University Of Utah Obstetrics & Gynecology 50 N Medical Dr, Salt Lake City, UT 84132 8015817647 (phone)
Intermountain Medical GroupMckay-Dee Hospital Center For Maternal Fetal Medicine 4401 Harrison Blvd STE 4600, Ogden, UT 84403 8013874647 (phone), 8013874657 (fax)
University Hospital Maternal Fetal Medicine 50 N Medical Dr, Salt Lake City, UT 84132 8015818425 (phone), 8015852594 (fax)
Education:
Medical School University of Utah School of Medicine Graduated: 1992
Procedures:
Cesarean Section (C-Section) Vaginal Delivery
Conditions:
Complicating Pregnancy or Childbirth Conditions of Pregnancy and Delivery Pregnancy-Induced Hypertension Uncomplicated or Low Risk Pregnancy and Delivery Abnormal Vaginal Bleeding
Languages:
English Spanish
Description:
Dr. Draper graduated from the University of Utah School of Medicine in 1992. He works in Ogden, UT and 2 other locations and specializes in Obstetrics & Gynecology. Dr. Draper is affiliated with Intermountain McKay-Dee Hospital Center, Logan Regional Hospital and University Of Utah Hospital.
This invention provides a method for treating or preventing malaria in a subject. The method includes administering to the subject an effective amount of a substituted tetracycline compound, such that malaria is treated or prevented. In one aspect, the invention relates to pharmaceutical compositions which include an effective amount of a tetracycline compound to treat malaria in a subject and a pharmaceutically acceptable carrier. The substituted tetracycline compounds of the invention can be used to in combination with one or more anti-malarial compounds or can be used to treat or prevent malaria which is resistant to one or more other anti-malarial compounds.
Substituted Tetracycline Compounds For The Treatment Of Malaria
Michael Draper - Plaistow NH, US Mark Nelson - Wellesley MA, US
International Classification:
A61K031/65 A61K031/473 A61K031/353 A61K031/385
US Classification:
514/152000, 514/284000, 514/434000, 514/453000
Abstract:
This invention provides a method for treating or preventing malaria in a subject. The method includes administering to the subject an effective amount of a substituted tetracycline compound, such that malaria is treated or prevented. In one aspect, the invention relates to pharmaceutical compositions which include an effective amount of a tetracycline compound to treat malaria in a subject and a pharmaceutically acceptable carrier. The substituted tetracycline compounds of the invention can be used to in combination with one or more anti-malarial compounds or can be used to treat or prevent malaria which is resistant to one or more other anti-malarial compounds.
Substituted Tetracycline Compounds As Antifungal Agents
Michael Draper - Plaistow NH, US Mark L. Nelson - Norfolk MA, US
Assignee:
Paratek Pharmaceuticals, Inc. - Boston MA
International Classification:
C12N 5/02
US Classification:
435375
Abstract:
The present invention relates, at least in part, to the use of substituted tetracycline compounds for regulation of expression of nucleic acids operably linked to a tetracycline operator system. The invention pertains to compounds used in a regulatory system which utilizes components of the Tet repressor/operator/inducer system of prokaryotes to regulate gene expression in cells. Use of certain substituted tetracycline compounds, as featured in the methods of the invention, result in improved dose-response results when compared to those for e.g., tetracycline and doxycycline. Certain methods of the invention thus allow for enhanced control of the Tet repressor/operator/inducer system in regulating gene expression in cells.
Substituted Tetracycline Compounds As Synergistic Antifungal Agents
The present invention relates to substituted tetracycline compounds and related methods for increasing the antifungal activity of an antifungal agent. The methods include administering to a subject an effective amount of a substituted tetracycline compound in combination with an antifungal agent such that the subject is treated for the fungal associated disorder.