-
1
-
-
85058999976
-
Antibodies to watch in 2019
-
Kaplon H, Reichert JM., Antibodies to watch in 2019. MAbs. 2019;11(2):219–24. doi:10.1080/19420862.2018.1556465.
-
(2019)
MAbs
, vol.11
, Issue.2
, pp. 219-224
-
-
Kaplon, H.1
Reichert, J.M.2
-
2
-
-
85040979948
-
Antibodies to watch in 2018
-
Kaplon H, Reichert JM. Antibodies to watch in 2018. MAbs. 2018;10(2):183–203. doi:10.1080/19420862.2018.1415671.
-
(2018)
MAbs
, vol.10
, Issue.2
, pp. 183-203
-
-
Kaplon, H.1
Reichert, J.M.2
-
3
-
-
85009967888
-
Antibodies to watch in 2017
-
Reichert JM. Antibodies to watch in 2017. MAbs. 2017;9(2):167–81. doi:10.1080/19420862.2016.1269580.
-
(2017)
MAbs
, vol.9
, Issue.2
, pp. 167-181
-
-
Reichert, J.M.1
-
4
-
-
84964523414
-
Antibodies to watch in 2016
-
Reichert JM. Antibodies to watch in 2016. MAbs. 2016;8(2):197–204. doi:10.1080/19420862.2015.1125583.
-
(2016)
MAbs
, vol.8
, Issue.2
, pp. 197-204
-
-
Reichert, J.M.1
-
5
-
-
84921345093
-
Antibodies to watch in 2015
-
Reichert JM. Antibodies to watch in 2015. MAbs. 2015;7(1):1–8. doi:10.4161/19420862.2015.988944.
-
(2015)
MAbs
, vol.7
, Issue.1
, pp. 1-8
-
-
Reichert, J.M.1
-
6
-
-
84903581591
-
Antibodies to watch in 2014: mid-year update
-
Reichert JM. Antibodies to watch in 2014: mid-year update. MAbs. 2014;6(4):799–802. doi:10.4161/mabs.29282.
-
(2014)
MAbs
, vol.6
, Issue.4
, pp. 799-802
-
-
Reichert, J.M.1
-
7
-
-
84892590856
-
Antibodies to watch in 2014
-
Reichert JM. Antibodies to watch in 2014. MAbs. 2014;6(1):5–14. doi:10.4161/mabs.27333.
-
(2014)
MAbs
, vol.6
, Issue.1
, pp. 5-14
-
-
Reichert, J.M.1
-
8
-
-
84880128705
-
Antibodies to watch in 2013: mid-year update
-
Reichert JM. Antibodies to watch in 2013: mid-year update. MAbs. 2013;5(4):513–17. doi:10.4161/mabs.24990.
-
(2013)
MAbs
, vol.5
, Issue.4
, pp. 513-517
-
-
Reichert, J.M.1
-
9
-
-
84872858296
-
Which are the antibodies to watch in 2013?
-
Reichert JM. Which are the antibodies to watch in 2013? MAbs. 2013;5(1):1–4. doi:10.4161/mabs.22976.
-
(2013)
MAbs
, vol.5
, Issue.1
, pp. 1-4
-
-
Reichert, J.M.1
-
10
-
-
84856800190
-
Which are the antibodies to watch in 2012?
-
Reichert JM. Which are the antibodies to watch in 2012? MAbs. 2012;4(1):1–3. doi:10.4161/mabs.4.1.18719.
-
(2012)
MAbs
, vol.4
, Issue.1
, pp. 1-3
-
-
Reichert, J.M.1
-
11
-
-
78651387929
-
Antibody-based therapeutics to watch in 2011
-
Reichert JM. Antibody-based therapeutics to watch in 2011. MAbs. 2011;3(1):76–99. doi:10.4161/mabs.3.1.13895.
-
(2011)
MAbs
, vol.3
, Issue.1
, pp. 76-99
-
-
Reichert, J.M.1
-
12
-
-
77951573241
-
Antibodies to watch in 2010
-
Reichert JM. Antibodies to watch in 2010. MAbs. 2010;2(1):84–100. doi:10.4161/mabs.2.1.10677.
-
(2010)
MAbs
, vol.2
, Issue.1
, pp. 84-100
-
-
Reichert, J.M.1
-
13
-
-
84944618044
-
-
[cited 2019 Dec 5]. Available from
-
U.S. Food and Drug Administration. Drug approval package: CABLIVI. [cited 2019 Dec 5]. Available from: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2019/761112Orig1s000TOC.cfm
-
Drug approval package: CABLIVI
-
-
-
14
-
-
84873424242
-
-
[cited 2019 Dec 5]. Available from
-
European Medicines Agency. Annex I summary of product characteristics. [cited 2019 Dec 5]. Available from: https://www.ema.europa.eu/en/documents/product-information/cablivi-epar-product-information_en.pdf.
-
Annex I summary of product characteristics
-
-
-
16
-
-
85077154396
-
-
2019 Apr 9. press release. [cited 2019 Dec 5]
-
U.S. Food and Drug Administration. FDA approves new treatment for osteoporosis in postmenopausal women at high risk of fracture. 2019 Apr 9. press release. [cited 2019 Dec 5]. Available from: https://www.fda.gov/news-events/press-announcements/fda-approves-new-treatment-osteoporosis-postmenopausal-women-high-risk-fracture.
-
FDA Approves New Treatment for Osteoporosis in Postmenopausal Women at High Risk of Fracture
-
-
-
18
-
-
85077141569
-
-
SKYRIZI approval letter, [cited 2019 Dec 5]
-
U.S. Food and Drug Administration. SKYRIZI approval letter. [cited 2019 Dec 5]. Available from: https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/761105s000ltr.pdf.
-
-
-
-
19
-
-
85070540421
-
Risankizumab compared with adalimumab in patients with moderate-to-severe plaque psoriasis (IMMvent): a randomised, double-blind, active-comparator-controlled phase 3 trial
-
Reich K, Gooderham M, Thaçi D, Crowley JJ, Ryan C, Krueger JG, Tsai TF, Flack M, Gu Y, Williams DA, et al. Risankizumab compared with adalimumab in patients with moderate-to-severe plaque psoriasis (IMMvent): a randomised, double-blind, active-comparator-controlled phase 3 trial. Lancet. 2019;394(10198):576–86. doi:10.1016/S0140-6736(19)30952-3.
-
(2019)
Lancet
, vol.394
, Issue.10198
, pp. 576-586
-
-
Reich, K.1
Gooderham, M.2
Thaçi, D.3
Crowley, J.J.4
Ryan, C.5
Krueger, J.G.6
Tsai, T.F.7
Flack, M.8
Gu, Y.9
Williams, D.A.10
-
20
-
-
85077154427
-
-
[cited 2019 Dec 5]. Available from
-
Langley RG, Blauvelt A, Gooderham M, Papp K, Philipp S, Wu JJ, Igarashi A, Geng Z, Wu T, Camez A, et al. Efficacy and safety of continuous Q12W risankizumab versus treatment withdrawal: results from the phase 3 IMMhance trial. [cited 2019 Dec 5]. Available from: https://server.aad.org/eposters/Submissions/getFile.aspx?id=10093&type=sub.
-
Efficacy and safety of continuous Q12W risankizumab versus treatment withdrawal: results from the phase 3 IMMhance trial
-
-
Langley, R.G.1
Blauvelt, A.2
Gooderham, M.3
Papp, K.4
Philipp, S.5
Wu, J.J.6
Igarashi, A.7
Geng, Z.8
Wu, T.9
Camez, A.10
-
21
-
-
85052121985
-
Efficacy and safety of risankizumab in moderate-to-severe plaque psoriasis (UltIMMa-1 and UltIMMa-2): results from two double-blind, randomised, placebo-controlled and ustekinumab-controlled phase 3 trials
-
Gordon KB, Strober B, Lebwohl M, Augustin M, Blauvelt A, Poulin Y, Papp KA, Sofen H, Puig L, Foley P, et al. Efficacy and safety of risankizumab in moderate-to-severe plaque psoriasis (UltIMMa-1 and UltIMMa-2): results from two double-blind, randomised, placebo-controlled and ustekinumab-controlled phase 3 trials. Lancet. 2018;392(10148):650–61. doi:10.1016/S0140-6736(18)31713-6.
-
(2018)
Lancet
, vol.392
, Issue.10148
, pp. 650-661
-
-
Gordon, K.B.1
Strober, B.2
Lebwohl, M.3
Augustin, M.4
Blauvelt, A.5
Poulin, Y.6
Papp, K.A.7
Sofen, H.8
Puig, L.9
Foley, P.10
-
22
-
-
85077158757
-
-
[cited 2019 Dec 5]. Available from
-
U.S. Food and Drug Administration. Polivy approval letter. [cited 2019 Dec 5]. Available from: https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/761121Orig1s000ltr.pdf.
-
Polivy Approval Letter
-
-
-
24
-
-
85066261962
-
HAWK and HARRIER: phase 3, multicenter, randomized, double-masked trials of brolucizumab for neovascular age-related macular degeneration
-
Dugel PU, Koh A, Ogura Y, Jaffe GJ, Schmidt-Erfurth U, Brown DM, Gomes AV, Warburton J, Weichselberger A, Holz FG,; HAWK and HARRIER Study Investigators. HAWK and HARRIER: phase 3, multicenter, randomized, double-masked trials of brolucizumab for neovascular age-related macular degeneration. Ophthalmology. 2019:S0161-6420(18)33018–5. doi:10.1016/j.ophtha.2019.04.017.
-
(2019)
Ophthalmology
-
-
Dugel, P.U.1
Koh, A.2
Ogura, Y.3
Jaffe, G.J.4
Schmidt-Erfurth, U.5
Brown, D.M.6
Gomes, A.V.7
Warburton, J.8
Weichselberger, A.9
Holz, F.G.10
-
26
-
-
85077172003
-
-
Nov, 15, press release,. [cited 2019 Dec 5]. Available from
-
US Food and Drug Administration. FDA approves first targeted therapy to treat patients with painful complication of sickle cell disease. 2019 Nov 15. press release. [cited 2019 Dec 5]. Available from: https://www.fda.gov/news-events/press-announcements/fda-approves-first-targeted-therapy-treat-patients-painful-complication-sickle-cell-disease.
-
(2019)
FDA approves first targeted therapy to treat patients with painful complication of sickle cell disease
-
-
-
28
-
-
85057262002
-
Effect of crizanlizumab on pain crises in subgroups of patients with sickle cell disease: A SUSTAIN study analysis
-
Kutlar A, Kanter J, Liles DK, Alvarez OA, Cançado RD, Friedrisch JR, Knight-Madden JM, Bruederle A, Shi M, Zhu Z, et al. Effect of crizanlizumab on pain crises in subgroups of patients with sickle cell disease: A SUSTAIN study analysis. Am J Hematol. 2019;94(1):55–61. doi:10.1002/ajh.25308.
-
(2019)
Am J Hematol
, vol.94
, Issue.1
, pp. 55-61
-
-
Kutlar, A.1
Kanter, J.2
Liles, D.K.3
Alvarez, O.A.4
Cançado, R.D.5
Friedrisch, J.R.6
Knight-Madden, J.M.7
Bruederle, A.8
Shi, M.9
Zhu, Z.10
-
29
-
-
85077144006
-
-
May, 7, press release,. [[cited 2019 Dec 5]. Available from
-
BIOCAD. BIOCAD registered the first Russian original therapeutic monoclonal antibody 2019 May 7. press release. [[cited 2019 Dec 5]. Available from: https://biocadglobal.com/post/Russian_original_therapeutic_monoclonal_antibody.
-
(2019)
BIOCAD registered the first Russian original therapeutic monoclonal antibody
-
-
-
30
-
-
85064659977
-
Fab fragment of VHH-based antibody netakimab: crystal structure and modeling interaction with cytokine IL-17A
-
Kostareva O, Kolyadenko I, Ulitin A, Ekimova V, Evdokimov S, Garber M, Tishchenko S, Gabdulkhakov A. Fab fragment of VHH-based antibody netakimab: crystal structure and modeling interaction with cytokine IL-17A. Crystals. 2019;9(3):177. doi:10.3390/cryst9030177.
-
(2019)
Crystals
, vol.9
, Issue.3
, pp. 177
-
-
Kostareva, O.1
Kolyadenko, I.2
Ulitin, A.3
Ekimova, V.4
Evdokimov, S.5
Garber, M.6
Tishchenko, S.7
Gabdulkhakov, A.8
-
31
-
-
85077150915
-
-
[cited 2019 Dec 5]. Available from
-
Zydus. Zydus to launch novel biologic for rabies, TwinrabTM. [cited 2019 Dec 5]. Available from: https://zyduscadila.com/public/pdf/pressrelease/Zydus%20to%20launch%20novel%20biologic%20for%20rabies_WHO.pdf.
-
Zydus to launch novel biologic for rabies, TwinrabTM
-
-
-
33
-
-
85077145972
-
-
Aug, 6, press release,. [cited 2019 Dec 5]. Available from
-
Alder BioPharmaceuticals, Inc. Alder BioPharmaceuticals reports second quarter 2019 financial and operating results. 2019 Aug 6. press release. [cited 2019 Dec 5]. Available from: https://investor.alderbio.com/news-releases/news-release-details/alder-biopharmaceuticalsr-reports-second-quarter-2019-financial.
-
(2019)
Alder BioPharmaceuticals reports second quarter 2019 financial and operating results
-
-
-
35
-
-
85019065038
-
Teprotumumab for thyroid-associated ophthalmopathy
-
Smith TJ, Kahaly GJ, Ezra DG, Fleming JC, Dailey RA, Tang RA, Harris GJ, Antonelli A, Salvi M, Goldberg RA, et al. Teprotumumab for thyroid-associated ophthalmopathy. N Engl J Med. 2017;376(18):1748–61. doi: 10.1056/NEJMoa1614949.
-
(2017)
N Engl J Med
, vol.376
, Issue.18
, pp. 1748-1761
-
-
Smith, T.J.1
Kahaly, G.J.2
Ezra, D.G.3
Fleming, J.C.4
Dailey, R.A.5
Tang, R.A.6
Harris, G.J.7
Antonelli, A.8
Salvi, M.9
Goldberg, R.A.10
-
38
-
-
85068489400
-
EV-201: results of enfortumab vedotin monotherapy for locally advanced or metastatic urothelial cancer previously treated with platinum and immune checkpoint inhibitors
-
June, 20
-
Petrylak DP, Balar AV, O’Donnell PH, McGregor BA, Heath EI, Yu EY, Galsky MD, Hahn NM, Gartner EM, Pinelli J, et al. EV-201: results of enfortumab vedotin monotherapy for locally advanced or metastatic urothelial cancer previously treated with platinum and immune checkpoint inhibitors. J Clin Oncol. 2019 June 20; 37(18_suppl):4505–4505. doi:10.1200/JCO.2019.37.18_suppl.LBA4505.
-
(2019)
J Clin Oncol
, vol.37
, pp. 4505
-
-
Petrylak, D.P.1
Balar, A.V.2
O’Donnell, P.H.3
McGregor, B.A.4
Heath, E.I.5
Yu, E.Y.6
Galsky, M.D.7
Hahn, N.M.8
Gartner, E.M.9
Pinelli, J.10
-
39
-
-
85065785802
-
The mechanism of action of the anti-cd38 monoclonal antibody isatuximab in multiple myeloma
-
Moreno L, Perez C, Zabaleta A, Manrique I, Alignani D, Ajona D, Blanco L, Lasa M, Maiso P, Rodriguez I, et al. The mechanism of action of the anti-cd38 monoclonal antibody isatuximab in multiple myeloma. Clin Cancer Res. 2019;25(10):3176–87. doi:10.1158/1078-0432.CCR-18-1597.
-
(2019)
Clin Cancer Res
, vol.25
, Issue.10
, pp. 3176-3187
-
-
Moreno, L.1
Perez, C.2
Zabaleta, A.3
Manrique, I.4
Alignani, D.5
Ajona, D.6
Blanco, L.7
Lasa, M.8
Maiso, P.9
Rodriguez, I.10
-
42
-
-
85077143154
-
-
Oct, 17, press release,. [cited 2019 Dec 5]. Available from
-
AstraZeneca and Daiichi Sankyo Company, Limited. Trastuzumab deruxtecan granted FDA priority review for treatment of patients with HER2-positive metastatic breast cancer. 2019 Oct 17. press release. [cited 2019 Dec 5]. Available from: https://www.astrazeneca.com/media-centre/press-releases/2019/trastuzumab-deruxtecan-granted-fda-priority-review-for-treatment-of-patients-with-her2-positive-metastatic-breast-cancer-17102019.html.
-
(2019)
Trastuzumab deruxtecan granted FDA priority review for treatment of patients with HER2-positive metastatic breast cancer
-
-
-
43
-
-
85077158129
-
-
May, 8, press release,. [cited 2019 Dec 5]. Available from
-
AstraZeneca and Daiichi Sankyo Company, Limited. Pivotal phase II DESTINY-Breast01 trial met primary endpoint, supporting global regulatory submission plan to start in H2 2019. 2019 May 8. press release. [cited 2019 Dec 5]. Available from: https://www.astrazeneca.com/media-centre/press-releases/2019/trastuzumab-deruxtecan-demonstrated-clinically-meaningful-response-in-patients-with-refractory-her2-positive-metastatic-breast-cancer-a-population-with-high-unmet-need-08052019.html.
-
(2019)
Pivotal phase II DESTINY-Breast01 trial met primary endpoint, supporting global regulatory submission plan to start in H2 2019
-
-
-
47
-
-
85072938913
-
Inebilizumab for the treatment of neuromyelitis optica spectrum disorder (N-MOmentum): a double-blind, randomised placebo-controlled phase 2/3 trial
-
Cree BAC, Bennett JL, Kim HJ, Weinshenker BG, Pittock SJ, Wingerchuk DM, Fujihara K, Paul F, Cutter GR, Marignier R, et al.; N-MOmentum study investigators. Inebilizumab for the treatment of neuromyelitis optica spectrum disorder (N-MOmentum): a double-blind, randomised placebo-controlled phase 2/3 trial. Lancet. 2019:S0140-6736(19)31817–3. doi:10.1016/S0140-6736(19)31817-3.
-
(2019)
Lancet
-
-
Cree, B.A.C.1
Bennett, J.L.2
Kim, H.J.3
Weinshenker, B.G.4
Pittock, S.J.5
Wingerchuk, D.M.6
Fujihara, K.7
Paul, F.8
Cutter, G.R.9
Marignier, R.10
-
49
-
-
85077166979
-
-
Sept, 25
-
CytoDyn Inc. Investor presentation. 2019 Sept 25.https://content.equisolve.net/_cb938b9f9372eed3b2f00594e8a2df74/cytodyn/db/193/2912/pdf/CytoDyn+-+Investor_presentation+-+Sep-25-2019-Final.pdf.
-
(2019)
Investor presentation
-
-
-
51
-
-
85070348417
-
Antibody-drug conjugates targeting TROP-2 and incorporating SN-38: A case study of anti-TROP-2 sacituzumab govitecan
-
Aug/Sep
-
Goldenberg DM, Sharkey RM. Antibody-drug conjugates targeting TROP-2 and incorporating SN-38: A case study of anti-TROP-2 sacituzumab govitecan. MAbs. 2019 Aug/Sep;11(6):987–95. doi:10.1080/19420862.2019.1632115.
-
(2019)
MAbs
, vol.11
, Issue.6
, pp. 987-995
-
-
Goldenberg, D.M.1
Sharkey, R.M.2
-
52
-
-
85077160850
-
-
Jan, 17, press release,. [cited 2019 Dec 5]. Available from
-
Immunomedics, Inc. Immunomedics receives complete response letter from FDA for sacituzumab govitecan biologics license application. 2019 Jan 17. press release. [cited 2019 Dec 5]. Available from: https://www.immunomedics.com/our-company/news-and-events/immunomedics-receives-complete-response-letter-from-fda-for-sacituzumab-govitecan-biologics-license-application/.
-
(2019)
Immunomedics receives complete response letter from FDA for sacituzumab govitecan biologics license application
-
-
-
53
-
-
85077158522
-
-
Dec, 3, press release,. [cited 2019 Dec 5]. Available from
-
Immunomedics, Inc. Immunomedics resubmits biologics license application to the FDA for sacituzumab govitecan. 2019 Dec 3. press release. [cited 2019 Dec 5]. Available from: https://www.immunomedics.com/our-company/news-and-events/immunomedics-resubmits-biologics-license-application-to-the-fda-for-sacituzumab-govitecan/.
-
(2019)
Immunomedics resubmits biologics license application to the FDA for sacituzumab govitecan
-
-
-
57
-
-
85075751523
-
Trial of satralizumab in neuromyelitis optica Spectrum disorder
-
Yamamura T, Kleiter I, Fujihara K, Palace J, Greenberg B, Zakrzewska-Pniewska B, Patti F, Tsai CP, Saiz A, Yamazaki H, et al. Trial of satralizumab in neuromyelitis optica Spectrum disorder. N Engl J Med. 2019;381(22):2114–24. doi:10.1056/NEJMoa1901747.
-
(2019)
N Engl J Med
, vol.381
, Issue.22
, pp. 2114-2124
-
-
Yamamura, T.1
Kleiter, I.2
Fujihara, K.3
Palace, J.4
Greenberg, B.5
Zakrzewska-Pniewska, B.6
Patti, F.7
Tsai, C.P.8
Saiz, A.9
Yamazaki, H.10
-
60
-
-
85077167854
-
-
Oct, 28, press release,. [cited 2019 Dec 5]. Available from
-
Omeros Corporation. Omeros corporation initiates BLA submission for narsoplimab for the treatment of HSCT-TMA. 2019 Oct 28. press release. [cited 2019 Dec 5]. Available from: https://investor.omeros.com/news-releases/news-release-details/omeros-corporation-initiates-bla-submission-narsoplimab.
-
(2019)
Omeros corporation initiates BLA submission for narsoplimab for the treatment of HSCT-TMA
-
-
-
61
-
-
85077298769
-
Improved survival following OMS721 treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathies (HCT-TMA)
-
Jun, 15, 215162,. [cited 2019 Dec 5]. Available from
-
Rambaldi A, Khaled S, Smith M, Zecca M, Kwong YM, Claes K, Leung N, Whitaker S. Improved survival following OMS721 treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathies (HCT-TMA). Eur Hematol Assoc Lib. 2018 Jun 15; 215162:PF724. [cited 2019 Dec 5]. Available from: https://library.ehaweb.org/eha/2018/stockholm/215162/alessandro.rambaldi.improved.survival.following.oms721.treatment.of.html
-
(2018)
Eur Hematol Assoc Lib
, pp. PF724
-
-
Rambaldi, A.1
Khaled, S.2
Smith, M.3
Zecca, M.4
Kwong, Y.M.5
Claes, K.6
Leung, N.7
Whitaker, S.8
-
62
-
-
84880296871
-
The Fc-engineered CD19 antibody MOR208 (XmAb5574) induces natural killer cell-mediated lysis of acute lymphoblastic leukemia cells from pediatric and adult patients
-
Kellner C, Zhukovsky EA, Pötzke A, Brüggemann M, Schrauder A, Schrappe M, Kneba M, Repp R, Humpe A, Gramatzki M, et al. The Fc-engineered CD19 antibody MOR208 (XmAb5574) induces natural killer cell-mediated lysis of acute lymphoblastic leukemia cells from pediatric and adult patients. Leukemia. 2013;27(7):1595–98. doi:10.1038/leu.2012.373.
-
(2013)
Leukemia
, vol.27
, Issue.7
, pp. 1595-1598
-
-
Kellner, C.1
Zhukovsky, E.A.2
Pötzke, A.3
Brüggemann, M.4
Schrauder, A.5
Schrappe, M.6
Kneba, M.7
Repp, R.8
Humpe, A.9
Gramatzki, M.10
-
63
-
-
85077153601
-
-
2019 Aug 6. press release. [cited 2019 Dec 5]. Available from
-
MorphoSys AG. MorphoSys AG reports second quarter 2019 financial results. 2019 Aug 6. press release. [cited 2019 Dec 5]. Available from: https://www.morphosys.com/media-investors/media-center/morphosys-ag-reports-second-quarter-2019-financial-results.
-
Morphosys AG Reports Second Quarter 2019 Financial Results
-
-
Morphosys, A.G.1
-
66
-
-
85057165662
-
Development of clinical-stage human monoclonal antibodies that treat advanced Ebola virus disease in nonhuman primates
-
Pascal KE, Dudgeon D, Trefry JC, Anantpadma M, Sakurai Y, Murin CD, Turner HL, Fairhurst J, Torres M, Rafique A, et al. Development of clinical-stage human monoclonal antibodies that treat advanced Ebola virus disease in nonhuman primates. J Infect Dis. 2018;218(suppl_5):S612–S626. doi:10.1093/infdis/jiy285.
-
(2018)
J Infect Dis
, vol.218
, pp. S612-S626
-
-
Pascal, K.E.1
Dudgeon, D.2
Trefry, J.C.3
Anantpadma, M.4
Sakurai, Y.5
Murin, C.D.6
Turner, H.L.7
Fairhurst, J.8
Torres, M.9
Rafique, A.10
-
67
-
-
85077164540
-
-
Nov, 5, press release,. [cited 2019 Dec 5]. Available from
-
Regeneron Pharmaceuticals, Inc. Regeneron reports third quarter 2019 financial and operating results. 2019 Nov 5. press release. [cited 2019 Dec 5]. Available from: https://investor.regeneron.com/news-releases/news-release-details/regeneron-reports-third-quarter-2019-financial-and-operating.
-
(2019)
Regeneron reports third quarter 2019 financial and operating results
-
-
-
68
-
-
85076449492
-
A randomized, controlled trial of Ebola virus disease therapeutics
-
Nov, 27
-
Mulangu S, Dodd LE, Davey RT, Jr, Tshiani Mbaya O, Proschan M, Mukadi D, Lusakibanza Manzo M, Nzolo D, Tshomba Oloma A, Ibanda A, et al. A randomized, controlled trial of Ebola virus disease therapeutics. N Engl J Med. 2019 Nov 27. doi:10.1056/NEJMoa1910993.
-
(2019)
N Engl J Med
-
-
Mulangu, S.1
Dodd, L.E.2
Davey, R.T.3
Tshiani Mbaya, O.4
Proschan, M.5
Mukadi, D.6
Lusakibanza Manzo, M.7
Nzolo, D.8
Tshomba Oloma, A.9
Ibanda, A.10
-
69
-
-
85077146456
-
-
Y-mAbs initiates rolling submission of biologics license application to U.S. FDA for naxitamab for treatment of neuroblastoma, Nov 29. press release. [cited 2019 Dec 5]
-
Y-mabs Therapeutics, Inc. Y-mAbs initiates rolling submission of biologics license application to U.S. FDA for naxitamab for treatment of neuroblastoma. 2019 Nov 29. press release. [cited 2019 Dec 5]. Available from: http://ir.ymabs.com/node/7156/pdf..
-
(2019)
-
-
-
70
-
-
85077158829
-
-
press release. [cited 2019 Dec 5]. Available from
-
Y-mabs Therapeutics, Inc. Y-mAbs announces naxitamab update. 2019 Oct 25. press release. [cited 2019 Dec 5]. Available from: http://ir.ymabs.com/news-releases/news-release-details/y-mabs-announces-naxitamab-update..
-
Y-Mabs Announces Naxitamab Update. 2019 Oct 25
-
-
-
73
-
-
85077165529
-
-
Jul, 30, press release,. [cited 2019 Dec 5]. Available from
-
Eli Lilly and Company. Lilly reports second-quarter 2019 financial results, raises 2019 EPS guidance. 2019 Jul 30. press release. [cited 2019 Dec 5]. Available from: https://investor.lilly.com/news-releases/news-release-details/lilly-reports-second-quarter-2019-financial-results-raises-2019.
-
(2019)
Lilly reports second-quarter 2019 financial results, raises 2019 EPS guidance
-
-
-
74
-
-
85068422731
-
Effect of tanezumab on joint pain, physical function, and patient global assessment of osteoarthritis among patients with osteoarthritis of the hip or knee: A randomized clinical trial
-
Schnitzer TJ, Easton R, Pang S, Levinson DJ, Pixton G, Viktrup L, Davignon I, Brown MT, West CR, Verburg KM. Effect of tanezumab on joint pain, physical function, and patient global assessment of osteoarthritis among patients with osteoarthritis of the hip or knee: A randomized clinical trial. JAMA. 2019;322(1):37–48. doi:10.1001/jama.2019.8044.
-
(2019)
JAMA
, vol.322
, Issue.1
, pp. 37-48
-
-
Schnitzer, T.J.1
Easton, R.2
Pang, S.3
Levinson, D.J.4
Pixton, G.5
Viktrup, L.6
Davignon, I.7
Brown, M.T.8
West, C.R.9
Verburg, K.M.10
-
75
-
-
85045873515
-
Structural and kinetic basis for the selectivity of aducanumab for aggregated forms of amyloid-β
-
23
-
Arndt JW, Qian F, Smith BA, Quan C, Kilambi KP, Bush MW, Walz T, Pepinsky RB, Bussière T, Hamann S, et al. Structural and kinetic basis for the selectivity of aducanumab for aggregated forms of amyloid-β. Sci Rep. 2018 23;8(1):6412. doi:10.1038/s41598-018-24501-0.
-
(2018)
Sci Rep
, vol.8
, Issue.1
, pp. 6412
-
-
Arndt, J.W.1
Qian, F.2
Smith, B.A.3
Quan, C.4
Kilambi, K.P.5
Bush, M.W.6
Walz, T.7
Pepinsky, R.B.8
Bussière, T.9
Hamann, S.10
-
78
-
-
85065901524
-
Cellular mechanisms of etrolizumab treatment in inflammatory bowel disease
-
Lichnog C, Klabunde S, Becker E, Fuh F, Tripal P, Atreya R, Klenske E, Erickson R, Chiu H, Reed C, et al. Cellular mechanisms of etrolizumab treatment in inflammatory bowel disease. Front Pharmacol. 2019;10:39. doi:10.3389/fphar.2019.00039.
-
(2019)
Front Pharmacol
, vol.10
, pp. 39
-
-
Lichnog, C.1
Klabunde, S.2
Becker, E.3
Fuh, F.4
Tripal, P.5
Atreya, R.6
Klenske, E.7
Erickson, R.8
Chiu, H.9
Reed, C.10
-
79
-
-
85077147988
-
-
[cited 2019 Dec 5]. Available from
-
Roche. Pipeline summary as of July 25, 2019 (slides 5, 72, 73). [cited 2019 Dec 5]. Available from: https://www.roche.com/dam/jcr:9fb4878c-e3a2-4fdc-80f6-62d435df7367/en/pharmahy19.pdf.
-
Pipeline summary as of July 25, 2019 (slides 5, 72, 73)
-
-
-
80
-
-
85021692509
-
Etrolizumab treatment leads to early improvement in symptoms and inflammatory biomarkers in anti-TNF-refractory patients in the open-label induction cohort of the phase 3 HICKORY study
-
[cited 2019 Dec 5]. Available from
-
Peyrin-Biroulet L, Feagan BG, Mansfield J, Rubin DT, Arulmani U, Maciuca R, Tyrrell H, Thommes J, Tole S. Etrolizumab treatment leads to early improvement in symptoms and inflammatory biomarkers in anti-TNF-refractory patients in the open-label induction cohort of the phase 3 HICKORY study. European Crohn’s and Colitis Organization meeting OP011. 2017. [cited 2019 Dec 5]. Available from: https://www.ecco-ibd.eu/publications/congress-abstract-s/abstracts-2017/item/op011-etrolizumab-treatment-leads-to-early-improvement-in-symptoms-and-inflammatory-biomarkers-in-anti-tnf-refractory-patients-in-the-open-label-induction-cohort-of-the-phase-3-hickory-study.html.
-
(2017)
European Crohn’s and Colitis Organization meeting OP011
-
-
Peyrin-Biroulet, L.1
Feagan, B.G.2
Mansfield, J.3
Rubin, D.T.4
Arulmani, U.5
Maciuca, R.6
Tyrrell, H.7
Thommes, J.8
Tole, S.9
-
82
-
-
85077162448
-
-
Jul, 29, press release,. [cited 2019 Dec 5]. Available from
-
Sanofi. Sanofi delivered solid growth in Q2 2019. 2019 Jul 29. press release. [cited 2019 Dec 5]. Available from: https://www.sanofi.com/en/media-room/press-releases/2019/2019-07-29-07-30-00.
-
(2019)
Sanofi delivered solid growth in Q2 2019
-
-
-
84
-
-
85077149530
-
-
Oct, 24, press release,. [cited 2019 Dec 5]. Available from
-
AstraZeneca PLC. Year-to-date and Q3 2019 results. 2019 Oct 24. press release. [cited 2019 Dec 5]. Available from: https://www.astrazeneca.com/content/dam/az/PDF/2019/q3/Year-to-date_and_Q3_2019_Results_announcement.pdf.
-
(2019)
Year-to-date and Q3 2019 results
-
-
-
85
-
-
85077167996
-
-
Aug, 29, press release,. [cited 2019 Dec 5]. Available from
-
AstraZeneca PLC. Anifrolumab phase III trial meets primary endpoint in systemic lupus erythematosus. 2019 Aug 29. press release. [cited 2019 Dec 5]. Available from: https://www.astrazeneca.com/media-centre/press-releases/2019/anifrolumab-phase-iii-trial-meets-primary-endpoint-in-systemic-lupus-erythematosus-29082019.html.
-
(2019)
Anifrolumab phase III trial meets primary endpoint in systemic lupus erythematosus
-
-
-
87
-
-
85077165152
-
-
Oct, 24, press release,. [cited 2019 Dec 5]. Available from
-
Provention Bio, Inc. Provention Bio announces PRV-031 (Teplizumab) granted PRIME designation by the European medicines agency. Oct 24, 2019 press release. [cited 2019 Dec 5]. Available from: http://investors.proventionbio.com/2019-10-24-Provention-Bio-Announces-PRV-031-Teplizumab-Granted-PRIME-Designation-by-the-European-Medicines-Agency.
-
(2019)
Provention Bio announces PRV-031 (Teplizumab) granted PRIME designation by the European medicines agency
-
-
-
88
-
-
85077159238
-
-
Sept 24. press release. [cited 2019 Dec 5]. Available from
-
Provention Bio, Inc. Provention Bio reiterates regulatory strategy for PRV-031 and announces completion of follow-on financing. 2019 Sept 24. press release. [cited 2019 Dec 5]. Available from: http://investors.proventionbio.com/2019-09-24-Provention-Bio-Reiterates-Regulatory-Strategy-for-PRV-031-and-Announces-Completion-of-Follow-on-Financing.
-
(2019)
Provention Bio Reiterates Regulatory Strategy for PRV-031 and Announces Completion of Follow-On Financing
-
-
-
89
-
-
85070816928
-
An anti-CD3 antibody, teplizumab, in relatives at risk for type 1 diabetes
-
Herold KC, Bundy BN, Long SA, Bluestone JA, DiMeglio LA, Dufort MJ, Gitelman SE, Gottlieb PA, Krischer JP, Linsley PS, et al.; Type 1 Diabetes TrialNet Study Group. An anti-CD3 antibody, teplizumab, in relatives at risk for type 1 diabetes. N Engl J Med. 2019;381(7):603–13. doi:10.1056/NEJMoa1902226.
-
(2019)
N Engl J Med
, vol.381
, Issue.7
, pp. 603-613
-
-
Herold, K.C.1
Bundy, B.N.2
Long, S.A.3
Bluestone, J.A.4
DiMeglio, L.A.5
Dufort, M.J.6
Gitelman, S.E.7
Gottlieb, P.A.8
Krischer, J.P.9
Linsley, P.S.10
-
90
-
-
85077140979
-
-
Third quarter 2019, Oct 30. press release. [cited 2019 Dec 5], Available from
-
GlaxoSmithKline plc. Third quarter 2019. 2019 Oct 30. press release. [cited 2019 Dec 5]. Available from: https://www.gsk.com/media/5735/q3-2019-results-announcement.pdf.
-
(2019)
-
-
-
92
-
-
85077170280
-
VISTA, phase 3 trial of Vicinium, an EPCAM-targeted Pseudomonas exotoxin, in BCG-unresponsive non-muscle invasive bladder cancer
-
Sep, 2021, Madrid, Spain:. [cited 2019 Dec 5]. Available from
-
Dickstein R, Wu N, Cowan B, Dunshee C, Franks M, Wolk F, Belkoff L, Castellucci S, Holzbeierlein J, Kulkarni G, et al. VISTA, phase 3 trial of Vicinium, an EPCAM-targeted Pseudomonas exotoxin, in BCG-unresponsive non-muscle invasive bladder cancer. Global Congress on Bladder Cancer 2018; 2018 Sep 20–21; Madrid, Spain. [cited 2019 Dec 5]. Available from: https://sesenbio.com/wp-content/uploads/2019/01/BLADDR_Congress_2018_Posterl.pdf.
-
(2018)
Global Congress on Bladder Cancer 2018
-
-
Dickstein, R.1
Wu, N.2
Cowan, B.3
Dunshee, C.4
Franks, M.5
Wolk, F.6
Belkoff, L.7
Castellucci, S.8
Holzbeierlein, J.9
Kulkarni, G.10
-
93
-
-
82255167636
-
Anti-tumor activity and toxicokinetics analysis of MGAH22, an anti-HER2 monoclonal antibody with enhanced Fcγ receptor binding properties
-
Nordstrom JL, Gorlatov S, Zhang W, Yang Y, Huang L, Burke S, Li H, Ciccarone V, Zhang T, Stavenhagen J, et al. Anti-tumor activity and toxicokinetics analysis of MGAH22, an anti-HER2 monoclonal antibody with enhanced Fcγ receptor binding properties. Breast Cancer Res. 2011;13(6):R123. doi:10.1186/bcr3069.
-
(2011)
Breast Cancer Res
, vol.13
, Issue.6
, pp. R123
-
-
Nordstrom, J.L.1
Gorlatov, S.2
Zhang, W.3
Yang, Y.4
Huang, L.5
Burke, S.6
Li, H.7
Ciccarone, V.8
Zhang, T.9
Stavenhagen, J.10
-
94
-
-
85077143346
-
-
Jul, 31, press release,. [cited 2019 Dec 5]. Available from
-
MacroGenics provides update on corporate progress and second quarter 2019 financial results. 2019 Jul 31. press release. [cited 2019 Dec 5]. Available from: http://ir.macrogenics.com/news-releases/news-release-details/macrogenics-provides-update-corporate-progress-and-second-3.
-
(2019)
-
-
-
95
-
-
85068895629
-
SOPHIA primary analysis: A phase 3 (P3) study of margetuximab (M) + chemotherapy (C) versus trastuzumab (T) + C in patients (pts) with HER2+ metastatic (met) breast cancer (MBC) after prior anti-HER2 therapies (Tx)
-
June, 4,; [cited 2019 Dec 5]. Available from:
-
Rugo HS, Im S-A, Wright GLS, Escriva-de-Romani S, DeLaurentiis M, Cortes J, Wazeen Bahadur S, Haley BB, Oyola RH, Riseberg DA, et al. SOPHIA primary analysis: A phase 3 (P3) study of margetuximab (M) + chemotherapy (C) versus trastuzumab (T) + C in patients (pts) with HER2+ metastatic (met) breast cancer (MBC) after prior anti-HER2 therapies (Tx). American Society of Clinical Oncology annual meeting; 2019 June 4; [cited 2019 Dec 5]. Available from: https://meetinglibrary.asco.org/record/170929/abstract.
-
(2019)
American Society of Clinical Oncology annual meeting
-
-
Rugo, H.S.1
Im, S.-A.2
Wright, G.L.S.3
Escriva-de-Romani, S.4
DeLaurentiis, M.5
Cortes, J.6
Wazeen Bahadur, S.7
Haley, B.B.8
Oyola, R.H.9
Riseberg, D.A.10
-
96
-
-
85077147679
-
-
Jul, 24, press release,. [cited 2019 Dec 5]. Available from
-
GlaxoSmithKline. Second quarter 2019 results. 2019 Jul 24. press release. [cited 2019 Dec 5]. Available from: https://www.gsk.com/media/5663/q2-2019-results-announcement.pdf.
-
(2019)
Second quarter 2019 results
-
-
-
98
-
-
85077165761
-
Q3 2019 results
-
Oct, 22,. p.,. [cited 2019 Dec 5]. Available from
-
Novartis. Q3 2019 results. investor presentation. 2019 Oct 22. p.20. [cited 2019 Dec 5]. Available from: https://www.novartis.com/sites/www.novartis.com/files/q3-2019-ir-presentation.pdf
-
(2019)
investor presentation
, pp. 20
-
-
-
99
-
-
85077143001
-
The anti–PD-1 antibody spartalizumab (S) in combination with dabrafenib (D) and trametinib (T) in previously untreated patients (pts) with advanced BRAF V600–mutant melanoma: updated efficacy and safety from parts 1 and 2 of COMBI-i. Abstract #9531
-
May 31-June 4, Chicago, [cited 2019 Dec 5]. Available from: IL
-
Long GV, Lebbe C, Atkinson V, Mandalà M, Nathan PD, Arance Fernandez AM, Richtig E, Yamazaki N, Robert C, Schadendorf D, et al. The anti–PD-1 antibody spartalizumab (S) in combination with dabrafenib (D) and trametinib (T) in previously untreated patients (pts) with advanced BRAF V600–mutant melanoma: updated efficacy and safety from parts 1 and 2 of COMBI-i. Abstract #9531. 2019 American Society of Clinical Oncology Annual Meeting; May 31-June 4; Chicago, [cited 2019 Dec 5]. Available from: IL.https://ascopubs.org/doi/abs/10.1200/JCO.2019.37.15_suppl.9531.
-
2019 American Society of Clinical Oncology Annual Meeting
-
-
Long, G.V.1
Lebbe, C.2
Atkinson, V.3
Mandalà, M.4
Nathan, P.D.5
Arance Fernandez, A.M.6
Richtig, E.7
Yamazaki, N.8
Robert, C.9
Schadendorf, D.10
-
100
-
-
85077154292
-
-
United States securities and exchange commission form 8-K, Nov 1. [cited 2019 Dec 5]
-
Y-mAbs Therapeutics, Inc. United States securities and exchange commission form 8-K. 2019 Nov 1. [cited 2019 Dec 5]. Available from: https://www.sec.gov/Archives/edgar/data/1722964/000110465919058623/a19-21369_38k.htm.
-
(2019)
-
-
-
101
-
-
85077141067
-
-
Sept, 6,. [cited 2019 Dec 5]. Available from
-
ADC Therapeutics SA. United States securities and exchange commission form F-1. 2019 Sept 6. [cited 2019 Dec 5]. Available from: https://www.sec.gov/Archives/edgar/data/1771910/000114036119016305/nt10002526x5_f1.htm.
-
(2019)
United States securities and exchange commission form F-1
-
-
-
102
-
-
84891634694
-
Retrocyte Display® technology: generation and screening of a high diversity cellular antibody library
-
Breous-Nystrom E, Schultze K, Meier M, Flueck L, Holzer C, Boll M, Seibert V, Schuster A, Blanusa M, Schaefer V, et al. Retrocyte Display® technology: generation and screening of a high diversity cellular antibody library. Methods. 2014;65(1):57–67. doi:10.1016/j.ymeth.2013.09.003.
-
(2014)
Methods
, vol.65
, Issue.1
, pp. 57-67
-
-
Breous-Nystrom, E.1
Schultze, K.2
Meier, M.3
Flueck, L.4
Holzer, C.5
Boll, M.6
Seibert, V.7
Schuster, A.8
Blanusa, M.9
Schaefer, V.10
-
104
-
-
85074276649
-
Efficacy and safety of rovalpituzumab tesirine in third-line and beyond patients with DLL3-expressing, relapsed/refractory small cell lung cancer: results from the phase II TRINITY study
-
Morgensztern D, Besse B, Greillier L, Santana-Davila R, Ready N, Hann CL, Glisson BS, Farago AF, Dowlati A, Rudin CM, et al. Efficacy and safety of rovalpituzumab tesirine in third-line and beyond patients with DLL3-expressing, relapsed/refractory small cell lung cancer: results from the phase II TRINITY study. Clin Cancer Res. 2019:clincanres.1133.2019. doi:10.1158/1078-0432.CCR-19-1133.
-
(2019)
Clin Cancer Res
-
-
Morgensztern, D.1
Besse, B.2
Greillier, L.3
Santana-Davila, R.4
Ready, N.5
Hann, C.L.6
Glisson, B.S.7
Farago, A.F.8
Dowlati, A.9
Rudin, C.M.10
-
105
-
-
85077142514
-
-
Aug, 29, press release,. [cited 2019 Dec 5]. Available from
-
AbbVie Inc. AbbVie discontinues rovalpituzumab tesirine (Rova-T) research and development program. 2019 Aug 29. press release. [cited 2019 Dec 5]. Available from: https://news.abbvie.com/news/press-releases/abbvie-discontinues-rovalpituzumab-tesirine-rova-t-research-and-development-program.htm.
-
(2019)
AbbVie discontinues rovalpituzumab tesirine (Rova-T) research and development program
-
-
|