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NCT04747964

A Safety Study of STSP-0601 in Adult Patients With Hemophilia A or B With Inhibitor

Completed Phase 1 Last updated 19 September 2024
What this trial tests

Phase 1 trial testing STSP-0601 for Injection in Hemophilia in 16 participants. Completed in 19 April 2021.

Timeline
15 January 2020
Primary endpoint
19 April 2021
19 April 2021

Quick facts

Lead sponsorStaidson (Beijing) Biopharmaceuticals Co., Ltd
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designsequential
Maskingnone
Primary purposetreatment
Enrollment16
Start date15 January 2020
Primary completion19 April 2021
Estimated completion19 April 2021
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Staidson (Beijing) Biopharmaceuticals Co., Ltd — full company profile →

Who can join

Adults 18 to 65, male only, with Hemophilia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will assess the pharmacokinetics and pharmacodynamics of STSP-0601 at six dose levels. The results will help identify the most optimal doses to treat bleedings in hemophilia patients with inhibitors.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of STSP-0601 for Injection

Trials testing the same drug.

Other recruiting trials for Hemophilia

Currently open trials in the same condition.

Other Staidson (Beijing) Biopharmaceuticals Co., Ltd trials

Trials by the same sponsor.

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Data sources for this page

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