NCT05438485

Brief Summary

The JUMP (Journey to Understand MMA and PA) Study is being conducted by HemoShear Therapeutics and AllStripes, a rare disease online research platform. JUMP is designed to accelerate understanding of the natural course of methylmalonic acidemia (MMA) and propionic acidemia (PA) disease and treatment for families, researchers, clinicians and industry. The study will collect and provide patient medical record information from multiple institutions for families to access in one place at no cost. AllStripes will remove identifying information like name and address from these medical records and aggregate this data for the HemoShear team to better understand the medical experience and progression of MMA and PA over time. In addition, academic researchers, healthcare practitioners and patient advocacy groups can apply to use the collective patient community data to answer specific research questions at no cost. HemoShear is collecting natural history data on MMA and PA because the company needs insight into the real-world experience of many patients to better understand the disease and be able to scientifically demonstrate whether the potential new treatment they are developing is effective in improving outcomes. This natural history study will include retrospective and prospective components. The retrospective component will consist of data abstracted from primarily electronic health records (eHR) and some paper records. The prospective component will include ongoing collection of medical records from enrolled participants, and participants may opt in to complete health-related questionnaires and an optional genetic testing sub-study. After signing informed consent, participants or their legal guardians will grant permission to AllStripes to collect their health records for data abstraction. Participants may opt into an optional no cost genetic testing sub-study. The JUMP (Journey to Understand MMA and PA) sub-study will help assess whether the genetic variant of the affected person may relate to disease severity and treatment response. Getting genetic testing will enable participants to understand the genetic mutation that causes their type of methylmalonic acidemia (MMA) or propionic acidemia (PA). Knowing the genetic mutations (whether from the MMUT, MMAA or MMAB gene or PCCA or PCCB) can help the impacted person, their caregivers and healthcare professionals understand the potential course of disease and select approaches to better manage the disease. The additional information will enable HemoShear and AllStripes to understand whether different genetic variants impact the disease journey and outcomes. A separate informed consent will be obtained for participating in the sub-study.

Trial Health

60
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
11

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Aug 2021

Typical duration for all trials

Geographic Reach
3 countries

3 active sites

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 27, 2021

Completed
10 months until next milestone

First Submitted

Initial submission to the registry

June 27, 2022

Completed
3 days until next milestone

First Posted

Study publicly available on registry

June 30, 2022

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 20, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 20, 2023

Completed
Last Updated

December 27, 2023

Status Verified

September 1, 2022

Enrollment Period

2.1 years

First QC Date

June 27, 2022

Last Update Submit

December 20, 2023

Conditions

Keywords

Methylmalonic AcidemiaPropionic AcidemiaOrganic AcidemiaInborn errors of metabolismPCCAPCCBPropionyl-coenzyme A carboxylaseMMUTMethylmalonyl-CoA mutaseMetabolic diseaseGenetic diseaseHemoShearNatural History StudyJUMP

Outcome Measures

Primary Outcomes (1)

  • Understanding of the natural course of methylmalonic acidemia (MMA) and propionic acidemia (PA) disease and treatment for families, researchers, clinicians and industry.

    5 years

Study Arms (2)

Methylmalonic Acidemia (MMA)

Approximately 60 subjects with Methylmalonic Acidemia

Other: Registry

Propionic Acidemia (PA)

Approximately 60 subjects with Propionic Acidemia

Other: Registry

Interventions

Observational (Registry)

Methylmalonic Acidemia (MMA)Propionic Acidemia (PA)

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Approximately 120 participants will be enrolled from the United States, Canada, and the United Kingdom.

You may qualify if:

  • Participant or participant's legal guardian must provide signed, informed eConsent/eAssent prior to releasing health records or performing any study-related procedures.
  • Confirmed diagnosis of MMA or PA.
  • Reside in the US, Canada, or United Kingdom and have all medical records available for abstraction.

You may not qualify if:

  • \. Participant or participant's legal guardian is unable to provide complete access to medical records.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (3)

AllStripes

San Francisco, California, 94551, United States

Location

AllStripes

Remote, Remote, Canada

Location

AllStripes

Remote, Remote, United Kingdom

Location

Related Links

MeSH Terms

Conditions

Methylmalonic acidemiaPropionic AcidemiaMetabolism, Inborn ErrorsMetabolic DiseasesGenetic Diseases, Inborn

Interventions

Registries

Condition Hierarchy (Ancestors)

Amino Acid Metabolism, Inborn ErrorsCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesNutritional and Metabolic Diseases

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesRecordsOrganization and AdministrationHealth Services AdministrationHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
OTHER
Target Duration
12 Months
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 27, 2022

First Posted

June 30, 2022

Study Start

August 27, 2021

Primary Completion

October 20, 2023

Study Completion

October 20, 2023

Last Updated

December 27, 2023

Record last verified: 2022-09

Data Sharing

IPD Sharing
Will not share

Locations