Trials / Recruiting
RecruitingNCT06745622
Long-term Safety and Tolerability of HSK39297 in Patients With Paroxysmal Nocturnal Hemoglobinuria
A Multicenter, Open-label Study to Evaluate the Long-term Safety, Tolerability and Efficacy of HSK39297 in Patients With Paroxysmal Nocturnal Hemoglobinuria(PNH)
- Status
- Recruiting
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 47 (estimated)
- Sponsor
- Haisco Pharmaceutical Group Co., Ltd. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is a multicenter, open-label study to evaluate the long-term safety, tolerability and efficacy of HSK39297. Adult patients with PNH who had previously received and completed HSK39297 study treatment will be included. Eligible subjects can maintain HSK39297 treatment until the end of the study.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | HSK39297 tablets | HSK39297 tablets until the end of treatment |
Timeline
- Start date
- 2025-01-03
- Primary completion
- 2027-06-01
- Completion
- 2027-06-01
- First posted
- 2024-12-20
- Last updated
- 2024-12-20
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT06745622. Inclusion in this directory is not an endorsement.