Clinical Experience With Sparsentan in Switzerland in IgA Nephropathy

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorWaid City Hospital, Zurich

About this trial

An observational study tracking the clinical course of patients with IgA nephropathy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

IgA Nephropathy, Use of Sparsentan

Disqualifiers

age < 18y

Trial population

Patients with IgA Nephropathy and therapy with sparsentan

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

  • sparsentan

    Drug

    Follow up observation of patients with IgA Nephropathy on sparsentan regarding Albuminuria and GFR

  • sparsentan

    Drug

    follow up observation of Albuminuria and GFR in IgA patients in therapy with sparsentan

Treatment groups

50 Participants
are divided into 1 treatment group
Group A: Patients with IgA Nephropathie and a therapy with Sparsentan1 intervention

Trial outcomes

Primary outcomes

1

Change of Albuminuria

What is the impact of sparsentan on Albuminuria

Time frame
36 months

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: