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NCT06802328

Intermediate-Size Patient Population Expanded Access: Foralumab in Non-Active Secondary Progressive MS Patients

AVAILABLE Last updated 6 June 2025
What this trial tests

trial testing Foralumab TZLS-401 50 µg in Non-Active Secondary Progressive Multiple Sclerosis. Available.

Quick facts

Lead sponsorTiziana Life Sciences LTD
StatusAVAILABLE
Study typeEXPANDED_ACCESS
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Tiziana Life Sciences LTD — full company profile →

Who can join

Adults 25 to 75, any sex, with Non-Active Secondary Progressive Multiple Sclerosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is an open-label, intermediate-size patient population expanded access treatment study utilizing 1 dose level of nasal Foralumab (50 µg/dosing day) with the possibility of increasing to 100 µg/dosing day. The goal of this expanded access clinical trial is to evaluate safety, tolerability, and immune effects of intranasal Foralumab in non-active secondary progressive multiple sclerosis patients. The primary objective is to treat patients who have failed current available therapy. Participants will visit the clinic for testing and follow-up every cycle (3 weeks) while administering the medication at home if able three times weekly.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Nasal Foralumab for the Treatment of Progression Independent of Relapses in Patients With Nonactive Secondary Progressive Multiple Sclerosis
    Chitnis T, Singhal T, Zurawski J, Saraceno T, et al · · 2026

Verify or expand the search:

Other recruiting trials for Non-Active Secondary Progressive Multiple Sclerosis

Currently open trials in the same condition.

Other Tiziana Life Sciences LTD trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06802328.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing