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Clinical Trials/NCT02692742
NCT02692742
Completed
Phase 2

A Randomised, Double-Blind, Placebo-Controlled, Parallel-Design, Multi-Center Study to Investigate the Efficacy To Reduce Chemotherapy-Induced Neutropenia (CIN), Effects on the Haematopoietic System, Safety and Pharmacokinetics of Myelo001 in Patients Receiving Adjuvant or Neoadjuvant Chemotherapy for the Treatment Of Breast Cancer

Myelo Therapeutics GmbH23 sites in 1 country137 target enrollmentMarch 2016

Overview

Phase
Phase 2
Intervention
Myelo001
Conditions
Chemotherapy-Induced Neutropenia
Sponsor
Myelo Therapeutics GmbH
Enrollment
137
Locations
23
Primary Endpoint
Threshold area over the curve (AOC1) of ANC: Area below the threshold line (ANC 2.0x10^9/L classified as grade 1 neutropenia) and above the individual ANC trajectory
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Neutropenia is the most serious hematologic toxicity of cancer chemotherapy, often limiting the doses and density of chemotherapy that can be tolerated. The degree and duration of neutropenia determine the risk of infection. Myelo001, a small orally bioavailable molecule, has been shown in chemotherapy- or radiotherapy-induced myelosuppression to stimulate differentiation of peripheral white blood cells (WBC) and bone marrow cells of the leucocytic, lymphocytic, and erythrocytic lineage. The purpose of the MyeloConcept study is to determine the safety and effectiveness of Myelo001 in preventing or reducing chemotherapy-induced neutropenia and myelosuppression in patients receiving chemotherapy due to breast cancer.

Detailed Description

Phase IIa study, 1:1 randomized, double-blind, placebo-controlled, parallel-design, multi-center study. Each breast cancer patient will be randomly assigned into one of two treatment arms receiving either Myelo001 or placebo as a tablet. Investigational medicinal product is taken as supportive care for 23 consecutive days during chemotherapy treatment. Hematologic and safety parameters as well as actual begin and doses of following chemotherapy cycles will be assessed. A single primary variable will be analyzed with test statistics based on frequent absolute neutrophil measurements. Additionally, in a subgroup of patients biomarkers and pharmacokinetics of Myelo001 will be investigated.

Registry
clinicaltrials.gov
Start Date
March 2016
End Date
November 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Female patient of any racial origin having fulfilled her 18th birthday on Visit 1 (Screening)
  • Histologically confirmed invasive breast cancer scheduled for neoadjuvant or adjuvant chemotherapy (patient with primary wound healing (\[R0\])
  • Already selected for neoadjuvant or adjuvant standard of care EC regimen (Epirubicin 90 mg/m2 BSA (body surface area) + Cyclophosphamide 600 mg/m2 BSA q21d (every 21 days)) (with or without treatment with taxanes afterwards)
  • Risk of chemotherapy-induced Febrile Neutropenia ≤20% according to ASCO Guidelines (2015)
  • More than 5 days remaining before the planned initiation of the 1st chemotherapy cycle
  • Performance status Grade 0-1 (ECOG)
  • Echocardiography: No contraindication for the scheduled chemotherapy
  • Haematologic, laboratory and chemistry thresholds at baseline:
  • Absolute neutrophil count (ANC) ≥2,000 cells/ mm3 (≥2.0 x 10/L)
  • Platelet count ≥100,000/mm3 (≥100 x 10exp9/L)

Exclusion Criteria

  • Suspected allergy to Myelo001 or its excipients
  • Prior chemotherapy
  • Prior or concomitant treatment with radiotherapy
  • Currently on or scheduled for other immunomodulatory or immunosuppressive therapies (e.g. TNF inhibitors) during the first chemotherapy cycle
  • Currently on or scheduled for other immunostimulatory or hematopoietic active therapies (e.g.G-CSF, GM-CSF)
  • Currently on or scheduled for primary prophylaxis with antibiotics in the first chemotherapy cycle
  • History of bone marrow transplantation or stem cell transplant
  • Administration of another investigational medicinal product / medical device within 30 days prior to screening. Participation in non-interventional, national or international cancer registries is allowed.
  • Already confirmed HIV, hepatitis B or C virus (HBV or HCV) infection
  • History of somatic disease/condition that may interfere with the objectives of the study

Arms & Interventions

Myelo001

Myelo001 100 mg QD

Intervention: Myelo001

Placebo

Matching Placebo QD

Intervention: Placebo

Outcomes

Primary Outcomes

Threshold area over the curve (AOC1) of ANC: Area below the threshold line (ANC 2.0x10^9/L classified as grade 1 neutropenia) and above the individual ANC trajectory

Time Frame: visit 3 to visit 10 (22 days)

Threshold area over the curve (AOC3) of ANC: Area below the threshold line (ANC 1.0x10^9/L classified as grade 3 neutropenia) and above the individual ANC trajectory

Time Frame: visit 3 to visit 10 (22 days)

Duration of ANC < 1.0x10^9/L classified as grade 3 neutropenia

Time Frame: visit 3 to visit 10 (22 days)

Secondary Outcomes

  • Change of Threshold Area over the Curve of thrombocytes(visit 3 to visit 10 (22 days))
  • Proportion of patients with neutropenia grade 1 and higher; 3 and higher, 4, and ANC ≤0.1x 10^9/L(visit 3 to visit 10 (22 days))
  • Duration of neutropenia grade 1 and higher; 3 and higher, 4, and ANC ≤0.1x 10^9/L(visit 3 to visit 10 (22 days))
  • ANC at nadir(visit 3 to visit 10 (22 days))
  • Time to ANC nadir (from start of chemotherapy)(visit 3 to visit 10 (22 days))
  • Time to ANC recovery from grade 3 neutropenia, i. e. time from onset to time of reaching neutropenia grade ≤2 (ANC ≥ 1.5x10^9/L)(visit 3 to visit 10 (22 days))
  • Time to ANC recovery from grade 4 neutropenia, i. e. time from onset to time of reaching neutropenia grade ≤2 (ANC ≥ 1.5x10^9/L)(visit 3 to visit 10 (22 days))
  • Time to ANC recovery from profound neutropenia (ANC ≥ 0.1x10^9/L), i. e. time from onset to time of reaching neutropenia grade ≤2 (ANC ≥1.5x10^9/L)(visit 3 to visit 10 (22 days))
  • Proportion of patients with rescue therapy(visit 3 to visit 10 (22 days))
  • Proportion of patients developing febrile neutropenia (body temperature ≥38.3°C by single tympanic or oral measurement) and ANC ≤0.5x 10^9/L (Grade 4)(visit 3 to visit 10 (22 days))
  • Proportion of patients with CTX dose reduction and/or delay of CTX cycle 2(visit 10 to visit 11)
  • Treatment success rate: a) Neutropenia grade ≤2, b) No need for G-CSF rescue therapy, c) No early withdrawal (drop-out).(visit 3 to visit 10 (22 days))
  • Threshold AOC of ANC (AOC4): Area below the threshold line (ANC 0.5x10^9/L classified as grade 4 neutropenia) and above the individual ANC trajectory(visit 3 to visit 10 (22 days))
  • Change of Threshold Area over the Curve of lymphocytes(visit 3 to visit 10 (22 days))
  • Change of Threshold Area over the Curve of leukocytes(visit 3 to visit 10 (22 days))

Study Sites (23)

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