WHO ICTRP trial

Platform Study of Novel Ruxolitinib Combinations in Myelofibrosis Patients

LBCTR2022035001 · Lebanon Clinical Trials Registry (LBCTR) · Not Recruiting

Key facts

Trial ID LBCTR2022035001
Public title Platform Study of Novel Ruxolitinib Combinations in Myelofibrosis Patients
Scientific title A Randomized, Open-label, Phase I/II Open Platform Study Evaluating Safety and Efficacy of Novel Ruxolitinib Combinations in Myelofibrosis Patients
Primary sponsor Novartis Pharmaceuticals
Registry Lebanon Clinical Trials Registry (LBCTR)
Recruitment status Not Recruiting
Study type Interventional
Phase 1 to 2
Countries Australia;Belgium;Canada;Denmark;Germany;Hungary;Italy;Netherlands;Russian Federation;Spain;Sweden;Switzerland;United Kingdom;Lebanon
Conditions Myelofibrosis Myelofibrosis;D75.8;Myelofibrosis
Interventions - Drug: Ruxolitinib 5 mg tablets for oral use Other Name: INC424, Jakavi - Drug: Siremadlin 10 mg, 20 mg, or 40 mg capsules for oral use Other Name: HDM201 - Drug: Crizanlizumab 100 mg/mL concentrate for infusion for intravenous use Other…
Registration date Dec 8, 2022
Target size 4
Secondary IDs NCT04097821
Registry page lbctr.moph.gov.lb

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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