IP Library Granted Patent US 12,478,625
Granted Patent B2
US 12,478,625 · App. 18/662,276 · Granted Nov 25, 2025

Pharmaceutical compositions and crushable tablets including amorphous solid dispersions of dasatinib and uses

Inventors: Christian F. Wertz (Saint Louis Park, MN); Tzehaw Chen (Corcoran, MN)
Assignee: Handa Therapeutics, LLC
A61K31/506A61K9/0053A61K9/2027
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,478,625
App. No.
18/662,276
Granted
Nov 25, 2025
Kind
B2
Abstract

Amorphous solid dispersions and pharmaceutical compositions of the protein kinase inhibitor dasatinib. The pharmaceutical compositions may be used in methods of treating a proliferative disorder such as cancer, or in methods of delivering dasatinib to patients without regard to whether the patient is concurrently administered a gastric acid-reducing agent, or without regard to whether the patient has an elevated gastric pH. The compositions may be particularly suitable for patients afflicted by achlorhydria or hypochlorhydria, or Helicobacter pylori infection. The compositions may be administered intact, or may be crushed prior to administration.

Claims (22)

1 . A method of delivering a therapeutically effective amount of dasatinib to a patient in need thereof, comprising:

(a) providing a pharmaceutical composition in the form of one or more crushable tablets;

(b) crushing the one or more crushable tablets to provide a powder; and

(c) orally administering the powder to the patient;

wherein the crushable tablets comprise an amorphous solid dispersion, the amorphous solid dispersion comprising dasatinib and a polymer that exhibits pH dependent solubility; and

wherein the dasatinib and the polymer that exhibits pH dependent solubility are present in the amorphous solid dispersion in a w/w ratio of 30:70 to 95:5 (dasatinib:polymer).

2 . The method of claim 1 , further comprising the step of dispersing the powder in a soft food prior to administration to the patient.

3 . The method of claim 1 , further comprising the step of dispersing the powder in a fruit preparation prior to administration to the patient.

4 . The method of claim 1 , further comprising the step of dispersing the powder in a fluid prior to administration to the patient.

5 . The method of claim 1 , further comprising the step of dispersing the powder in a juice prior to administration to the patient.

6 . The method of claim 1 , wherein the patient is a pediatric patient, a geriatric patient, or a patient that suffers from dysphagia.

7 . The method of claim 1 , wherein the patient is an adult patient, and the one or more crushable tablets comprise a total of 100 to 180 mg dasatinib.

8 . The method of claim 1 , wherein the patient is a pediatric patient, and the one or more crushable tablets comprise a total of 40 to 100 mg dasatinib.

9 . The method of claim 1 , wherein the polymer that exhibits pH dependent solubility comprises a methacrylic acid and ethyl acrylate copolymer.

10 . The method of claim 1 , wherein the polymer that exhibits pH dependent solubility comprises a methacrylic acid and ethyl acrylate copolymer that is insoluble in an aqueous medium at pH of 5 or lower, and soluble in an aqueous medium at pH 5.5 or greater.

11 . The method of claim 1 , wherein the dasatinib and the polymer that exhibits pH dependent solubility are present in the amorphous solid dispersion in a w/w ratio of 40:60 to 70:30 (dasatinib:polymer).

12 . The method of claim 1 , wherein the pharmaceutical composition is co-administered to the patient with a gastric acid-reducing agent.

13 . The method of claim 1 , wherein the pharmaceutical composition is co-administered to the patient with a standard dosage of a proton pump inhibitor.

14 . The method of claim 1 , wherein the patient has elevated gastric pH.

15 . The method of claim 1 , wherein the patient is suffering from a proliferative disorder.

16 . The method of claim 15 , wherein the proliferative disorder is Philadelphia chromosome-positive chronic myeloid leukemia.

17 . The method of claim 15 , wherein the proliferative disorder is Philadelphia chromosome-positive acute lymphoblastic leukemia.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 28, 2025
From: PXMMI, LLC
To: HANDA THERAPEUTICS, LLC
Reel/Frame 071084/0182 →
NUNC PRO TUNC ASSIGNMENT Recorded Apr 24, 2025
From: NANOCOPOEIA, LLC
To: PXMMI, LLC
Reel/Frame 070939/0374 →
AFFIDAVIT RE: ASSGNMENT FOR THE BENEFIT OF CREDITORS (MINNESOTA STATE COURT FILE NO. 62-CV-24-5879) Recorded Mar 11, 2025
From: NANOCOPOEIA, LLC
To: LIGHTHOUSE MANAGEMENT GROUP, INC.
Reel/Frame 070733/0519 →
AFFIDAVIT RE: ASSGNMENT FOR THE BENEFIT OF CREDITORS (MINNESOTA STATE COURT FILE NO. 62-CV-24-5879) Recorded Mar 11, 2025
From: LIGHTHOUSE MANAGEMENT GROUP, INC.
To: NANOCOPOEIA, LLC
Reel/Frame 070908/0001 →
Continuity (3)
Division 17876096 · Jul 28, 2022
Provisional Application 63226496 · Jul 28, 2021
Related Publication 20240299389A1 · Sep 12, 2024
References Cited (171)
US 6350786B1 · Albano et al. · 2002 [cited by applicant]
US 6596746B1 · Das et al. · 2003 [cited by applicant]
US 6746869B2 · Pui et al. · 2004 [cited by applicant]
US 6764720B2 · Pui et al. · 2004 [cited by applicant]
US 7125875B2 · Das et al. · 2006 [cited by applicant]
US 7153856B2 · Barrish et al. · 2006 [cited by applicant]
US 7279322B2 · Pui et al. · 2007 [cited by applicant]
US 7491725B2 · Lajeunesse et al. · 2009 [cited by applicant]
US 7498063B2 · Pui et al. · 2009 [cited by applicant]
US 7951428B2 · Hoerr et al. · 2011 [cited by applicant]
US 7972661B2 · Pui et al. · 2011 [cited by applicant]
US 7973045B2 · Šimo et al. · 2011 [cited by applicant]
US 8557995B2 · Miller et al. · 2013 [cited by applicant]
US 8680103B2 · Lajeunesse et al. · 2014 [cited by applicant]
US 8703196B2 · Babcock et al. · 2014 [cited by applicant]
US 8841303B2 · Breitenbach et al. · 2014 [cited by applicant]
US 8883209B2 · Babcock et al. · 2014 [cited by applicant]
US 8940800B2 · Babcock et al. · 2015 [cited by applicant]
US 8974827B2 · Bloom et al. · 2015 [cited by applicant]
US 8992471B2 · Dugas et al. · 2015 [cited by applicant]
US 8992603B2 · Dugas et al. · 2015 [cited by applicant]
US 9040816B2 · Gupta · 2015 [cited by applicant]
US 9050611B2 · Pui et al. · 2015 [cited by applicant]
US 9108217B2 · Hoerr et al. · 2015 [cited by applicant]
US 9211261B2 · Appel et al. · 2015 [cited by applicant]
US 9248217B2 · Hoerr et al. · 2016 [cited by applicant]
US 9249134B2 · Dwivedi · 2016 [cited by applicant]
US 9456992B2 · Brisander et al. · 2016 [cited by applicant]
US 9642694B2 · Hoerr et al. · 2017 [cited by applicant]
US 9827230B2 · Brisander et al. · 2017 [cited by applicant]
US 9833442B2 · Brisander et al. · 2017 [cited by applicant]
US 9833443B2 · Brisander et al. · 2017 [cited by applicant]
US 9884857B2 · Hafner et al. · 2018 [cited by applicant]
US 10023566B2 · Marvanyos et al. · 2018 [cited by applicant]
US 10143683B2 · Brisander et al. · 2018 [cited by applicant]
US 10252289B2 · Hoerr et al. · 2019 [cited by applicant]
US 10314829B2 · Brisander et al. · 2019 [cited by applicant]
US 10314830B2 · Brisander et al. · 2019 [cited by applicant]
US 10464933B2 · Thirunahari et al. · 2019 [cited by applicant]
US 10555937B2 · Brisander et al. · 2020 [cited by applicant]
US 10561643B2 · Brisander et al. · 2020 [cited by applicant]
US 10561644B2 · Brisander et al. · 2020 [cited by applicant]
US 10561645B2 · Brisander et al. · 2020 [cited by applicant]
US 10562048B2 · Chen et al. · 2020 [cited by applicant]
US 10772877B2 · Brisander et al. · 2020 [cited by applicant]
US 10799459B1 · Andersson et al. · 2020 [cited by applicant]
US 10821375B2 · Fonseca et al. · 2020 [cited by applicant]
US 10874671B2 · Jain et al. · 2020 [cited by applicant]
US 11202778B2 · Wertz et al. · 2021 [cited by applicant]
US 11298356B1 · Wertz et al. · 2022 [cited by applicant]
US 11324745B2 · Wertz et al. · 2022 [cited by applicant]
US 11413290B2 · Wertz et al. · 2022 [cited by applicant]
US 11633398B2 · Wertz et al. · 2023 [cited by applicant]
US 11980619B2 · Wertz et al. · 2024 [cited by applicant]
US 20090203709A1 · Steinberg et al. · 2009 [cited by applicant]
US 20100143459A1 · Liepold et al. · 2010 [cited by applicant]
US 20100256158A1 · Simo et al. · 2010 [cited by applicant]
US 20100266692A1 · Bloom et al. · 2010 [cited by applicant]
US 20110229627A1 · Hoerr et al. · 2011 [cited by applicant]
US 20110287096A1 · Gorukanti · 2011 [cited by applicant]
US 20130096116A1 · Dalziel et al. · 2013 [cited by applicant]
US 20130323403A1 · Hoerr et al. · 2013 [cited by applicant]
US 20140343073A1 · Dwivedi et al. · 2014 [cited by applicant]
US 20140356443A1 · Brisander et al. · 2014 [cited by applicant]
US 20150110871A1 · Wong · 2015 [cited by applicant]
US 20150190253A1 · Dugas et al. · 2015 [cited by applicant]
US 20160175881A1 · Lasch et al. · 2016 [cited by applicant]
US 20160235677A1 · Hoerr et al. · 2016 [cited by applicant]
US 20160361313A1 · Brisander et al. · 2016 [cited by applicant]
US 20170209372A1 · Temtem et al. · 2017 [cited by applicant]
US 20190040054A1 · Thirunahari et al. · 2019 [cited by applicant]
US 20190193109A1 · Hoerr et al. · 2019 [cited by applicant]
US 20190270735A1 · Rao et al. · 2019 [cited by applicant]
US 20200113903A1 · Liu et al. · 2020 [cited by applicant]
US 20200179963A1 · Chen et al. · 2020 [cited by applicant]
US 20200188400A1 · Liu et al. · 2020 [cited by applicant]
US 20220273656A1 · Wertz et al. · 2022 [cited by applicant]
US 20220273657A1 · Wertz et al. · 2022 [cited by applicant]
US 20220280512A1 · Wertz et al. · 2022 [cited by applicant]
DK 2802314T3 · 2021 [cited by applicant]
EP 0988863 · 2000 [cited by applicant]
JP 201970000 · 2019 [cited by applicant]
WO 2005077945 · 2005 [cited by applicant]
WO 2007035874 · 2007 [cited by applicant]
WO 2009053854 · 2009 [cited by applicant]
WO 2010081443 · 2010 [cited by applicant]
WO 2012035074 · 2012 [cited by applicant]
WO 2015181573 · 2015 [cited by applicant]
WO 2017108605 · 2017 [cited by applicant]
WO 2019010092 · 2019 [cited by applicant]
WO WO2019010092A1 · 2019 [cited by applicant]
WO 2019241504 · 2019 [cited by applicant]
WO 2022040446A1 · 2022 [cited by applicant]
WO 2022115464A1 · 2022 [cited by applicant]
WO 2022157308A1 · 2022 [cited by applicant]
Takahashi, Cancer Chemother. Pharamcol (2012) 69.999-1004 (Year: 2012). [cited by examiner]
Horinkova (Prague Medical Report, vol. 120, 2019, No. 2-3, p. 52-63 (Year: 2019). [cited by examiner]
Monschke et al., “Amorphous solid dispersions of weak bases with pH-dependent soluble polymers to overcome limited bioavailability due to gastric pH variability—An in-vtiro approach,” Apr. 13, 2019, [cited by applicant]
AIDHC Medications, https://www.nemours.org/content/dam/nemours/wwwv2/filebox/service/medical/oncology/AIDHC%20Medications%20by%20Mouth%20for%20Kids%20with%20Cancer.pdf published 2008 (Year: 2008). [cited by applicant]
Vaidhyanathan et al. Journal of Pharmaceutical Sciences, 108, 2019, 741-749 (Year: 2019). [cited by applicant]
Certified Copy of U.S. Appl. No. 63/288,752, filed Dec. 13, 2021. 92 pages. [cited by applicant]
Certified Copy of U.S. Appl. No. 63/140,043, filed Jan. 21, 2021. 56 pages. [cited by applicant]
Budha et al., “Drug Absorption Interactions Between Oral Targeted Anticancer Agents and PPIs: Is PH-Dependent Solubility the Achilles Heel of Targeted Therapy?”, Clinical Pharmacology & Therapeutics, vol. 92, No. 2, Aug… [cited by applicant]
Chen et al., “P-Glycoprotein and Breast Cancer Resistance Protein Influence Brain Distribution of Dasatinib”, The Journal of Pharmacology and Experimental Therapeutics, vol. 330, No. 3, pp. 956-963 (2009). [cited by applicant]
Chu et al., “Gastric Acid Suppression is Associated with Decreased Erlotinib Efficacy in Non-Small-Cell Lung Cancer”, Clinical Lung Cancer, vol. 16, No. 1, pp. 33-39 (2015). [cited by applicant]
Furmanski et al., “Contribution of Abcc4-Mediated Gastric Transport to the Absorption and Efficacy of Dasatinib”, Clin Cancer Res; 19(16) Aug. 15, 2013. [cited by applicant]
Gala et al., “Harnessing the Therapeutic Potential of Anticancer Drugs Through Amorphous Solid Dispersions”, BB—Reviews on Cancer 1873 (2020) 188319. [cited by applicant]
Gurunath et al., “Amorphous Solid Dispersion Method for Improving Oral Bioavailability of Poorly Water-Soluble Drugs”, Journal of Pharmacy Research 6 (2013) 476-480. [cited by applicant]
Ha et al., “Does Gastric Acid Suppression Affect Sunitinib Efficacy in Patients with Advanced or Metastatic Renal Cell Cancer?”, J Oncol Pharm Practice,, 2015, vol. 21(3), 194-200. [cited by applicant]
Haouala et al., “Drug Interactions with the Tyrosine Kinase Inhibitors Imatinib, Dasatinib, and Nilotinib”, Blood, Feb. 24, 2011, vol. 117, No. 8. [cited by applicant]
Herbrink, et al., “Inherent Formulation Issues of Kinase Inhibitors”, Journal of Controlled Release, 239 (2016) 118-127. [cited by applicant]
Herbrink, Maikel, Thesis of Pharmaceutics of Oral Anticancer Agents and Stimulants, Feb. 2, 1990, pp. 1-315. [cited by applicant]
Hoshino-Yoshino et al., “Bridging from Preclinical to Clinical Studies for Tyrosine Kinase Inhibitors Based on Pharmacokinetics/Pharmacodynamics and Toxicokinetics/Toxicdynamics”, Drug Metab. Pharmacokinet. 26(6):612-62… [cited by applicant]
Huang et al., “Fundamental Aspects of Solid Dispersion Technology for Poorly Soluble Drugs”, Acta Pharmaceutica Sinica B 2014; 4(1):18-25. [cited by applicant]
Jesson et al., “Carbon Dioxide-Mediated Generation of Hybrid Nanoparticles for Improved Bioavailability of Protein Kinase Inhibitors”, Pharm Res (2014) 31:694-705. [cited by applicant]
Kamath, et al., “Preclinical Pharmacokinetics and in Vitro Metabolism of Dasatinib (BMS-354825): A Potent Oral Multi-Targeted Kinase Inhibitor against SRC and BCR-ABL”, Cancer Chemother Pharmacol (2008) 61:365-376. [cited by applicant]
Karagianni et al., “Co-Amorphous Solid Dispersions for Solubility and Absorption Improvement of Drugs: Composition, Preparation, Characterization and Formulations for Oral Delivery”, Pharmaceutics 2018, 10, 98. [cited by applicant]
Koutake et al., “Influence of Proton Pump Inhibitors and H2-Receptor Antagonists on the Efficacy and Safety of Dasatinib in Chronic Myeloid Leukemia Patients”, International Journal of Hematology (2020) 111:826-832. [cited by applicant]
Lubach et al, “Investigation of the Rat Model for Preclinical Evaluation of pH-Dependent Oral Absorption in Humans”, Molecular Pharmaceutics, 2013, 10, 3997-4004. [cited by applicant]
Luo et al., “Dasatinib (BMS-354825) Pharmacokinetics and Pharmacodynamic Biomarkers in Animal Models Predict Optimal Clinical Exposure”, Clin Cancer Res 2006; 12(23) Dec. 1, 2006. [cited by applicant]
Matsuoka et al., “H2-Receptor Antagonist Influences Dasatinib Pharmacokinetics in a Patient with Philiadelphia-Positive Acute Lymphoblastic Leukemia”, Cancer Chemother Pharmacol (2012) 70:351-352. [cited by applicant]
Mitra et al., “Impaired Drug Absorption Due to High Stomach pH: A Review of Strategies for Mitigation of Such Effect to Enable Pharmaceutical Product Development”, Molecular Pharmaceutics, 2013, 10, 3970-3979. [cited by applicant]
Nguyen et al., “Pharmaceutical Applications of Electrospraying”, Journal of Pharmeutical Sciences 105 (2016) 2601-2620. [cited by applicant]
Pang et al., “Pharmacokinetics and Absorption of the Anticancer Agents Dasatinib and GDC-0941 Under Various Gastric Conditions in Dogs-Reversing the Effect of Elevated Gastric pH with Betaine HCI”, Mol. Pharmeutics 2013… [cited by applicant]
PCT International Search Report and Written Opinion for PCT/US2021/014742 dated Apr. 7, 2021 (12 pages). [cited by applicant]
Press Release, XSpray First Study Group Has Been Dosed in XSpray Pharma's Ongoing Pivotal Registration Studies with HyNap-Dasa, Jul. 3, 2020. [cited by applicant]
Press Release, XSpray Announces Positive Preliminary Results from the Study for its Lead Product Candidate HyNap-Dasa, Sep. 25, 2020. [cited by applicant]
Press Release, XSpray Announces Positive Stability Data on HyNap-Dasa Tablets, Aug. 31, 2020. [cited by applicant]
Press Release, XSpray Announces Preliminary Results from the First Study for Its Lead Product Candidate HyNap-Dasa, Aug. 12, 2020. [cited by applicant]
Press Release, XSpray First Batch of HyNap-Dasa Tablets Manufactured on Commercial Scale According to GMP, Dec. 19, 2019. [cited by applicant]
Press Release, Xspray Pharma Announces Positive Clinical Data for its Lead Product Candidate HyNap-Dasa, Sep. 9, 2018. [cited by applicant]
Press Release, XSpray Pharma Announces Results from Additional Bioequivalence Study and Provides Update Regarding Upcoming Regulatory Applications for ANDA and 505(b)(2), Jan. 14, 2021. [cited by applicant]
Press Release, XSpray Pharma has decided to Await the Result of Two Ongoing Clinical Studies Before Submitting its ANDA Application, Dec. 11, 2020. [cited by applicant]
Press Release, XSpray Pharma Initiates Pivotal Registration Studies with HyNap-Dasa for the Market Approval Application in the United States, May 29, 2020. [cited by applicant]
Press Release, XSpray Pharma Reports Positive Results from a Study with Dasatinib During Omeprazole Treatment, Dec. 30, 2020. [cited by applicant]
Press Release, XSpray Pharma's HyNap-Dasa Shows Formal Bioequivalanece, Oct. 10, 2018. [cited by applicant]
Press Release, XSpray Pharmas Study with Modified Formulation of HyNap-Dasa Has Now Started, Jan. 22, 2021. [cited by applicant]
Press Release, XSpray Stability Studies Initiated with XSpray's HyNap-Dasa Tablets, Feb. 11, 2020. [cited by applicant]
Press Release, XSpray, Both Groups in the Two Ongoing Bioequivalence Studies with XSpray Pharma's Product Candidate HyNap-Dasa Have Been Dosed, Mar. 5, 2021. [cited by applicant]
Sane et al., “Development and Evaluation of a Novel Microemulsion Formulation of Elacridar to Improve its Bioavailability”, J Pharm Sci., 2013; 102(4); 1343-1354. [cited by applicant]
Segal et al., “Oral Chemotherapy Food and Drug Interactions: A Comprehensive Review of the Literature”, Journal of Oncology Practice, vol. 10, Issue 4, 2014, pp. 255-268. [cited by applicant]
Smelick et al., “Prevalence of Acid-Reducing Agents (ARA) in Cancer Populations and ARA Drug-Drug Interaction Potential for Molecular Targeted Agents in Clinical Development”, Mol. Pharmaceutics 2013, 10, 4055-4062. [cited by applicant]
Sprycel-Dasatinib Tablet, E.R. Squibb & Sons, LLC, Highlights of Prescribing Information, 2018, 50 pages. [cited by applicant]
Sridhar et al., “Electrosprayed Nanoparticles for Drug Delivery and Pharmaceutical Applications”, Biomatter 3:3, e24281, Jul./Aug./Sep. 2013. [cited by applicant]
Takahashi et al., “Influence of H2-Receptor Antagonists and Proton Inhibitors on Dasatinib Pharmacokinetics in Japanese Leukemia Patients”, Cancer Chemother Pharmacol (2012) 69:999-1004. [cited by applicant]
Tran et al., “Overview of the Manufacturing Methods of Solid Dispersion Technology for Improving the Solubility of Poorly Water-Soluble Drugs and Application to Anticancer Drugs”, Pharmaceutics 2019, 11, 132. [cited by applicant]
Tsume et al., “In Vitro Dissolution Methodology, Mini-Gastrointestinal Simulator (mGIS), Predicts Better in Vivo Dissolution of a Weak Base Drug, Dasatinib”, European Journal of Pharmaceutical Sciences 76 (2015) 203-212. [cited by applicant]
van Leeuwen et al., “Drug-Drug Interactions with Tyrosine-Kinase Inhibitors: A Clinical Perspective”, Review, www.thelancet.com/oncology, vol. 15, Jul. 2014 e315-326. [cited by applicant]
Willemsen et al., “Effect of Food and Acid-Reducing Agents on the Absorption of Oral Targeted Therapies in Solid Tumors”, Drug Discovery Today, vol. 21, No. 6, Jun. 2016, pp. 962-976. [cited by applicant]
Yago et al., “Gastric Re-Acidification with Betaine HCI in Healthy Volunteers with Rabeprazole-Induced Hypochlorhydria”, Mol. Pharm., Mar. 8, 2014, 4032-4037. [cited by applicant]
Yago et al., “The Use of Betaine HCI to Enhance Dasatinib Absorption in Healthy Volunteers with Rabeprazole-Induced Hypochlorhydria”, The AAPS Journal, vol. 16, No. 6, Nov. 2014, 1358-1365. [cited by applicant]
Zhang et al., “pH-Dependent Drug-Drug Interactions for Weak Base Drugs: Potential Implications for New Drug Development”, Nature, vol. 96, No. 2, Aug. 2014, 266-277. [cited by applicant]
Zhang et al., “Processing Impact on Performance of Solid Dispersions”, Pharmaceutics 2018, 10, 142, 2018. [cited by applicant]
Bikiaris et al., “Solid Dispersions, Part 1: Recent Evolutions and Future Opportunities in Manufacturing Methods of Dissolution Rate Enhancement of Poorly Water-Soluble Drugs,” Expert Opin. Drug Deliv., (2011), 8(11), p… [cited by applicant]
Bikiaris et al., “Solid Dispersions, Part II: Recent Evolutions and Future Opportunities in Manufacturing Methods of Dissolution Rate Enhancement of Poorly Water-Soluble Drugs,” Expert Opin. Drug Deliv., (2011), 8(12), … [cited by applicant]
Nikghalb et al., “Solid Dispersion: Methods and Polymers to Increase the Solubility of Poorly Soluble Drugs,” Journal of Applied Pharmaceutical Science, vol. 2 (10), pp. 170-175, Oct. 2012. [cited by applicant]
Patel et al., “Revealing Facts Behind Spray Dried Solid Dispersion Technology used for Solubility Enhancement,” Saudi Pharmaceutical Journal, (2015), 23, 352-365. [cited by applicant]
Preliminary Amendment filed Dec. 13, 2021, for U.S. Appl. No. 17/549,104, filed Dec. 13, 2021. [cited by applicant]
Preliminary Amendment filed Dec. 15, 2021, for U.S. Appl. No. 17/551,512, filed Dec. 15, 2021. [cited by applicant]
Preliminary Amendment filed Dec. 8, 2021, for U.S. Appl. No. 17/545,370, filed Dec. 8, 2021. [cited by applicant]
Sawicki et al., “Inventory of Oral Anticancer Agents: Pharmaceutical Formulation Aspects with Focus on the Solid Dispersion Technique,” Cancer Treatment Reviews, 50 (2016) 247-263. [cited by applicant]
Shaukat et al., “Tackling the Challenges with Poorly Soluble Drugs,” Journal of Analytical & Pharmaceutical Research, 2015; 1(1) 1-3. [cited by applicant]
Vaidhyanathan et al., “Bioequivalence Comparison of Pediatric Dasatinib Formulations and Elucidation of Absorption Mechanisms Through Integrated PBPK Modeling,” Journal of Pharmaceutical Sciences, 108 (2019, 741-749. [cited by applicant]
Preliminary Amendment filed Dec. 8, 2021, for U.S. Appl. No. 17/545,324, filed Dec. 8, 2021. [cited by applicant]
Eley et al., Journal of Clinical Pharmacology, 2009, vol. 49, pp. 700-709. [cited by applicant]
U.S. Appl. No. 17/238,869, filed Apr. 23, 2021, Amorphous Nilotinib Nanoparticles and Uses thereof, Inventors: Chrisitan F. Wertz, Tzehaw Chan and Joseph McTarsney. [cited by applicant]
U.S. Appl. No. 17/328,548, filed May 24, 2021, Orally Disintegrating Tablet Comprising Amorphous Solid Dispersion of Nilotinib, Inventors: Christian F. Wertz, Tzehaw Chen, Joseph McTarsney, Sarah M. Rieschl and Limin Sh… [cited by applicant]
U.S. Appl. No. 17/545,324, filed Dec. 8, 2021, for Amorphous Solid Dispersions of Dasatinib and Uses thereof, Inventors: Christian F. Wertz and Tzehaw Chen. [cited by applicant]
U.S. Appl. No. 17/545,370, filed Dec. 8, 2021, for Amorphous Solid Dispersions of Dasatinib and Uses Thereof, Inventors: Christian F. Wertz and Tzehaw Chen. [cited by applicant]
U.S. Appl. No. 17/551,512, filed Dec. 15, 2021, for Amorphous Solid Dispersions of Dasatinib and Uses Thereof, Inventors: Christian F. Wertz and Tzehaw Chen. [cited by applicant]
U.S. Appl. No. 17/549,104, filed Dec. 13, 2021, for Amorphous Solid Dispersions of Dasatinib and Uses Thereof, Inventors: Christian F. Wertz and Tzehaw Chen. [cited by applicant]