PHILIP CINNAMON COMP
Medical Practice in Oklahoma City, OK

License number
Pennsylvania MD013726E
Category
Medicine
Type
Medical Physician and Surgeon
Address
Address 2
Oklahoma City, OK 73190
Pennsylvania

Personal information

See more information about PHILIP CINNAMON COMP at radaris.com
Name
Address
Phone
Philip Comp, age 80
5633 NW 121St Cir, Oklahoma City, OK 73162
Philip C Comp, age 80
2313 54Th St, Oklahoma City, OK 73112
(405) 842-0751
Philip C Comp, age 80
9805 Silver Lake Dr, Oklahoma City, OK 73162
(405) 720-9326

Professional information

Philip C Comp Photo 1

Dr. Philip C Comp, Oklahoma City OK - MD (Doctor of Medicine)

Specialties:
Internal Medicine, Allergy & Immunology
Address:
Peggy Charles Stephnsn Cncr Ctr
800 NE 10Th St SUITE 2500, Oklahoma City 73104
(405) 271-8299 (Phone)
Oklahoma Univ Hlh Sci Ctr Hm/On
800 NE 10Th St SUITE 2500, Oklahoma City 73104
(405) 271-8299 (Phone)
Certifications:
Allergy & Immunology, 1983, Internal Medicine, 1974
Awards:
Healthgrades Honor Roll
Languages:
English
Education:
Medical School
University of Washington
Graduated: 1971
Hospital Of The University Of Pennsylvania
University Of Oklahoma Health Sciences Center


Philip C Comp Photo 2

Philip C Comp, Oklahoma City OK

Specialties:
Internist
Address:
800 Ne 10Th St, Oklahoma City, OK 73104
825 Ne 10Th St, Oklahoma City, OK 73104
Board certifications:
American Board of Allergy and Immunology Certification in Allergy and Immunology, American Board of Internal Medicine Certification in Internal Medicine


Philip Comp Photo 3

Philip Comp, Oklahoma City OK

Work:
Oklahoma City VA Medical
921 NE 13Th St, Oklahoma City, OK 73104 Oklahoma Universtiy Physicians
825 NE 10Th St, Oklahoma City, OK 73104 Oklahoma Universtiy Physicians
800 NE 10Th St, Oklahoma City, OK 73104


Philip Comp Photo 4

Inhibition Of Tumor Growth By Blockade Of The Protein C System

US Patent:
6423313, Jul 23, 2002
Filed:
May 6, 1994
Appl. No.:
08/238987
Inventors:
Charles T. Esmon - Oklahoma City OK
Philip C. Comp - Oklahoma City OK
Assignee:
Oklahoma Medical Research Foundation - Oklahoma City OK
International Classification:
A61K 39395
US Classification:
4241381, 4241981, 435 723, 53038825, 53038826
Abstract:
Compositions, and methods of use thereof, for the inhibition of tumor growth and killing of solid tumors wherein the active agent is a compound blocking the Protein C system, preferably anti-Protein C antibody, anti-Protein S antibody, and C4b binding protein. In the most preferred embodiment, the Protein C blocking compound is provided in combination with a cytokine such as tumor necrosis factor (TNF), gamma interferon, interleukin-1, interleukin-2,p or granulocyte-macrophage colony stimulating factor, or a compound eliciting cytokine production such as endotoxin. Examples are provided demonstrating the administration of the Protein C blocking compound, alone or in combination with TNF or endotoxin, to animals having canine veneral tumors, a fibrosarcoma, and an adenocarcinoma, followed by significant tumor reduction.


Philip Comp Photo 5

Treatment Of Bleeding With Modified Tissue Factor In Combination With An Activator Of Fvii

US Patent:
5504064, Apr 2, 1996
Filed:
Feb 19, 1993
Appl. No.:
8/021615
Inventors:
James H. Morrissey - Oklahoma City OK
Philip C. Comp - Oklahoma City OK
Assignee:
Oklahoma Medical Research Foundation - Oklahoma City OK
International Classification:
A61K 3514, A61K 3848, A61K 3816, C07K 14745
US Classification:
514 8
Abstract:
It has been discovered that it is possible to administer truncated tissue factor (not having the transmembrane region) (tTF) in combination with factor VIIa (FVIIa) or an activator of endogenous factor VII to treat bleeding disorders such as those resulting from hemophilia or cirrhosis of the liver. The tTF is administered to produce up to 10. mu. g tTF/ml of plasma. The FVIIa or FVII activator is administered to produce levels of between 40 ng FVIIa/ml and 700 ng FVIIa/ml of plasma. The effective dosages of both tTF and FVIIa/factor VII activator are significantly and surprisingly less than the administration of either alone to stop bleeding. Examples demonstrate safety and efficacy in normal and hemophilic dogs.


Philip Comp Photo 6

Inhibition Of Tumor Growth By Blockade Of The Protein C System

US Patent:
5147638, Sep 15, 1992
Filed:
Aug 4, 1989
Appl. No.:
7/389617
Inventors:
Charles T. Esmon - Oklahoma City OK
Philip C. Comp - Oklahoma City OK
Assignee:
Oklahoma Medical Research Foundation - Oklahoma City OK
International Classification:
A61K 3700, A61K 3766, A61K 3900
US Classification:
424 858
Abstract:
Compositions, and methods of use thereof, for the inhibition of tumor growth and killing of tumors having extensive microcirculation wherein the active agent is a compound blocking the Protein C system, preferably anti-Protein C antibody, anti-Protein S antibody, and C4b binding protein. In the most preferred embodiment, the Protein C blocking compound is provided in combination with a cytokine such as tumor necrosis factor (TNF), gamma interferon, interleukin-1, interleukin-2 and granulocyte-macrophage colony stimulating factor. Examples are provided demonstrating the administration of the Protein C blocking compound, alone or in combination with TNF, to dogs having canine veneral tumors, or fibrosarcoma, and an adenocarcinoma, and pigs with melanoma followed by significant tumor reduction.


Philip Comp Photo 7

Treatment Of Bleeding With Modified Tissue Factor In Combination With Fviia

US Patent:
5374617, Dec 20, 1994
Filed:
May 13, 1992
Appl. No.:
7/882202
Inventors:
James H. Morrissey - Oklahoma City OK
Philip C. Comp - Oklahoma City OK
Assignee:
Oklahoma Medical Research Foundation - Oklahoma City OK
International Classification:
A61K 3702
US Classification:
514 8
Abstract:
It has been discovered that it is possible to administer truncated tissue factor (not having the transmembrane region) (tTF) in combination with factor VIIa (F VIIa) to treat bleeding disorders such as those resulting from hemophilia or cirrhosis of the liver. The tTF is administered to produce up to 10. mu. g tTF/ml of plasma. The F VIIa is administered to produce levels of between 40 ng VIIa/ml and 4. mu. g F VIIa/ml of plasma. The effective dosages of both tTF and VIIa are significantly and surprisingly less than the administration of either alone to stop bleeding. Examples demonstrate safety and efficacy in normal and hemophilic dogs.


Philip Comp Photo 8

Treatment Of Bleeding With Modified Tissue Factor In Combination With Fvii

US Patent:
5504067, Apr 2, 1996
Filed:
Oct 12, 1994
Appl. No.:
8/321777
Inventors:
James H. Morrissey - Oklahoma City OK
Philip C. Comp - Oklahoma City OK
Assignee:
Oklahoma Medical Research Foundation - Oklahoma City OK
International Classification:
A61K 3514, A61K 3848, A61K 3816, C07K 14745
US Classification:
514 8
Abstract:
It has been discovered that it is possible to administer truncated tissue factor, not having the transmembrane region (tTF) in combination with factor VIIa (FVIIa) to treat bleeding disorders such as those resulting from hemophilia or cirrhosis of the liver. Preferably, the tTF is administered to produce up to 10. mu. g tTF/ml of plasma. The FVIIa is administered to produce levels of between 40 ng FVIIa/ml and 4. mu. g FVIIa/ml of plasma. The effective dosages of both tTF and FVIIa are significantly and surprisingly less than the administration of either alone to stop bleeding. Examples demonstrate safety and efficacy in normal and hemophilic dogs.


Philip Comp Photo 9

Blockade Of Protein C Activation Reduces Microvascular Surgical Blood Loss

US Patent:
7291333, Nov 6, 2007
Filed:
Oct 14, 1994
Appl. No.:
08/323060
Inventors:
Philip C. Comp - Oklahoma City OK, US
Assignee:
Oklahoma Medical Research Foundation - Oklahoma City OK
International Classification:
A61K 39/395, C07K 16/44, C07K 16/18
US Classification:
4241451, 4241391, 4241521, 4241581, 4241721, 514 2, 514834, 53038825, 5303893, 435337
Abstract:
A method of inhibiting microvascular bleeding is provided. Antibody to protein C administered to a patient in a pharmaceutically acceptable carrier prevents anticoagulation by greater than 90% of activated protein C in human plasma.