To Assess the Safety, Tolerability and Efficacy of Itacitinib Immediate Release Tablets in Participants With Primary or Secondary Myelofibrosis Who Have Received Prior Ruxolitinib and/or Fedratinib Monotherapy (LIMBER-213)

PHASE2CompletedINTERVENTIONAL
Enrollment

4

Participants

Timeline

Start Date

July 12, 2021

Primary Completion Date

August 24, 2023

Study Completion Date

August 24, 2023

Conditions
MyelofibrosisPolycythemia VeraThrombocythemia
Interventions
DRUG

itacitinib

itacitinb Immediate Release (IR) will be dosed orally twice a day

Trial Locations (21)

17475

Universitaetsmedizin Greifswald, Greifswald

20132

Istituto Di Ricovero E Cura A Carattere Scientifico (Irccs) Ospedale San Raffaele, Milan

20817

Rcca Md, Llc, Bethesda

28041

Hospital Universitario 12 de Octubre, Madrid

31100

Treviso Hospital, Treviso

37235

Vanderbilt University, Nashville

38120

Baptist Cancer Center, Memphis

46000

Hospital Universitari I Politecnic La Fe, Valencia

64114

Midamerica Cancer Care, Kansas City

70112

Tulane University, New Orleans

70376

Interne 1 - Hematologie Mit Stammzelltransplantation, Hemostaseologie Und Medizinische Onkologie Ord, Linz

77380

Renovatio Clinical Consultants Llc, Spring

84131

Aou San Giovanni Di Dio E Ruggi, Salerno

08724-3009

New Jersey Hematology Oncology Associates Llc, Brick

75246-2092

Texas Oncology - Baylor Sammons Cancer Center, Dallas

01000

Cliniques Universitaires Ucl Saint-Luc, Brussels

03500

Jessa Ziekenhuis, Hasselt

08800

AZ DELTA, Roeselare

05530

Chu Ucl Namur University Hospital Mont-Godinne, Yvoir

06120

Universitatsklinikum Halle (Saale), Halle

40-519

Pratia Hematologia Katowice, Katowice

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Incyte Corporation

INDUSTRY

NCT04629508 - To Assess the Safety, Tolerability and Efficacy of Itacitinib Immediate Release Tablets in Participants With Primary or Secondary Myelofibrosis Who Have Received Prior Ruxolitinib and/or Fedratinib Monotherapy (LIMBER-213) | Biotech Hunter | Biotech Hunter