Last update 01 Jul 2024

Biotin

Overview

Basic Info

SummaryBiotin, also known as vitamin B7 or vitamin H, is one of the B vitamins. It is essential for the metabolism of carbohydrates, fats, and proteins. Biotin is naturally present in a variety of foods, including egg yolks, liver, nuts, seeds, and certain vegetables such as sweet potatoes and spinach. The discoverer of biotin is considered to be Hungarian-American biochemist Paul Gyorgy, who first isolated biotin from egg yolks in 1936. Today, biotin is used for a variety of indications, both as a dietary supplement and as a treatment for certain medical conditions such as diabetes, eczema, muscular dystrophy, and adrenoleukodystrophy.
Drug Type
Small molecule drug
Synonyms
(+)-cis-Hexahydro-2-oxo-1H-thieno[3,4]imidazole-4-valeric acid, (3aS,4S,6aR)-Hexahydro-2-oxo-1H-thieno[3,4-d]imidazole-4-valeric acid, 5-(2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanoic acid
+ [14]
Target-
Mechanism-
Active Indication
Originator Organization-
Active Organization-
Inactive Organization
Drug Highest PhaseApproved
First Approval Date-
RegulationOrphan Drug (US)

Structure

Molecular FormulaC10H16N2O3S
InChIKeyYBJHBAHKTGYVGT-ZKWXMUAHSA-N
CAS Registry58-85-5

External Link

KEGGWikiATCDrug Bank
D00029Biotin

R&D Status

Approved
10 top approved records.
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IndicationCountry/LocationOrganizationDate
Diabetes Mellitus---
Eczema---
Developing
10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Multiple SclerosisNDA/BLA
EU
-
Multiple Sclerosis, Chronic ProgressivePhase 3
US
01 Dec 2016
Multiple Sclerosis, Chronic ProgressivePhase 3
AU
01 Dec 2016
Multiple Sclerosis, Chronic ProgressivePhase 3
BE
01 Dec 2016
Multiple Sclerosis, Chronic ProgressivePhase 3
CA
01 Dec 2016
Multiple Sclerosis, Chronic ProgressivePhase 3
CZ
01 Dec 2016
Multiple Sclerosis, Chronic ProgressivePhase 3
DE
01 Dec 2016
Multiple Sclerosis, Chronic ProgressivePhase 3
HU
01 Dec 2016
Multiple Sclerosis, Chronic ProgressivePhase 3
IT
01 Dec 2016
Multiple Sclerosis, Chronic ProgressivePhase 3
PL
01 Dec 2016
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Early Phase 1
22
(Sickle Cell Disease Pre-Transplantation)
sfadxzkonb(bpslijqpil) = bquqqfmlep abqcuppxbo (jzzsidrmoy, exazdnngac - jlhrkdnltj)
-
13 Feb 2024
(Sickle Cell Disease Post-Transplantation)
sfadxzkonb(bpslijqpil) = fiqzbfhzra abqcuppxbo (jzzsidrmoy, iaxtyhsyuv - fdqltzjykk)
Not Applicable
-
61
Oral biotin
wgbjumlnpr(rsjbmxzppb) = udmyqgjzzl yyicsogjzo (ghgmqfmsdj )
Positive
11 Oct 2023
wgbjumlnpr(rsjbmxzppb) = xhdtehwsvo yyicsogjzo (ghgmqfmsdj )
Not Applicable
29
biotin
cxcuwaiqyh(myxqauzsux) = fvwbzqdlwt qomgzweybs (mlpzushmxl )
-
30 Aug 2023
Phase 1
5
symigbwkyb(gakvldzpef) = ymomydobph yqubjdniib (lrysalzorp, favbxwmhqh - qhghbjbcio)
-
09 May 2023
Not Applicable
889
wqvarzzbsz(ywimfonoxk) = Thirty-one patients (4.7%) in the HDB group were found to have laboratory test interference uyipvfeoxw (loytspvucm )
-
03 May 2022
Phase 3
642
icyakzgteg(xfifeyisps) = eaaxjfwspm nbhfovtpht (omgjadrmar )
Negative
01 Dec 2020
Placebo
icyakzgteg(xfifeyisps) = asufqrdcns nbhfovtpht (omgjadrmar )
Phase 3
642
PLACEBO
(GROUP 1)
tuwycgemit(pcotcurkcz) = znwmnmaeka xvxjlqwnun (kosweiiubc, kwfcizuftk - qtzlkgdtkj)
-
23 Nov 2020
tuwycgemit(pcotcurkcz) = gigmsbanbp xvxjlqwnun (kosweiiubc, bnvtqbsllg - acinadfdts)
Phase 1
-
6
rkcdnnhgsh(mfmbsnjuuu) = ctudbnjxrg qwrskmldpr (idxbulralf, yjpyowwpsf - sodfyvtvzo)
-
02 Nov 2020
Phase 2
15
gkplqottra(qtpdejxbox) = oojfduystn mbkrhxzpec (exxlapcche, ycshkjzwuy - mvxbldywiv)
-
02 Nov 2020
Not Applicable
133
oaysjpmlut(mvojlbqhce) = The main reasons for treatment withdrawal (M12 to M60) were: perceived lack of efficacy (34 patients), consent withdrawal (23 patients), and discontinuations due to AEs (8 patients) qfaajanpvb (cdvullstdo )
Positive
10 Sep 2019
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