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Clinical Trials/NCT03373877
NCT03373877
Terminated
Phase 1

A Phase Ib Study of Ruxolitinib in Combination With PU-H71 for the Treatment of Subjects With Primary Myelofibrosis (PMF), Post-Polycythemia Vera MF (Post-PV MF), and Post-EssentialThrombocythemia MF (Post-ET MF)

Samus Therapeutics, Inc.10 sites in 1 country4 target enrollmentMay 24, 2018

Overview

Phase
Phase 1
Intervention
PU-H71
Conditions
Myelofibrosis
Sponsor
Samus Therapeutics, Inc.
Enrollment
4
Locations
10
Primary Endpoint
Incidence of adverse events
Status
Terminated
Last Updated
3 years ago

Overview

Brief Summary

This is a multicenter 2-part, Phase 1b study designed to assess the safety, tolerability, pharmacokinetics (PK) and preliminary efficacy of PU-H71 in subjects taking concomitant ruxolitinib. The first part (Dose Escalation) will employ a standard 3+3 dose escalation design to determine Maximum Tolerated Dose (MTD). The second part of the study (Dose Confirmation) will confirm the recommended Phase 2 dose (RP2D) in an expanded population.

Detailed Description

This is a multicenter 2-part, Phase 1b study designed to assess the safety, tolerability, PK and preliminary efficacy of PU-H71 (dihydrochloride salt) in subjects taking concomitant ruxolitinib. The first part (Dose Escalation) will employ a standard 3+3 dose escalation design to determine MTD. The second part of the study (Dose Confirmation) will confirm the RP2D in an expanded population. Up to 30 subjects who have active disease despite having received a minimum of 6 months of ruxolitinib therapy (including last 2 months at a daily dose of ≥5 mg twice daily and no more than one dose reduction 2-8 weeks prior to the baseline visit)stable dose will be enrolled to evaluate the safety, PK, and MTD of IV PU-H71 administered in combination ruxolitinib. Four ascending dose levels are planned. The planned dose levels of PU-H71 are 225 mg/m2, 300 mg/m2, 400 mg/m2, and 600 mg/m2. Additional dosing cohorts may be added at the discretion of the Safety Review Committee (SRC). Following a 28-day screening period, eligible subjects will receive PU-H71 once weekly intravenously for three consecutive weeks, followed by one week off on a 28-day cycle (D1, D8, D15, every 28 days). Ruxolitinib will be administered twice daily per the package insert at the stable dose the subject had been receiving prior to enrolling in the study. Subjects will have pk samples taken and ECGs performed at various time points throughout the study. Subjects will have safety evaluations including physical examinations, vital signs, laboratory assessments, and AE reporting. If deemed necessary, additional safety measurements will be performed at the discretion of the Investigator or the SRC. Subjects will be treated until disease progression, DLT, death, or study termination. At each dose level, a 3+3 dose escalation design will be employed. If none of the initial 3 subjects in the cohort experience a DLT within the first cycle, a new cohort of 3 subjects will be treated at the next higher dose level. If 1 of the 3 subjects in a cohort experiences a DLT, then 3 additional subjects will be treated at the same dose level as described under Dose Limiting Toxicities. Once the MTD has been determined in the dose escalation portion of the study, up to 15 patients may be enrolled for further evaluation of safety, PK, and preliminary clinical activity in a dose confirmation phase. A safety review committee (SRC) will assess the safety, tolerability, and available PK information collected for each dose level, decide whether to proceed to the next cohort, and determine the dose for the cohort.

Registry
clinicaltrials.gov
Start Date
May 24, 2018
End Date
March 10, 2020
Last Updated
3 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Subject has a confirmed diagnosis of myelofibrosis, including PMF, post-PV MF, and post-ET MF.
  • Subject has been receiving ruxolitinib therapy for intermediate or high-risk myelofibrosis for \>6 months prior to enrollment with no more than 1 dose reduction of ruxolitinib in the 2-8 weeks prior to enrollment and a stable daily dose ≥5 mg twice daily (BID) \>2 months prior to enrollment.
  • Subject has MF with evidence of persistent disease despite ruxolitinib monotherapy treatment, consisting of:
  • Persistent or worsening disease-related symptoms, including but not limited to fatigue, pruritus, night sweats, early satiety, and other symptoms as determined by a MPN-SAF TSS score of \>20 points; AND
  • Documented splenomegaly of at least 5 cm below the costal margin as measured on inspiration by physical exam.
  • Subject has an Eastern Cooperative Oncology Group performance status of 0-
  • Acceptable pre-study organ function during screening defined as:
  • Absolute neutrophil count (ANC) ≥ 1000/uL
  • Hemoglobin (hgb) ≥ 8.0 g/dL (may be supported with transfusion)
  • Platelets (plt) ≥ 75,000/uL

Exclusion Criteria

  • Subject has known active liver disease, including viral hepatitis or cirrhosis.
  • Subject has known or suspected HIV or other active infections requiring acute or chronic treatment with systemic antibiotics. Conditions requiring topical antibiotics are acceptable.
  • Subject has a QTcF \> 480 ms (corrected) in the screening or baseline ECG.
  • Subject has left ventricular ejection fraction (LVEF) ≤ 50%, or below institution's lower limit of normal (whichever is lower) by echocardiogram (ECHO) or multigated acquisition (MUGA) scan.
  • Subject has a history (or family history) of long QT syndrome.
  • Subject has coronary artery disease with an ischemic event within 6 months prior to enrollment.
  • Subject has a permanent cardiac pacemaker.
  • Subject has history of a second primary malignancy within the past 2 year except for the following (if appropriately treated and considered cured): stage I endometrial, surgically treated cervical or prostate carcinoma, and non-melanoma skin cancer.
  • Subject has significant uncontrolled medical condition within 6 months prior to enrollment, as determined by the investigator.
  • Subject has concurrent participation in any interventional studies within 14 days of first dose of study drug.

Arms & Interventions

Dose 1: PU-H71 225 mg/m2 + ruxolitinib

Cohort 1

Intervention: PU-H71

Dose 1: PU-H71 225 mg/m2 + ruxolitinib

Cohort 1

Intervention: Ruxolitinib

Dose 2: PU-H71 300 mg/m2 + ruxolitinib

Cohort 2

Intervention: PU-H71

Dose 2: PU-H71 300 mg/m2 + ruxolitinib

Cohort 2

Intervention: Ruxolitinib

Dose 3: PU-H71 400 mg/m2 + ruxolitinib

Cohort 3

Intervention: PU-H71

Dose 3: PU-H71 400 mg/m2 + ruxolitinib

Cohort 3

Intervention: Ruxolitinib

Dose 4: PU-H71 600 mg/m2 + ruxolitinib

Cohort 4

Intervention: PU-H71

Dose 4: PU-H71 600 mg/m2 + ruxolitinib

Cohort 4

Intervention: Ruxolitinib

Outcomes

Primary Outcomes

Incidence of adverse events

Time Frame: 12 months

Safety of PU-H71 in combination with ruxolitinib as assessed by the incidence and severity of adverse events (AEs) and serious AEs as determined by the NCI CTCAE v4.03.

Recommended Phase 2 Dose of PU-H71 (RP2D)

Time Frame: 12 months

The RP2D is the dose with an acceptable risk/benefit ratio that warrant study in future trials

Maximum Tolerated Dose of PU-H71 (MTD)

Time Frame: 7 months

MTD as assessed by the occurrences of dose limiting toxicities of PU-H71 in combination with ruxolitinib. The MTD will be defined as the dose that does not exceed an acceptable threshold of toxicity.

Pharmacokinetic profile of PU-H71: Plasma half-life (T1/2)

Time Frame: 12 months

Plasma half-life (T1/2)

Pharmacokinetic profile of PU-H71: Area under the plasma concentration versus time curve (AUC)

Time Frame: 12 months

Area under the plasma concentration versus time curve (AUC)

Pharmacokinetic profile of PU-H71: Trough plasma concentration (Cmin)

Time Frame: 12 months

Trough plasma concentration (Cmin)

Pharmacokinetic profile of PU-H71: Peak plasma concentration (Cmax)

Time Frame: 12 months

Peak plasma concentration (Cmax)

Pharmacokinetic profile of PU-H71: Time to maximum plasma concentration (Tmax)

Time Frame: 12 months

Time to maximum plasma concentration (Tmax)

Secondary Outcomes

  • Biological Markers(12 months)
  • Treatment Response(12 months)
  • Symptom Burden Assessment(12 months)

Study Sites (10)

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