IP Library Granted Patent US 8,017,129
Granted Patent B2
US 8,017,129 · App. 11/734,592 · Granted Sep 13, 2011

Use of thymosin alpha 1 for preparing a medicament for the treatment of stage IV malignant melanoma

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Quick Facts
Patent No.
US 8,017,129
App. No.
11/734,592
Granted
Sep 13, 2011
Kind
B2
Abstract

It is described the use of thymosin alpha in combination with dacarbazine and optionally with Interferon alpha, for preparing a medicament for the treatment of malignant melanoma on stage IV characterized by distant unresectable metastases.

Claims (11)

1. A method of treating stage IV malignant melanoma classified as M1a, M1b or M1c, consisting of administering: thymosin alpha 1 in a dose of 3.2 mg/day/s.c., in combination with an effective amount of dacarbazine, to a human with said stage IV malignant melanoma.

2. Method according to claim 1 , in which dacarbazine is administered in a dose from 500 to 1100 mg/m 2 /day/i.v.

3. Method according to claim 1 , in which dacarbazine is administered in a dose of 800 mg/m 2 /day/i.v.

4. Method according to claim 1 , in which the human to be treated has a normal serum level of LDH.

5. A method of treating a stage IV malignant melanoma, consisting of administering thymosin alpha 1 in a dose of 3.2 mg/day/s.c. in combination with an effective amount of dacarbazine, to a human with stage IV malignant melanoma M1a, M1b or M1c.

6. The method of claim 5 , wherein the malignant melanoma is classified as M1a, M1b or M1c.

7. The method of claim 5 , in which dacarbazine is administered in a dose from 500 to 1100 mg/m 2 /day/i.v.

8. The method of claim 5 , in which dacarbazine is administered in a dose of 800 mg/m 2 /day/i.v.

9. A method of treating malignant melanoma in a human with stage IV malignant melanoma classified as M1a, M1b or M1c, consisting of administering a synergistic combination of thymosin alpha 1 and dacarbazine to a human in need thereof, wherein said combination is administered according to a protocol in which the dacarbazine is administered in a dose of 800 mg/m 2 /day/i.v. on day 1 thereof and the thymosin alpha 1 is administered in a dose of 3.2 mg/day/s.c. about one week and about two weeks thereafter.

10. The method of claim 5 , in which the human to be treated has a normal serum level of LDH.

11. Method according to claim 9 , in which the human to be treated has a normal serum level of LDH.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 4, 2024
From: SCICLONE PHARMACEUTICALS INTERNATIONAL LTD.
To: SCICLONE PHARMACEUTICALS INTERNATIONAL (SG) PTE. LTD.
Reel/Frame 066730/0332 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 22, 2020
From: SCICLONE PHARMACEUTICALS LLC
To: SCICLONE PHARMACEUTICALS INTERNATIONAL LTD.
Reel/Frame 053274/0935 →
CHANGE OF NAME Recorded Jul 22, 2020
From: SCICLONE PHARMACEUTICALS, INC.
To: SCICLONE PHARMACEUTICALS LLC
Reel/Frame 053275/0716 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 17, 2011
From: RUDOLPH, ALFRED R.; MARTINS, EDUARDO
To: SCICLONE PHARMACEUTICALS, INC.
Reel/Frame 026765/0902 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 10, 2010
From: SIGMA-TAU INDUSTRIE FARMACEUTICHE RIUNITE S.P.A.
To: SCICLONE PHARMACEUTICALS INTERNATIONAL LIMITED
Reel/Frame 024818/0017 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 29, 2007
From: CARMINATI, PAOLO; CAMERINI, ROBERTO
To: SIGMA-TAU INDUSTRIE FARMACEUTICHE RIUNITE S.P.A.
Reel/Frame 019351/0286 →