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

Bon USage Des ImmunoGlobulines Humaines Normales (IgHN) : Faisabilité de l'intégration Des critères de la hiérarchisation Lors Des Dispensations d'IgHN - BUS-IG

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06027450
Acronym
BUS-IG
Enrollment
250
Registered
2023-09-07
Start date
2023-09-01
Completion date
2023-12-01
Last updated
2023-09-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Immunoglobulins

Brief summary

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.

Interventions

OTHERNHIg prescription

Analysis of NHIg prescription

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Patients treated with NHIg for one of the following 3 indications between 01/10/2021 and 31/12/2021: TIP, CDIP and SID. * Patients 18 years of age and older

Exclusion criteria

* Patient Objection * Patients treated with NHIg- for another indication

Design outcomes

Primary

MeasureTime frameDescription
Number of patients with clinical and biological information in the medical recordAt inclusion* For TIP: Khellaf score present dating from less than a week * For CDIP: mention of at least one plasmapheresis since diagnosis and before NHIg prescription * For SID: mention of recent repeated infections (at least 2 infections that lead to hospitalization in the year before starting treatment) and rate of IgG dating from less than 3 months.

Secondary

MeasureTime frameDescription
Adequacy rate between NHIg indications noted in patients files and ANSM prioritization criteriaAt inclusion* For TIP: Ig prescription if Khellaf score \>8 dating from less than a week. * For CDIP: Ig prescription if plasmapheresis was executed in first intention * For SID: prescription of Ig if recent repeated infections (at least 2 infections that lead to hospitalization in the year before starting treatment) and rate of IgG dating from less than 3 months.
Number of patients prescribed treatment out of hierarchyAt inclusionDescription of the criteria out of hierarchy, justifying the prescription of NHIg in these 3 authorized indications

Contacts

Primary ContactLaure Deville, Dr
laure.deville@aphp.fr+33142494292
Backup ContactJérôme Lambert, Dr
jerome.lambert@u-paris.fr+33142499742

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026