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US4791101A Expired / Lapsed US ⏱️ 0.0 years remaining

Synergistic mixtures of interferons and tumor necrosis factor

Assignee: Boehringer Ingelheim GmbH
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Filing: 1985-06-20
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Granted: 1988-12-13
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Expires: 2005-06-20
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Abstract

Abstract Ternary compositions of an interferon of the alpha and/or beta type with an interferon of the gamma type and tumor necrosis factor having a surprising and unexpected synergistic anti-proliferative effect on neoplastic cells when compared to the activity of the individual components of this invention, said compositions being useful in the treatment of neoplasia in animals including humans.

Inventors

  • 👤 Gunther Adolf

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-09 22:13
CPC Classifications
A; A61; A61K; A61K38/00; A61K38/16; A61K38/17; A61K38/19; A61K38/21; Y; Y02; Y02A; Y02A50/00; Y02A50/30

Claims Analysis

Total Claims: 31
Claim 1
Independent Claim 36 words
A composition having a synergistic anti-proliferative effect on neoplastic animal cells, comprising a synergistically effective amount of (a) highly purified tumor necrosis factor; (b) highly purified type I interferon; and (c) highly purified type II interferon.
Claim 2
Dependent Claim 36 words
A composition having a synergistic anti-proliferative effect on neoplastic animal cells, comprising a synergistically effective amount of (a) highly purified tumor necrosis factor; (b) highly purified type I interferon; and (c) highly purified type II interferon.
Claim 3
Dependent Claim 53 words
A composition having a synergistic anti-proliferative effect on neoplastic animal cells selected from the group consisting of anal, breast, cervical, colorectal, head, lung, melanoma, and neck cancer cells, comprising a synergistically effective amount of (a) highly purified tumor necrosis factor; (b) highly purified type I inerferon; and (c) highly purified type II interferon.
Claim 4
Dependent Claim 53 words
A composition having a synergistic anti-proliferative effect on neoplastic animal cells selected from the group consisting of anal, breast, cervical, colorectal, head, lung, melanoma, and neck cancer cells, comprising a synergistically effective amount of (a) highly purified tumor necrosis factor; (b) highly purified type I inerferon; and (c) highly purified type II interferon.
Claim 5
Dependent Claim 30 words
The composition of claim 1 or 2, wherein said tumor necrosis factor, said type I interferon and said type II interferon each is greater than or equal to 90% pure.
Claim 6
Dependent Claim 14 words
The composition of claim 3, wherein said tumor necrosis factor is of mammalian origin.
Claim 7
Dependent Claim 15 words
The composition of claim 4, wherein said tumor necrosis factor is human tumor necrosis factor.
Claim 8
Dependent Claim 17 words
The composition of claim 3, said tumor necrosis factor being greater than or equal to 95% pure.
Claim 9
Dependent Claim 17 words
The composition of claim 6, said tumor necrosis factor being greater than or equal to 98% pure.
Claim 10
Dependent Claim 21 words
The composition of claim 3, wherein said type I interferon is alpha or beta or subtypes thereof, or a mixture thereof.
Claim 11
Dependent Claim 14 words
The composition of claim 8, wherein said type I interferon is of mammalian origin.
Claim 12
Dependent Claim 15 words
The composition of claim 9, wherein said type I interferon is human type I interferon.
Claim 13
Dependent Claim 13 words
The composition of claim 10, wherein said type I interferon is human interferon-alpha-2-arg.
Claim 14
Dependent Claim 17 words
The composition of claim 7, said type I interferon being greater than or equal to 95% pure.
Claim 15
Dependent Claim 17 words
The composition of claim 12, said type I interferon being greater than or equal to 98% pure.
Claim 16
Dependent Claim 16 words
The composition of claim 3, wherein said type II interferon is gamma or a subtype thereof.
Claim 17
Dependent Claim 14 words
The composition of claim 14, wherein said type II interferon is of mammalian origin.
Claim 18
Dependent Claim 14 words
The composition of claim 15, wherein said type II interferon is human interferon gamma.
Claim 19
Dependent Claim 17 words
The composition of claim 14, said type II interferon being greater than or equal to 95% pure.
Claim 20
Dependent Claim 14 words
The composition of claim 17, said type II inteferon being greater than 98% pure.
Claim 21
Dependent Claim 13 words
The composition of claim 3, further comprising a pharmaceutically acceptable carrier or carriers.
Claim 22
Dependent Claim 16 words
The composition of claim 3, wherein said type I interferon is produced by recombinant DNA methods.
Claim 23
Dependent Claim 16 words
The composition of claim 3, wherein said type II interferon is produced by recombinant DNA methods.
Claim 24
Dependent Claim 16 words
The composition of claim 3, wherein said tumor necrosis factor is produced by recombinant DNA methods.
Claim 25
Independent Claim 48 words
A method for the treatment of neoplastic disease in animals, comprising administering to an animal suffering from or suspected or suffering from said disease a synergistically effective amount of (a) highly purified tumor necrosis factor; (b) highly purified type I interferon; and (c) highly purified type II interferon.
Claim 26
Independent Claim 48 words
A method for the treatment of neoplastic disease in animals, comprising administering to an animal suffering from or suspected or suffering from said disease a synergistically effective amount of (a) highly purified tumor necrosis factor; (b) highly purified type I interferon; and (c) highly purified type II interferon.
Claim 27
Independent Claim 62 words
A method for the treatment of neoplastic disease selected from the group consisting of anal, breast, cervical, colorectal, head, lung, melanoma, and neck cancer, comprising administering to an animal suffering from or suspected of suffering from said disease a synergistically effective amount of (a) highly purified tumor necrosis factor; (b) highly purified type I interferon; and (c) highly purified type II interferon.
Claim 28
Independent Claim 62 words
A method for the treatment of neoplastic disease selected from the group consisting of anal, breast, cervical, colorectal, head, lung, melanoma, and neck cancer, comprising administering to an animal suffering from or suspected of suffering from said disease a synergistically effective amount of (a) highly purified tumor necrosis factor; (b) highly purified type I interferon; and (c) highly purified type II interferon.
Claim 29
Dependent Claim 13 words
The method of claim 23 or 24, wherein said animal is a mammal.
Claim 30
Dependent Claim 10 words
The method of claim 25, wherein said mammal is human.
Claim 31
Dependent Claim 41 words
The method of claim 23 or 24, wherein the dose of tumor necrosis factor is between 0.1-1000 mg/kg body weight, and wherein the dose of type I and/or type II interferon is between 10 3 and 10 6 IU/kg body weight.

References Cited (Backward Citations)

DE3227262A1 Cited
EP0128009A2 Cited
EP0131789A2 Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1991-12-13 1992-06-13 1992-12-13 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1995-12-13 1996-06-13 1996-12-13 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1999-12-13 2000-06-13 2000-12-13 $7700.00 Window Closed / Lapsed

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