U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Method for inhibiting infection of human T-cells

Patent 4840941 Issued on June 20, 1989. Estimated Expiration Date: Icon_subject January 15, 2008. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

Modulators of the complement system comprising polyhexaose arylene sulfate derivatives
Patent #: 4374832
Issued on: 02/22/1983
Inventor: Joseph ,   et al.

Composition of matter from Cryptosiphonia woodii useful for the treatment of herpes simplex virus
Patent #: 4522814
Issued on: 06/11/1985
Inventor: Nonomura ,   et al.

Synthetic immunoregulators and methods of use and preparation
Patent #: 4590181
Issued on: 05/20/1986
Inventor: McCarthy

Therapeutic agent for the use in cancer treatment
Patent #: 4710493
Issued on: 12/01/1987
Inventor: Landsberger

Membrane polysaccharides which are useful as immunostimulants Patent #: 4734403
Issued on: 03/29/1988
Inventor: Dussourd D'Hinterland ,   et al.

Inventors

Assignee

Application

No. 07/144131 filed on 01/15/1988

US Classes:

514/59, Dextran or derivative514/54, Polysaccharide514/55, Chitin or derivative514/56, Heparin or derivative514/60, Starch or derivative536/20, Chitin or derivative536/21, Heparin or derivative536/51, Dextran derivatives536/54, Sulfur containing536/58Esters

Examiners

Primary: Griffin, Ronald W.
Assistant: Carson, Nancy S.

Attorney, Agent or Firm

International Classes

A61K 31/715 (20060101)
C07H 11/00 (20060101)

Foreign Application Priority Data

1986-04-04 JP

Abstract

Method of treatment of diseases caused by retroviruses which comprises administering therapeutically effective amount of a natural or synthetic oligo- or polysaccharide having at least one S-oxoacid group attached to the saccharic carbon atom through a linking group of lower molecular weight or a pharmaceutically acceptable salt thereof to a subject in need of such treatment.

Other References

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  • Ehlers et al, J. Gen Virol (1984), 65, 423-428 and 1325-1330
  • Walton, British Journal Pharmacology, 7, 370 (1952), 8, 340 (1953) and 9, 1 (1954)
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