200 Participants Needed

TEV-56286 for Multiple System Atrophy

TU
Overseen ByTeva U.S. Medical Information
Age: 18+
Sex: Any
Trial Phase: Phase 2
Sponsor: Teva Branded Pharmaceutical Products R&D LLC
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests the safety and tolerability of a new oral medication, TEV-56286, for individuals with Multiple System Atrophy (MSA), a rare disorder affecting movement and balance. The goal is to assess how well patients manage long-term use of the medication. The trial spans about 100 weeks and suits those who have completed a previous related study with the same medication. Individuals with MSA who meet these criteria may find this trial suitable. As a Phase 2 trial, the research measures the treatment's effectiveness in an initial, smaller group of participants.

Do I have to stop taking my current medications for the trial?

The trial information mentions that some medications might be prohibited, but it doesn't specify which ones. It's best to contact the trial investigator for details about your specific medications.

Is there any evidence suggesting that TEV-56286 is likely to be safe for humans?

Research shows that the FDA has granted "fast track" status to TEV-56286, indicating it as a promising treatment for Multiple System Atrophy (MSA). This status often suggests that the drug has demonstrated potential benefits that outweigh risks in earlier tests, indicating a good safety profile.

In previous studies, researchers tested TEV-56286 on people with MSA. Although detailed safety data is not provided here, the continuation of trials suggests it was generally well-tolerated with manageable side effects. The ongoing research aims to confirm its long-term safety. So far, there have been no reports of serious side effects, which is encouraging for those considering joining the trial.12345

Why do researchers think this study treatment might be promising for MSA?

TEV-56286 is unique because it introduces a novel approach to treating Multiple System Atrophy (MSA), a condition for which there are currently limited treatment options mainly focusing on managing symptoms, such as autonomic dysfunction and movement disorders, rather than altering disease progression. Unlike current therapies, TEV-56286 may target the underlying disease mechanisms, offering potential neuroprotective benefits. Researchers are excited about TEV-56286 because it could provide a breakthrough in slowing down or even halting the progression of MSA, potentially improving quality of life for patients.

What evidence suggests that TEV-56286 might be an effective treatment for Multiple System Atrophy?

Studies have shown that TEV-56286, also known as Emrusolmin, is under development as a potential treatment for Multiple System Atrophy (MSA). The FDA has granted it fast track designation, recognizing it as a promising new therapy for this condition. The drug targets specific pathways in the body believed to be involved in MSA, aiming to slow the disease's progression. Although no treatment has been proven to completely stop MSA, TEV-56286 seeks to address this gap by altering the disease's development. Early signs suggest it could improve the management of MSA symptoms.12367

Who Is on the Research Team?

TM

Teva Medical Expert, MD

Principal Investigator

Teva Branded Pharmaceutical Products R&D LLC

Are You a Good Fit for This Trial?

This trial is for adults with Multiple System Atrophy who completed a previous TEV-56286 trial and were compliant. Women able to have children must test negative for pregnancy and use effective birth control, as should men with fertile partners.

Inclusion Criteria

I completed the treatment and follow-up for a previous trial without missing any requirements.
I understand there may be more criteria to meet.
I am using effective birth control because my partner is fertile.
See 2 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive TEV-56286 orally for the treatment of Multiple System Atrophy

100 weeks

Follow-up

Participants are monitored for safety and effectiveness after treatment

4-8 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • TEV-56286
Trial Overview The study tests the long-term safety of an oral drug called TEV-56286 in treating Multiple System Atrophy over approximately 100 weeks. It aims to understand if this treatment can be tolerated well over time.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: TEV-56286Experimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Teva Branded Pharmaceutical Products R&D LLC

Lead Sponsor

Citations

NCT06568237 | A Study to Test if TEV-56286 is Effective in ...The primary objective of the study is to evaluate the efficacy of TEV-56286 administered orally for the treatment of adult participants with Multiple System ...
Teva's Emrusolmin Granted U.S. FDA Fast Track Designation ...Emrusolmin (TEV-56286) is an investigational therapy being developed for the treatment of Multiple System Atrophy (MSA) that targets ...
Teva's Emrusolmin Granted Fast Track Designation for ...Teva's emrusolmin receives FDA fast track designation as a potential breakthrough treatment for multiple system atrophy, targeting ...
NCT07197866 | An Extension Trial to Test if TEV-56286 is ...The primary objective of the trial is to describe the long-term safety and tolerability of TEV-56286 administered orally for the treatment of adult participants ...
Next Era of Multiple System Atrophy TreatmentSymptomatic management remains the cornerstone of MSA care, as no disease-modifying medication has proven effective in halting its progression.
Finding Clinical TrialsA Study to Test if TEV-56286 is Effective in Relieving Multiple System Atrophy (MSA): A Safety and Efficacy Study (TOPAS-MSA). The primary objective of the ...
Emrusolmin FDA Fast Tracked for Multiple System AtrophyTeva Pharmaceuticals Industries Ltd announced that the FDA granted Fast Track designation for Teva's investigational therapy emrusolmin ...
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