IP Library Granted Patent US 8,394,365
Granted Patent B2
US 8,394,365 · App. 11/948,767 · Granted Mar 12, 2013

Multi-arm polymer prodrugs

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Quick Facts
Patent No.
US 8,394,365
App. No.
11/948,767
Granted
Mar 12, 2013
Kind
B2
Abstract

Provided herein are water-soluble prodrugs, compositions comprising such prodrugs, and related methods of making and administering the same. The prodrugs of the invention comprise a water-soluble polymer having three or more arms, at least three of which are typically covalently attached to an active agent, e.g., a small molecule. The conjugates of the invention provide an optimal balance of polymer size and structure for achieving improved drug loading, since the conjugates of the invention possess three or more active agents releasably attached to a multi-armed water-soluble polymer. The prodrugs of the invention are therapeutically effective, and exhibit improved properties in-vivo when compared to unmodified parent drug.

Claims (40)

1. A composition comprising a multi-arm polymer prodrug having the structure:

R(-Q-POLY 1 -X′-D 0,1 ) q   I

wherein

R is an organic radical possessing from 3 to 25 carbon atoms,

Q is a linker, wherein R, when taken together with Q, is a residue of a polyol or a polythiol after removal of “q” hydroxyl or thiol protons, respectively, to form a point of attachment for POLY 1 ,

POLY 1 is a water-soluble and non-peptidic polymer selected from the group consisting of poly(alkylene glycol), poly(olefinic alcohol), poly(vinylpyrrolidone), poly(hydroxylalkylmethacrylamide), poly(hydroxyalkyl-methacrylate), poly(α-hydroxy acid), poly(acrylic acid), poly(vinyl alcohol), polyphosphazene, polyoxazoline, poly(N-acryloylmorpholine), and copolymers or terpolymers thereof,

X is a spacer corresponding to —CH 2 C(O)NHCH 2 C(O)O—,

X′ is either (i) the spacer, X, or is (ii) X″, a terminal moiety,

D is a camptothecin attached at its 10-, 11- or 20-ring position, where D 1 indicates the presence of D and D 0 indicates its absence,

q has a value from 3 to 25,

wherein if X′ is X, then D is D 1 , and if X′ is X″, then D is D 0 , and

X′ is X in one or more of “q” polymer arms.

2. The composition of claim 1 , comprising one or more prodrug species having the structure:

R-(Q-POLY 1 -X-D 1 ) m (Q-POLY 1 -X″) s

wherein

m+s=q,

m has a value ranging from 1 to q and s has a value ranging from 0 to (q−1).

3. The composition of claim 2 , having an average number of D per multi-arm polymer ranging from 2.1-3.75.

4. The composition of claim 3 , having an average number of D per multi-arm polymer ranging from 2.3-3.5.

5. The composition of claim 1 , wherein X″ is —CH 2 COOH.

6. The composition of claim 2 , wherein POLY 1 is a poly(alkylene glycol).

7. A pharmaceutical composition comprising a prodrug of claim 1 and a pharmaceutically acceptable carrier.

8. A method of delivering a prodrug to a mammalian subject to a subject in need thereof, said method comprising administering to said mammalian subject a therapeutically effective amount of the composition of claim 1 .

9. The method of claim 8 , wherein said administering comprises administering said composition parenterally.

10. A method of treating a mammalian subject for a condition responsive to treatment with a camptothecin, said method comprising administering to said subject a therapeutically effective amount of a composition of claim 1 .

11. The composition of claim 1 , wherein R possesses a number of carbon atoms selected from the group consisting of 3, 4, 5, 6, 7, 8, 9, and 10.

12. The composition of claim 11 , wherein R is linear or cyclic.

13. The composition of claim 1 , wherein R, taken together with Q, is a residue of glycerol, trimethylolpropane, pentaerythritol, sorbitol, or glycerol oligomers after removal of “q” hydroxyl protons.

14. The composition of claim 1 , wherein Q is oxygen and POLY 1 is polyethylene glycol.

15. The composition of claim 14 , where q is 4.

16. A composition comprising a mixture of one or more prodrug species having the structure:

wherein O-Irinotecan is

m+s=4,

n has a value corresponding to a weight average molecular weight ranging from 3,000 to 20,000 daltons, and

the composition has an average number of irinotecan molecules per multi-arm polymer ranging from about 52% to about 94% of an idealized value of 4.

17. A composition comprising a mixture of one or more prodrug species having the structure:

wherein O-Irinotecan is

m+s=4,

n has a value corresponding to a weight average molecular weight ranging from 3,000 to 20,000 dalton, and

the composition has an average number of irinotecan molecules per multi-arm polymer greater than 94% therefor of an idealized value of 4.

Assignments (7)
RELEASE OF SECURITY INTEREST Recorded Apr 17, 2020
From: TC LENDING, LLC, AS COLLATERAL AGENT
To: NEKTAR THERAPEUTICS
Reel/Frame 053180/0009 →
RELEASE OF SECURITY INTEREST RECORDED AT REEL 28571, FRAME 0141 Recorded Oct 14, 2015
From: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
To: NEKTAR THERAPEUTICS
Reel/Frame 036866/0700 →
GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS Recorded Oct 6, 2015
From: NEKTAR THERAPEUTICS
To: TC LENDING, LLC, AS COLLATERAL AGENT
Reel/Frame 036796/0562 →
GRANT OF SECURITY INTEREST Recorded Jul 17, 2012
From: NEKTAR THERAPEUTICS
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 028571/0141 →
MERGER Recorded Aug 31, 2009
From: NEKTAR THERAPEUTICS AL, CORPORATION
To: NEKTAR THERAPEUTICS
Reel/Frame 023196/0394 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 15, 2008
From: ZHAO, XUAN; BENTLEY, MICHAEL DAVID; REN, ZHONGXU; VIEGAS, TACEY X.
To: NEKTAR THERAPEUTICS AL, CORPORATION
Reel/Frame 020519/0739 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 15, 2008
From: ZHAO, XUAN; BENTLEY, MICHAEL DAVID; REN, ZHONGXU; VIEGAS, TACEY X.
To: NEKTAR THERAPEUTICS AL. CORPORATION
Reel/Frame 020561/0298 →