Autopsy report · NCT00869856
Study to Evaluate the Efficacy, Safety and Immunogenicity of Subcutaneous HX575 in the Treatment of Anemia Associated With Chronic Kidney Disease (SWEEP)
Cause of deathSafety
“investigation of adverse events in a related clinical study”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Phase 3
- Sponsor
- Sandoz
- Sponsor type
- Industry
- Conditions
- Anemia; Chronic Renal Insufficiency
- Interventions
- HX575 solution for s.c. administration
- Participants
- 0
- Sites
- 19
- Countries
- Bulgaria, France, Germany, Romania, Spain
Trials that died the same way
- Safety and Bioactivity of AXT107 in Subjects With Diabetic Macular Edema
“Adverse Events” - Short Versus Long Interval to Ileostomy Reversal After Ileal Pouch Surgery
“Adverse Event” - Phase I Trial of AZD1775 and Belinostat in Treating Patients With Relapsed or Refractory Myeloid Malignancies or Untreated Acute Myeloid Leukemia
“Other - Adverse Events” - Ipilimumab + Androgen Depravation Therapy in Prostate Cancer
“Due to adverse events” - "Watch and Wait" After Neo-adjuvant Chemoradiotherapy for Primary Locally Advanced Rectal Cancer.
“Suspicion of adverse events”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.