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Gemtuzumab Ozogamicin in Induction and Glasdegib in Postremission Therapy in Patients With AML (Acute Myeloid Leukemia) (GnG)

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ClinicalTrials.gov Identifier: NCT04093505
Recruitment Status : Not yet recruiting
First Posted : September 18, 2019
Last Update Posted : September 18, 2019
Sponsor:
Information provided by (Responsible Party):
Prof. Dr. Richard F Schlenk, University Hospital Heidelberg

Brief Summary:
The study is a randomized phase III trial with a 2x2 factorial design with measurable residual disease and event-free survival as primary endpoints, respectively. Patients are upfront randomized for the two induction schedules (Gemtuzumab Ozogamicin (GO)-147 versus GO-1; ratio 1:1) and for Glasdegib or Placebo (double blinded, ratio 1:1) as adjunct to consolidation therapy and as single agent 6 months maintenance therapy. Chemotherapy backbone for induction therapy is standard 7+3 with cytarabine 200mg/m² continuously day 1 to day 7, daunorubicin 60mg/m² days 1, 2 and 3 and for consolidation therapy intermediate dose cytarabine (1g/m², bi-daily, days 1,2,3). The trial is designed to gain evidence of anti-leukemic activity of GO and Glasdegib in older patients with newly diagnosed acute myeloid leukemia.

Condition or disease Intervention/treatment Phase
Acute Myeloid Leukemia Drug: Gemtuzumab Ozogamicin 147 Drug: Gemtuzumab Ozogamicin 1 Drug: Glasdegib Drug: Placebo Oral Tablet Phase 3

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 252 participants
Allocation: Randomized
Intervention Model: Factorial Assignment
Intervention Model Description: The two research questions are addressed in a 2 by 2 factorial design. Patients are upfront randomized for the two induction schedules (GO-147 versus GO-1, ratio 1:1) and for Glasdegib or Placebo (double blinded, ratio 1:1) as adjunct to consolidation therapy and as single agent 6 months maintenance therapy.
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Randomized Phase-III Study to Compare Two Schedules of Gemtuzumab Ozogamicin as Adjunct to Intensive Induction Therapy and to Compare Intensive Postremission Therapy Double Blinded With or Without Glasdegib in Older Patients With Newly Diagnosed AML
Estimated Study Start Date : March 1, 2020
Estimated Primary Completion Date : December 1, 2023
Estimated Study Completion Date : March 1, 2024


Arm Intervention/treatment
Experimental: GO147_G

GO147: Induction therapy: Gemtuzumab Ozogamicin 3mg/m² on days 1,4 and 7

_G: Consolidation & Maintenance therapy Glasdegib 100mg on days 4 to 27

Drug: Gemtuzumab Ozogamicin 147
Induction therapy: Gemtuzumab Ozogamicin 3mg/m² on days 1,4 and 7
Other Name: GO147

Drug: Glasdegib
Consolidation & Maintenance therapy Glasdegib 100mg on days 4 to 27
Other Name: _G

Placebo Comparator: GO147_P

GO147: Induction therapy: Gemtuzumab Ozogamicin 3mg/m² on days 1,4 and 7

_P: Consolidation & Maintenance therapy Placebo 100mg on days 4 to 27

Drug: Gemtuzumab Ozogamicin 147
Induction therapy: Gemtuzumab Ozogamicin 3mg/m² on days 1,4 and 7
Other Name: GO147

Drug: Placebo Oral Tablet
Consolidation & Maintenance therapy Placebo 100mg on days 4 to 27
Other Name: _P

Experimental: GO1_G

GO1: Induction therapy: Gemtuzumab Ozogamicin 3mg/m² on day 1

_G: Consolidation & Maintenance therapy Glasdegib 100mg on days 4 to 27

Drug: Gemtuzumab Ozogamicin 1
Induction therapy: Gemtuzumab Ozogamicin 3mg/m² on day 1
Other Name: GO1

Drug: Glasdegib
Consolidation & Maintenance therapy Glasdegib 100mg on days 4 to 27
Other Name: _G

Placebo Comparator: GO1_P

GO1: Induction therapy: Gemtuzumab Ozogamicin 3mg/m² on day 1

_P: Consolidation & Maintenance therapy Placebo 100mg on days 4 to 27

Drug: Gemtuzumab Ozogamicin 1
Induction therapy: Gemtuzumab Ozogamicin 3mg/m² on day 1
Other Name: GO1

Drug: Placebo Oral Tablet
Consolidation & Maintenance therapy Placebo 100mg on days 4 to 27
Other Name: _P




Primary Outcome Measures :
  1. MRD-negativity [ Time Frame: Collected during the first MRD-analysis after the first induction therapy cycle (after 4 weeks) ]
    Minimal Residual Disease negativity (MRD-negativity) after induction therapy measured by flow cytometry.


Secondary Outcome Measures :
  1. EFS [ Time Frame: Collected after 2 years follow-up time ]
    Event-free survival



Information from the National Library of Medicine

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Ages Eligible for Study:   60 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients with newly diagnosed acute myeloid leukemia according to the 2016 WHO classification
  • Genetic and immunophenotypic assessment in one of the central laboratories
  • No prior chemotherapy for leukemia except hydroxyurea to control hyperleukocytosis (≤ 7 days)
  • Age ≥ 60 years, no upper age limit
  • ECOG performance status (ECOG PS) ≤ 2. See appendix 18.1
  • Pregnancy and childbearing potential:

    • Non-pregnant and non-nursing women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test within a sensitivity of at least 25 mIU/mL within 72 hours prior to registration ("Women of childbearing potential" is defined as a sexually active mature woman who has not undergone a hysterectomy or who has had menses at any time in the preceding 24 consecutive months).
    • Female patients of reproductive age must agree to avoid getting pregnant while on therapy.
    • WOCBP must either commit to continued abstinence from heterosexual intercourse or begin one acceptable method of birth control (IUD, tubal ligation, or partner's vasectomy) during study and 6 months after end of study/treatment. Hormonal contraception is an inadequate method of birth control.
    • Men must use a latex condom during any sexual contact with women of childbearing potential, even if they have undergone a successful vasectomy and must agree to avoid to father a child during study and 6 months after end of study/treatment
  • Signed written informed consent
  • Ability of patient to understand character and consequences of the clinical trial

Exclusion Criteria

  • AML with PML-RARA or BCR-ABL1
  • Patients with known active central nervous system leukemia (assessed clinically).
  • Prior treatment with a smoothened inhibitor (SMOi) and/or hypomethylating agent for AML. (Treatment of a preceding MDS (myelodysplastic syndrome) with HMA is not an exclusion criterion.)
  • Inadequate renal function: creatinine > 1.5 x upper normal serum level; estimated creatinine clearance ≤30 ml/min (calculated using the standard method for the institution).
  • Inadequate liver function: ALT and AST ≥ 2.5 x ULN), total bilirubin ≥ 1.5 x ULN; Alkaline phosphatase ≥ 2.5 x ULN. Known liver cirrhosis or history of veno-occlusive disease (VOD) or history of Sinusoidal Obstruction Syndrome (SOS)
  • Uncontrolled hypertension; severe obstructive or restrictive ventilation disorder
  • Any one of the following ongoing or in the previous 6 months: myocardial infarction, congenital long QT syndrome, Torsades de pointes, arrhythmias (including sustained ventricular tachyarrhythmia), right or left bundle branch block and bifascicular block, unstable angina, coronary/peripheral artery bypass graft, symptomatic congestive heart failure (CHF NYHA III/IV), cerebrovascular accident, transient ischemic attack or symptomatic pulmonary embolism; as well as bradycardia defined as <50 bpms
  • QTc interval >470 msec using the Fredericia correction (QTcF).
  • Uncontrolled infection
  • Patients known to be refractory to platelet or packed red cell transfusions as per institutional guidelines, or who are known to refuse or who are likely to refuse blood product support.
  • Patients with a "currently active" second malignancy other than non-melanoma skin cancer. Patients are not considered to have a "currently active" malignancy if they have completed therapy for more than one year and are considered by their physician to be at less than 30% risk of relapse within one year.
  • Severe neurologic or psychiatric disorder interfering with ability of giving informed consent
  • Known or suspected active alcohol or drug abuse
  • Known positivity for HIV, active HBV, HCV, or hepatitis A infection
  • Evidence or history of severe non-leukemia associated bleeding diathesis or coagulopathy
  • No consent for biobanking and for registration, storage and processing of the individual disease-characteristics and course as well as information of the family physician about study participation.
  • Pregnancy and lactation
  • History of hypersensitivity to the investigational medicinal product or to any drug with similar chemical structure or to any excipient present in the pharmaceutical form of the investigational medicinal product
  • Participation in a clinical study involving an investigational drug(s) (Phases 1-4) within 4 weeks prior to study entry.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04093505


Contacts
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Contact: Richard F Schlenk, Prof. Dr. 0049 6221 56 ext 6228 Richard.schlenk@nct-heidelberg.de

Sponsors and Collaborators
University Hospital Heidelberg

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Responsible Party: Prof. Dr. Richard F Schlenk, Head of NCT Trials Center and Clinical Trials Office Hematology/Oncology, University Hospital Heidelberg
ClinicalTrials.gov Identifier: NCT04093505     History of Changes
Other Study ID Numbers: NCT-2017-0537
First Posted: September 18, 2019    Key Record Dates
Last Update Posted: September 18, 2019
Last Verified: September 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Leukemia
Leukemia, Myeloid
Leukemia, Myeloid, Acute
Neoplasms by Histologic Type
Neoplasms
Gemtuzumab
Antineoplastic Agents, Immunological
Antineoplastic Agents