Trials / Withdrawn
WithdrawnNCT03801889
SP-420 in Subjects With Transfusion-dependent Beta-Thalassemia or Other Rare Anemias
Multicenter, Open-label, 52 Week, Dose-escalation Study of SP 420 in Subjects With Transfusion-dependent Beta-Thalassemia or Other Rare Anemias
- Status
- Withdrawn
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Abfero Pharmaceuticals, Inc · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to test the safety and tolerability of SP-420 and it's efficacy in terms of lowering iron in subjects with Beta-thalassemia or other rare anemias who need regular blood transfusions.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | SP-420 | Self-administered by mouth |
Timeline
- Start date
- 2020-08-01
- Primary completion
- 2022-09-01
- Completion
- 2023-01-01
- First posted
- 2019-01-14
- Last updated
- 2020-10-05
Locations
4 sites across 4 countries: Canada, Lebanon, Thailand, Turkey (Türkiye)
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03801889. Inclusion in this directory is not an endorsement.