Last update 21 Nov 2024

Autologous CD1c (BDCA-1)+ myDC(Universitair Ziekenhuis Brussel)

Overview

Basic Info

Drug Type
Cell therapy
Synonyms-
Target-
Mechanism
Cell replacements
Therapeutic Areas
Active Indication-
Inactive Indication
Originator Organization
Active Organization-
Inactive Organization
Drug Highest PhasePendingPhase 1
First Approval Date-
Regulation-
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Solid tumorPhase 1
BE
29 Jan 2018
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Phase 1
6
(nrnvopaued) = Treatment related adverse events (TRAE) included transient grade 1/2 injection site reactions and constitutional symptoms. One pt experienced a grade 3 systemic inflammatory syndrome with a lymphocytic peritoneal exudate (responsive to corticosteroids). There were no grade 4-5 TRAE. zcfyfwnmne (yvaiyeuznd )
Positive
14 Sep 2024
Phase 1
Refractory Melanoma
CD1c (BDCA-1) | CD141 (BDCA-3)
8
(ikeveqeplo) = zlsxaklnwx wcfiszxnyr (jjkikccjub )
Positive
11 Jan 2024
Phase 1
8
CD1c (BDCA-1)+/CD141 (BDCA-3)+ myDC(Universitair Ziekenhuis Brussel)+nivolumab+ipilimumab
(dcngeqesqr) = gqqbbnpxrf brvgwqivkk (damcuvymhd, 5.193 - 15.007)
Positive
01 Nov 2022
Phase 1
6
(soezgowhxj) = transient G 2 local pain at injection site in 2 pts, G1 pruritus in 2 pts, G2 pneumonitis in 1 pt, G1 rash in 1 pt, pruritus and redness of the skin overlaying the injected lesion in 1 pt udjlyjxiyu (cwwrpzbetg )
Positive
31 May 2019
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Regulation

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