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NCT04423367: BID-PERAL

Bortezomib Plus Dexamethasone for Acquired Pure Red Cell Aplasia Failure or Relapse After First-line Treatment

Completed Phase 2 Last updated 11 February 2026
What this trial tests

Phase 2 trial testing bortezomib/dexamethasone in Acquired Pure Red Cell Aplasia in 18 participants. Completed in 30 September 2024.

Timeline
13 September 2020
Primary endpoint
31 July 2024
30 September 2024

Quick facts

Lead sponsorInstitute of Hematology & Blood Diseases Hospital, China
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment18
Start date13 September 2020
Primary completion31 July 2024
Estimated completion30 September 2024
Sites3 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Institute of Hematology & Blood Diseases Hospital, China

Who can join

Adults 18 to 70, any sex, with Acquired Pure Red Cell Aplasia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is an open-label, single-arm study to evaluate the safety and efficacy of bortezomib plus dexamethasone for acquired pure red cell aplasia failure or relapse after first-line treatment.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Treatment-free survival to bortezomib combined with dexamethasone in patients with refractory/relapsed pure red cell aplasia: a prospective clinical study.
    Zhang L, Shen Y, Li R, Pan H, et al · · 2025 · PMID 40772317 · DOI 10.1080/07853890.2025.2540016

Verify or expand the search:

Other trials of bortezomib/dexamethasone

Trials testing the same drug.

Other recruiting trials for Acquired Pure Red Cell Aplasia

Currently open trials in the same condition.

Other Institute of Hematology & Blood Diseases Hospital, China trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04423367.

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