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Sunitinib 37.5, Pheochromocytoma / Paraganglioma

Protocol-ID: 2485 V1.0 (Mini), SUNI37.5, Pheochromocytoma/Paraganglioma

Indication(s)

  • Malignant Pheochromocytoma; ICD-10 C74.1
  • Paraganglioma; ICD-10 C75.5

Links

  • The FIRSTMAPPP study is a randomized, double-blind, phase II, international, multicenter study which aims to determine the efficacy of Sunitinib on the progression-free survival at 12 months in subjects with progressive malignant pheochromocytoma and paraganglioma treated with sunitinib at a starting dose of 37.5 mg daily (continuous dosing). [clinicaltrials.gov]
The publishers and authors assume no liability for the accuracy of the contents. The application is at the own responsibility of the treating physician. ©Onkopti.

Valid since: 11.11.2023