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NCT05605678

Hemophilia Non-Interventional Study Prior to SerpinPC Intervention (PRESent-5)

Terminated Last updated 7 February 2025
What this trial tests

trial testing No Intervention in Hemophilia a in 108 participants. Terminated before completion.

Timeline
9 December 2022
Primary endpoint
29 November 2024
29 November 2024

Quick facts

Lead sponsorApcinteX Ltd
StatusTerminated
Study typeOBSERVATIONAL
Enrollment108
Start date9 December 2022
Primary completion29 November 2024
Estimated completion29 November 2024
Sites45 locations across France, Italy, South Africa, Turkey (Türkiye), Taiwan, United Kingdom, Germany, Poland

Drugs / interventions tested

Conditions studied

Sponsor

ApcinteX Ltd — full company profile →

Who can join

Adults 12 to 65, male only, with Hemophilia a or Hemophilia B. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary objective of this study is to obtain prospective baseline documentation of annualized bleeding rates (ABRs) and treatment under standard-of-care (SOC) therapy among participants with hemophilia A or B. Participants in the study may be eligible to enroll in future planned interventional studies to be conducted by Sponsor.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of No Intervention

Trials testing the same drug.

Other recruiting trials for Hemophilia a

Currently open trials in the same condition.

Other ApcinteX Ltd trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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/NCT05605678.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing