IGFD Registry: A Patient Registry for Monitoring Long-term Safety and Efficacy of Increlex
Status
Conditions
Treatments
Details and patient eligibility
About
This project is a retrospective (beginning January 2006) and prospective patient registry program sponsored by Ipsen (formerly Tercica, Inc.). In collaboration with participating health care practitioners, the patient registry program is an observational study monitoring the long-term safety of patients treated with Increlex® (mecasermin [rDNA origin] injection). The IGFD (Increlex® Growth Forum Database) Registry is intended primarily to monitor the safety and efficacy of Increlex replacement therapy in children with growth failure.
Full description
The data collected for a patient will be those that exist in the patient's medical record as part of standard medical care. No additional patient procedures or activities are mandated by this study. The specific data to be collected at each visit and the schedule of data collection are listed in a schedule of assessments.
The collection of safety events is considered essential to the Registry. The website will provide the opportunity to report the occurrence of targeted adverse events (AEs), other important events considered to be related to Increlex administration and serious adverse events (SAEs).
Enrollment
Sex
Volunteers
Inclusion and exclusion criteria
Inclusion Criteria:
- Parents or legally authorized representatives must give signed informed consent before any Registry-related activities are conducted. Assent from the subject should also be obtained where appropriate.
- Patients receiving Increlex® by a qualified practitioner may be enrolled
Exclusion Criteria:
Trial design
1,378 participants in 1 patient group
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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