IP Library Granted Patent US 10,188,621
Granted Patent B2
US 10,188,621 · App. 15/668,236 · Granted Jan 29, 2019

Crystalline polymorphic forms of monosodium N-[-8-(2-hydroxybenzoyl)amino]caprylate

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Quick Facts
Patent No.
US 10,188,621
App. No.
15/668,236
Granted
Jan 29, 2019
Kind
B2
Abstract

The present invention relates to crystalline polymorphic forms of monosodium N-[8-(2-hydroxybenzoyl)amino]caprylate (“SNAC”), including two hydrates, a methanol solvate, and an ethanol solvate, of SNAC. More specifically, the present invention provide six polymorphic forms of SNAC (hereafter referred to as Forms I-VI). The present invention also provides an amorphous form of SNAC.

Claims (15)

1. A method for preparing a pharmaceutical composition comprising a monosodium N-[8-(2-hydroxybenzoyl)amino]caprylate exhibiting an X-ray powder diffraction pattern having a peak at 2.98±0.2° 2Θ and at least one active agent, wherein the active agent is a peptide, the method comprising

(i) wet granulating monosodium N-[8-(2-hydroxybenzoyl)amino]caprylate, in the presence of the at least one active agent and one or more pharmaceutically acceptable excipients, to yield a first mixture comprising a trihydrate of monosodium N-[8-(2-hydroxybenzoyl)amino]caprylate,

(ii) drying the first mixture comprising the trihydrate of monosodium N-[8-(2-hydroxybenzoyl)amino]caprylate to obtain a second mixture comprising monosodium N-[8-(2-hydroxybenzoyl)amino]caprylate exhibiting an X-ray powder diffraction pattern having a peak at 2.98±0.2° 2Θ , and

(iii) directly compressing the second mixture to form the pharmaceutical composition.

2. The method of claim 1 , wherein the dried monosodium N-[8-(2-hydroxybenzoyl)amino]caprylate formed in step (ii) exhibits an X-ray powder diffraction pattern having peaks at both 2.98±0.2° 2Θ and 15.72±0.2° 2Θ.

3. A pharmaceutical composition comprising a directly compressed mixture of (a) monosodium N-[8-(2-hydroxybenzoyl)amino]caprylate exhibiting an X-ray powder diffraction pattern having a peak at 2.98±0.2° 2Θ and (b) at least one active agent, wherein the active agent is a peptide.

4. The pharmaceutical composition of claim 3 , wherein the pharmaceutical composition is a tablet.

5. The pharmaceutical composition of claim 3 , wherein the pharmaceutical composition comprises from 50 to 98% by weight of crystalline anhydrous monosodium N-[8-(2-hydroxybenzoyl)amino]caprylate, based on the total weight of monosodium N-[8-(2-hydroxybenzoyl)amino]caprylate in the pharmaceutical composition.

6. The pharmaceutical composition of claim 3 , wherein the mixture is not prepared by or subjected to wet granulation.

7. The pharmaceutical composition of claim 3 , wherein the peptide is insulin.

8. The pharmaceutical composition of claim 3 , wherein the peptide is parathyroid hormone.

9. The method of claim 1 , wherein the pharmaceutical composition is a tablet.

10. The method of claim 1 , wherein the pharmaceutical composition comprises from 50 to 98% by weight of crystalline anhydrous monosodium N-[8-(2-hydroxybenzoyl)amino]caprylate, based on the total weight of monosodium N-[8-(2-hydroxybenzoyl)amino]caprylate in the pharmaceutical composition.

11. The method of claim 1 , wherein the peptide is insulin.

12. The method of claim 1 , wherein the peptide is parathyroid hormone.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 29, 2022
From: NOVO NORDISK NORTH AMERICA OPERATIONS A/S
To: NOVO NORDISK A/S
Reel/Frame 060352/0663 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 22, 2021
From: EMISPHERE TECHNOLOGIES, INC.
To: NOVO NORDISK NORTH AMERICA OPERATIONS A/S
Reel/Frame 056750/0169 →