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CompletedNCT04750785Updated Oct 14, 2021

A Study to Assess Choroideremia (CHM) Health Outcomes

An observational study in Choroideremia, sponsored by Biogen. Completed at 8 sites in United States. Open to male participants. Per ClinicalTrials.gov, last updated 2021-10-14.

Sponsored by Biogen · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
46
Sex
Male
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Study summary

The primary objectives of this study are to describe disease progression and severity by age in participants with CHM, to assess health-related quality-of-life, resource utilization and work productivity, and to assess quality-of-life, work productivity, and impact on daily activities in caregivers of participants with CHM at different stages of disease progression.

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Conditions studied

  • Choroideremia

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03

In context

Choroideremia

29 studies on the registry are indexed under Choroideremia; 6 are open to participants now.

Browse Choroideremia studies →

Lead sponsor

Biogen is the lead sponsor of 494 studies on the registry; 22 are open to participants now.

Of its 98 completed or terminated interventional studies of FDA-regulated products, 49 (50%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Male
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Participants who have been diagnosed with CHM. A minimum of approximately 50% of the participants will have an associated caregiver who will participate.

Participating physicians will enroll participants for inclusion in the study.

Eligibility criteria

Key Inclusion Criteria:

Physician Participants

  1. At least 60% of time spent in direct participant care.
  2. Board-certified or eligible with a Specialty in Ophthalmology, such as Retinal Specialist, IRD Specialist, Retinal Surgeon.

Patient Participants

  1. CHM diagnosis confirmed via genetic testing.
  2. Include any minimal disease severity requirement.
  3. Participant has at least one record of visual acuity measurement in the past 24 months, OR has be assigned by the treating clinician as having severe VA impairment of blind/legally blind by using one of the following methods: finger counting, hand movement, light perception / no light perception.

Key Exclusion Criteria:

Physician Participants

a. Participating physicians must not be affiliated with an approved management organization.

Patient Participants

a. Participants who received gene therapy or any other investigational treatment and participants who do not agree to informed consent.

NOTE: Other protocol defined Inclusion/Exclusion criteria may apply.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
46 participants (actual)
Patient registry
No

Groups and cohorts

  • All Participants

    Participants who have been diagnosed with CHM will be enrolled.

    Other: No Intervention

Interventions

  • OtherNo Intervention

    Administered as specified in the treatment arm.

06

What researchers measure

Primary outcomes

  1. Time to Disease Progression by Age in Participants with CHM

    Time frame: Up to 8 months

  2. Best Corrected Visual Acuity by Age

    Best corrected visual acuity will be used as an indicator to assess disease severity.

    Time frame: Up to 8 months

  3. Participants with CHM: EuroQol- 5 Dimension- 5 Level (EQ-5D-5L) Score

    EQ-5D is a self-report measure of health for clinical and economic appraisal. Participants complete the 5-level (no problems, slight problems, moderate problems, severe problems, and extreme problems), 5-dimension (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression) questionnaire concerning their current health state. A unique EQ-5D-5L health state scale ranges from 0 to 100 and is defined by combining 1 level from each of the 5 dimensions. Participants indicate their current health status by marking on a continuum ranging from 100 (best imaginable health state) to 0 (worst imaginable health state). The questionnaire will be implemented only one time per person in the study duration.

    Time frame: Up to 8 months

  4. Participants with CHM: Health Utilities Index (HUI3) Score

    Health Utilities Index (HUI3) is a family of generic preference-based systems for measuring comprehensive health status and health-related quality of life (HRQL). HUI® provides descriptive evidence on multiple dimensions of health status, a score for each dimension of health, and a HRQL score for overall health. Health dimensions include vision, hearing, speech, ambulation/mobility, pain, dexterity, self-care, emotion and cognition. Each dimension has 3- 6 levels. HUI® systems describe almost a million unique health states. HUI3 score ranges from 0.36 (worst) to 1 (best). The questionnaire will be implemented only one time per person in the study duration.

    Time frame: Up to 8 months

  5. Participants with CHM: Work Productivity and Activity Impairment (WPAI) Score

    The Work Productivity and Activity Impairment (WPAI) is a 6 questionnaire scale used to measure lost work productivity and impairment in daily activities over the past seven days. The WPAI yields four types of scores: 1. Absenteeism 2. Presenteesism 3. Work productivity loss 4. Activity Impairment, ranging from 0-100%. Higher numbers indicate greater impairment and less productivity. The questionnaire will be implemented only one time per person in the study duration.

    Time frame: Up to 8 months

  6. Participants with CHM: Visual Function Questionnaire (VFQ-25) Score

    VFQ-25 is a reliable and valid 25-item version of the 51-item National Eye Institute Visual Function Questionnaire (NEI-VFQ). It is especially useful in settings such as clinical trials, where interview length is a critical consideration. The global score derives from the summary of the scores deriving from each question. The total score has a minimum value "0" considered as the worst visual functionality, and the maximum value "100" considered as the better visual functionality. The questionnaire will be implemented only one time per person in the study duration.

    Time frame: Within 8 months

  7. Resource Utilization in Participants with CHM

    Healthcare Resource Utilization will be assessed by number of primary care provider visits, specialist visits, urgent care visits, emergency room (ER) visits, hospitalizations, and rehabilitation visits in past 12 months when stratified by all-cause \& CHM-related.

    Time frame: Up to 8 months

  8. Caregivers of Participants With CHM: Caregiver-reported Depression Via Patient Health Questionnaire-9 (PHQ-9) Score

    PHQ-9 can be used to screen for or diagnose depression, as well as measure depression severity. The PHQ-9 measures frequency of depression symptoms, with items scored on a 4-point scale (not at all=0 to nearly every day=3). The total score ranges from 0-27 where 0 is no depression and 27 is severe depression. The questionnaire will be implemented only one time per person in the study duration.

    Time frame: Up to 8 months

  9. Caregivers of Participants With CHM: Caregiver-reported Anxiety Via General Anxiety Disorder-7 (GAD-7) Score

    GAD-7 is a 7-item questionnaire that is used for screening, diagnosing, monitoring, and measuring the severity of anxiety. Each item can be answered on a 4 point scale running from 0= 'not at all sure' to 3= 'nearly every day'. The total score ranges from 0-21 where 0 is no anxiety and 27 is severe anxiety. The questionnaire will be implemented only one time per person in the study duration.

    Time frame: Up to 8 months

  10. Caregivers of Participants With CHM: Caregiver Reaction Assessment (CRA) Score

    Caregiver Reaction Assessment is a 24-item instrument assessing positive and negative aspects of caregiving (esteem, lack of family support, finances, schedule, and health). Each item is rated on a 1 to 4 scale. 1 (not at all) 2 (somewhat) 3 (quite a bit) 4 (completely). The questionnaire will be implemented only one time per person in the study duration.

    Time frame: Up to 8 months

  11. Caregivers of Participants With CHM: Work Productivity and Activity Impairment Caregiver (WPAI-CG) Score

    WPAI-CG is a 6 questionnaire scale used to measure lost work productivity and impairment in daily activities over the past seven days. The WPAI yields four types of scores: 1. Absenteeism 2. Presenteesism 3. Work productivity loss 4. Activity Impairment, ranging from 0-100%. Higher numbers indicate greater impairment and less productivity. The questionnaire will be implemented only one time per person in the study duration.

    Time frame: Up to 8 months

07

Study locations

8 sites
  • Research Site
    Los Angeles, California 90095, United States
  • Research Site
    San Francisco, California 94158, United States
  • Research Site
    Coral Gables, Florida 33146, United States
  • Research Site
    Gainesville, Florida 32607, United States
  • Research Site
    Portland, Oregon 97239, United States
  • Research Site
    Pittsburgh, Pennsylvania 15213, United States
  • Research Site
    Dallas, Texas 97239, United States
  • Research Site
    Madison, Wisconsin 53705, United States
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References and documents

Individual participant data

Plan to share: Yes — In accordance with Biogen's Clinical Trial Transparency and Data Sharing Policy on http://clinicalresearch.biogen.com/

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 14, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04750785
Lead sponsor
Biogen
Responsible party
Sponsor
First posted
Feb 11, 2021
Start date
Dec 15, 2020
Primary completion
Sep 27, 2021
Completion
Sep 27, 2021
Last update
Oct 14, 2021

Study contacts

Medical Director
study director · Biogen

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2021. You cannot join it, but the record below documents what was studied.

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