Method of treating diabetes mellitus using KGF

• US 5,858,977 A
• Filed: 04/11/1997
• Issued: 01/12/1999
• Est. Priority Date: 10/13/1994
• Status: Expired due to Term

• Current Assignee: Biovitrum AB (Swedish Orphan Biovitrum AB (publ))
• Original Assignee: Amgen Inc.
• Inventors: Aukerman, Sharon Lea, Pierce, Glenn Francis
• Primary Examiner(s): Ulm, John
• Assistant Examiner(s): SAOUD, CHRISTINE J
• Application Number:
  US08/817,260
• Time in Patent Office: 641 Days
• Field of Search: 514/2, 514/12, 514/866, 530/399
• US Class Current: 514/6.9
• CPC Class Codes: A61K 38/1825 Fibroblast growth factor [FGF]
• CPC Class Codes: C07K 14/50 Fibroblast growth factor [FGF]
• CPC Class Codes: Y02A 50/30 Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Abstract

A method and pharmaceutical compositions are described for the use of keratinocyte growth factor to treat diabetes mellitus in mammals.

Claims

1. A method of treating diabetes mellitus, comprising administering to a mammal having that condition an amount effective for reducing blood glucose levels compared to an untreated individual of a keratinocyte growth factor having amino acid residues 32-194 of SEQ ID NO:

2 (native KGF) or an analog thereof which comprises a difference from the sequence of native KGF by having an amino acid deletion of or having a residue other than cysteine substituted for Cys³² and Cys⁴⁶ of SEQ ID-NO;

2, wherein said keratinocyte growth factor exhibits at least 500-fold greater stimulation of BALB/MK keratinocyte cells than that of NIH/3T3 fibroblast cells and at least about 500-fold greater stimulation of BALB/MK keratinocyte cells than for BS/589 epithelial cells or for CC1208 epithelial cells, as determined by H-thymidine incorporation.

2. The method according to claim 1, wherein the keratinocyte growth factor is methionylated or nonmethionylated, native KGF, C(1,15)S, Δ

N15-Δ

N24, Δ

N3/C(15)S, Δ

N3/C(15)-, Δ

N8/C(15)S, Δ

N8/C(15)-, C(1,15)S/R(144)E, C(1,15) S/R(144)Q, Δ

N23/R(144)Q, C(1,15,40)S, C(1,15,102)S, C(1,15,102,106)S, Δ

N23/N(137)E, Δ

N23/K(139)E, Δ

N23/K(139)Q, Δ

N23/R(144)A, Δ

N23/R(144)E, Δ

N23/R(144)L, Δ

N23/K(147)E, Δ

N23/K (147)Q, Δ

N23/K(153)E, Δ

N23/K(153)Q and Δ

N23/Q(152)E/K(153)E.

3. The method according to any one of claims 1 or 2, wherein the keratinocyte growth factor is produced in bacterial cells.

4. The method according to claim 3, wherein the keratinocyte growth factor is produced in E. coli.

5. The method according to any one of claims 1 or 2, wherein the keratinocyte growth factor is formulated with a pharmaceutically acceptable carrier.

6. The method according to claim 5, wherein the pharmaceutically acceptable carrier is a long-term, slow release formulation.

7. The method according to any one of claims 1 or 2, wherein the keratinocyte growth factor is administered by parenteral injection.

8. The method according to claim 7, wherein the keratinocyte growth factor is administered in an amount from about 0.001 milligrams to about 10 milligrams per kilogram of body weight per day.

9. The method according to claim 8, wherein the amount of keratinocyte growth factor is from about 0.05 milligrams to about 5 milligrams per kilogram per day.

10. The method according to claim 7, wherein the mammal is a human.

11. The method of claim 7 wherein the parenteral injection is selected from the group consisting of subcutaneous, intravenous and intramuscular injection.