US 4410537A
· Kneen
· 1983
[cited by applicant]
US 4535183A
· Kneen
· 1985
[cited by applicant]
US 5607934A
· Tone et al.
· 1997
[cited by applicant]
US 5733888A
· Bryans et al.
· 1998
[cited by applicant]
US 5852018A
· Bryans et al.
· 1998
[cited by applicant]
US 5872151A
· Rhodes et al.
· 1999
[cited by applicant]
US 5874443A
· Kiely et al.
· 1999
[cited by applicant]
US 5886210A
· Rayle et al.
· 1999
[cited by applicant]
US 5891877A
· Brocchini et al.
· 1999
[cited by applicant]
US 5922683A
· Or et al.
· 1999
[cited by applicant]
US 5939098A
· Reidenberg et al.
· 1999
[cited by applicant]
US 5958980A
· Rhodes
· 1999
[cited by applicant]
US 6069146A
· Fenical et al.
· 2000
[cited by applicant]
US 6096786A
· Rhodes
· 2000
[cited by applicant]
US 6350759B1
· Casara et al.
· 2002
[cited by applicant]
US 6358957B1
· Fukumoto et al.
· 2002
[cited by applicant]
US 6500825B2
· Lan et al.
· 2002
[cited by applicant]
US 6506787B2
· Fujishita et al.
· 2003
[cited by applicant]
US 6509331B1
· Audia et al.
· 2003
[cited by applicant]
US 6583143B2
· Haddach
· 2003
[cited by applicant]
US 6713480B2
· Fukumoto et al.
· 2004
[cited by applicant]
US 6808710B1
· Wood et al.
· 2004
[cited by applicant]
US 6972289B1
· Kanzaki et al.
· 2005
[cited by applicant]
US 7026322B2
· Hayashi et al.
· 2006
[cited by applicant]
US 7064201B2
· Hayashi et al.
· 2006
[cited by applicant]
US 7488802B2
· Collins et al.
· 2009
[cited by applicant]
US 7629380B2
· McMorris et al.
· 2009
[cited by applicant]
US 7635757B2
· Freeman et al.
· 2009
[cited by applicant]
US 7674903B2
· Hayashi et al.
· 2010
[cited by applicant]
US 7700615B2
· Edwards et al.
· 2010
[cited by applicant]
US 7919497B2
· Palladino et al.
· 2011
[cited by applicant]
US 7935704B2
· Palladino et al.
· 2011
[cited by applicant]
US 7943743B2
· Korman et al.
· 2011
[cited by applicant]
US 7956058B2
· Hayashi et al.
· 2011
[cited by applicant]
US 8008449B2
· Korman et al.
· 2011
[cited by applicant]
US 8129527B2
· Palladino et al.
· 2012
[cited by applicant]
US 8168757B2
· Finnefrock et al.
· 2012
[cited by applicant]
US 8217149B2
· Irving et al.
· 2012
[cited by applicant]
US 8247552B2
· Palladino et al.
· 2012
[cited by applicant]
US 8618292B2
· Palladino et al.
· 2013
[cited by applicant]
US 9358289B2
· Korman et al.
· 2016
[cited by applicant]
US 9394368B2
· Brogdon et al.
· 2016
[cited by applicant]
US 20020028819A1
· Teng et al.
· 2002
[cited by applicant]
US 20020143021A1
· Fukumoto et al.
· 2002
[cited by applicant]
US 20040176372A1
· Suto et al.
· 2004
[cited by applicant]
US 20060079534A1
· Kanzaki et al.
· 2006
[cited by applicant]
US 20060167010A1
· Hayashi et al.
· 2006
[cited by applicant]
US 20060223822A1
· Hayashi et al.
· 2006
[cited by applicant]
US 20070293453A1
· Fisher et al.
· 2007
[cited by applicant]
US 20080199485A1
· Kundig et al.
· 2008
[cited by applicant]
US 20080255035A1
· Trieu et al.
· 2008
[cited by applicant]
US 20090170837A1
· Gourdeau et al.
· 2009
[cited by applicant]
US 20120041070A1
· Shengfan et al.
· 2012
[cited by applicant]
US 20130131018A1
· Leblond et al.
· 2013
[cited by applicant]
US 20150202291A1
· Bosch et al.
· 2015
[cited by applicant]
US 20160243153A1
· Sundaram et al.
· 2016
[cited by applicant]
US 20180028531A1
· Huang et al.
· 2018
[cited by applicant]
US 20200129504A1
· Mohanlal et al.
· 2020
[cited by applicant]
US 20200281921A1
· Huang
· 2020
[cited by applicant]
US 20210030843A1
· Mohanlal
· 2021
[cited by applicant]
US 20210161888A1
· Huang et al.
· 2021
[cited by applicant]
US 20210177952A1
· Mohanlal et al.
· 2021
[cited by applicant]
US 20220387365A1
· He
· 2022
[cited by applicant]
US 20230035763A1
· Tonra
· 2023
[cited by applicant]
US 20230181605A1
· Mohanlal et al.
· 2023
[cited by applicant]
US 20240197723A1
· Huang
· 2024
[cited by applicant]
US 20240299377A1
· Mohanlal
· 2024
[cited by applicant]
US 20240368126A1
· He
· 2024
[cited by applicant]
US 20240408082A1
· Lloyd et al.
· 2024
[cited by applicant]
US 20240425485A1
· Huang
· 2024
[cited by applicant]
US 20250073230A1
· Huang et al.
· 2025
[cited by applicant]
CN 110240592
· 2017
[cited by applicant]
EA 010198B1
· 2008
[cited by applicant]
EA 016817B1
· 2012
[cited by applicant]
EP 0054924
· 1982
[cited by applicant]
EP 0655060
· 1998
[cited by applicant]
GB 2143823
· 1985
[cited by applicant]
JP 059164
· 1993
[cited by applicant]
JP 05255106
· 1993
[cited by applicant]
JP 10130266
· 1998
[cited by applicant]
JP 2002507612A
· 2002
[cited by applicant]
JP 2012144512
· 2012
[cited by applicant]
JP 2013501791
· 2013
[cited by applicant]
JP 2014508167
· 2014
[cited by applicant]
JP 2015030679
· 2015
[cited by applicant]
JP 2016516523
· 2016
[cited by applicant]
JP 2016518879
· 2016
[cited by applicant]
JP 2018036233
· 2018
[cited by applicant]
JP 2020189806
· 2020
[cited by applicant]
RU 2258702
· 2005
[cited by applicant]
RU 2011148945A
· 2010
[cited by applicant]
WO WO8705297
· 1987
[cited by applicant]
WO WO9407479
· 1994
[cited by applicant]
WO WO9506077
· 1995
[cited by applicant]
WO WO9521832
· 1995
[cited by applicant]
WO WO9620190
· 1996
[cited by applicant]
WO WO9938844
· 1999
[cited by applicant]
WO WO99048889
· 1999
[cited by applicant]
WO WO00012121
· 2000
[cited by applicant]
WO WO01053290
· 2001
[cited by applicant]
WO WO01070663
· 2001
[cited by applicant]
WO WO03074550
· 2003
[cited by applicant]
WO WO03097164
· 2003
[cited by applicant]
WO WO04016600
· 2004
[cited by applicant]
WO WO04054498
· 2004
[cited by applicant]
WO WO04093831
· 2004
[cited by applicant]
WO WO05077940
· 2005
[cited by applicant]
WO WO06121168
· 2006
[cited by applicant]
WO WO07035841
· 2007
[cited by applicant]
WO WO07113648
· 2007
[cited by applicant]
WO WO08128169
· 2008
[cited by applicant]
WO WO09064444
· 2009
[cited by applicant]
WO WO09089260
· 2009
[cited by applicant]
WO WO10001169
· 2010
[cited by applicant]
WO WO10083439
· 2010
[cited by applicant]
WO WO10101627
· 2010
[cited by applicant]
WO WO11034954
· 2011
[cited by applicant]
WO WO11050344
· 2011
[cited by applicant]
WO WO11066389
· 2011
[cited by applicant]
WO WO11079507
· 2011
[cited by applicant]
WO WO11109625
· 2011
[cited by applicant]
WO WO11146382
· 2011
[cited by applicant]
WO WO11151423
· 2011
[cited by applicant]
WO WO12014549
· 2012
[cited by applicant]
WO WO12035436
· 2012
[cited by applicant]
WO WO12074904
· 2012
[cited by applicant]
WO WO12145493
· 2012
[cited by applicant]
WO WO13078537
· 2013
[cited by applicant]
WO WO13090552
· 2013
[cited by applicant]
WO WO13177633
· 2013
[cited by applicant]
WO WO14036412
· 2014
[cited by applicant]
WO WO14066834
· 2014
[cited by applicant]
WO WO14130657
· 2014
[cited by applicant]
WO WO14160183
· 2014
[cited by applicant]
WO WO14183066
· 2014
[cited by applicant]
WO WO14195852
· 2014
[cited by applicant]
WO WO15069770
· 2015
[cited by applicant]
WO WO15069790
· 2015
[cited by applicant]
WO WO15160641
· 2015
[cited by applicant]
WO WO16081281
· 2016
[cited by applicant]
WO WO16165007
· 2016
[cited by applicant]
WO WO17062505
· 2017
[cited by applicant]
WO WO21225908
· 2021
[cited by applicant]
Hardin (Expert Opinion on Pharmacotherapy, 2017 vol. 18, No. 7, 701-716). (Year: 2017).
[cited by examiner]
Tagliamento (Expert Opinion on Investigational Drugs 2019, vol. 28, No. 6, 513-523) (Year: 2019).
[cited by examiner]
Washington (Nivolumab and Plinabulin in Treating Patients With Stage IIIB-IV, Recurrent, or Metastatic Non-small Cell Lung Cancer , NCT02846792, Last Updated Mar. 4, 2019, 1-6). (Year: 2019).
[cited by examiner]
“Definition of ‘within’”. [Online] [2015 Archived version accessed on Aug. 13, 2020 from https://web.archive.org/web/20151030162428/https://dictionary.cambridge.org/us/dictionary/english/within. Cambridge English Dictio…
[cited by applicant]
Abels, Christoph, Targeting of the Vascular System of Solid Tumours by Photodynamic Therapy (PDT), Photochem Photobiol Sci., (Mar. 2004) 3: 765-771.
[cited by applicant]
Abolhasani et al., Jan. 2015, In-silico investigation of tubulin binding modes of a series of novel antiproliferative spiroisoxazoline compounds using docking studies, Iranian Journal of Pharmaceutical Research, 14(1):1…
[cited by applicant]
Abstracts of The 1999 Joint Chubu and Kansai Branch Conference and Symposia of Japan Society for Bioscience, Biotechnology, and Agrochemistry, (1999) p. 48.
[cited by applicant]
Acquaviva et al., “Targeting KRAS-Mutant Non-Small Cell Lung Cancer with the Hsp90 Inhibitor Ganetespib”, Mol Cancer Ther, Dec. 2012, 11(12), pp. 2633-2643.
[cited by applicant]
Agarwal et al., “OP449, a Novel SET Antagonist, is Cytotoxic to Leukemia Cells and Enhances Efficacy of Tyrosine Kinase Inhibitors in Drug-Resistant Myeloid Leukemias,” pursuant to an EMBASE record for a Conference ABST…
[cited by applicant]
Aggarwal et al., Antiangiogenic agents in the management of non-small cell lung cancer: Where do we stand now and where are we headed? Cancer Biology & Therapy (2012), 13(5), 247-263.
[cited by applicant]
Ahmed et al. “A new rapid and simple non-radioactive assay to monitor and determine the proliferation of lymphocytes: an alternative to [
[cited by applicant]
Akerlund et al., “Diketopiperazine-Based Polymers from Common Amino Acids,” Journal of Applied Polymer Science, (2000) 78 (12), 2213-2218.
[cited by applicant]
Algaier et al. “The effects of dimethyl sulfoxide on the kinetics of tubulin assembly.” Biochim. Biophys. Acta. 954, 235-43 (1988).
[cited by applicant]
Ali et al. “Toxicity of echinulin from Aspergillus chevalieri in rabbits.” Toxicology Letters. (1989) 48:235-41.
[cited by applicant]
Asahina, T., “Spectrochemical Study of Amino-acid Anhydrides,” Bulletin of the Chemical Society of Japan, (1930) 5, 354-365.
[cited by applicant]
Augustin, M. “Die Umsetzung des 2,5-Diketopiperazins mit Aldehyden und Nitrosoverbindungen” Journal für Praktische Chemie, (1966) 32(4), 158-166.
[cited by applicant]
Aviel-Ronen et al., “K-ras Mutations in Non-Small-Cell Lung Carcinoma: A Review,”
[cited by applicant]
Bankowska et al., Derivatives of 1,2,3-triazole. Potential drugs?, Wiadomosci Chemiczne (2012), 66(11-12), 993-1022.
[cited by applicant]
Bauer et al., Jan. 15, 2010, Identification of markers of taxane sensitivity using proteomic and genomic analyses of breast tumors from patients receiving neoadjuvant paclitaxel and radiation, Clinical Cancer Research, …
[cited by applicant]
Bazhenova, Feb. 21, 2021, Nivolumab in Combination With Plinabulin in Patients With Metastatic Non-Small Cell Lung Cancer (NSCLC), ClinicalTrials.gov, NCT02812667 version 7.
[cited by applicant]
Beavis et al., “Dual PD-1 and CTLA-4 Checkpoint Blockade Promotes Antitumor Immune Responses through CD4
[cited by applicant]
Berenbaum, Jun. 1989, What is synergy?, Pharmacol. Rev., 41(2):93-141.
[cited by applicant]
Bergman et al., Ariloxy Substituted N-arylpiperazinones as Dual Inhibitors of Farnesyltransferase and Geranylgeranyltransferase-1, Bioorg & Med Chem Lttrs. (Mar. 2001) 11: 1411-1415.
[cited by applicant]
Bertelsen et al., “Vascular effects of plinabulin (NPI-2358) and the influence on tumour response when given alone or combined with radiation,” International Journal of Radiation Biology (2011), 87(11), 1126-1134.
[cited by applicant]
Bertino J., et al., “Principles of Cancer Therapy.” Cecil Textbook of Medicine. Eds. Lee Goldman, et al. 21nd ed., (2000), Chapter 198, pp. 1060-1074.
[cited by applicant]
Bigioni et al., Sep. 2008, Antitumour effect of combination treatment with Sabarubicin (MEN 10755) and cis-platin (DDP) in human lung tumour xenograft, Cancer Chemother. Pharmacol., 62(4):621-629.
[cited by applicant]
Blankenstein et al., Mar. 1, 2012, The determinants of tumour immunogenicity, Nat. Rev. Cancer, 12(4):307-313.
[cited by applicant]
Blayney et al., “Plinabulin, a Novel Small Molecule That Ameliorates Chemotherapy-Induced Neutropenia, is Administered on the Same Day of Chemotherapy and Has Anticancer Efficacy”, Meeting Info.: 58th Annual Meeting and…
[cited by applicant]
Bond et al. “The Synthesis of Viridamine, a Penicillium Viridicatum Mycotoxin.” Synthetic Commun. 19 (13&14), 2551-2566 (1989).
[cited by applicant]
Borisy, G.G. “A Rapid Method for Quantitative Determination of Microtubule Protein using DEAE-Cellulose Filters.” Anal. Biochem. 50, 373-385 (1972).
[cited by applicant]
Braga et al. “Crystal Polymorphism and Multiple Crystal Forms,” Struct Bond (2009) 132:25-50.
[cited by applicant]
Brahmer et al., “Safety and Activity of Anti-PD-L1 Antibody in Patients with Advanced Cancer,” N Engl J Med (2012) 366:2455-2465.
[cited by applicant]
Buchbinder et al., Feb. 2016, CTLA-4 and PD-1 pathways: similarities, differences, and implications of their inhibition, American Journal of Clinical Oncology, 39(1):98-106.
[cited by applicant]
Burtles, Sally, “Transition from Preclinical to first-in-man Phase”, Expert Scientific Group on Phase One Clinical Trials Final Report, Presentation Jun. 19, 2006, pp. 35-38.
[cited by applicant]
Cai, Small molecule vascular disrupting agents: potential new drugs for cancer treatment, a 2009 update, Frontiers in Anti-Cancer Drug Discovery (2010), 1, 380-427.
[cited by applicant]
Cai, Sui X., “Small Molecule Vascular Disrupting Agents: Potential New Drugs for Cancer Treatment”, Recent Pat Anticancer Drug Discov. (2007) 2(1): 79-101.
[cited by applicant]
Caira, 1998, Crystalline polymorphism of organic compounds, Topics in Current Chemistry, 198:163-208.
[cited by applicant]
Callahan et al., “At the Bedside: CTLA-4- and PD-1-blocking antibodies in cancer immunotherapy”, J Leukocyte Biol, vol. 94, Jul. 2013, pp. 41-53.
[cited by applicant]
Carter et al., “No patient left behind: The promise of immune priming with epigenetic agents,” Oncoimmunology (2017) vol. 6, No. 10, e1315486 (13 pages).
[cited by applicant]
Champiat et al., Feb. 2014, Incorporating immune-checkpoint inhibitors into systemic therapy of NSCLC, J. Thorac. Oneal., 9(2):144-153.
[cited by applicant]
Chang et al., 1998, Changing residue 338 in human factor IX from arninine to alanine causes an increase in catalytic activity, J. Biol. Chem., 272(9):4929-4936.
[cited by applicant]
Chaplin et al., “Antivascular approaches to solid tumour therapy: evaluation of tubulin binding agents”, Br. J. Cancer 1996, 74 (Suppl. XXVII), S86-S88.
[cited by applicant]
Chen et al., “Adjuvant effect of docetaxel on the immune responses to influenza A H1N1 vaccine in mice,” BMC Immunology (2012) 13:36, pp. 1-12.
[cited by applicant]
Chin et al., “Immune Intervention with Monoclonal Antibodies Targeting CD152 (CTLA-4) for Autoimmune and Malignant Diseases,” Chang Gung Med J (Jan.-Feb. 2008) vol. 31, No. 1, pp. 1-15.
[cited by applicant]
Clezardin et al., Jan. 1, 2011, Bisphosphonates' antitumor activity: an unravelled side of a multifacted drug class, Bone, 48(1):71-79.
[cited by applicant]
ClinicalTrials.gov Identifier NCT00892931, “Phase 2 study MPC-6827 for recurrent glioblastoma multiforme,” (Oct. 14, 2011). [retrieved from internet on Jul. 30, 2019] <URL: https://clinicaltrials.gov/ct2/show/NCT0089293…
[cited by applicant]
ClinicalTrials.gov Identifier NCT02846792, “Nivolumab and Plinabulin in Treating Patients With Stage IIIB-IV, Recurrent, or Metastatic Non-small Cell Lung Cancer,” (Jul. 27, 2016). [retrieved from internet on Sep. 17, 2…
[cited by applicant]
ClinicalTrials.gov Identifier NCT03294577, “Plinabulin vs. pegfilgrastim in prevention of TAC induced neutropenia” (Sep. 27, 2107). <URL:ttps://clinicaltrials.gov/ct2/show/NCT3294577> 4 pp.
[cited by applicant]
Clinicaltrials.gov, NCT00151073, Estramustine, docetaxel and zoledronate treatment in hormone-refractory adenocarcinoma of the prostate, https//clinicaltrials.gov/ct2/show/NCT00151073?term=zoledronate%2C+tubulin&draw=2&…
[cited by applicant]
Cole, P., “Durvalumab, Human anti-PD-L1 monoclonal antibody Immune checkpoint inhibitor Oncolytic”, Drugs of the Future 2014, 39(12): pp. 843-847.
[cited by applicant]
Collins et al., 2014, Lipid tucaresol as an adjuvant for methamphetamine vaccine development, CHemComm, 50:4079-4081.
[cited by applicant]
Cooper et al., “Response to BRAF Inhibition in Melanoma is Enhanced When Combined with Immune Checkpoint Blockade,” Published OnlineFirst Apr. 29, 2014; DOI: 10.1158/2326-6066.CIR-13-0215; Cancer Immunol Res (Jul. 2014)…
[cited by applicant]
Costa et al., “Analyses of selected safety endpoints in phase 1 and late-phase clinical trials of anti-PD-1 and PD-L1 inhibitors: prediction of immune-related toxicities,” Oncotarget (2017) vol. 8, No. 40, pp. 67782-677…
[cited by applicant]
Crawford, Aug. 2003, Once-per-cycle pegilgrastim (neulata) for the management of chemotherapy-induced neutropenia, Seminars in Oncology 30(4)Suppl 13:23-30.
[cited by applicant]
Cui et al. “Novel Mammalian Cell Cycle Inhibitors, Tryprostatins A, B and Other Diketopiperazines Produced by Aspergillus fumigatus.” J. Antibiotics. 49(6), 534-40 (1996).
[cited by applicant]
Cui et al. “Novel Mammalian Cell Cycle Inhibitors, Tryprostatins A, B and Other Diketopiperazines Produced by Aspergillus fumigatus.” J. Antibiotics. 49(6): 527-33 (1996).
[cited by applicant]
Dale, Oct. 2015, Neutropenia, John Wiley & Sons Ltd., www.els.net, 8 pp.
[cited by applicant]
Dalgleish, 2015, Rationale for combining immunotherapy with chemotherapy, Immunotherapy, 7(3):309-316.
[cited by applicant]
Das et al., Feb. 1, 2015, Combination therapy with anti-CLTA4 and antiPD1 leads to distinct immunologic changes in-vivo, J. Immunolog, 194(3):950-959.
[cited by applicant]
Davies, Feb. 3, 2014, New modalities of cancer treatment for NSCLC: focus on immunotherapy, Cancer Manag. Res., 6:63-75.
[cited by applicant]
Davis et al., ZD6126: A Novel Vascular-targeting Agent That Causes Selective Destruction of Tumor Vasculature, Cancer Research (Dec. 15, 2002) 62: 7247-7253.
[cited by applicant]
Dennis, Aug. 17, 2006, Off by a whisker, Nature, 442:739-741.
[cited by applicant]
Dorwald, F., “Side Reactions in Organic Synthesis” Wiley-VCH Verlag Gmbh & Co. KgaA, Weinheim, (2005), book cover and preface p. IX only.
[cited by applicant]
Drug Approval and Licensing Procedures in Japan 2001, 2001, pp. 243-244.
[cited by applicant]
Du et al., Jul. 2018, docetaxel increases the risk of severe infections in the treatment of non-small cell lung cancer: a meta-analysis, Oncosciene, 5(7-8):220-238.
[cited by applicant]
Duarte et al., 2022, Evaluation of synergism in drug combinations and reference models for future orientations in oncology, Curr. Res. Pharmacol. Drug Discov., 3:100110; pp. 1-13.
[cited by applicant]
Dunitz et al., “Disappearing Polymorphs,” Acc. Chem. Res. (1995) vol. 28, No. 4, pp. 193-200.
[cited by applicant]
Dyson, Feb. 16, 2017, 4 Clinical Pearls for Granulocyte Colony Stimulating Factors (G-CSFs), Pharmacy Times, retrieved from the internet at URL <https://www.pharmacytimes.com/view/4-clinical-pearls-for-granulocyte-colon…
[cited by applicant]
El-Kenawi et al., Oct. 2013, Angiogenesis inhibitors in cancer therapy: mechanistic perspective on classification and treatment rationales, Br. J. Pharmacol., 170(4):712-729.
[cited by applicant]
Elliott et al., Oct. 15, 1989, Sequence and schedule-dependent synergy of trimetrexate in combination with 5-fluorouracil in vitro and in mice, Cancer Res., 49(20):5586-5590.
[cited by applicant]
Fan et al., 2021, Immunotherapy in colorectal cancer; current achievements and future perspective, Int. J. Biol. Sci., 17(14):3837-3849.
[cited by applicant]
Fernandez-Medarde et al., Mar. 2011, Ras in cancer and developmental diseases, Genes & Cancer, 2(3):344-358.
[cited by applicant]
Fernandez-Tejada et al., 2014, Design, synthesis, and immunologic evaluation of vaccine adjuvant conjugates based on QS-21 and tucaresol, Bioorganic & Medicinal Chemistry, 22:5917-5923.
[cited by applicant]
Fernandez-Tejada et al., 2016, Development of improved vaccine adjuvants based on the saponin natural product QS-21 through chemical synthesis, Accounts of Chemical Research 49:1741-1756.
[cited by applicant]
Ferrer et al., Plinabulin: tubulin polymerization inhibitor vascular-disrupting agent oncolytic, Drugs of the Future (2010), 35(1), 11-15.
[cited by applicant]
Fessas et al., 2017, A molecular and preclinical comparsion of the PC-1-targeted t-cell checkpoint inhibitors nivolumab and mebrolizumag, Seminars in Oncology, 44:136-140.
[cited by applicant]
Field et al., 2014, Microtubule-targeting agents are clinically successful due to both mitotic and interphase impairment of microtubule function, Bioorganic & Medicinal Chemistry, 22:5050-5059.
[cited by applicant]
Flanigan et al., Jan. 7, 2011, Melanoma brain metasteses: is it time ro reassess the bias?, Current Problems in Cancer, 35(4):200-210.
[cited by applicant]
Folkes et al., Synthesis and In Vitro Evaluation of a Series of Diketopiperazine Inhibitors of Plasminogen Activator Inhibitor-1, Bioorg & Med Chem Lttrs., (Jul. 2001) 11: 2589-2592.
[cited by applicant]
Folkman, Dec. 2002, Role of angiogenesis in tumor growth and metastasis, Semin Oncol, 29:15-18.
[cited by applicant]
Friedman et al., 2000, Schedule-dependent activity of irinotecan plus BCNU against malignant glioma xenografts, Cancer Chemother. Pharmacol., 45(4):345-349.
[cited by applicant]
Frost et al., Novel Syngeneic Pseudo-orthotopic Prostate Cancer Model: Vascular, Mitotic and Apoptotic Responses to Castration, Microvasc Research (Dec. 2004) 69: 1-9.
[cited by applicant]
Fukushima et al., “Biological Activities of Albonoursin,” J. Antibiotics, (1973) 26:175.
[cited by applicant]
Gallina et al., “Condensation of 1,4-diacetylpiperazine-2,5-dione with aldehydes”, Tetrahedron 1974, 30, 667-673.
[cited by applicant]
Gameiro et al., “Exploitation of differential homeostatic proliferation of T-cell subsets following chemotherapy to enhance the efficacy of vaccine-mediated antitumor responses,” Cancer Immunology Immunotherapy (2011) v…
[cited by applicant]
Garcia-Fuente et al., 2018, CISNA: an accurate description of dose-effect and synergism in combination therapies, Sci. Rep., 8:4964; pp. 1-9.
[cited by applicant]
Garris et al., “Successful Anti-PD-1 Cancer Immunotherapy Requires T Cell-Dendritic Cell Crosstalk Involving the Cytokines IFN-( and IL-12,” Immunity (Dec. 18, 2018) 49, pp. 1-14, e1-e7 (22 pages).
[cited by applicant]
Glisson et al., 2002, Phase II trial of docetaxel and cisplatin combination chemotherapy in patients with squamous cell carcinoma of the head and neck, Journal of Clinical Oncology 20:1593-1599.
[cited by applicant]
Goldani et al. “Treatment of murine pulmonary mucormycosis with SCH 42427, a broad-spectrum triazole antifungal drug”, Correspondence, J Antimicrob Chemother. 33, 369-372 (1994).
[cited by applicant]
Goldfarb et al., “Synthesis of β-2-thienylalanine,” Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, (1958) 98-100, as abstracted by CAPLUS.
[cited by applicant]
Gordon et al. “Reductive Alkylation on a Solid Phase: Synthesis of a Piperazinedione Combinatorial Library.” J. Bioorg. Med. Chem. Letters. 5, 47-50 (1995).
[cited by applicant]
Granville et al., Release of Cytochrome c1 Bax Migration, Bid Cleavage, and Activation of Caspases 2, 3, 6, 7, 8, and 9 during Endothelial Cell Apoptosis, Am J Path., (Oct. 1999) 155(4):1021-1025.
[cited by applicant]
Gridelli et al., Vascular disrupting agents: a novel mechanism of action in the battle against non-small cell lung cancer, Oncologist (2009), 14(6), 612-620.
[cited by applicant]
Gu et al., “Identification of CTLA-4 isoforms produced by alternative splicing and their association with myasthenia gravis,” Clinical Immunology (Sep. 2008) vol. 128, Issue 3, pp. 374-381.
[cited by applicant]
Gura, Trisha, “Cancer Models: Systems for Identifying New Drugs are Often Faulty”, Science 7(Nov. 1997) 278(5340): 1041-1042.
[cited by applicant]
Hamel, E. “Antimitotic Natural Products and Their Interactions with Tubulin.” Med. Res. Rev. (1996) 16(2): 207-31.
[cited by applicant]
Hartwell et al. “Checkpoints: Controls that Ensure the Order of Cell Cycle Events.” Science. 246, 629-34 (1989).
[cited by applicant]
Hayakawa, Structure-activity relationship analysis, Japanese Journal of Cancer and Chemotherapy, (2004), 31(4):526-528.
[cited by applicant]
Hayashi et al., “Total Synthesis of Anti-microtubule Diketopiperazine Derivatives: Phenylahistin and Aurantiamine,” J. Org. Chem., (2000) 65: 8402-8405.
[cited by applicant]
Hayashi et al., Medicinal chemistry and chemical biology of diketopiperazine-type antimicrotubule and vascular-disrupting agents, Chemical & Pharmaceutical Bulletin (2013), 61(9), 889-901.
[cited by applicant]
Hayashi et al., Small peptide-based medicinal chemistry for intractable disease, Peptide Science (2009), Volume Date 2008, 45th, 139-140.
[cited by applicant]
He et al., “Low-dose paclitaxel enhances the anti-tumor efficacy of GM-CSF surface-modified whole-tumor-cell vaccine in mouse model of prostate cancer,” Cancer Immunology Immunotherapy (2011) vol. 60, No. 5, pp. 715-730…
[cited by applicant]
Heist et al., “Abstract C30: Phase 1/2 study of the vascular disrupting agent (VCA) plinabulin (NPI-2358) combined with docetaxel in patients with non-small cell lung cancer (NSCLC),”
[cited by applicant]
Heist et al., “Randomized Phase 2 Trial of Plinabulin (NPI-2358) Plus Docetaxel in Patients with Advanced Non-Small Lung Cancer (NSCLC),” 2014 ASCO Annual Meeting. . . (abstr 8054) Poster Presentation. Retrieved from th…
[cited by applicant]
Helleman et al. “The International Journal of Biochemistry & Cell Biology,” vol. 42, pp. 25-30 (2010).
[cited by applicant]
Hellmann et al., May 31, 2018, Nivolumab plus ipilimumab in lung cancer with a high tumor mutational burden, N. Engl. J. Med., 378(22):2093-2104.
[cited by applicant]
Hellmann et al., Nov. 21, 2019, Nivolumab plus ipilimumab in advanced non-small-cell lung cancer, The New England Journal of Medicine, 381:2020-2031.
[cited by applicant]
Hodi et al., Nov. 2016, Combined nivolumab and ipilimumab versus ipilimumab alone in patients with advanced melanoma: 2-year overall survival outcomes in a multicentre, randomised, controlled, phase 2 trial, Lancet Onco…
[cited by applicant]
Horak et al. “Structures of the Austalides A-E, Five Novel Toxic Metabolites from Aspergillus ustus.” J Chem Soc Chem Commun. (1981) 1265-67.
[cited by applicant]
Http://scienceandresearch.homeoffice.gov.uk/animal-research/publications-and-reference/001-abstracts/abstracts2-2006/02november-2006/457?view=Html; “Abstract #457, Animals in Scientific Procedures (2006)”; (accessed on …
[cited by applicant]
Hursthouse et al., “Why Do Organic Compounds Crystallise Well or Badly or Ever so Slowly? Why is Crystallisation Nevertheless Such a Good Purification Technique?,” Organic Process Res & Devel (2009) vol. 13, No. 6, pp. …
[cited by applicant]
Hwang et al., 2019, Heat shock proteins: a dual carrier-adjuvant for an anti-drug vaccine against heroin, Bioorganic & Medicinal Chemistry, 27:125-132.
[cited by applicant]
Hyun et al., “Valine dehydrogenase from Streptomyces albus: gene cloning, heterologous expression and identification of active site by site-directed mutagenesis,” FEMS Microbiology Letters (Jan. 1, 2000) 182: 29-34.
[cited by applicant]
Intlekofer et al., Jul. 2013, At the bench: preclinical rationale for CTLA-4 and PD-1 blockade as cancer immunotherapy, J. Leukoc Biol., 94(1):25-39.
[cited by applicant]
Ishibashi et al., Sep. 1989, Interleukin-6 is a potent thrombopoietic factor in vivo in mice, Blood, 74(4):1241-1244.
[cited by applicant]
Iwasaki, S. “Antimitotic Agents: Chemistry and Recognition of Tubulin Molecule.” Med Res Rev. (1993) 13: 183-198.
[cited by applicant]
Iwasaki, S. “Bioactive Natural Products Interfering with Microtubule Function.” Kagaku to Seibutsu. 32(3): 153-159 (1994).
[cited by applicant]
Januchowski et al., Jan. 2014, Microarray-based detection and expression analysis of extracellular matrix proteins in drug-resistant ovarian cancer cell lines, Oncology Reports, 32:1981-1990.
[cited by applicant]
Ji et al., Tubulin Colchicine Binding Site Inhibitors as Vascular Disrupting Agents in Clinical Developments, Current Medicinal Chemistry (2015), 22(11), 1348-1360.
[cited by applicant]
Jiang et al., “A Novel Peptide Isolated from a Phage Display Peptide Library with Trastuzumab Can Mimic Antigen Epitope of HER-2*,” (Feb. 11, 2005) J Biol Chem, vol. 280, No. 6, pp. 4656-4662.
[cited by applicant]
Jin et al., Feb. 28, 2022, Different syngeneic tumors show distinctive intrinsic tumor-immunity and mechanisms of actions (MOA) of anti-PD-1 treatment, Sci. Rep., 12: 3278, pp. 1-18.
[cited by applicant]
Johnson et al. “Kinetic Analysis of Microtubule Self-assembly in Vitro.” J. Mol. Biol. 117, 1-31 (1977).
[cited by applicant]
Jure-Kunkel M. et al., “Synergy between chemotherapeutic agents and CTLA-4 blockade in preclinical tumor models”, Cancer Immunol. Immunother. 2013, vol. 62, pp. 1533-1545.
[cited by applicant]
Kakoulidou et al., “Human Soluble CD80 is Generated by Alternative Splicing, and Recombinant Soluble CD80 Binds to CD28 and CD152 Influencing T-cell Activation,” Scandinavian J. Immunol (Nov. 2007) 66(5):529-537.
[cited by applicant]
Kamb, Alexander, “What's wrong with our cancer models?”, Nature Reviews Drug Discovery (Feb. 2005) 4: 161-165.
[cited by applicant]
Kanoh et al., “(−)- Phenylahistin: A New Mammalian Cell Cycle Inhibitor Produced by Aspergillus USTUS,” Bioorganic & Medicinal Chemistry Letters, (1997) 7: 2847-2852.
[cited by applicant]
Kanoh et al., “(−)-Phenylahistin Arrests Cells in Mitosis by Inhibiting Tubulin Polymerization,” The Journal of Antibiotics, (1999) 52: 134-141.
[cited by applicant]
Kanoh et al., “Antitumor Activity of Phenylahistin in Vitro and in Vivo,” Bioscience Biotechnology Biochemistry, (1999) 63(6): 1130-1133.
[cited by applicant]
Kanoh et al., “Synthesis and Biological Activities of Phenylahistin Derivatives,” Bioorganic & Medicinal Chemistry, (1999) 7: 1451-1457.
[cited by applicant]
Kanojia et al., May 2015, βIII-tubulin regulates breast cancer meastases to the brain, Mol Cancer Ther., 14(5):1152-1161.
[cited by applicant]
Kanthou et al., Microtubule depolymerizing vascular disrupting agents: novel therapeutic agents for oncology and other pathologies, International Journal of Experimental Pathology(2009), 90(3), 284-294.
[cited by applicant]
Kanzaki et al., A Novel Potent Cell Cycle Inhibitor Dehydrophenylahistin-Enzymatic Synthesis and Inhibitory Activity toward Sea Urchin Embryo, The Journal of Antibiotics, (Dec. 2002) 55(12):1042-1047.
[cited by applicant]
Kanzaki et al., “Effective Production of Dehydro Cyclic Dipeptide Albonoursin Exhibiting Pronuclear Fusion Inhibitory Activity, I. Taxonomy and Fermentation,” The Journal of Antibiotics, (1999) 52: 1017-1022.
[cited by applicant]
Kanzaki et al., “Effective Production of Dehydro Cyclic Dipeptide Albonoursin Exhibiting Pronuclear Fusion Inhibitory Activity, II. Biosynthetic and Bioconversion Studies,” The Journal of Antibiotics, (2000) 53(1): 58-6…
[cited by applicant]
Kanzaki et al., “Enzymatic dehydrogenation of cyclo(L-Phe-L-Leu) to a bioactive derivative, albonoursin,” Journal of Molecular Catalysis B: Enzymatic (1999) 6(3): 265-270.
[cited by applicant]
Kanzaki et al., “Enzymatic Synthesis of Physiologically Active Substances Utilizing a Novel System for the Synthesis of Diketopiperazines Comprising Dehydroamino Acids as Constituents,” Abstracts of Papers Presented at …
[cited by applicant]
Kanzaki et al., “Novel Cyclic Dipeptide Dehydrogenase and Assay Method for Its Activity,” Scientific Reports of the Faculty of Agriculture, Okayama University, (1999) 88: 7-11.
[cited by applicant]
Kashyap et al., Sep. 24, 2019, GEF-H1 signaling upon microtubule destabilization is required for dendritic cell activation and specific anti-tumor responses, Cell Reports, 28:3367-3380.
[cited by applicant]
Keepers et al. “Comparison of the Sulforhodamine B Protein and Tetrazolium (MTT) Assays for in vitro Chemosensitivity Testing.” Eur. J. Cancer. 27, 897-900 (1991).
[cited by applicant]
Kim et al. “Polymer attached cyclic peptides, tetrahedron: Asymmetry.” 3(11):1421-1430 (1992).
[cited by applicant]
Kingston, Correction to Tubulin-interactive natural products as anticancer agents, Journal of Natural Products (2011), 74(5), 1352.
[cited by applicant]
Kingston, Tubulin-Interactive Natural Products as Anticancer Agents, Journal of Natural Products (2009), 72(3), 507-515.
[cited by applicant]
Kobayashi et al., “Microtubule Assembly Regulators of Microbial Origin,” Abstract of Paper Read at the 1989 Symposium on the Chemistry of Natural Products, (1989) 51.
[cited by applicant]
Kola et al., “Can the pharmaceutical industry reduce attrition rates?”, Nature Reviews Drug Discovery (2004) 3: 711-715.
[cited by applicant]
Kondoh et al. “Effects of Tryprostatin Derivatives on Microtubule Assembly In Viro and In Situ.” J. Antibiotics. 51, 801-04 (1998).
[cited by applicant]
Kopple et al., “A Convenient Synthesis of 2,5-Piperazinediones1a,” The Journal of Organic Chemistry, (1967) 33: 862-864.
[cited by applicant]
Kreamer K., “Immune checkpoint blockade: A New Paradigm in Treating Advanced Cancer”, J. Adv. Pract. Oncol., 2014, vol. 5, pp. 418-431.
[cited by applicant]
Krendel et al., Apr. 2002, Nucelotide exchange factor GEF-H1 mediates cross-talk between microtubules and the actin cytoskeleton, Nature Cell Biology, 4:294-301 and supplementary information.
[cited by applicant]
Krishan, A. “Rapid Flow Cytofluorometric Analysis of Mammalian Cell Cycle by Propidium Iodide Staining.” J. Cell Biol. 66, 188-193 (1975).
[cited by applicant]
Kupchan et al. “Steganacin and Steganangin, Novel Antileukemic Lignan Lactones from Steganotaenia araliacea 1-3.” J. Am. Chem. Soc. (1973) 95(4): 1335-36.
[cited by applicant]
Küster & Koeppenhöfer, “Über eininge Pyrrolderivate,” Z. Physiol, Chem., (1927) 172:126-137.
[cited by applicant]
Kwon et al., Apr. 2013, Mouse models for lung cancer, Mol. Oneal., 7(2):165-177.
[cited by applicant]
La-Beck, 2021, Repurposing amino-bisphosphonates by liposome formulation for a new reole in cancer treatment, Seminars in Cancer Biology, 68:175-185.
[cited by applicant]
Lacey et al. “Interaction of Phomopsin A and Related Compounds with Purified Sheep Brain Tubulin.” Biochem. Pharmacol. 36, 2133-38 (1987).
[cited by applicant]
Laemmli, U.K. “Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4.” Nature. 227, 680-85 (1970).
[cited by applicant]
Larsen et al. “Aurantiamine, A Kiketopiperazine from Two Varieties of Penicillium Aurantiogriseum.” Phytochemistry. 31, 1613-1615 (1992).
[cited by applicant]
Leaf, Clifton, “Why are we losing the war on cancer (and how to win it)?”, Health Administrator (2005) XVII(1): 172-183.
[cited by applicant]
Lee et al. “The Reconstitution of Microtubules from Purified Calf Brain Tubulin.” Biochemistr. 14(23), 5183-87 (1975).
[cited by applicant]
Lee et al., “A practical guide to pharmaceutical polymorph screening & selection,” Asian Journal of Pharmaceutical Sciences (2014) vol. 9, pp. 163-175.
[cited by applicant]
Lee et al., Colchicine site inhibitors of microtubule integrity as vascular disrupting agents, Drug Development Research (2008), 69(6), 352-358.
[cited by applicant]
Li et al., May-Jun. 2017, Epitope mapping reveals the binding mechanism of a functional antibody cross-reactive to both human and murine programmed death 1, MABS, 9(4):628-637.
[cited by applicant]
Li, Y., et al. “Interaction of marine toxin dolastatin 10 with porcine brain tubulin: competitive inhibition of rhizoxin and phomopsin A binding.” Chem. Biol. Interact. 93, 175-83 (1994).
[cited by applicant]
Liao et al., “Design and synthesis of novel soluble 2,5-diketopiperazine derivatives as potential anticancer agents,” European J Med Chem (2014) 83:236-244.
[cited by applicant]
Liou et al., Aug. 12, 2004, Concise synthesis and structure-activity relationships of combretastatin A-4 analogues, 1-aroylindoles and 3-aroylindoles, as novel classes of potent antitubulin agents, Journal of Medicial C…
[cited by applicant]
Liu et al., “The BRAF and MEK Inhibitors Dabrafenib and Trametinib: Effects on Immune Function and in Combination with Immunomodulatory Antibodies Targeting PD-1, PD-L1, and CTLA-4,” Clin Cancer Res (2015) 21(7) 1639-16…
[cited by applicant]
Liu et al., Dec. 31, 2019, Spectrum of EGFR aberrations and potential clinical implications, insights from integrative pan-cancer analysis, Cancer Communications, 40(1):43-59.
[cited by applicant]
Liwo et al. “Origin of the Ring-Ring Interaction in Cyclic Dipeptides Incorporating an Aromatic Amino Acid.” Tetrahedron Lett. 26, 1873-1876 (1985).
[cited by applicant]
Lloyd et al. Dec. 2003, NPI-2358 and 2386: two new vascular/tubulin modifying agents greatly potentiate standard chemotherapy in xenograft models, Clin. Cancer Res., 9 6153s; Abstract #B59, 1 p.
[cited by applicant]
Lloyd et al., 2015, Abstract A184: Activity of plinabulin in tumor models with kras mutations, Mol. Can. Thera. 14(12):Suppl. 2.
[cited by applicant]
Lloyd et al., Abstract A07: Plinabulin: Evidence for an immune-mediated mechanism of action, In: Proceedings of the AACR Special Conference: Function of Tumor Microenvironment in Cancer Progression; Jan. 7-10, 2016; San…
[cited by applicant]
Lu et al., Nov. 2012, An overview of tubulin inhibitors that interact with the colchicine binding site, Pharmaceutical Research, 29(11):2943-2971.
[cited by applicant]
Luduena, R.F. “Contrasting Roles of Tau and Microtubule-associated Protein 2 in the Vinblastine-induced Aggregation of Brain Tubulin.” J. Biol. Chem. 259:12890-98 (1984).
[cited by applicant]
Lyman et al., “Risk Models for Predicting Chemotherapy-Induced Neutropenia,” The Oncologist (2005) 10:427-437.
[cited by applicant]
Lyman, 2011, Neutropenia, Encyclopedia of Cancer, pp. 2506-2509.
[cited by applicant]
Lynch et al., “Ipilimumab in Combination With Paclitaxel and Carboplatin as First-Line Treatment in Stage IIIB/IV Non-Small-Cell Lung Cancer: Results From a Randomized, Double-Blind, Multicenter Phase II Study,” (Jun. 1…
[cited by applicant]
Mahindroo et al., “Antitubulin Agents for the Treatment of Cancer—A Medicinal Chemistry Update”, Expert Opin. Ther. Patents (2006) 16(5): 647-691.
[cited by applicant]
Mahoney et al., “The Next Immune-Checkpoint Inhibitors: PD-1/PD-L1 Blockade in Melanoma,” Clinical Therapeutics (Apr. 2015) vol. 37, Issue 4, pp. 764-782. Abstract.
[cited by applicant]
Malhotra, J., “A Phase I/II Study of Nivolumab, Ipilimumab and Plinabulin in Patients With Recurrent Small Cell Lung Cancer”, ClinicalTrials.gov, NCT03575793 version 9, Apr. 15, 2020, <URL: https://clinicaltrials.gov/ct…
[cited by applicant]
Malhotra, J., Abstract 8570: “A phase I trial of plinabulin in combination with nivolumab and ipilimumab in patients with relapsed small cell lung cancer (SCLC): Big Ten Cancer Research Consortium (BTCRC-LUN17-127) stud…
[cited by applicant]
Martin et al., Sep. 2014, The microtubule-depolymerizing agent ansamitocin P3 programs dendritic cells toward enhanced anti-tumor immunity, Cancer Immunol. Immunother., 63(9):925-938.
[cited by applicant]
Massarelli et al., Feb. 2014, Immunotherapy in lung cancer, Transl. Lung Cancer Res., 3(1):53-63.
[cited by applicant]
Matsuda et al., “Pilot study of WT1 peptide-pulsed dendritic cell vaccination with docetaxel in esophageal cancer,” Oncology Letters (Jul. 2018) vol. 16, No. 1, pp. 1348-1356.
[cited by applicant]
Mazza et al., 2017, Treating EGFR mutation resistance in non-small cell lung cancer—role of osimertinib, The Application of Clinical Genetics, 10:49-56.
[cited by applicant]
Melero et al., Aug. 2015, Evolving synergistic combinations of targeted immunotherapies to combat cancer, Nature Reviews Cancer, 15:457-472.
[cited by applicant]
Millward et al., “Phase I trial of NPI-2358 (a novel vascular disrupting agent) plus docetaxel,” J. Clin. Oncol. (May 2009) 27(15S): 3571-3571, Abstract.
[cited by applicant]
Millward et al., “Phase 1 study of the novel vascular disrupting agent plinabulin (NPI-2358) and docetaxel,” The Journal of New Anticancer Agents, vol. 3, No. 30, Feb. 16, 2011 plinabulin (NPI-2358) and docetaxel, Inves…
[cited by applicant]
Mita et al., “Phase 1 First-in-Human Trial of the Vascular Disrupting Agent Plinabulin (NPI-2358) in Patients with Solid Tumors or Lymphomas,” Clinical Cancer Research (2010), 16(23), 5892-5899.
[cited by applicant]
Mita et al., “Phase II study of docetaxel with or without plinabulin (NPI-2358) in patients with non-small cell lung cancer (NSCLC)”,
[cited by applicant]
Mita et al., Randomized Phase 2 Study of Docetaxel +/− Plinabulin (NPI-2358) in Patients with Non-Small Cell Lung Cancer (NSCLC),
[cited by applicant]
Mitsudomi et al., “Mutations of ras genes distinguish a subset of non-small-cell lung cancer cell lines from small-cell lung cancer cell lines,”
[cited by applicant]
Mizumoto et al., Nov. 1, 2005, Discovery of novel immunostimulants by dendritic-cell-based functional screening, Blood, 106(9):3082-3089.
[cited by applicant]
Mohanlal et al., “The plinabulin/docetaxel combination to mitigate the known safety concerns of docetaxel,” J Clin Oncol (2016) 34(15_suppl), Abstract e20595.
[cited by applicant]
Mohanlal et al., Feb. 10, 2018, Plinabulin, a novel small molecule clinical stage 10 agent with anti-cancer activity, to prevent chemo-induced neutropenia and immune related AEs, Journal of Clinical Oncology, 36(5 Suppl…
[cited by applicant]
Mohanlal et al., Mar. 1, 2017, Plinabulin as a novel small molecule clinical stage immuno-oncology agent for NSCLC, Journal of Clinical Oncology, 35(7), Supplement 1, Abstract 139.
[cited by applicant]
Muguruma et al., 2016, Novel Hybrid Compound of a Plinabulin Prodrug with an IgG Binding Peptide for Generating a Tumor Selective Noncovalent-Type Antibody-Drug Conjugate; Bioconjugate Chem. 27(7):1606-1613.
[cited by applicant]
Muguruma et al., OP-20: “Application of Fc-selective Z33-peptide to the preparation of non-covalent-type antibody-antimocrotubule plinabulin conjugate,” 34th European Peptide Symposium 2016 & 8th International Peptide S…
[cited by applicant]
Muller et al., 2014, Cancer chemotherapy agents target intratumoral dendritic cells to potentiate antitumor immunity, Oncoimmunology, 3(8):e954460; 4 pp.
[cited by applicant]
Nabholz, 2001, Phase II study of docetaxel, doxorubiin, and cyclophosphamide as first-line chemotherapy for metastatic breast cancer, Journal of Clinical Oncology, 19:314-321.
[cited by applicant]
Nagaria et al., “Flavopiridol Synergizes with Sorafenib to Induce Cytotoxicity and Potentiate Antitumorigenic Activity in EGFR/HER02 and Mutant RAS/RAF Breast Cancer Model Systems,” NEOPLASIA (Aug. 2013) vol. 15, No. 8,…
[cited by applicant]
Natoli et al., Mar. 3, 2021. Plinabulin, a distinct microtubule-targeting chemotherapy, promotes M1-like macrophage polarization and anti-tumor immunity, Frontiers in Oncology, 11:1-14.
[cited by applicant]
Neidle, Stephen, ed., Cancer Drug Design and Discovery , 9th Edition, Elsevier/Academic Press, (2008) Chapter 18, pp. 427-431.
[cited by applicant]
Nema et al., Excipients and Their Role in Approved Injectable Products: Current Usage and Future Directions, PDA J Pharm Sci and Tech 2011, 65 287-332.
[cited by applicant]
Nereus Pharmaceuticals, Inc., Aug. 16, 2011, Phase 1/2 study of vascular disrupting agent NPI-2358 + docetaxel in patients with advanced non-small cell lung cancer, ClinicalTrials.gov, NCT00630110 <URL: https://www.clin…
[cited by applicant]
Neuteboom et al., “450 Poster NPI-2358, a novel tumor vascular disrupting agent potentiates the anti-tumor activity of docetaxel in the non small cell lung cancer model MV522,” EJC Supplements (2008) 6(12):141.
[cited by applicant]
Nicholson et al., NPI-2358 is a tubulin-depolymerizing agent: in-vitro evidence for activity as a tumor vascular-disrupting agent, Anti-Cancer Drugs (2005), Volume Date 2006, 17(1), 25-31.
[cited by applicant]
Nielsen et al., Jun. 2005, Alternative splice variants of the human PD-1 gene, Cell Immunol., 235(2):109-116.
[cited by applicant]
Niemann et al., “The Synthesis of the Three Isomeric dl-β-Pyridylalanines” Journal of the American Chemical Society, (1942) 64(7):1678-1682.
[cited by applicant]
Nihei et al., “Evaluation of antivascular and antimitotic effects of tubulin binding agents in solid tumor therapy”, Jpn. J. Cancer. Res. 1999, 90, 1387-1395.
[cited by applicant]
Nitecki et al., “A Simple Route to Sterically Pure Diketopiperazines1,” The Journal of Organic Chemistry, (1968) 33:864-866.
[cited by applicant]
Ohaegbulam et al., “Human cancer immunotherapy with antibodies to the PD-1 and PD-L1 pathway,” Trends Mol Med, (Oct. 30, 2014) 21(1): pp. 24-33.
[cited by applicant]
Ott et al., “CTLA-4 and PD-1/PD-L1 Blockade: New Immunotherapeutic Modalities with Durable Clinical Benefit in Melanoma Patients,” Clin Cancer Res (Oct. 1, 2013) 19(19): pp. 5300-5309.
[cited by applicant]
Ouyang et al., Mar. 2024, Overcoming cold tumors: a combination strategy of immune checkpoint inhibors, Front. Immunol., 15: 1344272, pp. 1-8.
[cited by applicant]
Oxford English Dictionary Online, 2010, Definition of prevent, http://dictionary.oed.com/, 4 pp.
[cited by applicant]
Paik et al., “A Phase 2 Study of Weekly Albumin-Bound Paclitaxel (Abraxane®) Given as a Two-Hour Infusion”, Cancer Chemother. Pharmacol., Nov. 2011, vol. 68, No. 5, pp. 1331-1337.
[cited by applicant]
Pardoll et al., “The blockade of immune checkpoints in cancer immunotherapy,” Nat Rev Cancer (May 4, 2016) 12(4): 252-264.
[cited by applicant]
Pattingre et al., “Amino Acids Interfere with the ERK1/2-dependent Control of Macroautophagy by Controlling the Activation of Raf-1 in Human Colon Cancer HT-29 Cells,” J Biol Chem (May 9, 2003) vol. 278, No. 19, pp. 166…
[cited by applicant]
Perez, Edith A., “Paclitaxel in Breast Cancer,”
[cited by applicant]
Peters et al., Oct. 9, 2020, Schedule-dependent synergy between the histone deacetylase inhibitor belinostat and the dihydrofolate reductase inhibitor pralatrexate in T-and B-cell lymphone cells in vitro, (Front. Cell D…
[cited by applicant]
Peterson et al., 2004, Integrating pharmacology and in vivo cancer models in preclinical and clinical drug development, Eur. J. Cancer., 40:837-844.
[cited by applicant]
Petrillo et al., Novel VEGF-independent strategies targeting tumor vasculature: clinical aspects, Current Pharmaceutical Design (2012), 18(19), 2702-2712.
[cited by applicant]
Pettit et al. “Antineoplastic Agents. 291. Isolation and Synthesis of Combretastatins A-4, A-5, and A-6 1a.” J. Med. Chem. (1995) 38: 1666-1672.
[cited by applicant]
Plunkett et al., Aug. 1995, Gemcitabine: metabolism, mechanisms of action, and self-potentiation, Semin Oncol., 22(4 Suppl 11):3-10.
[cited by applicant]
Prior et al., “A Comprehensive Survey of Ras Mutations in Cancer” Cancer Res. (2012) vol. 72, No. 10, pp. 2457-2467.
[cited by applicant]
PRNewswire.com, Jun. 22, 2010, Nereus Pharmaceuticals completes enrollment of phase 2 advance clinical trial of plinabulin in non-small cell lung cancer, 4 pp.
[cited by applicant]
Rajan et al., Dec. 2014, Nivolumab (anti-PD-1, BMS-936558, ONO-4538) in patients with advanced non-small cell lung cancer, Transl. Lung Cancer Res. 3(6):403-405.
[cited by applicant]