drugset / Trial / NCT07517185

The HIt HArd and hiT Early in Multiple Sclerosis Trial

NCT07517185

Phase 2 Not yet recruiting 60 enrolled Uppsala University
NaSingle-groupOpen-labelTreatment

Summary

The HiHat trial is a Phase 2 study aimed at evaluating the safety and feasibility of sequential treatment with rituximab and cladribine in patients with relapsing-remitting multiple sclerosis (RRMS). The study follows a prospective, open-label, single-arm design, with 60 RRMS patients receiving both treatments in a controlled regimen: two cycles of rituximab (1,000 mg each, biweekly) followed by two cycles of cladribine (30 mg per cycle for three days per cycle) spaced one month apart. Participants are monitored over 24 months through clinical assessments, MRI, and biomarker analyses. The primary objective is to evaluate whether the rate of serious adverse events (SAE) is acceptably low. Secondary objectives include assessing impacts on MRI lesion count, relapse rates, disability progression, quality of life, and safety.

Timeline

Start
2026-04-15
Primary completion
2030-12-31
Completion
2030-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Cladribine Small molecule 30 mg
Subject Rituximab Monoclonal antibody 1000 mg