IP Library Granted Patent US 11,376,309
Granted Patent B2
US 11,376,309 · App. 16/397,944 · Granted Jul 5, 2022

Lipoprotein complexes and manufacturing and uses thereof

Inventors: Jean-Louis Dasseux (Toulouse, FR); Rose Ackermann (Northville, MI); Daniela Carmen Oniciu (Toulouse, FR)
Assignee: Cerenis Therapeutics Holding S.A.
A61K38/1709A61K38/17A61K38/18A61K45/00A61K47/50C07K1/04C07K1/042C07K14/775Y10T428/2982
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Quick Facts
Patent No.
US 11,376,309
App. No.
16/397,944
Granted
Jul 5, 2022
Kind
B2
Abstract

The present disclosure relates to lipoprotein complexes and lipoprotein populations and their use in the treatment and/or prevention of dyslipidemic diseases, disorders, and/or conditions. The disclosure further relates to recombinant expression of apolipoproteins, purification of apolipoproteins, and production of lipoprotein complexes using thermal cycling-based methods.

Claims (29)

1. A composition comprising:

(A) a population of lipoprotein complexes, each comprising

(a) a lipid fraction consisting of a sphingomyelin and, optionally, 1,2-dipalmitoyl-sn-glycero-3-[phospho-rac-(1-glycerol)] (DPPG), and

(b) an apolipoprotein fraction comprising an Apolipoprotein A-I (“ApoA-I”),

wherein

(i) at least 95% by weight of the apolipoprotein in the population is in complexed form;

(ii) at least 95% by weight of the lipid in the population is in complexed form;

(iii) at least 95% of the population is in a single peak in a gel permeation chromatogram;

(iv) the population has an apolipoprotein fraction-to-phospholipid fraction ratio of 1:2.7 by weight; and

(v) the weight ratio of the sphingomyelin to DPPG, when present, is 97:3;

which has been loaded with

(B) a hydrophobic, lipophilic, or apolar active agent.

2. The composition of claim 1 , wherein the active agent is hydrophobic.

3. The composition of claim 1 , wherein the active agent is lipophilic.

4. The composition of claim 1 , wherein the active agent is apolar.

5. The composition of claim 1 , wherein the active agent comprises a fatty acid, a drug, a nucleic acid, a vitamin, a nutrient, or a combination thereof.

6. The composition of claim 1 , wherein the active agent comprises an analgesic, an anti-inflammatory agent, an anthelmintic, an anti-arrhythmic agent, an anti-bacterial agent, an anti-viral agent, an anti-coagulant, an anti-depressant, an anti-diabetic, an anti-epileptic, an anti-fungal agent, an anti-gout agent, an anti-hypertensive agent, an anti-malarial, an anti-migraine agent, an anti-muscarinic agent, an anti-neoplastic agent, an erectile dysfunction improvement agent, an immunosuppressant, an anti-protozoal agent, an anti-thyroid agent, an anxiolytic agent, a sedative, a hypnotic, a neuroleptic, a β-blocker, a cardiac inotropic agent, a corticosteroid, a diuretic, an anti-parkinsonian agent, a gastrointestinal agent, a histamine receptor antagonist, a keratolytic, a lipid regulating agent, an anti-anginal agent, a COX-2 inhibitor, a leukotriene inhibitor, a macrolide, a muscle relaxant, a nutritional agent, a nucleic acid, an opioid analgesic, a protease inhibitor, a sex hormone, a stimulant, a muscle relaxant, an anti-osteoporosis agent, an anti-obesity agent, a cognition enhancer, an anti-urinary incontinence agent, a nutritional oil, an anti-benign prostate hypertrophy agent, an essential fatty acid, a non-essential fatty acid, or a combination thereof.

7. The composition of claim 1 , wherein the active agent comprises acetretin, albendazole, albuterol, aminoglutethimide, amiodarone, amlodipine, amphetamine, amphotericin B, atorvastatin, atovaquone, azithromycin, baclofen, beclomethasone, benezepril, benzonatate, betamethasone, bicalutanide, budesonide, bupropion, busulfan, butenafine, calcifediol, calcipotriene, calcitriol, camptothecin, candesartan, capsaicin, carbamezepine, carotenes, celecoxib, cerivastatin, cetirizine, chlorpheniramine, cholecalciferol, cilostazol, cimetidine, cinnarizine, ciprofloxacin, cisapride, clarithromycin, clemastine, clomiphene, clomipramine, clopidogrel, codeine, coenzyme Q10, cyclobenzaprine, cyclosporin, danazol, dantrolene, dexchlorpheniramine, diclofenac, dicoumarol, digoxin, dehydroepiandrosterone, dihydroergotamine, dihydrotachysterol, dirithromycin, donezepil, efavirenz, eposartan, ergocalciferol, ergotamine, essential fatty acid sources, etodolac, etoposide, famotidine, fenofibrate, fentanyl, fexofenadine, finasteride, fluconazole, flurbiprofen, fluvastatin, fosphenytoin, frovatriptan, furazolidone, gabapentin, gemfibrozil, glibenclamide, glipizide, glyburide, glimepiride, griseofulvin, halofantrine, ibuprofen, irbesartan, irinotecan, isosorbide dinitrate, isotretinoin, itraconazole, ivermectin, ketoconazole, ketorolac, lamotrigine, lansoprazole, leflunomide, lisinopril, loperamide, loratadine, lovastatin, L-thryroxine, lutein, lycopene, medroxyprogesterone, mifepristone, mefloquine, megestrol acetate, methadone, methoxsalen, metronidazole, miconazole, midazolam, miglitol, minoxidil, mitoxantrone, montelukast, nabumetone, nalbuphine, naratriptan, nelfinavir, nifedipine, nilsolidipine, nilutanide, nitrofurantoin, nizatidine, omeprazole, oprevelkin, oestradiol, oxaprozin, paclitaxel, paracalcitol, paroxetine, pentazocine, pioglitazone, pizofetin, pravastatin, prednisolone, probucol, progesterone, pseudoephedrine, pyridostigmine, rabeprazole, raloxifene, rofecoxib, repaglinide, rifabutine, rifapentine, rimexolone, ritanovir, rizatriptan, rosiglitazone, saquinavir, sertraline, sibutramine, sildenafil citrate, simvastatin, sirolimus, spironolactone, sumatriptan, tacrine, tacrolimus, tamoxifen, tamsulosin, targretin, tazarotene, telmisartan, teniposide, terbinafine, terazosin, tetrahydrocannabinol, tiagabine, ticlopidine, tirofibran, tizanidine, topiramate, topotecan, toremifene, tramadol, tretinoin, troglitazone, trovafloxacin, ubidecarenone, valsartan, venlafaxine, verteporfin, vigabatrin, vitamin A, vitamin D, vitamin E, vitamin K, zafirlukast, zileuton, zolmitriptan, zolpidem, zopiclone, a salt of any of the foregoing, or a combination of any of the foregoing.

8. The composition of claim 1 , wherein at least 97% of the population is in a single peak in gel permeation chromatogram.

9. The composition of claim 1 , wherein said ApoA-I is a human ApoA-I protein.

10. The composition of claim 1 , wherein said ApoA-I is a recombinant ApoA-I.

11. The composition of claim 1 , wherein said ApoA-I has at least 95% sequence identity to a protein corresponding to amino acids 25 to 267 of SEQ ID NO: 1.

12. The composition of claim 1 , wherein said lipid fraction consists of sphingomyelin.

13. The composition of claim 12 , wherein the sphingomyelin is egg sphingomyelin.

14. The composition of claim 12 , wherein the sphingomyelin is palmitoyl sphingomyelin.

15. The composition of claim 1 , wherein said lipid fraction consists of 97 weight % sphingomyelin and 3 weight % DPPG.

16. The composition of claim 15 , wherein the sphingomyelin is egg sphingomyelin.

17. The composition of claim 15 , wherein the sphingomyelin is palmitoyl sphingomyelin.

18. A pharmaceutical composition comprising the composition of claim 1 , and one or more pharmaceutically acceptable carriers, diluents and/or excipients.

Assignments (2)
CHANGE OF NAME Recorded Jun 4, 2025
From: CERENIS THERAPEUTICS HOLDING S.A.
To: ABIONYX PHARMA S.A.
Reel/Frame 071495/0745 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 2, 2025
From: DASSEUX, JEAN-LOUIS; ONICIU, DANIELA CARMEN; ACKERMANN, ROSE
To: CERENIS THERAPEUTICS HOLDING S.A.
Reel/Frame 071289/0158 →
Continuity (7)
Division 14884115 · Oct 15, 2015
Continuation 14103686 · Dec 11, 2013
Division 13367237 · Feb 6, 2012
Provisional Application 61487263 · May 17, 2011
Provisional Application 61452630 · Mar 14, 2011
Provisional Application 61440371 · Feb 7, 2011
Related Publication 20190298800A1 · Oct 3, 2019
Cited By (1)
US 12,364,735