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NOT YET RECRUITING
NCT07749157
PHASE1

A Study of Subcutaneously Administered RO7845860 in Participants With Relapsing Multiple Sclerosis

Sponsor: Hoffmann-La Roche

View on ClinicalTrials.gov

Summary

The purpose of this study is to assess the safety, tolerability, pharmacokinetics (PK) and, pharmacodynamics (PD) of subcutaneously administered RO7845860 in participants with relapsing multiple sclerosis (RMS).

Official title: An Open-Label, Multicenter, Dose Escalation Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Subcutaneously Administered RO7845860 in Participants With Relapsing Multiple Sclerosis

Key Details

Gender

All

Age Range

18 Years - 60 Years

Study Type

INTERVENTIONAL

Enrollment

85

Start Date

2026-11-23

Completion Date

2031-02-28

Last Updated

2026-08-06

Healthy Volunteers

No

Interventions

DRUG

RO7845860

Participants will receive RO7845860 as an subcutaneous (SC) injection per the schedule in the protocol.