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NCT03852407RecruitingPhase 2

Allogeneic Hematopoietic Cell Transplantation From HLA-matched Donor After Flu-Mel-PTCy Versus Flu-Mel-ATG Reduced-intensity Conditioning

Allogeneic Hematopoietic Cell Transplantation From HLA-matched Donor After Flu-Mel-PTCy Versus Flu-Mel-ATG Reduced-intensity Conditioning: a Phase II Randomized Study From the Belgian Hematology Society (BHS)

Source: ClinicalTrials.gov · Last updated 12 Oct 2022 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The present project aims at comparing two conditioning regimens (FM-PTCy vs FM-ATG). The hypothesis is that one or the two regimens will lead to a 2-year cGRFS rate improvement from 30% (the cGRFS rate with FM without ATG/PTCy) to 45% (Pick-a-winner phase 2 randomized study).

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
114 (estimated)
First submitted
21 Jan 2019
Start date
4 Feb 2019
Primary completion date
1 Nov 2033
Lead sponsor
University of Liege
NCT number
NCT03852407
EU CT number
2024-518568-11-00
EudraCT number
2017-000824-91

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 114
  • From 4 Feb 2019 to the primary completion date, 1 Nov 2033
  • 9 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Any condition not fulfilling inclusion criteria;
  • Life expectancy severely limited by disease other than malignancy;
  • Central Nervous System involvement with disease refractory to intrathecal chemotherapy.
  • Uncontrolled infection;
  • Any condition precluding the use of melphalan or Thymoglobulin;
    • Donors
  • Any condition not fulfilling inclusion criteria;

Lab values

  • Terminal organ failure, except for renal failure (dialysis acceptable)
    • Cardiac: Symptomatic coronary artery disease; ejection fraction \<40%; uncontrolled arrhythmia, uncontrolled hypertension;
    • Pulmonary: Diffusing Capacity of the Lung for Carbon Monoxide (DLCO)\< 40% and/or receiving supplementary continuous oxygen, Forced Expiratory Volume in 1 Second (FEV1)\< 40%;
    • Hepatic: Fulminant liver failure, cirrhosis of the liver with evidence of portal hypertension, alcoholic hepatitis, esophageal varices, a history of bleeding esophageal varices, hepatic encephalopathy, uncorrectable hepatic synthetic dysfunction evinced by prolongation of the prothrombin time, ascites related to portal hypertension, bacterial or fungal liver abscess, biliary obstruction, chronic viral hepatitis with total serum bilirubin \>3 mg/dL, and symptomatic biliary disease;

Age

  • Non-hematological malignancy(ies) (except non-melanoma skin cancer) active \< 3 years before Hematopoietic Cell Transplantation (HCT).

Other

  • Patients
  • Human Immunodeficiency Virus positive;
  • Karnofsky Performance Score \<70%;
  • Patient is a fertile man or woman who is unwilling to use contraceptive techniques during and for 12 months following treatment;
  • Patient is a female who is pregnant or breastfeeding;
  • Unable to undergo leukapheresis because of poor vein access or other reasons.

Who the study is looking for

  • Patients V.1.1. Diseases
  • Hematological malignancies confirmed histologically:
  • AML in morphological CR or not in morphological CR but not rapidly progressing (i.e. no need to give treatments such as hydroxyurea to maintain WBC count \< 10 000 x109/mL);
  • MDS;
  • CML in CP or AP;
  • MPD not in blast crisis,
  • MDS/MPD overlap,
  • ALL in CR;
  • Multiple myeloma;
  • CLL;
  • Non-Hodgkin's lymphoma (aggressive NHL should have chemosensitive disease);
  • Hodgkin's disease with chemosensitive disease or responding to checkpoint inhibitors.
    • \* Clinical situations
    • Theoretical indication for a standard allo-transplant, but not feasible because:
  • Age \> 50 yrs;
  • Unacceptable end organ performance;
  • The physician's decision;
  • The patient's decision
    • Underlying 'lower risk' disease, for which Reduced Intensity Conditioning is preferred (eg CLL, MCL)
    • \* Other inclusion criteria
    • Male or female; fertile patients must use a reliable contraception method;
    • Age 18-75 yrs (children of any age are not allowed in the protocol);
    • Informed consent given by patient or his/her guardian if indicated.
    • Donors
  • Male or female;
  • Any age;
  • Human Leukocyte Antigen (HLA)-identical sibling donor or 10 of 10 (HLA-A, -B, -C, -DRB1, and -DQB1) HLA allele matched unrelated donor;
  • Weight \> 15 Kg (because of leukapheresis);
  • Fulfills criteria for allogeneic Peripheral Blood Stem Cell (PBSC) donation according to standard procedures;
  • Informed consent given by donor or his/her guardian if indicated, as per donor center standard procedures.

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (9)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Institut Jules Bordet
Coordinator of this site? Confirm its status
AnderlechtBelgiumRecruiting
Ziekenhuis Aan De Stroom
Coordinator of this site? Confirm its status
AntwerpBelgiumRecruiting
Az St-Jan Brugge-Oostende A.V.
Coordinator of this site? Confirm its status
BruggeBelgiumRecruiting
Universiteit Gent
Coordinator of this site? Confirm its status
GentBelgiumRecruiting
Vrije Universiteit Brussel
Coordinator of this site? Confirm its status
JetteBelgiumRecruiting
UZ Leuven
Coordinator of this site? Confirm its status
LeuvenBelgiumRecruiting
Algemeen Ziekenhuis Delta
Coordinator of this site? Confirm its status
RoeselareBelgiumRecruiting
Cliniques Universitaires Saint-Luc
Coordinator of this site? Confirm its status
Sint-Lambrechts-WoluweBelgiumRecruiting
Centre Hospitalier Universitaire Dinant Godinne Sainte-Elisabeth-UCL-Namur
Coordinator of this site? Confirm its status
YvoirBelgiumRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.