Last update 21 Jun 2024

Cobomarsen

Overview

Basic Info

Drug Type
Antisense oligonucleotides
Synonyms
Cobomarsen (USAN/INN), LNA-antimiR-155, MRG-106
Target
Mechanism
miR-155 antagonists(microRNA 155 antagonists)
Active Indication
Originator Organization
Active Organization
Inactive Organization-
Drug Highest PhasePhase 2
First Approval Date-
RegulationOrphan Drug (US)

External Link

KEGGWikiATCDrug Bank
D11163--

R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Cutaneous T-Cell LymphomaPhase 2--
Adult T-Cell Leukemia-LymphomaPhase 1
US
09 Feb 2016
Chronic Lymphocytic LeukemiaPhase 1
US
09 Feb 2016
Diffuse Large B-Cell LymphomaPhase 1
US
09 Feb 2016
Mycosis FungoidesPhase 1
US
09 Feb 2016
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Phase 2
37
Cobormarsen+Cobomarsen
(Cobomarsen (Randomized))
jzkmedbvmo(hubzimrknu) = uwpwucoobo wpnrjeqpxa (ggoovppdzp, xnvghmygsz - ifngllvduk)
-
08 Apr 2022
(Vorinostat (Randomized))
jzkmedbvmo(hubzimrknu) = nwsocemwiq wpnrjeqpxa (ggoovppdzp, ixmepivpki - trmunmocud)
Phase 2
37
xgymnuncqo(uuqkawyppd) = Based on investigator assessments, these preliminary data in 37 patients suggest that cobomarsen lacks a compelling result for the study's primary endpoint, objective skin response of at least four months duration (ORR4) relative to the vorinostat control arm. dyswodpyxn (hdqlpqpnxp )
Negative
05 Oct 2020
Phase 1
15
dagrcqrale(tzwwivnldi) = One patient at the 900 mg SC dose level had a possible flare of their disease after 3 doses that resolved after 3 weeks. riclumedyu (rtxenkzzni )
Positive
30 May 2017
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Regulation

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