7 research outputs found
The role of peptides in bone healing and regeneration: A systematic review
- Author
- A Au
- A Bitschnau
- A Horii
- A Kasaj
- A Kubler
- A Memeo
- A Mesfin
- A Mota
- A Oteo-Alvaro
- A Rezania
- A Rezania
- A Saito
- A Scarano
- A Shekaran
- A Spreafico
- A Verheyen
- A Vignery
- AA Sawyer
- AC Karaplis
- AM Wojtowicz
- Anastasios Lampropoulos
- AR El-Ghannam
- AU Dignass
- B Elmengaard
- B Elmengaard
- B Mognetti
- B Olszewska-Pazdrak
- BH Vickery
- BK Culpepper
- BK Culpepper
- BM Hanratty
- BP Sherman
- C Trasatti
- CC Wu
- CD Reyes
- CD Reyes
- CG Trejo
- CT Yu
- D Moher
- D Paridis
- DJ Hak
- DM Ferris
- E Garreta
- E Jimi
- E Mrak
- E Peggion
- E Ruoslahti
- E Smith
- EA Cavalcanti-Adam
- ED Karagiannis
- EF Morgan
- EL Hedberg
- Elena Jones
- EM Lindley
- EP Barboza
- F Butz
- F Fukuda
- F Gelain
- F Gomar
- FA Suaid
- G An
- G Balasundaram
- G Balasundaram
- G Cakmak
- G Li
- G Li
- G Tian
- G Xu
- G Zimmermann
- Giorgio Maria Calori
- GM Calori
- GN Onuoha
- H Ceylan
- H Drissi
- H Drissi
- H Egusa
- H Emam
- H Huang
- H Misawa
- H Nakahara
- H Nguyen
- H Shin
- H Tachiiri
- H Wang
- HH Rowshan
- I Bab
- I Bab
- I El-Madany
- I Millet
- I Pountos
- I Pountos
- I Pountos
- I Pountos
- I Pountos
- I Villa
- IJ Ezquerro
- Ippokratis Pountos
- J Guan
- J Guo
- J Holm
- J Jo
- J Jo
- J Li
- J Strnad
- JA Guimaraes
- JA Lee
- JC Chang
- JD Bashutski
- JD Smucker
- JE Madsen
- JF Whitfield
- JM Anderson
- JM Latzman
- JS Suh
- JT Ryaby
- JW Calland
- JW Park
- JY Lee
- JY Lee
- JY Lee
- JY Lee
- JY Lee
- K Nozaka
- K Ochi
- K Sarahrudi
- K Tamai
- KC Dee
- KC Dee
- KD Hankenson
- KL Ong
- KM Hennessy
- KM Hennessy
- KM Park
- L Kruger
- L Pietrogrande
- L Wang
- L Zhang
- LB Priddy
- LF Castro de
- LR Amir
- M Amling
- M Degidi
- M Deng
- M Gelbart
- M Gilbert
- M Giorgio Calori
- M Ikeno
- M Kantlehner
- M Komrakova
- M Nelson
- M Ozeki
- M Panteli
- M Roberto-Rodrigues
- M Ronga
- M Schuler
- M Shuqiang
- M Thorwarth
- M Thorwarth
- MA Brager
- MB Murphy
- MC Durrieu
- MC Simmonds
- ME Cupp
- Michalis Panteli
- MK Shin
- ML Bhongade
- MM Martino
- MP Bostrom
- MP Bostrom
- MR Sheller
- N Fukushima
- N Gabarin
- N Mardas
- N Tomomatsu
- O Ashman
- P Aspenberg
- P Aspenberg
- P Du
- P Philippart
- Peter V. Giannoudis
- PT Rubery
- PV Giannoudis
- Q Fei
- Q Liu
- Q Zhao
- R Ballica
- R Visser
- R Yoshimi
- R Yukna
- R Zura
- RA Stile
- RA Yukna
- RA Yukna
- RA Yukna
- RE Dent-Acosta
- RE Jung
- RN Palchesko
- RR Barros
- RS Bhatnagar
- S Cakarer
- S Chintamaneni
- S Dai
- S Hofmann
- S Komatsubara
- S Matos
- S Rammelt
- S Schutzenberger
- S Sun
- S Vastardis
- S Zhang
- S Zheng
- SG Amara
- SH Park
- SJ Gomberg
- SJ Sample
- SP Massia
- SY Yoo
- T Fujita
- T Goff
- T Hanks
- T Hayashibara
- T Hou
- T Manabe
- T Schinke
- T Vordemvenne
- TD Sargeant
- TJ Martin
- W Li
- W Schneiders
- W Thein-Han
- X Li
- XB Yang
- Y Furuya
- Y Gabet
- Y Hamada
- Y Hamada
- Y Song
- Y Wang
- YH Wang
- YJ Kim
- YJ Kim
- YM Alkhiary
- YQ Sun
- Z Artzi
- Z Artzi
- Z Chen
- Z Dahabreh
- Z Greenberg
- Z Li
- ZX Chen
- ZY Zhao
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2016
- Field of study
Background: Bone tissue engineering and the research surrounding peptides has expanded significantly over the last few decades. Several peptides have been shown to support and stimulate the bone healing response and have been proposed as therapeutic vehicles for clinical use. The aim of this comprehensive review is to present the clinical and experimental studies analysing the potential role of peptides for bone healing and bone regeneration. Methods: A systematic review according to PRISMA guidelines was conducted. Articles presenting peptides capable of exerting an upregulatory effect on osteoprogenitor cells and bone healing were included in the study. Results: Based on the available literature, a significant amount of experimental in vitro and in vivo evidence exists. Several peptides were found to upregulate the bone healing response in experimental models and could act as potential candidates for future clinical applications. However, from the available peptides that reached the level of clinical trials, the presented results are limited. Conclusion: Further research is desirable to shed more light into the processes governing the osteoprogenitor cellular responses. With further advances in the field of biomimetic materials and scaffolds, new treatment modalities for bone repair will emerge
Comparison of PCSK9 Inhibitor Evolocumab vs Ezetimibe in Statin-Intolerant Patients: Design of the Goal Achievement After Utilizing an Anti-PCSK9 Antibody in Statin-Intolerant Subjects 3 (GAUSS-3) Trial.
- Publication venue
- Publication date
- Field of study
Statins are the accepted standard for lowering low-density lipoprotein cholesterol (LDL-C). However, 5% to 10% of statin-treated patients report intolerance, mostly due to muscle-related adverse effects. Challenges exist to objective identification of statin-intolerant patients. Evolocumab is a monoclonal antibody that binds proprotein convertase subtilisin/kexin type 9 (PCSK9), resulting in marked LDL-C reduction. We report the design of Goal Achievement After Utilizing an Anti-PCSK9 Antibody in Statin-Intolerant Subjects 3 (GAUSS-3), a phase 3, multicenter, randomized, double-blind, ezetimibe-controlled study to compare effectiveness of 24 weeks of evolocumab 420 mg monthly vs ezetimibe 10 mg daily in hypercholesterolemic patients unable to tolerate an effective statin dose. The study incorporates a novel atorvastatin-controlled, double-blind, crossover phase to objectively identify statin intolerance. Eligible patients had LDL-C above the National Cholesterol Education Project Adult Treatment Panel III target level for the appropriate coronary heart disease risk category and were unable to tolerate ≥3 statins or 2 statins (one of which was atorvastatin ≤10 mg/d) or had a history of marked creatine kinase elevation accompanied by muscle symptoms while on 1 statin. This trial has 2 co-primary endpoints: mean percent change from baseline in LDL-C at weeks 22 and 24 and percent change from baseline in LDL-C at week 24. Key secondary efficacy endpoints include change from baseline in LDL-C, percent of patients attaining LDL-C <70 mg/dL (1.81 mmol/L), and percent change from baseline in total cholesterol, non-high-density lipoprotein cholesterol, and apolipoprotein B. Recruitment of 511 patients was completed on November 28, 201
Thigh-length compression stockings and DVT after stroke
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- Abbas M
- Abbasi S
- Abbasi S
- Abdelaziz A
- Abdelfattah M
- Abdul B
- Abdulmumeen A
- Abdulshukkoor N
- Abdusamad K
- Aboaba A
- Abouibrahim M
- Abraham M
- Abraham T
- Abrams J
- Abung A
- Acharya D
- Acharya D
- Acheson J
- Acosta A
- Acosta A
- Acton C
- Adam M
- Adams C
- Adams K
- Adamus M
- Adegoke K
- Adenwalla S
- Adeyeye E
- Adnan A
- Agbo C
- Aggarwal S
- Agwada-Akeru J
- Agyapong K Ansu
- Ah-Chuen J
- Ahmad M
- Ahmed I
- Ahmed I
- Ahmed L
- Ahmed L
- Ahmed M
- Ahmed M Cecilia
- Ahmed N
- Ahmed N
- Ahmed R
- Ahmed RA
- Ahmed S
- Ahmed S Haris
- Ail D
- Ainsley A
- Ainsworth M
- Aitken L
- Ajibode A
- Ajmi A
- Ajmi A
- Akhtar N
- Akili S
- Akindolie O
- Al Balushi A
- Al-Asadi A
- Al-Hakim B
- Al-Jibury M
- Al-Rabahi A
- Al-Ramadhani B
- Al-Shamkhani W
- Al-Sheklly B
- Alam S
- Aldana A
- Aldouri R
- Aldridge N
- Alegria A
- Alexander A
- Alexander J
- Alexander PDG
- Ali F Runa
- Ali M
- Ali O
- Ali S
- Ali S
- Ali S
- Alkhusheh M
- Alkhusheh M
- Allanson A
- Allen L
- Allen R
- Allen S
- Allison K
- Allsop L
- Alomari L
- Alzetani M
- Ambler S
- Ambrogetti R
- Ambrose C
- Amezaga M
- Amin A
- Amosun V
- Amosun V
- Amsha K
- Anand A
- Anderson J
- Anderson L
- Anderson N
- Anderson R
- Andreou P
- Andrews A
- Andrews J
- Aneke K
- Ang A
- Angel T
- Antill P
- Antonina Z
- Anu V
- Appleby S
- Appleyard D
- Archer A
- Ardley C
- Arimoto R
- Arkley C
- Armah C
- Armstrong C
- Armstrong S
- Armtrong P
- Arnison-Newgass C
- Arora D
- Arter A
- Arter A
- Asghar A
- Ashbrook-Raby C
- Ashish A
- Ashish A
- Ashraf S
- Ashton D
- Asrar A
- Assaf O
- Astin-Chamberlain R
- Athorne D
- Atkinson J
- Atkinson V
- Aubrey P
- Aung K Thu
- Aung N
- Aung Z Myo
- Austin E
- Avery M
- Avram C
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- Aziz G
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- Babatunde F
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- Babs-Osibodu A Obaloluwa
- Bacon G
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- Balachandran N
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- Waterstone M
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- Webster T
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- Wilde M
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- Wiliams T
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- Wilkinson S
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- Williams A
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- Williams J
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- Williams S
- Williams T
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- Williamson D
- Williamson J
- Willis E
- Willis H
- Willis H
- Willis J
- Willis J
- Wilson A
- Wilson A
- Wilson A
- Wilson D
- Wilson J
- Wilson J
- Wilson K
- Wilson L
- Wilson T
- Win M
- Winder L
- Winder P
- Winn S
- Winstanley M
- Winter H
- Winter J
- Wiselka M
- Wittes J
- Wolodimeroff E
- Wong N
- Wood C
- Wood F
- Wood J
- Wood L
- Wood T
- Woodford J
- Woodhead L
- Woodland P
- Woodward Z
- Wooldridge G
- Woollen L
- Woosey D
- Wootton D
- Worton S
- Wright D
- Wright R
- Wroe C
- Wu P
- Wyness K
- Wynter I
- Xavier B
- Xia Z
- Yan M
- Yanney M
- Yasmin S
- Yates B
- Yates B
- Yates D
- Yates H
- Yein K
- Yelnoorkar F
- Yip K
- Ynter I
- Yorke J
- Youssouf S
- Yousuf A
- Yung B
- Zafar A-M
- Zaher S
- Zalewska K
- Zaman M
- Zaman S
- Zammit L
- Zammit-Mangion M
- Zdanaviciene A
- Zehnde D
- Zhixin J
- Zhu D
- Zia M
- Zin E Thant
- Zinyemba V
- Zipitis C
- Zmierczak A
- Zuhra N
- Zulaikha R
- Zullo C
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/07/1994
- Field of study
Controversy exists as to whether neoadjuvant chemotherapy improves survival in patients with invasive bladder cancer, despite randomised controlled trials of more than 3000 patients. We undertook a systematic review and meta-analysis to assess the effect of such treatment on survival in patients with this disease
PTH1-34 improves bone healing by promoting angiogenesis and facilitating MSCs migration and differentiation in a stabilized fracture mouse model
- Author
- A Donneys
- A Oskowitz
- AA Naik
- AP Kusumbe
- Cuidi Xu
- DJ Hak
- E Wernike
- F Paino
- G Robertson
- GB Adams
- Gianpaolo Papaccio
- Hongli Shi
- I Mortada
- J Westgeest
- JA Rytlewski
- KD Hankenson
- KK Sivaraj
- M Guan
- M La Noce
- M Wang
- M Yuasa
- NK Kanakaris
- P Aspenberg
- Qun Cheng
- R Prisby
- RE Dent-Acosta
- RS Dhillon
- S Kakar
- SG Ball
- SK Ramasamy
- SK Ramasamy
- TW Axelrad
- W Chen
- X Sun
- Xin Jiang
- Y Jung
- Y Ogata
- Y Ren
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- Field of study
Anomalien des Phenylalanin-Stoffwechsels
- Author
- A Bentovim
- A Fois
- A Fölling
- A Fölling
- A Fölling
- A Lütcke
- A Lütcke
- A Lütcke
- A Meister
- A Neuberger
- A Szeinberg
- A Szeinberg
- A Wallner
- AA Moncrieff
- AE Garrod
- AEH Emery
- AJ Brenndorff von
- AJ Schneider
- AJ Terr
- AL Prensky
- AN Davison
- AN Davison
- AP Beddard
- AR Moss
- AS Beckman
- AS Breatnach
- AV Lorenzo
- B Blechova
- B Clayton
- B Cohen
- B Gerstl
- B Umbarger
- BA Smith
- BB Blivaiss
- BB Gallagher
- BE Cohen
- BE Cohen
- BE Cohen
- BE Cohen
- BK Koe
- BM Rouse
- BN Du La
- BN Du La
- BN Du La
- BN Du La
- BN Du La
- BN Du La
- BN Du La
- BN Du La
- BS Sutherland
- BS Sutherland
- BS Sutherland
- C Boedeker
- C Heiden van der
- C Mitoma
- CA Larson
- CC Huntley
- CC Mabry
- CC Mabry
- CC Mabry
- CC Mabry
- CE Dent
- CF Johnson
- CH Ménibus De
- CJ Clow
- CL Clow
- CM McKean
- CM McKean
- CM Poser
- CMB Pare
- CMB Pare
- CO Carter
- CO Mabry
- CR Grau
- CR Scriver
- CR Scriver
- CR Scriver
- CR Scriver
- CR Scriver
- CS Shear
- CW Hassel
- D Ingall
- D Lonsdale
- D Murphy
- D Murphy
- D Murphy
- D Rosenblatt
- DB Windhorst
- DDY Hsia
- DE Clader
- DG Grahame-Smith
- DJ O’Grady
- DM Brown
- DS Kleinman
- DUY Hsia
- DW Woolley
- DYY Hsia
- DYY Hsia
- DYY Hsia
- DYY Hsia
- DYY Hsia
- DYY Hsia
- DYY Hsia
- DYY Hsia
- E Abderhalden
- E Borek
- E Layne
- E Lund
- E Lund
- E Schmid-Rüter
- ECC Lin
- ECC Lin
- EL Coodley
- ES Kang
- F Güttler
- F Lanyar
- F Linneweh
- F Linneweh
- F Schulte
- F Vasella
- FA Horner
- FB Goldstein
- FH Horner
- FL Siegel
- FP Hudson
- FP Hudson
- FP Hudson
- FP Hudson
- FSW Brimblecombe
- G Embden
- G Fekete
- G Guroff
- G Machill
- G Medes
- G Takada
- G Weber
- G Weber
- G Weber
- GA Jervis
- GA Jervis
- GA Jervis
- GA Jervis
- GA Jervis
- GA Jervis
- GA Jervis
- GE Gaull
- GR Kerr
- GS Lo
- GT Pryor
- H Albrecht
- H Berendes
- H Bickel
- H Bickel
- H Bickel
- H Bickel
- H Bickel
- H Forssman
- H Schmidt
- H Schmidt
- H Schönenberg
- H Weil-Malherbe
- HA Waisman
- HA Waisman
- HA Waisman
- HC Agrawal
- HC Agrawal
- HD Grümer
- HD Grümer
- HF Falls
- HH Brühl
- HJ Bremer
- HJ Bremer
- HJ Bremer
- HJ Bremer
- HK Berry
- HK Berry
- HK Berry
- HK Kornreich
- HL Levy
- HL Levy
- HL Wang
- HM Myers
- HP Chase
- HP Chase
- HR Bloxam
- HV Candle
- HW Wallace
- IJ Light
- J Brodehl
- J Cowie
- J Dancis
- J Delay
- J Dobbing
- J Dobbing
- J Dobbing
- J Gentz
- J Gentz
- J Larochelle
- J Mathews
- JA Anderson
- JA Anderson
- JA Anderson
- JA Anderson
- JA Lowden
- JA Munro
- JA Munro
- JB Colombo
- JB Longenecker
- JBP Stephenson
- JC Denniston
- JC Dobson
- JC Dobson
- JD Allan
- JD Blainey
- JD Sherman
- JE Sisken
- JG Gostomzyk
- JH Fellman
- JH Fellman
- JH French
- JH Menkes
- JH Menkes
- JH Menkes
- JH Menkes
- JH Menkes
- JH Renwick
- JK Dittrich
- JK Visakorpi
- JL Berman
- JL Berman
- JL Kennedy
- JL Kennedy
- JM Berg
- JM Hackney
- JM Thompson
- JN Cumings
- JP Roscoe
- JS Yu
- JS Yu
- JW Farquhar
- JW MacInnes
- K Aoki
- K Lang
- K Lang
- K Sakai
- K Sakai
- K Schreier
- K Shizume
- K Tada
- K Tada
- K Taniguchi
- K Winkler
- KD Neame
- KH Drummond
- KS Holt
- L Barbato
- L Crome
- L Crome
- L Crome
- L Penrose
- L Volicer
- LE Holt
- LE Rosenberg
- LJ Woolf
- LJ Woolf
- LJ Woolf
- LJ Woolf
- LJ Woolf
- LJ Woolf
- LJ Woolf
- LJ Woolf
- LJ Woolf
- LJH Arthur
- LM Barbato
- LS Penrose
- LS Penrose
- LS Penrose
- M Bechar
- M Blaskowics
- M Blaskowics
- M Galdston
- M Rhein
- M Roth
- M Winick
- M Winick
- M Winick
- M Wolkow
- MA Lipton
- MD Armstrong
- MD Armstrong
- MD Armstrong
- MD Armstrong
- MD Baber
- MD Blumenthal
- MD Kogut
- MD Milne
- ME Avery
- ME Blaskowics
- ME O’Flynn
- ME Smith
- MG Wilson
- MJ Carver
- MJ Carver
- MK Wilson
- ML Efron
- ML Williamson
- ML Williamson
- MM Boyd
- MM Hunt
- MM Murdoch
- MM Pomeranz
- MND Goswami
- MS McBean
- MT Yarbo
- MW McCaman
- MW Partington
- MW Partington
- MW Partington
- MW Partington
- MW Partington
- MW Partington
- MW Partington
- MW Partington
- MW Partington
- N Kretchmer
- N Kretchmer
- N Kretchmer
- N Kretchmer
- N Malamtjd
- NA Peterson
- NA Peterson
- NJW Royston
- NK Gibbs
- NL Low
- NRM Buist
- O Hjalmarsson
- O Neubauer
- O Neubauer
- O Schrappe
- O Thalhammer
- P Frogatt
- P Justice
- PA Friedman
- PB Acosta
- PB Dent
- PB Reed
- PJ Waardenburg
- PR Dodge
- PW Anders
- PWK Wong
- PWK Wong
- R Fuller
- R Grüttner
- R Grüttner
- R Guthrie
- R Koch
- R Koch
- R Lindemann
- R Virchow
- R Williams
- RA Campbell
- RA MacCready
- RC Baldridge
- RE Counsell
- RE Stevenson
- RG Daniel
- RJ Allen
- RJ Allen
- RJ Glazer
- RJ Glazer
- RL Geison
- RO Fisch
- RO Fisch
- RO Fisch
- RO Fisch
- RO Fisch
- RO Fisch
- RR Howell
- RR Sealock
- RR Sealock
- RS Paine
- RW Coffelt
- RW Lippmann
- S Aronsson
- S Berlow
- S Castells
- S Farber
- S Grubel-Kaiser
- S Halvorsen
- S Halvorsen
- S Halvorsen
- S Jablonska
- S Kaiser
- S Kaufman
- S Kaufman
- S Kaufman
- S Kaufman
- S Kaufman
- S Kaufman
- S Kaufman
- S Kaufman
- S Kaufman
- S Kaufman
- S Kaufman
- S Kaufman
- S Rampini
- S Rampini
- S Scheibenreiter
- S Udenfriend
- S Udenfriend
- S Udenfriend
- SB Feinberg
- SE Snyderman
- SF Cahalane
- SH Appel
- SK Wadman
- SK Wadman
- SK Wadman
- SN Shah
- SN Shah
- SN Shah
- SP Bessman
- SP Bessman
- SW Wright
- SZ Levine
- TB Fitzpatrick
- TE Young
- TJ Fleisher
- TJ Moran
- TL Perry
- TL Perry
- TL Perry
- TL Perry
- TL Perry
- V Cowie
- VA Cowie
- VA Cowie
- VG Zannoni
- VG Zannoni
- VG Zannoni
- VG Zannoni
- VH Auerbach
- VH Auerbach
- VH Auerbach
- VH Stadler
- VJ Polidora
- VY Cremata
- W Dihlmann
- W Grüter
- W Schwenke
- WB Hanley
- WE Knox
- WE Knox
- WE Knox
- WE Knox
- WHO Techn. Rep. Ser. No. 401
- WK Frankenburg
- WM Diedrich
- WM O’Brien
- WR Centerwall
- WT McLean
- Y Kotake
- Y Sakamoto
- YM Bhende
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/1974
- Field of study
A search for pair production of new light bosons decaying into muons
- Author
- A. Abdulsalam
- A. Ackert
- A. Adair
- A. Adiguzel
- A. Agapitos
- A. Ahmad
- A. Aleksandrov
- A. Ali
- A. Apresyan
- A. Apyan
- A. Askew
- A. Attikis
- A. Aubin
- A. Avetisyan
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- V. Karimäki
- V. Karjavin
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- W.J. Spalding
- W.J. Womersley
- W.L. Aldá Júnior
- W.L. Prado Da Silva
- W.T. Ford
- X. Janssen
- X. Niu
- X. Quan
- X. Shi
- Y. Assran
- Y. Ban
- Y. Chao
- Y. Chen
- Y. Choi
- Y. Erdogan
- Y. Eshaq
- Y. Gershtein
- Y. Go
- Y. Guler
- Y. Hsiung
- Y. Iiyama
- Y. Ivanov
- Y. Kim
- Y. Kubota
- Y. Kuessel
- Y. Lu
- Y. Mao
- Y. Mao
- Y. Maravin
- Y. Musienko
- Y. Onel
- Y. Pakhotin
- Y. Roh
- Y. Sirois
- Y. Takahashi
- Y. Tu
- Y. Weng
- Y. Xin
- Y. Yang
- Y. Yilmaz
- Y.-J. Lee
- Y.D. Oh
- Y.F. Liu
- Y.H. Chang
- Y.H. Shin
- Y.J. Lu
- Y.K. Choi
- Y.M. Tzeng
- Y.O. Günaydin
- Y.S. Lai
- Y.W. Chang
- Yu. Andreev
- Z. Antunovic
- Z. Chen
- Z. Demiragli
- Z. Hu
- Z. Lesko
- Z. Mao
- Z. Meng
- Z. Szillasi
- Z. Tsamalaidze
- Z. Tu
- Z. Wang
- Z. Wu
- Z. Xu
- Z.A. Ibrahim
- Z.L. Trocsanyi
- Publication venue
- Publication date
- 01/01/2015
- Field of study
A search for the pair production of new light bosons, each decaying into a pair of muons, is performed with the CMS experiment at the LHC, using a dataset corresponding to an integrated luminosity of 20.7 fb-1 collected in proton-proton collisions at center-of-mass energy of √s=8 TeV. No excess is observed in the data relative to standard model background expectation and a model independent upper limit on the product of the cross section, branching fraction, and acceptance is derived. The results are compared with two benchmark models, the first one in the context of the next-to-minimal supersymmetric standard model, and the second one in scenarios containing a hidden sector, including those predicting a nonnegligible light boson lifetime. © 2015 CERN for the benefit of the CMS Collaboration
Azithromycin in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial
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- Publication venue
- 'Elsevier BV'
- Publication date
- 01/02/2021
- Field of study
Background Azithromycin has been proposed as a treatment for COVID-19 on the basis of its immunomodulatory actions. We aimed to evaluate the safety and efficacy of azithromycin in patients admitted to hospital with COVID-19. Methods In this randomised, controlled, open-label, adaptive platform trial (Randomised Evaluation of COVID-19 Therapy [RECOVERY]), several possible treatments were compared with usual care in patients admitted to hospital with COVID-19 in the UK. The trial is underway at 176 hospitals in the UK. Eligible and consenting patients were randomly allocated to either usual standard of care alone or usual standard of care plus azithromycin 500 mg once per day by mouth or intravenously for 10 days or until discharge (or allocation to one of the other RECOVERY treatment groups). Patients were assigned via web-based simple (unstratified) randomisation with allocation concealment and were twice as likely to be randomly assigned to usual care than to any of the active treatment groups. Participants and local study staff were not masked to the allocated treatment, but all others involved in the trial were masked to the outcome data during the trial. The primary outcome was 28-day all-cause mortality, assessed in the intention-to-treat population. The trial is registered with ISRCTN, 50189673, and ClinicalTrials.gov, NCT04381936. Findings Between April 7 and Nov 27, 2020, of 16 442 patients enrolled in the RECOVERY trial, 9433 (57%) were eligible and 7763 were included in the assessment of azithromycin. The mean age of these study participants was 65·3 years (SD 15·7) and approximately a third were women (2944 [38%] of 7763). 2582 patients were randomly allocated to receive azithromycin and 5181 patients were randomly allocated to usual care alone. Overall, 561 (22%) patients allocated to azithromycin and 1162 (22%) patients allocated to usual care died within 28 days (rate ratio 0·97, 95% CI 0·87–1·07; p=0·50). No significant difference was seen in duration of hospital stay (median 10 days [IQR 5 to >28] vs 11 days [5 to >28]) or the proportion of patients discharged from hospital alive within 28 days (rate ratio 1·04, 95% CI 0·98–1·10; p=0·19). Among those not on invasive mechanical ventilation at baseline, no significant difference was seen in the proportion meeting the composite endpoint of invasive mechanical ventilation or death (risk ratio 0·95, 95% CI 0·87–1·03; p=0·24). Interpretation In patients admitted to hospital with COVID-19, azithromycin did not improve survival or other prespecified clinical outcomes. Azithromycin use in patients admitted to hospital with COVID-19 should be restricted to patients in whom there is a clear antimicrobial indication. Funding UK Research and Innovation (Medical Research Council) and National Institute of Health Research