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Tolerability of the intravenous immunoglobulin Octagam® 10%

Tolerability of the intravenous immunoglobulin Octagam® 10%

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN58800347
Enrollment
600
Registered
2008-12-03
Start date
2008-09-15
Completion date
Unknown
Last updated
2022-11-28

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

Conditions

Primary or secondary immunodeficiencies, immunomodulation in autoimmune diseases Haematological Disorders Other immunodeficiencies

Interventions

Treatment with Octagam® 10% will be documented. This includes data about the patient's disease, age, gender, weight, concomitant medication or illness. For each application, the date and duration of i

Sponsors

Octapharma GmbH (Germany)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients of any age and gender who receive treatment with Octagam® 10%

Exclusion criteria

Exclusion criteria: Patients with known contraindications to Octagam® 10%

Design outcomes

Primary

MeasureTime frame
To observe the tolerability of Octagam® 10% in different indication groups in routine clinical practice

Secondary

MeasureTime frame
Data about the efficacy of Octagam® 10%

Countries

Germany

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 26, 2026