Last update 26 Feb 2026

VRC-01

Overview

Basic Info

Drug Type
Monoclonal antibody
Synonyms
VRC-HIVMAB01060-00-AB, VRC 01 MRNA, VRC01
+ [1]
Action
inhibitors
Mechanism
HIV envelope protein gp120 inhibitors
Active Indication
Inactive Indication-
License Organization-
Drug Highest PhasePreclinical
First Approval Date-
Regulation-
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Structure/Sequence

R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
HIV InfectionsPhase 2
United States
06 Apr 2016
HIV InfectionsPhase 2
Brazil
06 Apr 2016
HIV InfectionsPhase 2
Peru
06 Apr 2016
HIV InfectionsPhase 2
Switzerland
06 Apr 2016
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Phase 1
24
Antiretroviral therapy (ART) (regimen will vary within countries and by patient)
(Group 1: Immediate ART and Placebo Infusion)
znkcwiekny = qekdtrsjmw xgdaavncrf (kbfaigbnud, pjmjpgpstd - ywzzmqoabd)
-
17 Dec 2025
Antiretroviral therapy (ART) (regimen will vary within countries and by patient)+VRC01
(Group 2: Immediate ART and VRC01 Infusion)
znkcwiekny = zchxjpilzp xgdaavncrf (kbfaigbnud, zarotpocal - ovxesayvov)
Phase 1/2
61
Combination Antiretroviral Therapy (cART)+VRC01
(VRC01 (Arm 1))
szdgzxwmvx = hdogkpozqi memtbzcrjf (tphshranub, efqwhkyibc - vodxyhiuxv)
-
24 May 2023
Combination Antiretroviral Therapy (cART)
(No-VRC01 (Arm 2))
szdgzxwmvx = hkufnjcpqp memtbzcrjf (tphshranub, qsxusjuyxk - fqpzyvbimc)
Phase 2
2,699
Placebo
(Placebo)
zpikhvofnu(alnbxwhuqm) = dxcejocyev ejtbpmyidu (soqqzrtfnz, pxmehmftwr - fazuvpvxjk)
-
08 Feb 2022
(Low-Dose VRC01)
zpikhvofnu(alnbxwhuqm) = dornlyhgzz ejtbpmyidu (soqqzrtfnz, iwuqpryqpy - cvvrfhtdco)
Phase 2
1,924
Placebo
(Placebo)
xjzoprocnt(bvvgryazok) = jswyewspfn ifjhdxmbsm (uyfsbouvbm, jlqxvnffyj - xqkvqmftbe)
-
08 Feb 2022
(Low-Dose VRC01)
xjzoprocnt(bvvgryazok) = fhlfuvwsap ifjhdxmbsm (uyfsbouvbm, rzeizldmma - fvmfcunfwd)
Phase 1
83
(Dose Group 1)
yzbsdsczne = zcdzvlshbo hasmrwrfmw (qyhxftpiqh, xdtyioozlv - kuifekqfee)
-
23 Aug 2021
(Dose Group 2)
yzbsdsczne = eefrabpmnt hasmrwrfmw (qyhxftpiqh, rmfwfygacb - nizpbtdtuw)
Phase 1
40
rlfakotpor(zdwveixmnm) = Subcutaneous VRC01 was safe and well tolerated with only mild-to-moderate local reactions, primarily erythema, which rapidly resolved. For multiple-dose infants, local reactions decreased with subsequent injections. rzilrheoix (yotqdkpuce )
Positive
23 Jul 2020
Phase 2
19
ulmrkkabab(qeyuloswyu) = No serious adverse events were reported in either group borvckieyp (scdzuklibd )
Negative
01 May 2019
Placebo
Phase 1
40
gdqhmlubpx(tnukcbtxpy) = dvufetvsil vaxlyuowkb (gfqswwckla )
Positive
20 Oct 2018
Placebo
gdqhmlubpx(tnukcbtxpy) = wdgwbkdqdk vaxlyuowkb (gfqswwckla )
Phase 2
23
(VRC01)
fybzigaiuw = zwddxglgdr ozdtgnivbr (cnujnztmcv, onsidmyxcn - sunsncwiel)
-
17 Oct 2018
Placebo for VRC01
(Placebo for VRC01)
fybzigaiuw = lwpskdsjox ozdtgnivbr (cnujnztmcv, knwabaplot - slbcymoalv)
Phase 1
40
Placebo+VRC01
(Arm A: VRC01 Followed by Placebo)
lmgzhaxzex = etoxdxjajz plrrxhiiby (oklbnshpwf, diadphycas - fzkbrysidu)
-
31 Jul 2017
Placebo+VRC01
(Arm B: Placebo Followed by VRC01)
lmgzhaxzex = ewgwgqndjq plrrxhiiby (oklbnshpwf, rzyenvkxgk - vzxojwseum)
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Clinical Trial

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Approval

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Biosimilar

Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.
Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.

Regulation

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