PhuturdexDrug Pipeline Intelligence

Phuturdex › Drugs › Vidofludimus

Drugs in development · updated 11 November 2026

Vidofludimus: clinical trials and development status

Other names and codes: IMU-838

FDA substance registryNot approved in the USNo EMA authorisationEstimated US launch Jan 2028 – Nov 2028 (Phuturdex estimate)

As of 11 November 2026 Vidofludimus is in 3 active clinical trials (recruiting or ongoing, phases I–III) for 2 diseases. The most advanced phase is III.

Authorisation

Sources: EMA, AIFA register (open data), FDA. For Germany only the EU centralised authorisation is shown: the national BfArM register is not one of our sources.

Where Vidofludimus trials are recruiting

Map of sites in Europe with recruitment status, every trial and an email when something changes. Full access free until 31 March 2027, no card needed.

Sign up free →
3Active trials
IIIMost advanced phase
2Diseases studied

Diseases studied

For each disease: the drug’s most advanced phase and active trials, with the reference trial on ClinicalTrials.gov.

DiseaseMost advanced phaseActive trialsReference trial
Multiple sclerosisIII2NCT05134441
Relapsing-remitting multiple sclerosisIII2NCT05201638

Sites in Europe

65 sites of the active trials in 7 European countries, 0 recruiting.

Sites declared by the sponsors on ClinicalTrials.gov; region worked out by Phuturdex from the geographic point. The list of sites with city and recruitment status is in the app. See the sites →

Everything on Vidofludimus

In Phuturdex you get every trial with sponsors, countries and dates, development events, FDA and EMA approvals, patents and exclusivities, orphan designations and safety alerts, with PDF and Excel export. Free until 31 March 2027.

Open in Phuturdex →

Source: Phuturdex analysis of ClinicalTrials.gov (U.S. National Library of Medicine), FDA and EMA data, updated 11 November 2026. Active trials = recruiting or ongoing, phases I–III. Diseases are those named by each trial (NLM MeSH terms). The estimated launch, when shown, refers to the United States and is a Phuturdex calculation described on the Method page, not official data: the drug may already be marketed in other countries.

ItalianoFrançaisDeutsch