The Chimerix CMX001 Registry
Purpose
The prospective observational study is to establish a registry database to evaluate the potential impact of prior treatment with CMX001 on the long-term incidence of specific events, such as outcomes, late CMV and other Double-stranded DNA virus associated events, s well as survival rates in subjects previously enrolled in selected clinical studies of CMX001. Each Registry participant will be followed for a period of approximately 3 years from their enrollment in the Registry.
Conditions
- Outcomes
- Survival Rates
Eligibility
- Eligible Ages
- Between 6 Months and 100 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Have previously completed study CMX001-301 through the Week 24 visit, or participated in another qualifying clinical study with CMX001. - Willing and able to understand and provide written informed consent to participate in this observational study - Willing and able to participate in all required study activities for the entire duration of the observational study (i.e., agreeable to being contacted at periodic intervals over the course of approximately 10 years following the completion of study CMX001-301 or other qualifying clinical study.
Exclusion Criteria
- None
Study Design
- Phase
- Study Type
- Observational [Patient Registry]
- Observational Model
- Case-Only
- Time Perspective
- Prospective
Arm Groups
Arm | Description | Assigned Intervention |
---|---|---|
CMX001 | Subjects who have previously participated in CMX001-301 or other CMX001 study. |
|
More Details
- Status
- Terminated
- Sponsor
- Chimerix