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1 se of bivalent HPV vaccine (2vHPV; Cervarix, GlaxoSmithKline).
2 egistry maintained by the drug manufacturer (GlaxoSmithKline).
3 itute of Mental Health, ViiV Healthcare, and GlaxoSmithKline.
4 titute of Mental Health, and ViiV Healthcare-GlaxoSmithKline.
5 chard Therapeutics, Fondazione Telethon, and GlaxoSmithKline.
6 -Aventis, Boehringer Ingelheim, Servier, and GlaxoSmithKline.
7 itute of Allergy and Infectious Diseases and GlaxoSmithKline.
8 identical to those of DELSM manufactured by GlaxoSmithKline.
9 ion, the Roger de Spoelberch Foundation, and GlaxoSmithKline.
10 National Institute for Health Research, GlaxoSmithKline.
11 ubunit protein vaccine candidate provided by GlaxoSmithKline.
12 iclovir was provided for trial 3 for free by GlaxoSmithKline.
13 Hospital Center and by a research grant from GlaxoSmithKline.
14 ntroduce the oral rotavirus vaccine Rotarix (GlaxoSmithKline), 1 of 2 recently developed vaccines aga
15 se (MEK) inhibitors (PD0325901 or trametinib/GlaxoSmithKline 1120212) significantly prolonged surviva
19 efficacy studies (assessing the 3-component GlaxoSmithKline and 5-component Sanofi-Pasteur formulati
20 Two live oral vaccines being prepared by GlaxoSmithKline and Merck have completed large-scale cli
21 d to model 5-HT type 3 antagonist (Lotronex, GlaxoSmithKline) and 5-HT type 4 agonist (Zelnorm, Novar
22 received oral valacyclovir 2 g tid (Valtrex, GlaxoSmithKline) and one patient with impaired renal fun
25 0 through collaboration between AstraZeneca, GlaxoSmithKline, and the University of Cambridge, with C
26 misation list that was computer generated at GlaxoSmithKline, and was stratified, in a block size of
27 oratories in the nonprofit sector, Merck and GlaxoSmithKline are developing commercial versions of th
28 United Kingdom (Grant Number G0700654); and GlaxoSmithKline as part of an MRC-CASE studentship (gran
29 Council (grant number G1000417/94909), ICON, GlaxoSmithKline, AstraZeneca, and the Medical Evaluation
30 P vaccine (DTaP-Hib-HepB-IPV, Infanrix hexa, GlaxoSmithKline, Australia) at approximately 6 weeks old
38 ion to product-specific results for Rotarix (GlaxoSmithKline Biologicals, Rixensart, Belgium) or Rota
41 is Vaccines and Diagnostics), AS03 and AS04 (GlaxoSmithKline Biologics), AF03 (Sanofi), and liposomes
42 ception occurring after Rotarix vaccination (GlaxoSmithKline Biologics, Research Triangle Park, North
43 l population structure and vaccine (Bexsero, GlaxoSmithKline, Brentford, Middlesex, UK) antigen varia
44 ivated protein kinase inhibitor (Losmapimod; GlaxoSmithKline, Brentford, United Kingdom), which reduc
45 oehringer Ingelheim, Novartis, and Sepracor; GlaxoSmithKline; Centers for Medicare and Medicaid Servi
48 eidentified individual participant data from GlaxoSmithKline clinical trials were obtained through Cl
49 cted at a specialist early psychosis clinic, GlaxoSmithKline Clinical Unit, and magnetic resonance im
51 attenuated, oral rotavirus vaccine (Rotarix, GlaxoSmithKline) efficacy trial conducted among infants
53 ized clinical trials conducted by Janssen or GlaxoSmithKline for one of nine disorders (N = 10,743 pa
54 nal Development, the Rockefeller Foundation, GlaxoSmithKline, Gilead Sciences, Boehringer-Ingelheim,
55 dation, Eli Lilly, GE Healthcare, Genentech, GlaxoSmithKline, Golub Capital, Insitro, Janssen Neurosc
56 es and Diagnostics division (now part of the GlaxoSmithKline group of companies), Wellcome Trust UK,
58 omized controlled trials (RCTs) conducted by GlaxoSmithKline (GSK) and the NCIC Clinical Trials Group
59 distributed to more than 300 laboratories by GlaxoSmithKline (GSK) between 2011 and 2015 and by SGC-U
60 ical study (BAT117213 study) is sponsored by GlaxoSmithKline (GSK) with associated exploratory studie
61 gs for Neglected Diseases initiative (DNDi), GlaxoSmithKline (GSK), and the University of Dundee.
66 women, were combined in a post-hoc analysis (GlaxoSmithKline [GSK] e-track number 202142) to investig
69 ew Cruzipain inhibitory scaffolds within the GlaxoSmithKline HAT (Human African Trypanosomiasis) and
70 d at SmithKline Beecham Pharmaceuticals (now GlaxoSmithKline) have allowed us to analyze the relative
72 independent case-control studies of MDD: the GlaxoSmithKline-High-Throughput Disease-specific target
73 (6/21 [29%]), intradermal IPV (9/16 [56%]), GlaxoSmithKline intramuscular IPV (19/22 [86%]), and Pan
74 egative, 42 (100%) of 42 seroconverted after GlaxoSmithKline intramuscular IPV, and 24 (59%) of 41 af
76 ction of a replacement MMR vaccine (Priorix; GlaxoSmithKline, London, United Kingdom) in 1998, active
77 ritish Heart Foundation, Cancer Research UK, GlaxoSmithKline, Medical Research Council, and Wellcome
81 ger Ingelheim (Germany and Canada), Servier, GlaxoSmithKline, Novartis, King Pharma, and national or
83 al-dose inactivated poliovirus vaccine (IPV, GlaxoSmithKline), or intramuscular full-dose IPV from tw
85 and Genomic Epidemiology (ENGAGE) and Oxford-GlaxoSmithKline (Ox-GSK) consortia to follow up the 15 m
86 ared the efficacy of rosiglitazone (Avandia; GlaxoSmithKline, Philadelphia, PA) 4 mg orally twice dai
87 FabI inhibitors began with screening of the GlaxoSmithKline proprietary compound collection, which i
92 one-based interactive voice-response system (GlaxoSmithKline Registration and Medication Ordering Sys
95 y assigned to standard therapy (Nicoderm CQ [GlaxoSmithKline, Research Triangle Park, North Carolina]
96 d (1:1) to receive an HPV vaccine (Cervarix, GlaxoSmithKline, Rixensart, Belgium) or a control hepati
98 Individual-level data on 5074 infants in 9 GlaxoSmithKline Rotarix Phase 2/3 clinical trials from 1
99 ree-step asymmetric and racemic syntheses of GlaxoSmithKline's highly potent PDE IVb inhibitor 1 were
105 iversity Research Foundation, Astra, Pfizer, GlaxoSmithKline, Servier, HemoCue, Wellcome Trust, UK Me
107 everal examples (use cases) from programs at GlaxoSmithKline that demonstrate the utility of mTPA thr
108 ata for a large set of compounds reported by GlaxoSmithKline (the Tres Cantos AntiMalarial Set, TCAMS
111 nt trial with funding provided by Sanofi and GlaxoSmithKline (TRIO-US B07, Clinical Trials NCT0076947
112 recombinant shingles vaccine (RZV; Shingrix, GlaxoSmithKline) vaccination program in adults aged >=65
114 ation schedule was generated by means of the GlaxoSmithKline validated randomisation software RANDALL
116 000 copies per mL) and sex at birth and used GlaxoSmithKline-verified randomisation software (RandAll
117 al virus (RSV) vaccine for older adults from GlaxoSmithKline was the first RSV vaccine approved by th
119 ritish Heart Foundation, Cancer Research UK, GlaxoSmithKline, Wellcome Trust, Medical Research Counci