US 5652138A
· Burton et al.
· 1997
[cited by applicant]
US 7612181B2
· Wu et al.
· 2009
[cited by applicant]
US 8088376B2
· Chamberlain et al.
· 2012
[cited by applicant]
US 8217148B2
· Davies
· 2012
[cited by examiner]
US 8258268B2
· Wu et al.
· 2012
[cited by applicant]
US 8394925B2
· Chamberlain et al.
· 2013
[cited by applicant]
US 8586714B2
· Ghayur et al.
· 2013
[cited by applicant]
US 8716450B2
· Ghayur et al.
· 2014
[cited by applicant]
US 8722855B2
· Ghayur et al.
· 2014
[cited by applicant]
US 8735546B2
· Ghayur et al.
· 2014
[cited by applicant]
US 8822645B2
· Ghayur et al.
· 2014
[cited by applicant]
US 20110111406A1
· Igawa
· 2011
[cited by examiner]
US 20130243775A1
· Papadopoulos et al.
· 2013
[cited by applicant]
US 20160161500A1
· Lee et al.
· 2016
[cited by applicant]
US 20170348429A1
· Reilly et al.
· 2017
[cited by applicant]
US 20180208658A1
· Liu et al.
· 2018
[cited by applicant]
US 20180230218A1
· Chittenden et al.
· 2018
[cited by applicant]
US 20220281984A1
· Nichols et al.
· 2022
[cited by applicant]
US 20240197906A1
· Fiske et al.
· 2024
[cited by applicant]
CN 102174106
· 2011
[cited by applicant]
CN 102918057
· 2013
[cited by applicant]
CN 103002916
· 2013
[cited by applicant]
EP 2552955
· 2013
[cited by applicant]
JP 2015502397A
· 2015
[cited by applicant]
KR 20180025865
· 2018
[cited by applicant]
WO WO2009125825
· 2009
[cited by applicant]
WO WO2011111007
· 2011
[cited by applicant]
WO WO2011122011
· 2011
[cited by applicant]
WO WO2011151412
· 2011
[cited by applicant]
WO WO2013093809A1
· 2013
[cited by applicant]
WO WO2013138400
· 2013
[cited by applicant]
WO WO2017134197
· 2017
[cited by applicant]
WO WO2017201204
· 2017
[cited by applicant]
WO WO2018044619
· 2018
[cited by applicant]
WO WO2018062402
· 2018
[cited by applicant]
WO WO2018093669
· 2018
[cited by applicant]
WO WO2018129029
· 2018
[cited by applicant]
WO WO2018136455
· 2018
[cited by applicant]
WO WO2019189453
· 2019
[cited by applicant]
WO WO2020014306
· 2020
[cited by applicant]
WO WO2020092385A1
· 2020
[cited by applicant]
WO WO2021022039
· 2021
[cited by applicant]
WO WO2022169975
· 2022
[cited by applicant]
Zhou. Site-specific antibody conjugation for ADC and Beyond. Biomedicines 2017, 5, 64; doi:10.3390/biomedicines5040064 (Year: 2017).
[cited by examiner]
Dimasi et al. Efficient preparation of site specifici antibody drug conjugates using cysteine insertion. Mol/ Pharmaceutics 2017, 14, 1501-1516; DOI: 10.1021/acs.molpharmaceut.6b00995 (Year: 2017).
[cited by examiner]
Li et al. 2019. Evaluation and use of an anti-cynomolgus monkey CD79b surrogate antibody-drug conjugate to enable clinical development of polatuzumab vedotin. Br J Pharmacol. 2019; 176: 3805-3818. https://doi.org/10.111…
[cited by examiner]
Abdiche et al., “Exploring blocking assays using Octet, ProteOn, and Biacore biosensors”, Anal Biochem., Mar. 2009, 386(2):172-180.
[cited by applicant]
Amini, “Hospital Adminstration Routine,” Sanqin Publishing House, 2013, pp. 397-398.
[cited by applicant]
Bonvin et al., “De novo isolation of antibodies with pH-dependent binding properties,” MABS, Mar. 11, 2015, 7(2):294-302.
[cited by applicant]
Borrok et al., “pH-dependent Binding Engineering Reveals an FcRn Affinity Threshold That Governs IgG Recycling,” The Journal of Biological Chemistry, Feb. 13, 2015, 290(7):4282-4290.
[cited by applicant]
BroadInstitute.Org [online], “Cancer Cell Line Encyclopedia”, available on or before Jul. 2016, retrieved on Mar. 29, 2022, retrieved from URL <https://portals.broadinstitute.org/ccle>, 6 pages.
[cited by applicant]
Carter et al., “Antibody-Drug Conjugates for Cancer Therapy”, Cancer J., May 2008, 14(3):154-169.
[cited by applicant]
Catcott et al., “Microscale screening of antibody libraries as maytansinoid antibody-drug conjugates”, mAbs, 2016 8(3):513-523.
[cited by applicant]
Chandna, “Single-Cell Gel Electrophoresis Assay Monitors Precise Kinetics of DNA Fragmentation Induced During Programmed Cell Death”, Cytometry, 2004, 61A:127-133.
[cited by applicant]
Chari, “Targeted Cancer Therapy: Conferring Specificity to Cytotoxic Drugs”, Acc. Chem. Res., Jan. 2008, 41(1):98-107.
[cited by applicant]
Cromie et al., “Nanobodies and their use in GPCR drug discovery”, Curr. Top. Med. Chem., 2015, 15(24):2543-2557.
[cited by applicant]
Dall et al., “Increasing the Affinity of a Human IgG1 for the Neonatal Fc Receptor: Biological Consequences”, J Immunol., 2002, 169:5171-5180.
[cited by applicant]
De Genst et al., “Antibody repertoire development in camelids”, Dev. Comp.Immunol., 2006, 30(1-2):187-198.
[cited by applicant]
De Meyer et al., “Nanobody-based products as research and diagnostic tools”, Trends Biotechnol., May 2014, 32(5):263-270.
[cited by applicant]
DiGiammarino et al., “Design and generation of DVD-Ig™ molecules for dual-specific targeting”, Methods Mol. Biol., 2012, 899:145-156.
[cited by applicant]
Fischer et al., “The assay design used for measurement of therapeutic antibody concentrations can affect pharmacokinetic parameters”, mAbs, 2012, 4(5):623-631.
[cited by applicant]
Fujita et al., “A Novel Non-Agonist c-Met Antibody Drug Conjugate with Superior Potency Over a c-Met Tyrosine Kinase Inhibitor in c-Met Amplified and Non-Amplified Cancers”, Cancer Biol. Ther., 2002, 21(6):549-559.
[cited by applicant]
Garber, “Bispecific antibodies rise again”, Nat. Rev. Drug Discov., Nov. 2014, 13:799-801.
[cited by applicant]
Gera et al., “Design of pH Sensitive Binding Proteins from the Hyperthermophilic Sso7d Scaffold”, PLoS One, Nov. 2012, 7(11):e48928.
[cited by applicant]
Gupta et al., “Preclinical pharmacokinetics of MHAA4549A, a human monoclonal antibody to influenza A virus, and the prediction of its efficacious clinical dose for the treatment of patients hospitalized with influenza A…
[cited by applicant]
Huang et al., “Assessment of Histone H2AX Phosphorylation Induced by DNA Topoisomerase I and II Inhibitors Topotecan and Mitoxantrone and by the DNA Cross-Linking Agent Cisplatin”, Cytometry Part A., 2004, 58A:99-110.
[cited by applicant]
Igawa et al., “pH-dependent antigen-binding antibodies as a novel therapeutic modality,” Proteomics, , 2014, 1844(11):1943-1950.
[cited by applicant]
International Preliminary Report on Patentability in International Appln. No. PCT/US2020/044263, dated Feb. 10, 2022, 15 pages.
[cited by applicant]
International Search Report and Written Opinion in International Application No. PCT/US2022/015116, dated Jun. 30, 2022, 21 pages.
[cited by applicant]
International Search Report and Written Opinion in International Appln. No. PCT/US2020/044263, dated Dec. 23, 2020, 25 pages.
[cited by applicant]
Invitation to Pay Additional Fees in International Appln. No. PCT/US2020/044263, dated Oct. 30, 2020, 19 pages.
[cited by applicant]
Invitation to Pay Additional Fees in International Appln. No. PCT/US2022/015116, May 9, 2022, 22 pages.
[cited by applicant]
Jakob et al., “Structure reveals function of the dual variable domain immunoglobulin (DVD-Ig™) molecule”, mAbs, 2013, 5(3):358-363.
[cited by applicant]
Jamur et al., “Permeabilization of cell membranes”, Methods Mol Biol., 2010, 588:63-66.
[cited by applicant]
Kijanka et al., “Nanobody-based cancer therapy of solid tumors”, Nanomedicine, 2015, 10:161-174.
[cited by applicant]
Kovaleva et al., “Shark variable new antigen receptor biologics—a novel technology platform for therapeutic drug development”, Expert. Opin. Biol. Ther., 2014, 14(10):1527-1539.
[cited by applicant]
Krah et al., “Single-domain antibodies for biomedical applications”, Immunopharmacol. Immunotoxicol., 2016, 38:21-28.
[cited by applicant]
Labrijn et al., “Controlled Fab-arm exchange for the generation of stable bispecific IgG1”, Nature Protcols, 2014, 9(10):2450-2463.
[cited by applicant]
Lefranc, “The IMGT unique numbering for Immunoglobulins, T cell receptors and Ig-like domains”, Immunologist, Jul. 1999, 7(4):132-136.
[cited by applicant]
Li et al., “A Biparatopic HER2-Targeting Antibody-Drug Conjugate Induces Tumor Regression in Primary Models Refractory to or Ineligible for HER2-Targeted Therapy”, Jan. 2016, Cancer Cell 29:117-29.
[cited by applicant]
Lu et al., “Linkers Having a Crucial Role in Antibody-Drug Conjugates”, Int. J. Mol. Sci., Apr. 2016, 17(4):561, 22 pages.
[cited by applicant]
Mahmutefendic et al., “Segregation of open Major Histocompatibility Class I conformers at the plasma membrane and during endosomal trafficking reveals conformation-based sorting in the endosomal system”, Int. J. Biochem…
[cited by applicant]
McCombs et al., “Antibody drug conjugates: design and selection of linker, payload and conjugation chemistry”, Aaps J., Mar. 2015, 17(2):339-351.
[cited by applicant]
Mendoza et al., “Inhibition of Ligand-mediated HER2 Activation in Androgen-independent Prostate Cancer”, Cancer Res., Oct. 2002, 62:5485-5488.
[cited by applicant]
Mujic-Delic et al., “GPCR-targeting nanobodies: attractive research tools, diagnostics, and therapeutics”, Trends Pharmacol. Sci., May 2014, 35(5):247-255.
[cited by applicant]
Muyldermans et al., “Recognition of antigens by single-domain antibody fragments: the superfluous luxury of paired domains”, Trends Biochem. Sci., Apr. 2001, 26(4):230-235.
[cited by applicant]
Muyldermans, “Nanobodies: Natural Single-Domain Antibodies”, Annu. Rev. Biochem., Jun. 2013, 82:775-797.
[cited by applicant]
Muyldermans, “Single domain camel antibodies: current status”, Rev. Mol. Biotechnol., 2001, 74:277-302.
[cited by applicant]
Office Action in Chinese Appln. No. 114746123, mailed on Oct. 31, 2023, 85 pages (with Machine translation).
[cited by applicant]
Oflazoglu et al., “Potent Anticarcinoma Activity of the Humanized Anti-CD70 Antibody h1F6 Conjugated to the Tubulin Inhibitor Auristatin via an Uncleavable Linker”, Clin. Cancer Res., 2008, 14(19): 6171-6180.
[cited by applicant]
Promega Corporation, “CellTiter-Glo™ Luminescent Cell Viability Assay,” Technical Bulletin #TB288, revised Mar. 2015, 15 pages.
[cited by applicant]
Rahbarizadeh et al., “Nanobody; an Old Concept and New Vehicle for Immunotargeting”, Immunol. Invest., 2011, 40:299-338.
[cited by applicant]
Sanderson et al., “In vivo Drug-Linker Stability of an Anti-CD30 Dipeptide-Linked Auristatin Immunoconjugate”, Clin. Cancer Res., Jan. 2005, 11(2 Pt1):843-852.
[cited by applicant]
Schneider et al., “Quantification of human Alu sequences by real-time PCR—an improved method to measure therapeutic efficacy of anti-metastatic drugs in human xenotransplants”, Clin. Exp. Metas., 2002, 19:571-582.
[cited by applicant]
Singh et al., “Measurement and Mathematical Characterization of Cell-Level Pharmacokinetics of Antibody-Drug Conjugates: A Case Study with Trastuzumab-vc-MMAE”, Drug Metabolism and Disposition, 2017, 45(11):1120-1132.
[cited by applicant]
Sorkin et al., “Quantitative analysis of endocytosis and turnover of epidermal growth factor (EGF) and EGF receptor”, Curr. Protoc. Cell Biol., Mar. 2010, Chapter 15, Unit-15.14.
[cited by applicant]
Spiess et al., “Alternative molecular formats and therapeutic applications of bispecific antibodies”, Mol. Immunol., 2015, 67(2 Pt A):95-106.
[cited by applicant]
Tiberghien et al., “Design and Synthesis of Tesirine, a Clinical Antibody-Drug Conjugate Pyrrolobenzodiazepine Dimer Payload”, ACS Med Chem Lett, Nov. 2016, 7(11):983-987.
[cited by applicant]
Tillotson et al., “Engineering an Anti-Transferrin Receptor ScFv for pH-Sensitive Binding Leads to Increased Intracellular Accumulation,” Plos One, Dec. 29, 2015, 10(12): e0145820.
[cited by applicant]
Vainshtein et al., “Quantitative Measurement of the Target-Mediated Internalization Kinetics of Biopharmaceuticals”, Pharm Res., 2015, 32:286-299.
[cited by applicant]
Van Audenhove et al., “Nanobodies as Versatile Tools to Understand, Diagnose, Visualize and Treat Cancer”, EBioMedicine, Jun. 2016, 8:40-48.
[cited by applicant]
Van Bockstaele et al., “The development of nanobodies for therapeutic applications”, Curr. Opin. Investig. Drugs, 2009, 10(11):1212-1224.
[cited by applicant]
Vincke et al., “Introduction to heavy chain antibodies and derived Nanobodies”, Methods Mol. Biol., 2012, 911:15-26.
[cited by applicant]
Wang et al., “ABBV-399, a c-Met Antibody—Drug Conjugate that Targets Both MET-Amplified and c-Met-Overexpressing Tumors, Irrespective of MET Pathway Dependence”, Clin Cancer Res, Feb. 2017, 23(4):992-1000.
[cited by applicant]
Wesolowski et al., “Single domain antibodies: promising experimental and therapeutic tools in infection and immunity”, Med. Microbiol. Immunol., Aug. 2009, 198(3):157-174.
[cited by applicant]
Wiley et al., “The Role of Tyrosine Kinase Activity in Endocytosis, Compartmentation, and Down-regulation of the Epidermal Growth Factor Receptor”, J. Biol. Chem., 1991, 266(17):11083-11094.
[cited by applicant]
Wustner, “Steady State Analysis and Experimental Validation of a Model for Hepatic High-Density Lipoprotein Transport”, Traffic, 2006, 7(6):699-715.
[cited by applicant]
Awad, “Impaired c-Met Receptor Degradation Mediated by MET Exon 14 Mutations in Non-Small-Cell Lung Cancer,” Journal of Clinical Oncology, Mar. 10, 2016, 34(8):879-881.
[cited by applicant]
Cappuzzo et al., “Epidermal growth factor receptor gene and protein and gefitinib sensitivity in non-small-cell lung cancer,” Journal of the National Cancer Institute, May 4, 2005, 97(9):643-655.
[cited by applicant]
Castañeda-González et al., “Multiple mutations in the EGFR gene in lung cancer: a systematic review,” Translational Lung Cancer Research, Oct. 2022, 11(10):2148-2163.
[cited by applicant]
Chang et al., “Whole-Body Pharmacokinetics and Physiologically Based Pharmacokinetic Model for Monomethyl Auristatin E (MMAE),” Journal of Clinical Medicine, Mar. 23, 2021, 10(6):1332, 18 pages.
[cited by applicant]
Chon et al., “FDA Approval Summary: Amivantamab for the Treatment of Patients with Non-Small Cell Lung Cancer with EGFR Exon 20 Insertion Mutations, ” Clinical Cancer Research, Sep. 1, 2003, 29(17):3262-3266.
[cited by applicant]
Coleman et al., “Antibody-drug conjugates in lung cancer: dawn of a new era?, ” NPJ Precision Oncology, Jan. 2023, 7(5):1-12.
[cited by applicant]
De George et al., “Guidance for Industry: S9 Nonclinical Evaluation for Anticancer Pharmaceuticals,” U.S. Department of Health and Human Services, Mar. 2010, 12 pages.
[cited by applicant]
Dong et al., “MET-Targeted Therapies and Clinical Outcomes: A Systematic Literature Review,” Molecular Diagnosis & Therapy, Mar. 10, 2022, 26(2):203-227.
[cited by applicant]
Doronina et al., “Novel peptide linkers for highly potent antibody-auristatin conjugate,” Bioconjugate chemistry, Oct. 15, 2008, 19(10):1960-3.
[cited by applicant]
Dubowchik et al., “Cathepsin B-sensitive dipeptide prodrugs. 1. A model study of structural requirements for efficient release of doxorubicin, ” Bioorganic & Medicinal Chemistry Letters, Dec. 1, 1998, 8(23):3341-3346.
[cited by applicant]
Fernandes et al., “When the MET receptor kicks in to resist targeted therapies,” Oncogene, Jun. 2021, 40(24):4061-4078.
[cited by applicant]
Fisher Jr., “Considerations for the Nonclinical Safety Evaluation of Antibody-Drug Conjugates,” Antibodies, Apr. 19, 2021, 10(2):15.
[cited by applicant]
Francisco et al., “cAC10-vcMMAE, an anti-CD30-monomethyl auristatin E conjugate with potent and selective antitumor activity,” Aug. 15, 2003, Blood, 102(4):1458-1465.
[cited by applicant]
Fujino et al., “Lung Cancer with MET exon 14 Skipping Mutation: Genetic Feature, Current Treatments, and Future Challenges,” Lung Cancer: Targets and Therapy, May 20, 2021, 35-50.
[cited by applicant]
Gera et al., “Abstract 5000: MYTX:011: A novel cMET_targeting antibody drug conjugate (ADC) engineered to increase on-target uptake in and efficacy against cMET expressing tumors,” Poster, Presented for the American Ass…
[cited by applicant]
Gymnopoulos et al., “TR1801-ADC: a highly potent cMet antibody-drug conjugate with high activity in patient-derived xenograft models of solid tumors,” Molecular Oncology, Dec. 3, 2019, 14(1):54-68.
[cited by applicant]
Han et al., “CYP3A-mediated drug-drug interaction potential and excretion of brentuximab vedotin, an antibody-drug conjugate, in patients with CD30-positive hematologic malignancies,” Journal of Clinical Pharmacology, A…
[cited by applicant]
International Search Report and Written Opinion in International Appln. No. PCT/US2023/083354, mailed on Mar. 20, 2024, 16 pages.
[cited by applicant]
Jackman et al., “Exon 19 Deletion Mutations of Epidermal Growth Factor Receptor Are Associated with Prolonged Survival in Non-Small Cell Lung Cancer Patients Treated with Gefitinib or Erlotinib,” Clinical Cancer Researc…
[cited by applicant]
Junutula et al., “Site-specific conjugation of a cytotoxic drug to an antibody improves the therapeutic index,” Nature biotechnology, Aug. 2008, 26(8):925-932.
[cited by applicant]
Kinoshita et al., “Safety and pharmacokinetics of polatuzumab vedotin in Japanese patients with relapsed/refractory B-cell non-Hodgkin lymphoma: a phase 1 dose-escalation study,” Japanese Journal of Clinical Oncology, J…
[cited by applicant]
Koeppen et al., “Biomarker Analyses from a Placebo-Controlled Phase II Study Evaluating Erlotinib + Onartuzumab in Advanced Non-Small Cell Lung Cancer: MET Expression Levels Are Predictive of Patient Benefit,” Clinical …
[cited by applicant]
Kontermann et al., “Bispecific antibodies,” Drug Discovery Today, Jul. 2015, 20(7):838-847.
[cited by applicant]
Lai et al., “Preclinical Evaluation of a New, Non-Agonist ADC Targeting MET-Amplified Tumors with a Peptide-linked Maytansinoid,” Poster, AACR Annual Meeting, Mar. 29-Apr. 3, 2019, 1 page.
[cited by applicant]
Lee et al., “MET in gastric carcinomas: comparison between protein express and gene copy number and impact on outcome,” British Journal of Cancer, Jul. 2012, 107(2):325-333.
[cited by applicant]
Lv et al., “Soluble c-Met is a Reliable and Sensitive Marker to Detect c-Met Expression Level in Lung Cancer,” BioMed Research International, Jan. 1, 2015, 2015(626578):1-9.
[cited by applicant]
Okamoto et al., “Pharmacokinetics of trastuzumab deruxtecan (T-DXd), a novel anti-HER2 Adc, in HER2-positive tumor-bearing mice,” Xenobiotica, Oct. 2, 2020, 50(10):1242-1250.
[cited by applicant]
Park et al., “MET amplification, protein expression, and mutations in pulmonary adenocarcinoma,” Lung Cancer, Dec. 2015, 90(3):381-387.
[cited by applicant]
Pastuskovas et al., “Tissue distribution, metabolism, and excretion of the antibody-drug conjugate Herceptin-monomethyl auristatin E in rats,” Cancer Res, May 1, 2005, 65(9 Supplement):1195-6, 1 page (abstract only).
[cited by applicant]
Resnick et al., “Epidermal growth factor receptor, cMET, B-catenin, and p53 expression as prognostic indicators in stage II colon cancer: a tissue microarray study,” Clinical Cancer Research, May 2004, 10(9):3069-3075.
[cited by applicant]
Saber et al., “An FDA oncology analysis of antibody-drug conjugates,” Regulatory Toxicology and Pharmacology, Apr. 2015, 71(3):444-52.
[cited by applicant]
Salgia, “MET in Lung Cancer: Biomarker Selection Based on Scientific Rationale,” Molecular Cancer Therapeutics, Apr. 2017, 16(4):555-565.
[cited by applicant]
Scagliotti et al., “A Randomized-Controlled Phase 2 Study of the MET Antibody Emibetuzumab in Combination with Erlotinib as First-Line Treatment for EGFR Mutation-Positive NSCLC Patients,” Journal of Thoracic Oncology, …
[cited by applicant]
Shen et al., “Conjugation site modulates the in vivo stability and therapeutic activity of antibody-drug conjugates,” Nature Biotechnology, Feb. 2012, 30(2):184-189.
[cited by applicant]
Sierra Jr. et al., “c-MET as a potential therapeutic target and biomarker in cancer,” Therapeutic advances in medical oncology, Nov. 2011, 3(1 Suppl):S21-35.
[cited by applicant]
Spigel et al., “Randomized Phase II trial of onartuzumab in combination with erlotinib in patients with advanced non-small-cell lung cancer,” Journal of Clinical Oncology, Nov. 2013, 31(32):4105-4114.
[cited by applicant]
Strickler et al., “Phase 1 dose-escalation and -expansion study of telisotuzumab (ABT-700), an Anti-c-met antibody, in patients with advanced solid tumors,” Molecular cancer therapeutics, May 2020, 19(5):1210-1217.
[cited by applicant]
Takahashi et al., “A phase I study of enfortumab vedotin in Japanese patients with locally advanced or metastatic urothelial carcinoma,” Investigational new drugs, Aug. 2020, 38:1056-1066.
[cited by applicant]
Toki et al., “Protease-mediated fragmentation of p-amidobenzyl ethers: a new strategy for the activation of anticancer prodrugs,” The Journal of organic chemistry, Mar. 22, 2002, 67(6):1866-72.
[cited by applicant]
Walker et al., “Monoclonal antibody mediated intracellular targeting of tallysomycin S10b,” Bioorganic & medicinal chemistry letters, Aug. 16, 2004, 14(16):4323-7.
[cited by applicant]
Walker et al., “Synthesis of an immunoconjugate of camptothecin,” Bioorganic & medicinal chemistry letters, Jan. 2002, 12(2):217-219.
[cited by applicant]
Wolf et al., “Capmatinib in MET Exon 14-Mutated or MET-Amplified Non-Small- Cell Lung Cancer,” New England Journal of Medicine, Sep. 2020, 383(10):944-957.
[cited by applicant]
Yang et al., “SHR-A1403, a novel c-Met antibody-drug conjugate, exerts encouraging anti-tumor activity in c-Met-overexpressing models,” Acta Pharmacologica Sinica, Jan. 14, 2019, 40(7):971-979.
[cited by applicant]
Yang et al., “EGFR-tyrosine kinase inhibitor treatment in a patient with advanced non-small cell lung cancer and concurrent exon 19 and 21 EGFR mutations: A case report and review of the literature,” Oncol Lett. May 201…
[cited by applicant]
Yuan et al., “Bayesian Optimal Interval Design: A Simple and Well-Performing Design for Phase I Oncology Trials,” Clinical Cancer Research, Jul. 2016, 22(17):4291-4301.
[cited by applicant]
Zalevsky et al., “Enhanced antibody half-life improves in vivo activity,” Nature biotechnology, Feb. 2010, 28(2):157-9.
[cited by applicant]
Lee et al., “An engineered human Fc domain that behaves like a pH-toggle switch for ultra-long circulation persistence,” Nature Communications, Nov. 6, 2019, 10(1):5031, 11 pages.
[cited by applicant]
Majumdar et al., “Correlations between changes in conformational dynamics and physical stability in a mutant IgG1 mAb engineered for extended serum half-life,” Mabs, Jan. 2, 2015, 7(1);84-95, 13 pages.
[cited by applicant]