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Clinical trial information and results are updated daily from ClinicalTrials.gov. The latest data update was conducted on 04/16/2021.

A Study of Fedratinib in Japanese Subjects With DIPSS (Dynamic International Prognostic Scoring System)- Intermediate or High-risk Primary Myelofibrosis (PMF), Post-polycythemia Vera Myelofibrosis (Post-PV MF), or Post-essential Thrombocythemia Myelofibrosis (Post-ET MF)

Clinicaltrials.gov identifier NCT04446650

Recruitment Status Not yet recruiting

First Posted June 25, 2020

Last update posted June 25, 2020

Study Description

Brief summary:

The study will be conducted in compliance with the International Council for Harmonisation (ICH) of Technical Requirements for Registration of Pharmaceuticals for Human Use/Good Clinical Practice (GCP) and applicable regulatory requirements. This is a Phase 1/2 multicenter, single arm, open-label study in Japanese subjects with DIPSS intermediate or high-risk PMF, post-PV or post-ET MF. The study consists of 2 parts: Phase 1 part to determine safety and tolerability and a RP2D. The Phase 1 portion of the study will explore one or more drug doses for fedratinib (300 mg and 400 mg) using a mTPI-2 design. Following completion of dose escalation and determination of MTD and/or a RP2D, the study will progress into the Phase 2 part to further evaluate the efficacy and safety. The study will consist of 3 periods: a Screening Period, a Treatment Period including a 30-day follow-up after last dose visit and a survival follow-up period.

  • Condition or Disease:Primary Myelofibrosis
  • Intervention/Treatment: Drug: Fedratinib
  • Phase: Phase 1/Phase 2
Detailed Description

N/A

Study Design
  • Study Type: Interventional
  • Estimated Enrollment: 31 participants
  • Intervention Model: Single Group Assignment
  • Masking: None (Open Label) ()
  • Primary Purpose: Treatment
  • Official Title: A Phase 1/2, Multicenter, Single-arm, Open-label Study to Evaluate the Efficacy and Safety of Fedratinib in Japanese Subjects With DIPSS (Dynamic International Prognostic Scoring System)- Intermediate or High-risk Primary Myelofibrosis (PMF), Post-polycythemia Vera Myelofibrosis (Post-PV MF), or Post-essential Thrombocythemia Myelofibrosis (Post-ET MF)
  • Estimated Study Start Date: June 2020
  • Estimated Primary Completion Date: July 2022
  • Estimated Study Completion Date: July 2024
Arms and interventions
Arm Intervention/treatment
Experimental: Fedratinib Administration
The fedratinib dose is 300 or 400 mg/day PO (3 or 4 x 100 mg capsules) to be self-administered orally once daily continuously on an outpatient basis, preferably together with food during an evening meal, the same time each day.
Drug: Fedratinib
Oral
Outcome Measures
  • Primary Outcome Measures: 1. Maximum Tolerated Dose (MTD) [ Time Frame: Up to Cycle 1 (each cycle is 28 days) ]
    is the highest dose that causes DLTs in not more than 33% of the subjects treated with fedratinib in the first cycle with at least 3 evaluable subjects treated at this dose.
  • 2. Recommended Phase 2 dose (RP2D) [ Time Frame: Up to Cycle 1 (each cycle is 28 days) ]
    is a recommended Phase 2 dose that is determined as safe and tolerable by the Safety Review Committee based on the data from the first cycle with at least 3 evaluable subjects treated at each dose of the Phase 1 part.
  • 3. Response Rate (RR) [ Time Frame: Up to Cycle 6 (each cycle is 28 days) ]
    Proportion of subjects who have ≥ 35% SVR at end of Cycle 6 from baseline
  • Secondary Outcome Measures: 1. Spleen and Disease Progression Free Survival (SDPFS) [ Time Frame: Up to 4 years ]
    Time from the start of fedratinib treatment to death due to any reason or disease progression (modified IWGMRT 2013 including ≥ 25% increase in spleen volume by MRI/CT)
  • 2. Adverse Events (AEs) [ Time Frame: From ICF signature up until 30 days after last dose of IP ]
    An AE is any noxious, unintended, or untoward medical occurrence that may appear or worsen in a subject during the course of a study. It may be a new intercurrent illness, a worsening concomitant illness, an injury, or any concomitant impairment of the subject's health, including laboratory test values, regardless of etiology. Any worsening (ie, any clinically significant adverse change in the frequency or intensity of a preexisting condition) should be considered an AE.
  • 3. Pharmacokinetics - Cmax [ Time Frame: Up to Cycle 1 (each cycle is 28 days) ]
    Peak (maximum) plasma concentration of the drug
  • 4. Pharmacokinetics - AUC [ Time Frame: Up to Cycle 1 (each cycle is 28 days) ]
    Area under the plasma concentration curve
  • 5. Pharmacokinetics - Tmax [ Time Frame: Up to Cycle 1 (each cycle is 28 days) ]
    Time to maximum plasma concentration
  • 6. Symptom response rate (SRR) [ Time Frame: Up to Cycle 6 (each cycle is 28 days) ]
    Proportion of subjects with ≥ 50% reduction in total symptom scores measured by MFSAF version 2.0 (Appendix C) at end of Cycle 6
  • 7. Spleen volume response rate 25 (RR25) [ Time Frame: Up to Cycle 6 (each cycle is 28 days) ]
    Proportion of subjects who have ≥ 25% reduction in spleen volume at the end of Cycle 6
  • 8. Spleen Response Rate by Palpation (RRP) [ Time Frame: Up to Cycle 6 (each cycle is 28 days) ]
    Proportion of subjects who have ≥ 50% reduction in spleen size by palpation at end of Cycle 6
  • 9. Duration of spleen volume response (DR) [ Time Frame: Up to 4 years ]
    Duration of ≥ 35% SVR by MRI/CT
  • 10. Duration of spleen response by palpation (DRP) [ Time Frame: Up to 4 years ]
    Time from the first documented palpable spleen response, according to the IWGMRT 2013 to the time of the first documented loss of response according to the IWG-MRT 2013.
  • 11. Duration of symptoms response (DSR) [ Time Frame: Up to 4 years ]
    Duration of ≥ 50% reduction in total symptom scores measured by MFSAF version 2.0
  • 12. Gastrointestinal adverse events [ Time Frame: From ICF signature to the 30-day follow-up after last dose of IP ]
    Incidence of subjects with Grade 3 or higher Gastrointestinal events (nausea, diarrhea, or vomiting) according to CTCAE v5.0
  • 13. Wernicke encephalopathy (WE) events [ Time Frame: From ICF signature to the 30-day follow-up after last dose of IP ]
    Occurrence of confirmed Wernicke encephalopathy events
  • 14. Overall Survival (OS) [ Time Frame: Up to 4 years ]
    Time from the start of fedratinib treatment to death due to any reason
Eligibility Criteria
  • Ages Eligible for Study: 20 Years and older (Adult, Older Adult)
  • Sexes Eligible for Study: All
  • Accepts Healthy Volunteers: No
Criteria

Inclusion Criteria:

Subjects must satisfy the following criteria to be enrolled in the study:

1. Subject is ≥ 20 years of age at the time of signing the informed consent form (ICF)

2. Subject has an Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) of 0,
1 or 2

3. Subject has diagnosis of Primary myelofibrosis (PMF) according to the 2016 World
Health Organization (WHO) criteria, or diagnosis of post-ET or post- Polycythemia vera
(PV) Myelofibrosis (MF) according to the IWG-MRT 2007 criteria, confirmed by the most
recent local pathology report

4. Subject has a Dynamic International Prognostic Scoring System (DIPSS) Risk score of
Intermediate-1 with symptom(s), Intermediate-2 or High

5. Subject has a measurable splenomegaly during the screening period as demonstrated by
spleen volume of ≥ 450 cm3 by magnetic resonance imaging (MRI) or computed tomography
(CT) scan or by palpable spleen measuring ≥ 5 cm below the left costal margin.

6. Subject must meet at least one of the following criteria of (a or b).

Note: reason to discontinue ruxolitinib treatment (lack of efficacy and/or
intolerability, etc) and physician decision as to the study participation as being
appropriate should be recorded in the case report form:

1. Previously received ruxolitinib treatment for PMF or post-PV MF or post-ET MF for
at least 14 days (exposure of < 14 days is allowed for subjects who discontinued ruxolitinib due to intolerability or allergy). 2. Never received ruxolitinib treatment and is expected to derive clinical benefit from this study participation based on the clinical judgement of the Investigator Only those subjects who previously received ruxolitinib treatment are eligible for the Phase 1 part of the study to avoid overestimating tolerability of fedratinib. 7. Subject must have treatment-related toxicities from prior therapy resolved to Grade 1 or pretreatment baseline before start of last therapy prior to starting the fedratinib treatment. 8. Subject must understand and voluntarily sign an ICF prior to any study-related assessments/procedures being conducted. 9. Subject is willing and able to adhere to the study visit schedule and other protocol requirements. 10. A female of childbearing potential (FCBP) must: 1. Have 2 negative pregnancy tests as verified by the Investigator during screening prior to starting fedratinib treatment. She must agree to ongoing pregnancy testing during the course of the study, and after end of fedratinib treatment. This applies even if the subject practices true abstinence* from heterosexual contact. 2. Either commit to true abstinence* from heterosexual contact (which must be reviewed on a monthly basis and source documented) or agree to use and be able to comply with highly effective contraception** without interruption, -14 days prior to starting investigational product, during the fedratinib treatment (including dose interruptions), and for 30 days after discontinuation of fedratinib treatment. 3. If breastfeeding, agree to stop breastfeeding prior to the participation in the study and not to resume breastfeeding for at least 30 days after treatment discontinuation of the fedratinib treatment. Note: A female of childbearing potential (FCBP) is a female who: 1) has achieved menarche at some point, 2) has not undergone a hysterectomy or bilateral oophorectomy, or 3) has not been naturally postmenopausal (amenorrhea following cancer therapy or amenorrhea due to other medical reasons does not rule out childbearing potential) for at least 24 consecutive months (ie, has had menses at any time in the preceding 24 consecutive months). 11. A male subject must: Practice true abstinence (which must be reviewed on a monthly basis) or agree to use a condom during sexual contact with a pregnant female or a female of childbearing potential while participating in the study, during dose interruptions and for at least 30 days following fedratinib discontinuation, or longer if required by local regulations, even if he has undergone a successful vasectomy. True abstinence is acceptable when this is in line with the preferred and usual lifestyle of the subject. (Periodic abstinence [eg, calendar, ovulation, symptothermal, postovulation methods] and withdrawal are not acceptable methods of contraception). Agreement to use highly effective methods of contraception that alone or in combination resulting in a failure rate of a Pearl index of less than 1% per year when used consistently and correctly throughout the course of the study. Such methods include combined (estrogen and progestogen containing) hormonal contraception (oral), progestogen-only hormonal contraception associated with inhibition of ovulation (oral), placement of an intrauterine device, placement of an intrauterine hormone-releasing system, bilateral tubal occlusion, and vasectomized partner. Exclusion Criteria: The presence of any of the following will exclude a subject from enrollment: 1. Any of the following laboratory abnormalities: 1. Platelets < 50 x 109/L (without platelet transfusion) 2. Absolute neutrophil count (ANC) 100 x 109/L

4. Myeloblasts ≥ 5 % in peripheral blood

5. Estimated creatinine clearance 1.5 x upper limit of normal

7. Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 3 x upper
limit of normal (ULN)

8. Total bilirubin > 1.5 x ULN, subject's total bilirubin between 1.5 - 3.0 x ULN
are eligible if the direct bilirubin fraction is
10 mg/day prednisone or equivalent. Subjects who have had prior exposure to
hydroxyurea (eg, Hydrea) in the past may be enrolled into the study as long as it has
not been administered within 14 days prior to starting the fedratinib treatment.

10. Subject on treatment with myeloid growth factor (eg, granulocyte-colony stimulating
factor [G-CSF]) within 14 days prior to starting the fedratinib treatment

11. Subject with previous exposure to JAK inhibitor(s) other than ruxolitinib treatment

12. Subject has received ruxolitinib within 14 days prior to starting the fedratinib
treatment

13. Subject on treatment with aspirin with doses > 150 mg daily

14. Subject with major surgery within 28 days prior to starting the fedratinib treatment

15. Subject with diagnosis of chronic liver disease (eg, chronic alcoholic liver disease,
autoimmune hepatitis, sclerosing cholangitis, primary biliary cirrhosis,
hemochromatosis, non-alcoholic steatohepatitis)

16. Subject with prior malignancy other than the disease under study unless the subject
has not required treatment for the malignancy for at least 3 years prior to the start
of fedratinib treatment. However, subject with the following history/concurrent
conditions provided successfully treated may enroll: non-invasive skin cancer, in situ
cervical cancer, carcinoma in situ of the breast, incidental histologic finding of
prostate cancer (T1a or T1b using the tumor, nodes, metastasis [TNM] clinical staging
system), or is free of disease and on hormonal treatment only

17. Subject with uncontrolled congestive heart failure (New York Heart Association
Classification 3 or 4)

18. Seropositive for and with evidence of active viral infection with hepatitis B virus
(HBV)

1. Subject who are hepatitis B surface antigen (HBsAg) negative but HB core
anti-body (HBcAb) positive or HBsAb positive are eligible in case HBV viral
deoxyribonucleoside (DNA) negative

2. Subject who had HBsAg positive but show non-detectable viral DNA for at least 6
months prior to starting the fedratinib treatment where appropriate anti-viral
treatment should have been given/considered to prevent HBV reactivation based on
the standard practice are eligible

3. Subject who are seropositive because of hepatitis B virus vaccine are eligible

19. Seropositive for and with active viral infection with hepatitis C virus (HCV)

• Subject who had hepatitis C but show no detectable HCV viral ribonucleotide (RNA)
for at least 6 months prior to starting the fedratinib treatment are eligible.

20. Evidence of human immunodeficiency virus (HIV) infection.

21. Subject with serious active infection

22. Subject with presence of any significant gastric or other disorder that would inhibit
absorption of oral medication

23. Subject is unable to swallow capsule

24. Subject with any significant medical condition, laboratory abnormality, or psychiatric
illness that would prevent the subject from participating in the study

25. Subject has any condition including the presence of laboratory abnormalities, which
places the subject at unacceptable risk if the subject were to participate in the
study

26. Subject has any condition that confounds the ability to interpret data from the study

27. Subject with participation in any study of an investigational agent (drug, biologic,
device) within 30 days prior to starting the fedratinib treatment

28. Subject with a life expectancy of less than 6 months from the planned first dose of
fedratinib.

Contacts and Locations
Contacts

Contact: Associate Director Clinical Trial Disclosure 1-888-260-1599 clinicaltrialdisclosure@celgene.com

Locations
Sponsors and Collaborators

Celgene

Investigators

Study Director: Kiyoshi Okazuka, MD Celgene

More Information
  • Responsible Party: Celgene
  • ClinicalTrials.gov Identifier: NCT04446650 History of Changes
  • Other Study ID Numbers: FEDR-MF-003, U1111-1252-2577
  • First Posted: June 25, 2020 Key Record Dates
  • Last Update Posted: June 25, 2020
  • Last Verified: June 2020
  • Individual Participant
    Data (IPD) Sharing
    Statement:
  • Plan to Share IPD: Yes
  • Plan Description: https://www.celgene.com/research-development/clinical-trials/clinical-trials-data-sharing/
  • Supporting Materials: Study Protocol, Statistical Analysis Plan (SAP), Informed Consent Form (ICF), Clinical Study Report (CSR), Analytic Code
  • Time Frame: See Plan Description
  • Access Criteria: See Plan Description
  • URL: https://www.celgene.com/research-development/clinical-trials/clinical-trials-data-sharing/
  • Studies a U.S. FDA-regulated Drug Product: No
  • Studies a U.S. FDA-regulated Device Product: No
  • Keywords provided by Celgene: Fedratinib
    Myelofibrosis
    Japanese
  • Additional relevant MeSH terms: Polycythemia
    Thrombocythemia, Essential
    Polycythemia Vera
    Primary Myelofibrosis
    Thrombocytosis