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Study Evaluating Rapamune in Transplant Recipients in the Nordic Countries

A Rapamune Follow-up Registry in Transplant Recipients in the Nordic Countries, Wrap-up

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00195195
Enrollment
66
Registered
2005-09-19
Start date
2005-01-31
Completion date
2008-06-30
Last updated
2012-01-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Transplantation

Keywords

Transplantation

Brief summary

The purpose of this study is to gather information about the long-term effects and safety of treatment with Rapamune in transplant patients.

Interventions

DRUGSirolimus

Transplantation patients treated with sirolimus who consent to participate in the study (register)

Sponsors

Wyeth is now a wholly owned subsidiary of Pfizer
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Transplantation patients treated with sirolimus (Rapamune).

Exclusion criteria

* Patients must be able to give informed consent.

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026