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NCT04913597
A Study of Switching Avatrombopag and Rh-TPO in ITP
trial in Corticosteroid-resistant or Relapsed ITP in 100 participants. Status unknown.
31 December 2022
Quick facts
| Lead sponsor | Peking University People's Hospital |
|---|---|
| Status | Status unknown |
| Study type | OBSERVATIONAL |
| Enrollment | 100 |
| Start date | 20 June 2021 |
| Primary completion | 31 December 2022 |
| Estimated completion | 31 December 2023 |
Conditions studied
- Corticosteroid-resistant or Relapsed ITP — all drugs for Corticosteroid-resistant or Relapsed ITP →
Sponsor
Peking University People's Hospital
Who can join
Adults 18 to 75, any sex, with Corticosteroid-resistant or Relapsed ITP. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Thrombopoietin receptor agonists (TPO-RAs) represent a highly effective and well-tolerated second-line ITP treatment that provides excellent responses.If there is cross-resistance between 2 drugs for the treatment of adult ITP is still unkonwn.The purpose of this study is to investigate the efficacy and safety of switching avatrombopag and rh-TPO in adults with ITP.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT04913597
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04913597 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Peking University People's Hospital
- Last refreshed: 4 June 2021
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/NCT04913597.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing