US 2033909A
· Cox et al.
· 1936
[cited by applicant]
US 4691034A
· Sanderson et al.
· 1987
[cited by applicant]
US 5133974A
· Paradissis et al.
· 1992
[cited by applicant]
US 5166174A
· Ueno et al.
· 1992
[cited by applicant]
US 5648387A
· Bisgaier et al.
· 1997
[cited by applicant]
US 6410802B1
· Dasseux et al.
· 2002
[cited by applicant]
US 6500457B1
· Midha et al.
· 2002
[cited by applicant]
US 6861555B2
· Ando et al.
· 2005
[cited by applicant]
US 6909014B2
· Dasseux et al.
· 2005
[cited by applicant]
US 7510729B2
· Kolter et al.
· 2009
[cited by applicant]
US 7777071B2
· Goel
· 2010
[cited by applicant]
US 8563761B2
· Armand et al.
· 2013
[cited by applicant]
US 9486446B2
· KurasaWa et al.
· 2016
[cited by applicant]
US 9849104B2
· Bisgaier et al.
· 2017
[cited by applicant]
US 20040137054A1
· Hager et al.
· 2004
[cited by applicant]
US 20040167229A1
· Bakker-Arkema et al.
· 2004
[cited by applicant]
US 20040192771A1
· Dasseux et al.
· 2004
[cited by applicant]
US 20050004196A1
· Kowala
· 2005
[cited by applicant]
US 20070116758A1
· Dafna et al.
· 2007
[cited by applicant]
US 20080241240A1
· Kim et al.
· 2008
[cited by applicant]
US 20090036414A1
· Du et al.
· 2009
[cited by applicant]
US 20090208539A1
· Penhasi et al.
· 2009
[cited by applicant]
US 20090220611A1
· Dargelas et al.
· 2009
[cited by applicant]
US 20090226515A1
· Schmitt et al.
· 2009
[cited by applicant]
US 20100015220A1
· Wetterau et al.
· 2010
[cited by applicant]
US 20100196569A1
· Scanlin et al.
· 2010
[cited by applicant]
US 20120164221A1
· Bova et al.
· 2012
[cited by applicant]
US 20130123354A1
· Currie et al.
· 2013
[cited by applicant]
US 20130273157A1
· Ishii et al.
· 2013
[cited by applicant]
US 20150094303A1
· Bachovchin et al.
· 2015
[cited by applicant]
US 20170158601A9
· Oniciu et al.
· 2017
[cited by applicant]
US 20180194713A1
· Oniciu et al.
· 2018
[cited by applicant]
US 20180297929A1
· Oniciu et al.
· 2018
[cited by applicant]
US 20180325825A1
· Oniciu et al.
· 2018
[cited by applicant]
US 20190008779A1
· Oniciu et al.
· 2019
[cited by applicant]
CA 1197242
· 1985
[cited by applicant]
CN 1182415A
· 1998
[cited by applicant]
CN 104127391A
· 2014
[cited by applicant]
CN 105434391A
· 2016
[cited by applicant]
EA 015519B1
· 2011
[cited by applicant]
EP 2604256A1
· 2013
[cited by applicant]
JP 2003520835
· 2003
[cited by applicant]
JP 2006501238
· 2006
[cited by applicant]
JP 2007500690
· 2007
[cited by applicant]
JP 2015503588
· 2015
[cited by applicant]
RU 2008118974
· 2009
[cited by applicant]
RU 2404767C1
· 2010
[cited by applicant]
RU 2491070C2
· 2013
[cited by applicant]
SU 324740A3
· 1971
[cited by applicant]
WO WO1996030328
· 1996
[cited by applicant]
WO WO9630328A1
· 1996
[cited by examiner]
WO WO2000059855
· 2000
[cited by applicant]
WO WO2001055078
· 2001
[cited by applicant]
WO WO2002030922
· 2002
[cited by applicant]
WO WO2003004470
· 2003
[cited by applicant]
WO WO2003088962
· 2003
[cited by applicant]
WO WO2004017952
· 2004
[cited by applicant]
WO WO2004045596
· 2004
[cited by applicant]
WO WO2005009431
· 2005
[cited by applicant]
WO WO2007058664
· 2007
[cited by applicant]
WO WO2008018877
· 2008
[cited by applicant]
WO WO2008106901
· 2008
[cited by applicant]
WO WO2009024889
· 2009
[cited by applicant]
WO WO2009135949
· 2009
[cited by applicant]
WO WO2009140341
· 2009
[cited by applicant]
WO WO2012002919
· 2012
[cited by applicant]
WO WO2012117071
· 2012
[cited by applicant]
WO WO2013084237
· 2013
[cited by applicant]
WO WO2016077832
· 2016
[cited by applicant]
WO WO2017079755
· 2017
[cited by applicant]
WO WO2018195163
· 2018
[cited by applicant]
Office Action for U.S. Appl. No. 14/942,765, mailed Sep. 21, 2017, 41 pages.
[cited by applicant]
Office Action for U.S. Appl. No. 14/942,765, mailed Feb. 8, 2018, 39 pages.
[cited by applicant]
Office Action for U.S. Appl. No. 14/942,765, mailed May 2, 2017, 36 pages.
[cited by applicant]
Office Action for U.S. Appl. No. 14/942,765, mailed Sep. 20, 2016, 30 pages.
[cited by applicant]
Office Action for U.S. Appl. No. 14/942,765, mailed Sep. 4, 2018, 30 pages.
[cited by applicant]
International Search Report and Written Opinion for International Application No. PCT/US2015/060917, mailed May 13, 2016, 13 pages.
[cited by applicant]
International Search Report and Written Opinion for International Application No. PCT/US2016/060849, mailed Mar. 13, 2017, 21 pages.
[cited by applicant]
International Preliminary Report on Patentability for International Application No. PCT/US2016/060849, dated May 8, 2018, 17 pages.
[cited by applicant]
International Search Report and Written Opinion for International Application No. PCT/US2018/028113, mailed Jun. 21, 2018, 9 pages.
[cited by applicant]
Office Action for U.S. Appl. No. 15/977,226, mailed Dec. 14, 2018, 35 pages.
[cited by applicant]
International Search Report and Written Opinion for International Application No. PCT/US2018/032351, mailed Aug. 8, 2018, 9 pages.
[cited by applicant]
6.2 Direct Alkylation of Simple Enolates (Online), Retrieved from the Internet: <URL:http://chem.yonsei.ac.kr/chem/upload/CHE6402-01/119665643430625.pdf>, Aug. 2010, 9 pages.
[cited by applicant]
Amer, A, “What is a simple way to convert an ester into carboxylic acid?” (Online), Feb. 19, 2014, Retrieved from the Internet: Apr. 17, 2017, 1 page.
[cited by applicant]
Ballantyne, C. M. et al., “Effect of Ezetimibe Coadministered With Atorvastatin in 628 Patients WithPrimary Hypercholesterolemia. A Prospective, Randomized, Double-Blind Trial.” Circulation, 2003;107:2409-2415.
[cited by applicant]
Bhasin, R. K. et al., “Design & Development of Atorvastatin Orally Disintegrating Tablets & Their Evaluationby Electronic Tongue,” Drug Development & Delivery [Online], Retrieved from the Internet: <URL:http://www.drug-…
[cited by applicant]
Billecke, S. et al., “Human serum paraoxonase (PON1) isozymes Q and R hydrolyze lactones and cycliccarbonate esters,” Drug Metabolism and Disposition, vol. 28, No. 11, pp. 1335-1342 (2000).
[cited by applicant]
Bisgaier, C. L. et al., “A novel compound that elevates high density lipoprotein and activates theperoxisome proliferator activated receptor,” Journal of Lipid Research, 39:17-30 ( 1998).
[cited by applicant]
Blonk, M. et al., “Pharmacokinetic Drug-Drug Interaction Study Between Raltegravir and Atorvastatin 20 mgin Healthy Volunteers,” J Acquir Immune Defic Syndr 2015;69:44-51.
[cited by applicant]
Boyd, R. A. et al., “Atorvastatin coadministration may increase digoxin concentrations by inhibition ofintestinal P-glycoprotein-mediated secretion,” Journal of Clinical Pharmacology, 2000; 40:91-98.
[cited by applicant]
Castaneda, P. S. et al., “Design and evaluation of a transdermal patch with atorvastatin,” Farmacia,2017, vol. 65, No. 6, pp. 908-916.
[cited by applicant]
Chemguide, Hydrolysing Esters (Online), (2004), Retrieved from the Internet: <http://www.chemguide.co.uk/organicprops/esters/hydrolysis.html>, Retrieved from the Internet on: Aug. 25, 2016, 4 pages.
[cited by applicant]
Bisgaier, C. L. et al., “125: 328104r Preparation of terminal carboxy or tetrazole group-containing dialkylethers as anticholesteremics and antidiabetics,” Chemical Abstracts, 23-Aliphatic Compounds 328108, vol. 125, No…
[cited by applicant]
Clayden, “Alkylation of Enolates,” Chapter 26, pp. 663-688 (2008).
[cited by applicant]
Clayden, “Nucleophilic Substitution at Saturated Carbon,” Chapter 15, p. 348 (2012).
[cited by applicant]
Clayden et al., Organic Chemistry, Chapter 25: Alkylation of Enolates, pp. 588-589 (2012).
[cited by applicant]
Di Stasi, S. L. et al., “Effects of Statins on Skeletal Muscle: A Perspective for Physical Therapists,” PhysTher. Oct. 2010; 90(10): 1530-1542.
[cited by applicant]
Dressman, J. B., “Comparison of canine and human gastrointestinal physiology,” Pharmaceutical Research, vol. 3, No. 3, 1986, pp. 123-131.
[cited by applicant]
Fallingborg, J. et al., “pH-Profile and regional transit times of the normal gut measured by aradiotelemetry device,” Aliment Pharmacol Ther., Dec. 1989, 3(6)605-613.
[cited by applicant]
Gite, S. et al., “Development and Validation of a Discriminating Dissolution Method for Atorvastatin Delayed-Release Nanoparticles Using a Flow-Through Cell: A Comparative Study Using USP Apparatus 4 and 1,”Dissolution …
[cited by applicant]
Gleiter, R. et al. “Synthesis of 5,5, 10, 10-Tetramethyl-1-oxacyclotridecane-6,7,8,9-tetrone—on theMechanism of the Rubottom Reaction,” Liebigs Annalen, vol. 1995, Issue 9, Aug. 1995, pp. 1655-1661.
[cited by applicant]
Gomez-Bombarelli, R., et al. “Mechanisms of Lactone Hydrolysis in Acidic Conditions,” The Journal ofOrganic Chemistry, 2013, vol. 78, pp. 6880-6889.
[cited by applicant]
Gomez-Bombarelli, R., et al. “Mechanisms of Lactone Hydrolysis in Neutral and Alkaline Conditions,” TheJournal of Organic Chemistry, 2013, vol. 78, pp. 6868-6879.
[cited by applicant]
Hajir, M. et al., “Stable amorphous calcium oxalate: synthesis and potential intermediate inbiomineralization,” Chem. Commun. 2014, 50:6534-6536.
[cited by applicant]
Hayashi, K. et al., “Studies on angiotensin converting enzyme inhibitors. II. Syntheses and angiotensinconverting enzyme inhibitory activities of carboxyethylcarbamoyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylicacid der…
[cited by applicant]
Hermann, M. et al., “Exposure of atorvastatin is unchanged but lactone and acid metabolites are increasedseveral-fold in patients with atorvastatin-induced myopathy,” Clin. Pharmacol. Ther. 2006;79(6):532-539.
[cited by applicant]
Ireland, R. E. et al., “132. Diels-Alder Approach to Highly Functionalized Tertiary a-Hydroxy Ketones: ANovel Route to the Hexahydrobenzofuran Portion of the Avermectins and Milbemycins,” Helv. Chim. Acta1986, 69:1273-1…
[cited by applicant]
Kakurkin, N. P. et al., “Solutions in the Calcium Oxide-Ethylene Glycol-Water System,” ISSN 1070-4272, Russian Journal of Applied Chemistry, 2007, vol. 80, No. 5, pp. 722-725, Pleiades Publishing, Ltd., 2007.Original Ru…
[cited by applicant]
Kantola, T. et al., “Effect of itraconazole on the pharmacokinetics of atorvastatin,” Clin. Pharmacol. Ther.,1998, 64:58-65.
[cited by applicant]
Kearney, A. S. et al., “The interconversion kinetics, equilibrium, and solubilities of the lactone andhydroxyacid forms of the HMG-COA reductase inhibitor, Cl-981,” Pharmaceutical Research, vol. 10, No. 10,1993, pp. 146…
[cited by applicant]
Khare, A. R. et al., “Swelling/deswelling of anionic copolymer gels,” Biomaterials 16 (1995) 559-567.
[cited by applicant]
Konig, J. et al., “Localization and Genomic Organization of a New HepatocellularOrganic Anion Transporting Polypeptide,” The Journal of Biological Chemistry, vol. 275, No. 30, Jul. 28, 2000, pp. 23161-23168.
[cited by applicant]
Kot Ame, R. N. et al., “Formulation and Evaluation of Microspheres of Atorvastatin Calcium by ParticleEngineering Through Spherical Crystalisation,” Research Journal of Pharmaceutical, Biological and ChemicalSciences, J…
[cited by applicant]
Kumar, N. et al., “Atorvastatin calcium encapsulated eudragit nanoparticles with enhanced oralbioavailability, safety and efficacy profile,” Pharmaceutical Development and Technology, Mar. 2017;22(2): 156-167. doi: 10.3…
[cited by applicant]
Lennernas, H., “Clinical Pharmacokinetics of Atorvastatin,” Clin Pharmacokinet 2003; 42( 13): 1141-1160.
[cited by applicant]
Lew, G., “Effect of Particle Size on Dissolution and Gastrointestinal Absorption Rates of Pharmaceuticals, ”American Journal of Pharmacy and the Sciences Supporting Public Health, 135:78-92 (Mar. 1963).
[cited by applicant]
“Making Soap—Saponification,” Aug. 29, 2003, 3 pages.
[cited by applicant]
McShane, M. et al., “An Oral, Rising, Multiple-Dose Tolerance, Pharmacokinetic, and PharmacodynamicStudy of Gemcabene in Healthy Volunteers,” Gemphire Therapeutics Inc., Poster, ATVB May 2016, Nashville, TN, Abstract No…
[cited by applicant]
MIT Department of Chemistry X-Ray Diffraction Facility, “Growing Quality Crystals,” (Online), (2004),Retrieved from the Internet: <URL: http://web.mit.edu/x-ray/cystallize.html>, Retrieved on Sep. 1, 2016,5 pages.
[cited by applicant]
Mudie, D. M. et al., “Physiological Parameters for Oral Delivery and In vitro Testing,” Mol Pharm. Oct. 4, 2010; 7(5): 1388-1405. doi: 10.1021/mp100149j.
[cited by applicant]
Mueller, R. et al., “Long Hydrocarbon Chain Ether Diols and Ether Diacids That Favorably Alter LipidDisorders in Vivo,” J. Med. Chem. 2004, 47(21):5183-5197.
[cited by applicant]
Narayanan, V. S. et al., “Design and evaluation of bi-layer drug delivery system of atorvastatin andglipizide,” Int. J. Chem. Sci.: 7(3), 2009, 1802-1816.
[cited by applicant]
Pang, K. S., “Modeling of intestinal drug absorption: roles of transporters and metabolic enzymes (for theGillette review series),” Drug Metabolism and Disposition, vol. 31, No. 12, 2003, pp. 1507-1519.
[cited by applicant]
Pasanen, M. K. et al., “Different Effects of SLCO1 B1 Polymorphism on the Pharmacokinetics of Atorvastatinand Rosuvastatin,” Clinical Pharmacology & Therapeutics, vol. 82, No. 6, Dec. 2007, pp. 726-733.
[cited by applicant]
Prueksaritanont, T. et al., “Glucuronidation of Statins in Animals and Humans: A Novel Mechanism ofStatin Lactonization,” Drug Metabolism and Disposition May 2002, 30(5):505-512; DOI:https://doi.org/10.1124/dmd.30.5.505.
[cited by applicant]
Schwindeman, J. A et al., “Safe handling of organolithium compounds in the laboratory,” Chemical Healthand Safety, vol. 9, Issue 3, May/Jun. 2002, pp. 6-11.
[cited by applicant]
Shanmukaraj, D. et al., “Boron Esters as Tunable Anion Carriers for Non-Aqueous BatteriesElectrochemistry,” J. Am. Chem. Soc. 2010, 132(9):3055-3062.
[cited by applicant]
Sisido, K. et al., “Condensation oft-Butyl Esters with Organic Halides in the Presence of Alkali Amides,” J.Am. Chem. Soc., 81(21):5817-5819 (Nov. 1959).
[cited by applicant]
Skottheim, I. B. et al., “Atorvastatin Metabolite Measurements as a Diagnostic Tool for Statin-InducedMyopathy,” Mol. Diagn. Ther. 2011:15(4): 221-227.
[cited by applicant]
Srivastava, R. A K et al., “Gemcabene, a first-in-class lipid-lowering agent in late- stage development, down-regulates acute-phase C-reactive protein via C/EBP-o-mediated transcriptional mechanism,” Molecularand Cellul…
[cited by applicant]
Taylor, E. P., “30. Synthetic Neuromuscular Blocking Agents. Part II. Bis(quaternary Ammonium Salts)derived from Laudanosine,” J. Chem. Soc. (Resumed), 1952, Issue 0, 142-145.
[cited by applicant]
Vitthal, K. V. et al., “Melt extrusion based solid dispersions for enhanced solubility and physical stability ofatorvastatin calcium,” International Journal of Biopharmaceutics, 2016; 7(1): 35-47.
[cited by applicant]
Weber, E, “Neutralliganden mit Tensidstruktur—Synthase, Komplexierung, lonentransfer,” Liebigs Ann.Chem., D 1983, pp. 770-801.
[cited by applicant]
Wu, X. et al., “Atorvastatin transport in the Caco-2 cell model: contributions of P-glycoprotein and protonmonocarboxylicacid co-transporter,” Pharmaceutical Research, Feb. 2000, vol. 17, No. 2, pp. 209-215.
[cited by applicant]
Wuts, P. G. M. et al., Chapter 5. Protection for the Carboxyl Group, In: Greene's Protective Groups inOrganic Synthesis, Fourth Edition, John Wiley & Sons, Inc., Published online Apr. 10, 2006, pp. 582-588.
[cited by applicant]
Yang, J. et al., “Kilogram-Scale Synthesis of bis(6-Hydroxy-5,5-Dimethylhexyl)ether (ESP24232), a NovelLipid Lowering Agent,” Organic Preparations and Procedures International, The New Journal for OrganicSynthesis, vol.…
[cited by applicant]
Zhang, T., “Physiologically based pharmacokinetic modeling of disposition and drug-drug interactions foratorvastatin and its metabolites,” European Journal of Pharmaceutical Sciences 77 (2015) 216-229.
[cited by applicant]
Dalko, P. I. et al., “Stereoselective Synthesis of Quaternary Benzylic Carbons Using C2 Symmetriclmidazolines and Tetrahydrofuran as Electrophile,” J. Org. Chem., 1998, vol. 63, No. 23, pp. 8107-8117.
[cited by applicant]
The fourth series of Experimental Chemistry 22, Organic Synthesis IV, Acid, Amino Acid, and Peptide, 1994, 2nd issue, pp. 6-11.
[cited by applicant]
Assmus, M. et al., “Accurate GI targeting with EUDRAGIT FS 30 D/L 30 D-55 mixtures,” Evonik Industries, [Online], 2008. Retrieved from the Internet: <URL:http://www.pharmapolymers.com/pharmapolymers/MCMSbase/Pages/Provi…
[cited by applicant]
DeBunne, A. et al., “Development and in vitro evaluation of an enteric-coated multiparticulate drug deliverysystem for the administration of piroxicam to dogs,” European Journal of Pharmaceutics andBiopharmaceutics, 54(…
[cited by applicant]
Dreu, R. et al., “Development of a multiple-unit tablet containing enteric-coated pellets,” PharmaceuticalDevelopment and Technology, 16(2):118-126 (Apr. 2011).
[cited by applicant]
Fyles, T. M. et al., “Solid-phase synthesis of a library of linear oligoester ion- channels,” Organic &Biomolecular Chemistry, vol. 7, pp. 725-732 (2009).
[cited by applicant]
Oniciu, D. C. et al., “Long hydrocarbon chain diols and diacids with central ether or ketone moieties thatfavorably alter lipid disorders,” Pharmazie, 61(2):157-165 (2006).
[cited by applicant]
Watson, T. G. et al., “Long-Acting Contraceptive Agents: Esters of Norethisterone with a- and/or ˜-ChainBranching,” Steroids, vol. 41, No. 3 (Mar. 1983) pp. 255-266.
[cited by applicant]
Zhang, Y. et al., “The preparation of carbon-14 and tritium radio-labeled PD-72953,” Journal of LabelledCompounds and Radiopharmaceuticals, vol. 50, Issue 5-6 (2007) pp. 602-604.
[cited by applicant]
Gemcabene, PubChem CID: 157692, Aug. 2005, 1 page.
[cited by applicant]
Extended European Search report for European Application No. 18788278.2, mailed Sep. 17, 2020, 10 pages.
[cited by applicant]
Stein, E. et al., “Efficacy and safety of gemcabene as add-on to stable statin therapy in hypercholesterolemic patients”, Journal of Clinical Lipidology, 2016, 10: 1212-1222.
[cited by applicant]
Brittain H G: “Developing an Appropriate Salt Form for an Active Pharmaceutical Ingredient | American Pharmaceutical Review—The Review of American Pharmaceutical Business & Technology”, American Pharmaceutical Review, J…
[cited by applicant]
Bastin R J, et al., “Salt Selection and Optimisation for Pharmaceutical New Chemical Entities”, Organic Process Research and Development, Jan. 1, 2000, vol. 4, No. 5, pp. 427-435, XP008154792.
[cited by applicant]