WHO ICTRP trial

A Clinical Trial to compare the effectiveness of the study drug IMO-2125 given…

EUCTR2017-002454-36-SE · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2017-002454-36-SE
Public title A Clinical Trial to compare the effectiveness of the study drug IMO-2125 given in combination with Ipilimumab (a drug indicated for the treatment of advanced melanoma) compared to Ipilimumab given alone in subjects with Refractory Melanoma
Scientific title A Randomized Phase 3 Comparison of IMO-2125 with Ipilimumab versus Ipilimumab Alone in Subjects with Anti-PD-1 Refractory Melanoma
Primary sponsor Idera Pharmaceuticals, Inc.
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): yes Therapeutic use (Phase IV): no
Countries United States;France;Czech Republic;Canada;Spain;Australia;Netherlands;Germany;United Kingdom;Italy;Sweden
Conditions Refractory melanoma is a malignant tumor of melanocytes which originates predominantly from skin. MedDRA version: 20.0 Level: LLT Classification code 10027481 Term: Metastatic melanoma System Organ Class: 100000004864 ;Therapeutic area…
Interventions Product Name: IMO-2125 Product Code: IMO-2125 Pharmaceutical Form: Solution for injection INN or Proposed INN: tilsotolimod Current Sponsor code: tilsotolimod Other descriptive name: IMO-2125 Concentration unit: mg/ml…
Registration date Mar 13, 2018
Target size 454
Secondary IDs 2125-MEL-301;125515
Registry page clinicaltrialsregister.eu

At a glance

  • Yes Results available

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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