application
    Filed: May 1, 2006
    Publication date: November 1, 2007
    Applicant: NeuroSystec Corporation
    Inventors: Thomas Lobl, Stephen McCormack, Anna Nagy, Jacob Pananen, John Schloss
  • Publication number: 20060264897
    Abstract: An apparatus may include a needle for sustained delivery of drugs and other agents to the inner ear or other tissues of a human or an animal. The needle can include an insertion stop, and can be placed through the round window membrane or through a surgically-prepared hole in a bone. The needle can be in fluid communication with a port and/or with a micro-infusion or osmotic pump. A cochlear implant electrode can be used instead of a needle.
    Type: Application
    Filed: January 24, 2006
    Publication date: November 23, 2006
    Applicant: NeuroSystec Corporation
    Inventors: Thomas Lobl, Stephen McCormack, Thomas Lenarz, John Schloss, Anna Nagy, Jacob Pananen
  • Publication number: 20060205789
    Abstract: Improved formulations of gacyclidine for direct administration to the inner or middle ear.
    Type: Application
    Filed: March 6, 2006
    Publication date: September 14, 2006
    Applicant: NeuroSystec Corporation
    Inventors: Thomas Lobl, John Schloss, Stephen McCormack, Anna Nagy, Jacob Pananen