TrialPath
Multiple sclerosis · Denver

Multiple sclerosis clinical trials in Denver

5 recruiting multiple sclerosis studies within range of Denver. Click any trial for full eligibility criteria and contact info.

TSC Biosample Repository and Natural History Database

NCT05676099 · Tuberous Sclerosis, Lymphangioleiomyomatosis
Recruiting

The TSC Biosample Repository collects and stores samples of blood, DNA, and tissues that scientists can request to use in their research. The samples we collect are all linked to clinical data in the TSC Natural History Database. The TSC Natural History Database captures clinical data to document the impact of the disease on a person's health over his or her lifetime. This data may be collected retrospectively or prospectively.

Phase
TypeObservational
AgeAny
WhereBirmingham, Alabama, United States + 23 more
SponsorNational Tuberous Sclerosis Association
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A Study Evaluating the Real World Experience of Participants Treated With BRIUMVI® (Ublituximab-xiiy) for Relapsing Multiple Sclerosis (RMS)

NCT06433752 · Relapsing Multiple Sclerosis, Multiple Sclerosis
Recruiting

The purpose of this study is to evaluate safety, effiectiveness, and to gain insight into the treatment experience of participants prescribed BRIUMVI® (ublituximab-xiiy) in the real-world setting

Phase
TypeObservational
Age18 Years
WhereBirmingham, Alabama, United States + 84 more
SponsorTG Therapeutics, Inc.
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A Long-Term Follow-Up Study for Participants Previously Treated With KYV-101

NCT07403188 · Refractory Lupus Nephritis, Myasthaenia Gravis, Stiff Person Syndrome
Recruiting

The purpose of this long-term follow-up (LTFU) study is to collect delayed adverse events (AEs) and understand the persistence of KYV-101 (autologous CAR T cell product; gene-modified product), in participants who have been administered KYV-101 (gene-modified product; autologous CAR T cell product). This LTFU protocol will be open to any participant who received at least one infusion of KYV-101 in a previous Kyverna sponsored clinical trial or Investigator Initiated Trial (IIT).

Phase
TypeObservational
Age18 Years
WhereDenver, Colorado, United States
SponsorKyverna Therapeutics
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A Study to Evaluate the Safety, Tolerability, Efficacy, and Drug Levels of CC-97540 in Participants With Relapsing Forms of Multiple Sclerosis, Progressive Forms of Multiple Sclerosis or Refractory Myasthenia Gravis (MG) (Breakfree-2)

NCT06220201 · Multiple Sclerosis, Myasthenia Gravis
Recruiting

The purpose of this study is to evaluate the safety, tolerability, efficacy, and drug levels of CC-97540 in participants with Relapsing Forms of Multiple Sclerosis (RMS), Progressive Forms of Multiple Sclerosis (PMS) or Refractory Myasthenia Gravis (MG).

PhasePhase 1
TypeInterventional
Age18 Years – 60 Years
WhereBirmingham, Alabama, United States + 34 more
SponsorJuno Therapeutics, Inc., a Bristol-Myers Squibb Company
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Care in Multiple Sclerosis (MS)

NCT07011914 · Multiple Sclerosis
Recruiting

This study is structured around three main aims. In Aim 1, investigators will conduct community-based participatory research (CBPR) to develop culturally tailored methods to assess childhood adversity in multiple sclerosis (MS). Aim 2 will investigate the impact of childhood adversity on MS outcomes among individuals with relapsing-remitting MS (RRMS), among whom 70% belong to a group historically under-represented in MS research: Black, Hispanic, or poverty-impacted. Aim 2 procedures involve two visits that include a research blood draw and an MRI scan. In Aim 3, investigators will conduct interviews and surveys to explore environmental and social factors affecting quality of life for minority MS patients.

Phase
TypeObservational
Age18 Years
WhereBirmingham, Alabama, United States + 5 more
SponsorNYU Langone Health
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