Revolade Tablets Specified Drug-use Survey

Status Not yet recruiting

Clinical Trial Summary

This is a multicenter, single-arm, non-interventional study (NIS) to confirm the safety and efficacy of eltrombopag in Anti-Thymocyte Globulin (ATG) treatment naive pediatric patients with aplastic anemia (AA).

Clinical Trial Description

The objective of this survey is to confirm the safety and efficacy of eltrombopag in ATG treatment naive pediatric patients with AA. Eltrombopag should be administered according to the dosage and administration specified in the latest version of the package insert. The observation period is 1 year (364 days) from the start of treatment with this product, regardless of whether treatment with eltrombopag is continued or not. However, if hematopoietic stem cell transplantation is performed within 1 year after the start of treatment with eltrombopag, the observation period shall be until the date of hematopoietic stem cell transplantation. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06287268
Study type	Observational
Source	Novartis
Contact	Novartis Pharmaceuticals
Phone	+81337978748
Email	novartis.email@novartis.com
Status	Not yet recruiting
Phase
Start date	June 28, 2024
Completion date	October 31, 2028

View Details

See also
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