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NCT06027450: BUS-IG

Good Use of Normal Human ImmunoGlobulins (NHIg): Feasibility of Integrating the Criteria of Hierarchy During of NHIg Dispensations

Status unknown Last updated 7 September 2023
What this trial tests

trial testing NHIg prescription in Immunoglobulins in 250 participants. Status unknown.

Timeline
1 September 2023
Primary endpoint
1 December 2023
1 December 2023

Quick facts

Lead sponsorAssistance Publique - Hôpitaux de Paris
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment250
Start date1 September 2023
Primary completion1 December 2023
Estimated completion1 December 2023

Drugs / interventions tested

Conditions studied

Sponsor

Assistance Publique - Hôpitaux de Paris — full company profile →

Who can join

Adults 18 to 100, any sex, with Immunoglobulins. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Supply of Normal Human Immunoglobulins (NHIg) has been in steady tension for almost 15 years in the world. The scarcity of raw material, manufacturing time by industries, and increase consumptions are some of the causes. These phenomena has been accentuated for two years in the context of pandemic. Faced these difficulties, the french National Medication Security Agency (ANSM) , in collaboration with health professionals and patients associations concerned, established a hierarchy of indications of NHIg to prioritize NHIg for patients without therapeutic alternative (2013 and 2019). Its use is sometimes complex, particularly in the indications where the use of NHIg must combine clinico-biological criteria and/or previous treatment lines.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Assistance Publique - Hôpitaux de Paris trials

Trials by the same sponsor.

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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/NCT06027450.

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