Patents by Inventor Miikka Vikkula

Miikka Vikkula has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Publication number: 20230277522
    Abstract: The present disclosure relates to methods for inhibiting TIE2 kinase useful in the treatment of growth of venous malformations.
    Type: Application
    Filed: August 12, 2020
    Publication date: September 7, 2023
    Inventors: Daniel L. Flynn, Bryan D. Smith, Miikka Vikkula
  • Publication number: 20220047573
    Abstract: The present disclosure relates to methods for inhibiting TIE2 kinase useful in the treatment of growth of venous malformations.
    Type: Application
    Filed: August 12, 2020
    Publication date: February 17, 2022
    Inventors: Daniel L. Flynn, Bryan D. Smith, Miikka Vikkula
  • Patent number: 7700748
    Abstract: The present invention relates to genes responsible for disorders with a vascular component, the identification of mutations in said genes and the detection of their sequences as well as methods for detection and treatment for disorders with a vascular component. This invention further relates to proteins encoded by said genes and their applications.
    Type: Grant
    Filed: February 16, 2001
    Date of Patent: April 20, 2010
    Assignee: Universite Catholique de Louvain
    Inventor: Miikka Vikkula
  • Publication number: 20060141472
    Abstract: The invention relates to the field of vascular anomalies and methods for diagnosing and treating them. The invention provides for the causative gene (RASA1) and mutations therein which are useful for diagnosis of inherited capillary malformations. The invention further provides RASA1 antagonists for use in treatment of capillary malformations.
    Type: Application
    Filed: March 20, 2003
    Publication date: June 29, 2006
    Inventors: Miikka Vikkula, Laurence Boon, Liro Eerola
  • Publication number: 20030176649
    Abstract: The present invention relates to genes responsible for disorders with a vascular component, the identification of mutations in said genes and the detection of their sequences as well as methods for detection and treatment for disorders with a vascular component. This invention further relates to proteins encoded by said genes and their applications.
    Type: Application
    Filed: August 27, 2002
    Publication date: September 18, 2003
    Inventor: Miikka Vikkula