CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 125 enrolled
Drug / intervention
RO7490677 +1 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01981850
NCT01981850Phase 2Completed

A Phase 2, Prospective Study Of PRM-151 In Subjects With Primary Myelofibrosis (PMF), Post-Polycythemia Vera MF (Post-PV MF), Or Post-Essential Thrombocythemia MF (Post-ET MF)

Hoffmann-La Roche·interventional·Posted Nov 13, 2013·Updated Jan 5, 2022

In Brief

A Phase 2 clinical trial evaluating RO7490677 and Ruxolitinib for Primary Myelofibrosis and 2 related conditions. Completed, enrolled 125 participants across 23 sites in 8 countries.

Detailed Summary

RO7490677 is an investigational drug that is being developed for possible use in the treatment of myelofibrosis (MF), a disease in which the bone marrow, which is the organ in the body that makes blood cells, is replaced by fibrosis, or excess scar tissue. The purpose of this study is to gather information on whether RO7490677 has an effect on the MF disease, whether it is safe in patients with MF, and how well it is tolerated.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, France, Germany, Israel, Italy, Netherlands, United Kingdom, United States
Collaborators--

Timeline

Phase 2CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedNov 13, 2013
Enrollment StartOct 1, 2013
Primary CompletionJul 10, 2020
TodayJul 2, 2026
Enrollment to primary: 6.8 yearsPosted 12.6 years ago

Interventions

RO7490677biological

IV infusion

Ruxolitinibdrug

IV infusion