Muscular Atrophy clinical trials at University of California Health
9 in progress, 5 open to eligible people
Blood Flow Restriction After Meniscus Repair
open to eligible people ages 18-60
The purpose of this study is to evaluate post-operative outcomes after meniscus surgery in participants undergoing blood flow restriction training as a rehabilitative adjunct compared to those with standard rehabilitation.
at UCSF
NMD670 in Ambulatory Adult Patients With Type 3 Spinal Muscular Atrophy
open to eligible people ages 18-75
The purpose of this study is to evaluate the efficacy, safety, tolerability and pharmacokinetics of NMD670 in the treatment of ambulatory adults with spinal muscular atrophy type 3
at UCLA
Intrathecal Port and Catheter System for Subjects With Spinal Muscular Atrophy
open to eligible people ages 3 years and up
The primary objective of the clinical investigation is to demonstrate successful clinical use of the ThecaFlex DRx™ System in delivering nusinersen in subjects with spinal muscular atrophy (SMA). All enrolled subjects will undergo implantation of…
at UCSD
Clinical Procedures to Support Research in ALS
open to eligible people ages 18 years and up
The purpose of the Clinical Procedures To Support Research (CAPTURE) study is to utilize information collected in the medical record to learn more about a disease called amyotrophic lateral sclerosis (ALS) and related disorders.
at UC Irvine
Registry of Patients With a Diagnosis of Spinal Muscular Atrophy (SMA)
open to all eligible people
Spinal muscular atrophy (SMA) is a neurogenetic disorder caused by a loss or mutation in the survival motor neuron 1 gene (SMN1) on chromosome 5q13, which leads to reduced SMN protein levels and a selective dysfunction of motor neurons. SMA is an…
at UC Davis UCLA UCSD
Taldefgrobep Alfa in Participants With Spinal Muscular Atrophy
Sorry, in progress, not accepting new patients
This trial will study the efficacy and safety of taldefgrobep alfa as an adjunctive therapy for participants who are already taking a stable dose of nusinersen or risdiplam or have a history of onasemnogene abeparvovec-xioi, compared to placebo.
at UCSD UCSF
Risdiplam in Participants With Spinal Muscular Atrophy (SMA)
Sorry, in progress, not accepting new patients
A multi-center, longitudinal, prospective, non-comparative study to investigate the long-term safety and effectiveness of risdiplam, prescribed based on clinician judgment as per the Evrysdi® U.S. Package Insert (USPI) in adult and pediatric…
at UC Davis UC Irvine
Long-Term Safety & Efficacy of Apitegromab in Patients With SMA Who Completed Previous Trials of Apitegromab
Sorry, in progress, not accepting new patients
The ONYX study is an Open-Label, Multicenter, Extension study that will evaluate the long-term safety and efficacy of Apitegromab in Patients with Type 2 and Type 3 SMA who have completed TOPAZ or SAPPHIRE.
at UCSD
Phenotype, Genotype & Biomarkers in ALS and Related Disorders
Sorry, accepting new patients by invitation only
The goals of this study are: (1) to better understand the relationship between the phenotype and genotype of amyotrophic lateral sclerosis (ALS) and related diseases, including primary lateral sclerosis (PLS), hereditary spastic paraplegia (HSP),…
at UCSD
Our lead scientists for Muscular Atrophy research studies include Nanette Joyce, DO Namita Goyal, MD Perry B. Shieh, MD, PhD.
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