IMO-2125
Sponsors
Amsterdam UMC, Idera Pharmaceuticals, Inc.
Conditions
Hepatitis CHepatitis C, Treatment Naïve, Genotype 1 PatientsMelanomaMetastatic MelanomaRefractory Solid TumorspT3-4 cN0M0 Melanoma
Phase 1
Placebo-controlled, Dose-escalation Study of the Safety of IMO-2125 (Immunomodulatory Oligonucleotide) in Hepatitis C-infected Patients
CompletedNCT00728936
Start: 2007-09-30End: 2010-05-31Updated: 2019-02-15
Study of Combination Treatment With IMO-2125 and Ribavirin in Naïve Hepatitis C-infected, Genotype 1 Patients
CompletedNCT00990938
Start: 2009-09-30End: 2011-01-31Updated: 2019-02-15
A Study of Intratumoral IMO-2125 in Patients With Refractory Solid Tumors
CompletedNCT03052205
Start: 2017-06-09End: 2019-10-04Updated: 2020-02-11
Phase 2
A Phase 2 Study to Assess the Safety and Efficacy of IMO-2125 With 8 mg Ipilimumab in Patients With Metastatic Melanoma
CompletedNCT02644967
Start: 2015-12-31End: 2021-05-31Updated: 2022-08-03
A Randomized Controlled Phase II Clinical Trial with Intradermal IMO-2125 (Tilsotolimod) in clinical cT3-4N0M0 Melanoma (Intrim 1 study)
Active, not recruitingCTIS2023-509461-20-00
Start: 2020-01-22Target: 214Updated: 2024-12-06