Phase 1b Safety Study of IMSB301 in Type 1 Interferonopathies
A Phase 1b Open-Label Study of IMSB301 in Subjects With a Type 1 Interferonopathy
ImmuneSensor Therapeutics Inc.
6 participants
Jan 12, 2026
INTERVENTIONAL
Conditions
Summary
Open-Label Study (Phase Ib) of Type 1 Interferonopathy patients receiving IMSB301 monotherapy.
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
Twice daily administration for 28 days. Subjects will be treated as out-patient and will return to the clinic at least once weekly on Days 8, 15, 22 and 29. Continued treatment beyond Day 28 may be considered on a case-by-case basis for subjects benefiting from treatment.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07364513