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Not Yet RecruitingNCT07266155

Efficacy, Safety, and Pharmacokinetics of LP-005 Injection in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)

A Phase Ⅱ Extension Clinical Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of LP-005 Injection in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)

Status
Not Yet Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Longbio Pharma · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This is an extension study for patients who have completed a prior P10-LP005-02 clinical study. The aim of this study is to evaluate the long-term safety, efficacy, and pharmacokinetics of LP-005 injection in adult patients with paroxysmal nocturnal hemoglobinuria (PNH).

Conditions

Interventions

TypeNameDescription
BIOLOGICALLP-005 InjectionIV infusion, Q4W

Timeline

Start date
2025-12-05
Primary completion
2027-12-30
Completion
2028-05-01
First posted
2025-12-05
Last updated
2025-12-05

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07266155. Inclusion in this directory is not an endorsement.