№ lp_1_11444
Year: 2024
Region / City: Australia
Topic: Medicinal Product Registration
Document Type: Submission Report
Agency: Therapeutic Goods Administration (TGA)
Author: GlaxoSmithKline Australia
Target Audience: Medical Practitioners
Treatment Phase: Initial Treatment
Indication: Myelofibrosis, including primary, post-polycythaemia vera, and post-essential thrombocythaemia myelofibrosis
Approval Status: Pending
Date of Submission: May 2024
Date of Approval: Not yet approved
Background: Momelotinib is currently approved in the UK, US, Japan, and the EU.
Description: Clinical submission for listing momelotinib under the Australian PBS for the treatment of myelofibrosis in patients with moderate to severe anaemia.
Price: 8 / 10 USD
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