Not medical advice. This website is not medical advice, a diagnosis, a match to a trial, or a recommendation to join a study. Listings are plain-English rewrites of public ClinicalTrials.gov records. Whether a site is still enrolling, and whether you qualify, can only be confirmed by the study team and your clinician. Source registry: ClinicalTrials.gov. Editorial rules: methodology.
PlainTrials
RecruitingPhase 4interventionalRules rewrite

Phase 4: testing Ocrelizumab at home for Multiple Sclerosis

The goal is to assess the safety and effectiveness of home ocrelizumab infusion.

Official registry: https://clinicaltrials.gov/study/NCT04650321 · University of Colorado, Denver · enrollment listed as 110

What this phase means

Phase 4: the treatment is already approved. This study asks new questions — longer-term effects, other diseases, or how it compares in everyday care.

Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

What the registry says happens

If you join, the listed intervention(s) are Ocrelizumab at home. The registry lists allocation as na. The goal is to assess the safety and effectiveness of home ocrelizumab infusion.

They plan to enroll about 110 people at Centennial. Taking part typically means taking a study drug (or dummy pill) plus check-ins.

Official title (unrewritten)

Evaluating the Feasibility of Pandemic Forward, Telehealth Based Home Based Infusions

Interventions: Ocrelizumab at home

Primary outcome (registry wording): Severe infusion reactions

Who it is for (from inclusion criteria)

  • Ages 18 Years to 55 Years
  • Current active patient of Rocky Mountain MS Center at the time of final study consent
  • Between 18-55 years of age at the time of final study consent
  • Diagnosis of primary progressive or relapsing MS as defined by the 2017 McDonald criteria.19
  • Has at minimum completed their first 600 mg dose of ocrelizumab
  • Is physically residing in the Denver metro, Fort Collins or Colorado Springs area at the time of final study consent
  • Has a Patient Determined Disease Steps (PDDS) between 0 to 6.5 20
  • Can complete patient reported outcomes developed and validated as English written scales

Public study contact (from the registry)

Brooke Valdez, BS

303-724-2635

brooke.valdez@cuanshutz.edu

Published on ClinicalTrials.gov. Contact them as a possible participant. They decide eligibility.

Sites listed on ClinicalTrials.gov

1 listed

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FAQ about this NCT record

Is NCT04650321 still recruiting?

The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.

What phase is NCT04650321?

Phase 4. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

Can PlainTrials tell me if I qualify for NCT04650321?

No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.

How to read a ClinicalTrials.gov record · Questions to ask the coordinator · Glossary