Oh Sang Kwon

Dr. Oh Sang Kwon

orcid

Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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5 May 2022 in New England Journal of Medicine
Verified
Journal Article
Closed access
BKBrett King
Brett King
MOManabu Ohyama
Manabu Ohyama
OKOh Sang Kwon
Oh Sang Kwon
AZAbraham Zlotogorski
Abraham Zlotogorski
JKJustin Ko
Justin Ko
RSRodney Sinclair
Rodney Sinclair
Alopecia areata is an autoimmune condition characterized by rapid hair loss in the scalp, eyebrows, and eyelashes, for which treatments are limited. Baricitinib, an oral, selective, reversible inhibitor of Janus kinases 1 and 2, may interrupt cytokine signaling implicated in the pathogenesis of alopecia areata.

2 June 2013 in Nature Medicine
Verified
Journal Article
Closed access
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DGDenise Gay
Denise Gay
OKOh Sang Kwon
Oh Sang Kwon
ZZZhikun Zhang
Zhikun Zhang
MSMichelle Spata
Michelle Spata
MPMaksim V Plikus
Maksim V Plikus
GCGeorge Cotsarelis
George Cotsarelis

1 April 2004 in Journal of Dermatological Science
Verified
Journal Article
Closed access
JHJi Hyun Han
Ji Hyun Han
OKOh Sang Kwon
Oh Sang Kwon
JCJin Ho Chung
Jin Ho Chung
KCKwang Hyun Cho
Kwang Hyun Cho
HEHee Chul Eun
Hee Chul Eun
KKKyu Han Kim
Kyu Han Kim

1 July 2007 in Journal of the American Academy of Dermatology
Verified
Journal Article
Closed access
WLWon-Soo Lee
Won-Soo Lee
BRByung In Ro
Byung In Ro
SHSeung Phil Hong
Seung Phil Hong
HBHana Bak
Hana Bak
WSWoo-Young Sim
Woo-Young Sim
TOTak Heon Oh
Tak Heon Oh

1 March 2023 in American Journal of Clinical Dermatology
Verified
Journal Article
Open access
PDF file
OKOh Sang Kwon
Oh Sang Kwon
MSMaryanne M. Senna
Maryanne M. Senna
RSRodney Sinclair
Rodney Sinclair
TITaisuke Ito
Taisuke Ito
YDYves Dutronc
Yves Dutronc
BKBrett King
Brett King
Background The oral Janus kinase (JAK) inhibitor baricitinib has demonstrated efficacy for severe alopecia areata (AA) over 36 weeks. There are limited data on the longer-term treatment of AA. Objective The aim of this study was to evaluate the efficacy and safety of baricitinib for AA in adults with ≥50% scalp hair loss through 52 weeks of continuous therapy in two phase III trials (BRAVE-AA1 and BRAVE-AA2). Methods Patients randomized to baricitinib at baseline in BRAVE-AA1 (N = 465) and BRAVE-AA2 (N = 390) retained their treatment allocation through Week 52. Efficacy outcomes included the proportion of patients achieving a Severity of Alopecia Tool (SALT) score ≤ 20 (≤ 20% scalp hair loss). Data were censored after permanent treatment discontinuation or if collected remotely due to the coronavirus disease 2019 (COVID-19) pandemic. Results Response rates for hair regrowth increased over the 52-week period. Of patients treated with baricitinib 4 mg and 2 mg, respectively, 40.9% and 21.2% in BRAVE-AA1 and 36.8% and 24.4% in BRAVE-AA2 achieved a SALT score ≤ 20 at Week 52. The most frequent treatment-emergent adverse events included upper respiratory tract infection, headache, nasopharyngitis, acne, urinary tract infection, creatine phosphokinase elevation, and COVID-19 infection. Limitation There were no comparisons with placebo. Conclusion Efficacy of baricitinib for adults with severe AA continuously improved over 52 weeks, indicating that long-term treatment may be necessary to observe maximum clinical benefit. There were no new safety signals. ClinicalTrials Registration ClinicalTrials.gov NCT03570749 and NCT03899259. Video abstract Efficacy and Safety of Baricitinib in Patients with Severe Alopecia Areata: Week-52 Results from BRAVE-AA1 and BRAVE-AA2

1 August 2007 in Phytomedicine
Verified
Journal Article
Closed access
OKOh Sang Kwon
Oh Sang Kwon
JHJ.H. Han
J.H. Han
HYH.G. Yoo
H.G. Yoo
JCJ.H. Chung
J.H. Chung
KCK.H. Cho
K.H. Cho
KKK.H. Kim
K.H. Kim