IP Library Granted Patent US 6,911,200
Granted Patent B2
US 6,911,200 · App. 09/814,357 · Granted Jun 28, 2005

Methods of treating neoplasia with combination of target-cell specific adenovirus, chemotherapy and radiation

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Quick Facts
Patent No.
US 6,911,200
App. No.
09/814,357
Granted
Jun 28, 2005
Kind
B2
Abstract

The invention provides methods of treating neoplasia using combinations of target cell-specific replication competent adenoviral vectors and chemotherapy, radiation therapy or combinations thereof. The adenoviral vectors are target cell-specific for the particular type of neoplasia for which treatment is necessary and the combination with the chemotherapy and/or radiation leads to synergistic treatment over existing adenoviral therapy or traditional chemotherapy and radiation therapy.

Claims (12)

1. A method for suppressing tumor growth in a mammal comprising:

administering to a mammal a synergistic combination of

a replication competent, target tumor cell-specific adenovirus, said adenovirus comprising an adenoviral gene essential for replication under transcriptional control of a prostate-specific antigen (PSA)-TRE wherein said target tumor cell-specific adenovirus results in virus replication-dependent cytolysis; and

at least one antineoplastic agent selected from the group consisting of paclitaxel and docetaxel, in a combined dosage effective to substantially reduce the numbers of said targeted solid tumor cell population to a level more than additive when compared to administration of the adenovirus and antineoplastic agent alone, wherein said tumor growth in said mammal is suppressed.

2. The method according to claim 1 , wherein said adenovirus is administered by site-specific injection.

3. The method according to claim 1 , wherein said adenovirus is administered by intravenous injection.

4. The method according to claim 1 , wherein said adenoviral gene essential for replication is an adenoviral early gene.

5. The method of claim 4 , wherein the adenoviral early gene is E1A.

6. The method of claim 4 , wherein the adenoviral early gene is E1B.

7. The method of claim 6 , wherein E1B has a deletion of the 19-kDa region.

8. The method of claim 1 , wherein said at least one antineoplastic agent is paclitaxel.

9. The method of claim 1 , wherein said at least one antineoplastic agent is docetaxel.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 26, 2001
From: YU, DE-CHAO; CHEN, YU; HENDERSON, DANIEL R.
To: CALYDON, INC.
Reel/Frame 012395/0761 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 17, 2001
From: CALYDON, INC
To: CELL GENESYS, INC
Reel/Frame 012243/0012 →
SECURITY INTEREST Recorded Jun 19, 2001
From: CALYDON, INC.
To: PERSEUS CAPTIAL, L.L.C.
Reel/Frame 011679/0302 →