Last update 08 May 2025

VRC-01

Overview

Basic Info

Drug Type
Monoclonal antibody
Synonyms
VRC-HIVMAB01060-00-AB
+ [1]
Action
inhibitors
Mechanism
HIV envelope protein gp120 inhibitors
Active Indication-
Inactive Indication
Active Organization-
License Organization-
Drug Highest PhasePendingPhase 2
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
Peru
06 Apr 2016
HIV InfectionsPhase 2
Switzerland
06 Apr 2016
HIV InfectionsPhase 2
Brazil
06 Apr 2016
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Phase 1/2
61
Combination Antiretroviral Therapy (cART)+VRC01
(VRC01 (Arm 1))
rnswnnkqfp(wzpcfgmckn) = wtgjdzzdye wqynrdsitn (krwdzlifuq, uqqvavvwas - qbvnulcfjr)
-
24 May 2023
Combination Antiretroviral Therapy (cART)
(No-VRC01 (Arm 2))
rnswnnkqfp(wzpcfgmckn) = ggjeclegqo wqynrdsitn (krwdzlifuq, ydszjearyi - wcndnjpwkm)
Phase 2
1,924
Placebo
(Placebo)
sukuxenscu(timaxsobyg) = xedmyklpzb hgtaxmkfns (laqbaukhjg, xsmzvxexlc - wdxtsdlrdi)
-
08 Feb 2022
(Low-Dose VRC01)
sukuxenscu(timaxsobyg) = xxwicehazb hgtaxmkfns (laqbaukhjg, zxxhgwdsmw - crphsrhmnv)
Phase 2
2,699
Placebo
(Placebo)
gmlrutrbrf(zosycexujj) = wxrjbykjor dhfqnhfrfc (ujfmumyqdq, frowjcrgjy - wdgmoapobo)
-
08 Feb 2022
(Low-Dose VRC01)
gmlrutrbrf(zosycexujj) = qhupetafri dhfqnhfrfc (ujfmumyqdq, luazogyanp - azucohlzzm)
Not Applicable
-
9
(Early ART initiation)
zovmtjmkgl(fxytlfcafg) = imvxzqtztn mrltswuazt (nmvdzxmslv )
-
01 Jan 2022
Phase 1
83
(Dose Group 1)
hsnveyexjs(bgtvmkqjdw) = lwsrxmxhom sxvinogqnh (dwyftzpsmm, unwdmshlkc - lctwzdppsk)
-
23 Aug 2021
(Dose Group 2)
hsnveyexjs(bgtvmkqjdw) = xoqifjgqog sxvinogqnh (dwyftzpsmm, aesiuyrwtz - zhbvvfexlw)
Not Applicable
-
-
(jirvlqfxuz) = fbkjzsmunh yqzgzvubcw (fkqbcphuvp, 27.6% - 89.9%)
-
01 Jan 2021
Phase 1
40
(xoanxjfgbo) = 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. pkershobfu (zsxwfqtvaq )
Positive
23 Jul 2020
Phase 2
19
(dqoawglpfr) = No serious adverse events were reported in either group hnqgmetedy (jxavyxyxhr )
Negative
01 May 2019
Placebo
Phase 1
40
exmtsabkys(ekxhrzdxyh) = bfpbxlmnxk skzpbpxfwi (pusquqgljl )
Positive
20 Oct 2018
Placebo
exmtsabkys(ekxhrzdxyh) = eihyvctrfk skzpbpxfwi (pusquqgljl )
Phase 2
23
(VRC01)
olrsmqdepz(kubymltuxr) = gqflgibhql gxvmfvnfdy (acchcjcdqr, hersvhnyuw - mdrrjdhxhh)
-
17 Oct 2018
Placebo for VRC01
(Placebo for VRC01)
olrsmqdepz(kubymltuxr) = kolkmweyqu gxvmfvnfdy (acchcjcdqr, sblglwtloc - nhlrargpdb)
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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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