IP Library Granted Patent US 8,507,518
Granted Patent B2
US 8,507,518 · App. 13/078,272 · Granted Aug 13, 2013

Method of treating mantle cell lymphoma

Inventors: Thomas E. Witzig (Rochester, MN); Scott H. Kaufmann (Rochester, MN)
Assignee: Mayo Foundation for Medical Education and Research
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Quick Facts
Patent No.
US 8,507,518
App. No.
13/078,272
Granted
Aug 13, 2013
Kind
B2
Abstract

This invention provides the use of rapamycin 42-ester with 3-hydroxy-2-(hydroxymethyl)-2-methylpropionic acid (CCI-779) in the treatment or inhibition of mantle cell lymphoma.

Claims (13)

1. A regimen for treating mantle cell lymphoma in a human patient, said regimen comprising delivering to the patient rapamycin 42-ester with 3-hydroxy-2-(hydroxymethyl)-2-methylpropionic acid (CCI-779) as a single active agent in a monthly cycle of treatment, said monthly cycle comprising administering a first intravenous dosage of CCI-779 comprising about 175 mg to about 250 mg per week for at least one week in the cycle followed by a decreased intravenous dose of CCI-779 of about 25 mg to 75 mg for at least one week of the cycle.

2. The regimen according to claim 1 , wherein the CCI-779 is delivered via a parenteral formulation comprising from 2.5 mg/mL to 10 mg/mL CCI-779, an antioxidant comprising d,l-tocopherol, ethanol, polyethylene glycol, a surfactant, and citric acid at a concentration of less than 0.01% w/v.

3. The regimen according to claim 1 , wherein the monthly cycle comprises at least one week where no CCI-779 is administered.

4. The regimen according to claim 1 , wherein the monthly cycle comprises weekly dosage administrations.

5. The regimen according to claim 1 , wherein the CCI-779 is delivered for two to twelve cycles.

6. The regimen according to claim 1 , wherein the monthly cycles are continuous.

7. The regimen according to claim 1 , wherein the first dosage of CCI-779 is about 175 mg.

8. A regimen for reducing tumor size in a relapsed mantle cell lymphoma human patient, said regimen comprising intravenously delivering to the patient a monthly cycle which comprises an intravenous dosage of about 175 to about 250 mg of CCI-779 per week as a single active agent followed by at least one weekly administration of a decreased intravenous dosage of about 75 mg per week.

9. The regimen according to claim 8 , wherein the CCI-779 is delivered via a parenteral formulation comprising from 2.5 mg/mL to 10 mg/mL CCI-779, an antioxidant comprising d,l-tocopherol, ethanol, polyethylene glycol, a surfactant, and citric acid at a concentration of less than 0.01% w/v.

10. The regimen according to claim 8 , wherein the dosage of CCI-779 differs from week to week within the cycle.

11. The regimen according to claim 8 , wherein the monthly cycle comprises weekly or bi-weekly dosage administrations.

12. The regimen according to claim 11 , wherein the CCI-779 is delivered for two to twelve cycles.

13. The regimen according to claim 8 , wherein the first dosage of CCI-779 is about 175 mg.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 8, 2013
From: WITZIG, THOMAS E; KAUFMANN, SCOTT H
To: MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH
Reel/Frame 030751/0141 →
CONFIRMATORY LICENSE Recorded Apr 22, 2011
From: MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 026169/0998 →
Continuity (3)
Continuation 10979284 · Nov 2, 2004
Provisional Application 60517329 · Nov 4, 2003
Related Publication 20110184010A1 · Jul 28, 2011