CClinicalTrials.gg
CompletedNCT00195195Updated Jan 31, 2012

Study Evaluating Rapamune in Transplant Recipients in the Nordic Countries

An observational study in Transplantation, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer. Completed at 3 sites in Sweden. Per ClinicalTrials.gov, last updated 2012-01-31.

Sponsored by Wyeth is now a wholly owned subsidiary of Pfizer · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
66
Sex
All
01

Study summary

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

02

Conditions studied

  • Transplantation

Keywords

  • Transplantation
03

In context

Lead sponsor

Wyeth is now a wholly owned subsidiary of Pfizer is the lead sponsor of 472 studies on the registry; none are open to participants now.

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

04

Who can participate

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

Study population

Transplantation patients treated with sirolimus.

Inclusion criteria

  • Transplantation patients treated with sirolimus (Rapamune).

Exclusion criteria

Exclusion Criteria:

  • Patients must be able to give informed consent.
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
66 participants (actual)

Groups and cohorts

  • 1

    Sirolimus

    Drug: Sirolimus

Interventions

  • DrugSirolimus

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

    Also known as: Rapamune

06

Study locations

3 sites
  • Gothenburg, SE-413 45, Sweden
  • Stockholm, SE-141 86, Sweden
  • Uppsala, SE-751 85, Sweden
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 31, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00195195
Lead sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Responsible party
Sponsor
First posted
Sep 19, 2005
Start date
Jan 2005
Primary completion
Jun 2008
Completion
Jun 2008
Last update
Jan 31, 2012

Study contacts

Pfizer CT.gov Call Center
study director · Wyeth is now a wholly owned subsidiary of Pfizer

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2012. You cannot join it, but the record below documents what was studied.

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Discussion

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