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US4959353A Expired / Lapsed US ⏱️ 0.0 years remaining

Promotion of corneal stroma wound healing with human epidermal growth factor prepared from recombinant DNA

Assignee: Novartis Vaccines and Diagnostics Inc
•
Filing: 1987-04-23
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Granted: 1990-09-25
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Expires: 2007-04-23
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Abstract

Abstract A method for treating corneal stromal wounds to promote regeneration of the affected tissue is provided. This method employs recombinant human epidermal growth factor.

Inventors

  • 👤 Gregory L. Brown
  • 👤 Richard Eiferman
  • 👤 Gregory L. Schultz
  • 👤 Pablo D. T. Valenzuela

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-10 02:15
CPC Classifications
C; C07; C07K; C07K14/00; C07K14/435; C07K14/475; C07K14/485; A; A61; A61P; A61P17/00; A61P27/00; A61P27/02; A61P43/00; A61K; A61K38/00

Claims Analysis

Total Claims: 23
Claim 1
Independent Claim 61 words
A method for treating corneal stromal wounds to promote healing, said method comprising applying human epidermal growth factor (hEGF) to the wound, where said hEGF is produced by expressing an hEGF gene encoding a polypeptide having at least substantially the same amino acid sequence and the same corneal stromal wound-healing activity as naturally occurring human epidermal growth factor in a microorganism.
Claim 2
Independent Claim 61 words
A method for treating corneal stromal wounds to promote healing, said method comprising applying human epidermal growth factor (hEGF) to the wound, where said hEGF is produced by expressing an hEGF gene encoding a polypeptide having at least substantially the same amino acid sequence and the same corneal stromal wound-healing activity as naturally occurring human epidermal growth factor in a microorganism.
Claim 3
Dependent Claim 13 words
A method as in claim 1, wherein the hEGF is produced in yeast.
Claim 4
Dependent Claim 38 words
A method as in claim 2, wherein the yeast is transformed with a DNA construct carrying a hEGF gene under the transcriptional and translational control of regulatory sequences including secretory leader and processing signal sequences functional in yeast.
Claim 5
Dependent Claim 23 words
A method as in claim 1, wherein the hEGF is present in a physiologically acceptable carrier at from 1 μg/ml to 10 μg/ml.
Claim 6
Dependent Claim 20 words
A method as in claim 1 wherein the hEGF is applied continually to the wound over an extended time period.
Claim 7
Dependent Claim 18 words
A method as in claim 5 wherein the continual application is achieved via a sustained release dosage form.
Claim 8
Dependent Claim 14 words
A method as in claim 6 wherein the sustained release dosage form is liposomes.
Claim 9
Dependent Claim 12 words
A method as in claim 7 wherein the liposomes are multilamellar liposomes.
Claim 10
Dependent Claim 20 words
A method as in claim 5 wherein the sustained release dosage form comprises the hEGF incorporated into a semipermeable polymer.
Claim 11
Dependent Claim 14 words
A method as in claim 9 wherein the semipermeable polymer is ethylene-vinyl acetate copolymer.
Claim 12
Dependent Claim 18 words
A method as in claim 5 wherein the continual application is achieved via a multiplicity of intermittent doses.
Claim 13
Independent Claim 106 words
A method for treating corneal stromal wounds to promote healing, said method comprising applying to the wound a polypeptide capable of stimulating the proliferation of epithelial and stromal cells, where said polypeptide is produced by growing, in a culture medium suitable for growth of yeast, a yeast host which has been transformed by an extrachromosomal element carrying a gene encoding a polypeptide having at least substantially the same amino acid sequence and the same corneal stromal wound-healing activity as naturally occurring human epidermal growth factor under the transcriptional and translational control of regulatory sequences including secretory leader and processing signal sequences functional in said yeast host.
Claim 14
Independent Claim 106 words
A method for treating corneal stromal wounds to promote healing, said method comprising applying to the wound a polypeptide capable of stimulating the proliferation of epithelial and stromal cells, where said polypeptide is produced by growing, in a culture medium suitable for growth of yeast, a yeast host which has been transformed by an extrachromosomal element carrying a gene encoding a polypeptide having at least substantially the same amino acid sequence and the same corneal stromal wound-healing activity as naturally occurring human epidermal growth factor under the transcriptional and translational control of regulatory sequences including secretory leader and processing signal sequences functional in said yeast host.
Claim 15
Dependent Claim 16 words
A method as in claim 12, wherein the hEGF gene is composed of preferred yeast codons.
Claim 16
Dependent Claim 23 words
A method as in claim 12, wherein the polypeptide is present in a physiologically acceptable carrier at from 1 μg/ml to 10 μg/ml.
Claim 17
Dependent Claim 20 words
A method as in claim 12 wherein the hEGF is applied continually to the wound over an extended time period.
Claim 18
Dependent Claim 18 words
A method as in claim 15 wherein the continual application is achieved via a sustained release dosage form.
Claim 19
Dependent Claim 14 words
A method as in claim 16 wherein the sustained release dosage form is liposomes.
Claim 20
Dependent Claim 12 words
A method as in claim 18 wherein the liposomes are multilamellar liposomes.
Claim 21
Dependent Claim 20 words
A method as in claim 16 wherein the sustained release dosage form comprises the hEGF incorporated into a semipermeable polymer.
Claim 22
Dependent Claim 14 words
A method as in claim 20 wherein the semipermeable polymer is ethylene-vinyl acetate copolymer.
Claim 23
Dependent Claim 18 words
A method as in claim 15 wherein the continual application is achieved via a multiplicity of intermittent doses.

References Cited (Backward Citations)

EP0046039A1 Cited
US4526938A Cited
US4588684A Cited
US4708861A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1993-09-24 1994-03-26 1994-09-25 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1997-09-24 1998-03-26 1998-09-25 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2001-09-24 2002-03-26 2002-09-25 $7700.00 Window Closed / Lapsed

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